Sunday, March 28, 2010

Refrence for test of aldehyde and ketone





1.http://www.cem.msu.edu/~reusch/VirtualText/aldket1.htm
2.http://www.chemguide.co.uk/organicprops/carbonyls/background.html
3.http://www.wellesley.edu/Chemistry/chem211lab/Orgo_Lab_Manual/
4.http://www.chemistry.ccsu.edu/glagovich/teaching/316/qualanal/tests/benedict.html
5.http://www.chemistry.ccsu.edu/glagovich/teaching/316/qualanal/tests/tollens.html
6.http://www.chemistry.ccsu.edu/glagovich/teaching/316/qualanal/tests/jones.html
7.http://en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine
8.http://www.chemistry.ccsu.edu/glagovich/teaching/316/qualanal/tests/fehling.html
9.http://www.chemistry.ccsu.edu/glagovich/teaching/316/qualanal/tests/schiff.html
10.http://www.chemistry.ccsu.edu/glagovich/teaching/316/qualanal/tests/bisulfite.html
11.http://www.rsc.org/ej/AN/1998/a708351c.pdf
12.http://www.chemtradelogistics.com/MSDS/Sodium_Bisulfite-English.pdf
13.http://en.wikipedia.org/wiki/Iodoform
14.http://www.chem.ucalgary.ca/courses/351/Carey/Ch18/ch18-3-2b.html
15. http://www.jtbaker.com/msds/englishhtml/S3074.htm
16. http://cheville.okstate.edu/photonicslab/Safety/safety/MSDS/hcl_msds.htm
17. http://www.oldbridgechem.com/msdscuso4.html
1. 18. www.cliffsnotes.com

Tollens Test ,MSDS








Procedure:

Add one drop or a few crystals of unknown to the freshly prepared Tollens reagent. Gentle heating can be employed if no reaction is immediately observed.
Tollens reagent: Into a test tube which has been cleaned with 10% sodium hydroxide, place 2 mL of a 5% silver nitrate solution, and add a drop of 10% sodium hydroxide. Add 2% ammonia solution, drop by drop, with constant shaking, until the precipitate of silver oxide just dissolves.

Positive Test

Formation of silver mirror or black precipitate is a positive test.

Complications

The test tube must be clean and free of oil if a silver mirror is to be observed.
Easily oxidized compounds give a positive test. For example: aromatic amine, some phenols, -alkoxy and -dialkylaminoketones.


Safety data for silver nitrate

________________________________________
General:

Synonyms: lunar caustic, silver (I) nitrate, silver (1+) nitrate, nitric acid silver salt
Molecular formula: AgNO3
CAS No: 7761-88-8
EC No: 231-853-9
EC Index No: 047-001-00-2

Physical data

Appearance: colourless crystals or white powder
Melting point: 212 C
Boiling point: ca. 444 C (decomposes)
Specific gravity: 4.33
Vapour pressure:
Flash point: n/a
Explosion limits: n/a
Autoignition temperature:

Stability

Stable. Substances to be avoided include nonmetals, organic substances, alkali hydroxides, acetylidene, acetylene, aldehydes, nitriles, ammonia, alcohols, ammonium compounds, combustible materials, hydrazine and its derivatives, carbides, magnesium in powder form, alcohols. Light-sensitive. Strong oxidizing agent.

Toxicology

Poisonous. Causes burns. Long-term exposure can cause permanent blue-grey staining of eyes, mouth, throat and skin, (argyria) and may cause eye damage. Short contact can lead to deposition of black silver stains on the skin. Very destructive of mucous membranes. Skin and eye irritant. Experimental equivocal tumorigenic agent.

Toxicity data

(The meaning of any abbreviations which appear in this section is given here.)
ORL-MUS LD50 50 mg kg-1
UNR-MAN LDLO 29 mg kg-1
ORL-RBT LDLO 800 mg kg-1
SCU-GPG LDLO 62 mg kg-1
IVN-RBT LDLO 9 mg kg-1
Risk phrases
(The meaning of any risk phrases which appear in this section is given here.)
R22 R34 R50 R53.

Environmental information

Harmful in the environment - may cause long-term damage.
Transport information
(The meaning of any UN hazard codes which appear in this section is given here.)
UN No 1493. Hazard class 5.1. Packing group II. EMS No 5.1-06.

Personal protection

Safety glasses, gloves.
Safety phrases
(The meaning of any safety phrases which appear in this section is given here.)
S26 S45.

Benedict's Solution test, MSDS








Benedict's reagent:
(also called Benedict's solution or Benedict's test) is a chemical reagent named after an American chemist, Stanley Rossiter Benedict.[1]
Benedict's reagent is used as a test for the presence of reducing sugars. This includes all monosaccharides and the disaccharides , lactose and maltose. Even more generally, Benedict's test will detect the presence of aldehydes (except aromatic ones), and alpha-hydroxy-ketones, including those that occur in certain ketoses. Thus, although the ketose fructose is not strictly a reducing sugar, it is an alpha-hydroxy-ketone, and gives a positive test because it is converted to the aldoses glucose and mannose by the base in the reagent.[2].
One litre of Benedict's reagent can be prepared from 100 g of anhydrous sodium carbonate, 173 g of sodium citrate and 17.3 g of copper(II) sulfate pentahydrate.[3] It is often used in place of Fehling's solution.
Benedict's reagent contains blue copper(II) ions (Cu2+) which are reduced to copper(I) (Cu+). These are precipitated as red copper(I) oxide which is insoluble in water.

Procedure


To a solution or suspension of 0.2 g of unknown in 5 mL of water, add 5 mL of Benedict's solution. If no precipitate is formed, heat the mixture to boiling and cool.
Benedict's solution:
A solution of 17.3 g of sodium citrate and 10.0 g of anhydrous sodium carbonate in 80.0 mL of water is heated until the salts are dissolved. Additional water is added to bring the volume up to 85.0 mL. A solution of 1.73 g of hydrated copper sulfate in 10.0 mL of water is poured slowly with stirring into the solution of the citrate and the carbonate. Add water to make a final volume of 100 mL.

Positive Test

Precipitation of copper(I) oxide as a red, yellow, or yellowish-green solid is a positive test.

Complications

Not general for simple aldehydes and ketones.
Hydrazine derivatives give a positive test.



MSDS FOR Copper Sulfate:

Common Name Copper Sulfate
Manufacturer Old Bridge Chemicals, Inc.
P.O. Box 194
Old Bridge, New Jersey 08857
Telephone (732) 727-2225
Emergency Telephone 1(800) 275-3924
This document is prepared pursuant to the OSHA Hazard Communication Standard (29 CFR 1910.1200).
________________________________________
SECTION I. MATERIAL IDENTIFICATION

Common Name Copper Sulfate
Synonyms Blue Vitrol, Bluestone, Cupric Sulfate
Molecular Formula CuSO4 • 5H20
EPA Reg. Number 46923-4
CAS Number 7758-99-8
SIC Number 28199 C 29
________________________________________
SECTION II. PHYSICAL DATA

Physical State Blue crystals or powder
Boiling Point -5 H2O @ 150 C
Melting Point -4 H2O @ 110 C
Specific Gravity 2.284
Solubility in H2O 22.37% @ 0 C
117.95% @ 100 C
Solubility in other solvents Soluble in methanol, glycerol and slightly soluble in ethanol
Appearance Blue crystals or powder
Odor Odorless
________________________________________
SECTION III. FIRE AND EXPLOSION DATA

Flash Point Not applicable
Flammable Limits Not flammable. If heated above 400 C it can decompose to emit toxic fumes of oxide and sulfur.
Extinguishing Media Copper Sulfate does not burn nor will it support combustion. If stored with other combustible products use water, CO2 or dry chemical.
Special Fire Fighting Instructions If dry heated above 600 C, SO2 is evolved. If water is used it will solubalize the Copper Sulfate and care should be taken to keep such water out of streams or other water bodies.
Fire and Explosion Hazards None
________________________________________
SECTION IV. REACTIVITY DATA

Stability Stable
Conditions to Avoid Product is highly soluble, but does not react with water.
Incompatibility None know when product remains dry. Product readily dissolves in water. Solutions are mildly corrosive to steel. Store solutions in plastic or rubber or 304, 347 or 316 stainless steel. Iron and moisture should be avoided. Store in a dry area. With exposure to air it will oxidize and turn whitish.
Hazardous Decomposition Products None at normal production temperatures and pressures. If dry heated above 600 C toxic sulfur may evolve.
Polymerization Will not occur.
________________________________________
SECTION V. HEALTH AND HAZARD INFORMATION

Swallowing Toxic orally in accordance with FHSLA regulations. Acute oral LD50 (male rats) = 472 mg/kg.
Skin Non-toxic. Skin irritation index is zero in accordance with FHSLA regulations.
Eyes Corrosive in accordance with FHSLA regulations. Eye irritation score: 24 hours = 41.67; 48 hours = corrosive
Inhalation Inhalation of dust may cause irritation to the upper respiration tract.
Carcinogenicity None as per NTP, OSHA, and IARC.
This product contains Copper Sulfate subject to the reporting requirements of Section 13 of the Emergency Planning and Community-right-to-Know-Act of 1986 (40 CFR 372).
________________________________________
SECTION VI. FIRST AID PROCEDURES

Swallowing Give large amounts of milk or water. Induce vomiting. Call Poison Control Center or a physician.
Skin Wash thoroughly with soap and water. Remove and wash contaminated clothing before reuse.
Eyes Immediately flush eyes with plenty of water for 15 minutes. Hold eyelids apart during irrigation. Call a physician.
Inhalation Remove person to fresh air and call a physician.
Carcinogenicity None
________________________________________
SECTION VII. HANDLING PRECAUTIONS

Personal Protective Equipment Chemical safety goggles. Rubber gloves and rubber apron may be worn.
Ventilation TWA = 1 mg/l for Copper Sulfate. When TWA exceeds this limit in the workplace, provide appropriate ventilation. Wear an approved respirator for dusts or mists: MSHA/NIOSH approved number prefix TC-21C, or a NIOSH approved respirator with any R, P or HE filter.
Alternatively, provide respiratory protection equipment in accordance with Paragraph 1910.134 of Title 29 of the Code of Federal Regulations.
________________________________________
SECTION VIII. ENVIRONMENTAL AND DISPOSAL INFORMATION

Aquatic Toxicity LC50, 24 hours, Daphnia magna equals 0.182 mg/l. Rainbow Trout equals 0.17 mg/l. Blue Gill equals 1.5 mg/l. All values are expressed as Copper Sulfate Pentahydrate. Test water was soft.
Spills and Leaks Comply with Federal, State and local regulations on reporting spills. Do not wash away crystals or powder. Recover dry if possible. If product is in a confined solution, react with soda ash to form an insoluble Copper Carbonate solid that can be scooped up.
Waste Disposal Do not reuse container. Comply with Federal, State and local regulations. Sweep up crystals, powder or insoluble Copper Carbonate and dispose of in an approved landfill.
Environmental Effects May be dangerous if it enters the public water systems. Follow local regulation. Toxic to fish and plants. Fish toxicity critical concentration is 235 mg/l and plant toxicity is 25 mg/l.
________________________________________
SECTION IX. SPECIAL PRECAUTIONS

Storage Store in a dry place.
Other Precautions None other than those stated in the MSDS or on the package.
________________________________________
SECTION XI. REGULATORY INFORMATION

NOTICE: The information herein is presented in good faith and believed to be accurate. However, no warranty, expressed or implied, is given. Regulatory requirements are subject to change and may differ from one location to another. It is the buyer’s responsibility to ensure that its activities comply with Federal, State and local laws.
U.S. REGULATIONS: SARA 313 Information. This product contain the following substance subject to the reporting requirements of Section 313 of Title III of the Superfund Amendments and Reauthorization Act of 1986 and 40 CFR Part 372: COPPER COMPOUND 63.3%.
SARA HAZARD CATEGORY: This product has been reviewed according to the EPA "Hazard Categories" promulgated under Sections 311 and 312 of the Superfund Amendments and Reauthorization Act of 1986 (SARA Title III) and is considered, under applicable definitions, to meet the following category: AN IMMEDIATE HEALTH HAZARD.

Fuchsin-Aldehyde Reagent , MSDS








Fuchsin-Aldehyde Reagent (Schiff's Reagent)
________________________________________

Procedure

Place 2 mL of Schiff's reagent in a test tube and add 2 drops or a few crystals of the unknown. Shake the tube gently, and observe the color that is developed in 3-4 min. Aldehydes react with Schiff's reagent to form a complex which has a wine-purple color.
Schiff's Reagent: Dissolve 0.05 g of pure fuchsin (4-rosaline hydrochloride) in 50 mL of distilled water. Add 2 mL of saturated sodium bisulfite solution. After allowing the solution to sit for 1 hr, add 1 mL of concentrated hydrochloric acid. Allow to stand overnight. This reagent is practically colorless and very sensitive.

Positive Test

Formation of a violet-purple solution is a positive test.

Complications

In this test the reagent should not be heated, and the solution tested should not be alkaline. When the test is used on an unknown, a simultaneous test on a known aldehyde and a known ketone should be performed for comparison.





MSDS FOR HYDROCHLORIC ACID (10%-33%)MSDS Number: H3886 ---


Effective Date: 11/17/99

1. Product Identification

Synonyms: This MSDS applies to the concentrated standard used to make laboratory solutions and any solution that contains more than 10% but less than 33% Hydrochloric acid. For diluted product, see MSDS for Hydrochloric Acid (less than 10%). For saturated solution
CAS No.: 7647-01-0
Molecular Weight: 36.46
Chemical Formula: HCl in H2O
Product Codes:
J.T. Baker: 0323, 0327, 4654, 4657, 4658, 5618, 5619
Mallinckrodt: 2608, 2609, 2625, H151, H168, V024, V035, V328

2. Composition/Information on Ingredients


Ingredient CAS No Percent Hazardous
--------------------------------------- ------------ ------- ---------

Hydrogen Chloride 7647-01-0 10 - 33% Yes
Water 7732-18-5 67 - 90% No


3. Hazards Identification
Emergency Overview--------------------------

POISON! DANGER! CORROSIVE. LIQUID AND MIST CAUSE SEVERE BURNS TO ALL BODY TISSUE. MAY BE FATAL IF SWALLOWED OR INHALED.

J.T. Baker SAF-T-DATA(tm) Ratings (Provided here for your convenience)
-----------------------------------------------------------------------------------------------------------
Health Rating: 3 - Severe (Poison)
Flammability Rating: 0 - None
Reactivity Rating: 2 - Moderate
Contact Rating: 3 - Severe (Corrosive)
Lab Protective Equip: GOGGLES & SHIELD; LAB COAT & APRON; VENT HOOD; PROPER GLOVES
Storage Color Code: White (Corrosive)
-----------------------------------------------------------------------------------------------------------

Potential Health Effects
----------------------------------

Inhalation:
Corrosive! Inhalation of vapors can cause coughing, choking, inflammation of the nose, throat, and upper respiratory tract, and in severe cases, pulmonary edema, circulatory failure, and death.
Ingestion:
Corrosive! Swallowing hydrochloric acid can cause immediate pain and burns of the mouth, throat, esophagus and gastrointestinal tract. May cause nausea, vomiting, and diarrhea, and in severe cases, death.
Skin Contact:
Corrosive! Can cause redness, pain, and severe skin burns. Concentrated solutions cause deep ulcers and discolor skin.
Eye Contact:
Corrosive! Vapors are irritating and may cause damage to the eyes. Contact may cause severe burns and permanent eye damage.
Chronic Exposure:
Long-term exposure to concentrated vapors may cause erosion of teeth. Long term exposures seldom occur due to the corrosive properties of the acid.
Aggravation of Pre-existing Conditions:
Persons with pre-existing skin disorders or eye disease may be more susceptible to the effects of this substance.


4. First Aid Measures


Inhalation:
Remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical attention immediately.
Ingestion:
DO NOT INDUCE VOMITING! Give large quantities of water or milk if available. Never give anything by mouth to an unconscious person. Get medical attention immediately.
Skin Contact:
In case of contact, immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse. Thoroughly clean shoes before reuse. Get medical attention immediately.
Eye Contact:
Immediately flush eyes with plenty of water for at least 15 minutes, lifting lower and upper eyelids occasionally. Get medical attention immediately.


5. Fire Fighting Measures


Fire:
Not considered to be a fire hazard. May react with metals or heat to release flammable hydrogen gas.
Explosion:
Not considered to be an explosion hazard.
Fire Extinguishing Media:
Water or water spray. Neutralize with soda ash or slaked lime.
Special Information:
In the event of a fire, wear full protective clothing and NIOSH-approved self-contained breathing apparatus with full facepiece operated in the pressure demand or other positive pressure mode. Structural firefighter's protective clothing is ineffective for fires involving hydrochloric acid. Stay away from ends of tanks. Cool tanks with water spray until well after fire is out.

6. Accidental Release Measures

Ventilate area of leak or spill. Wear appropriate personal protective equipment as specified in Section 8. Isolate hazard area. Keep unnecessary and unprotected personnel from entering. Contain and recover liquid when possible. Neutralize with alkaline material (soda ash, lime), then absorb with an inert material (e. g., vermiculite, dry sand, earth), and place in a chemical waste container. Do not use combustible materials, such as saw dust. Do not flush to sewer! US Regulations (CERCLA) require reporting spills and releases to soil, water and air in excess of reportable quantities. The toll free number for the US Coast Guard National Response Center is (800) 424-8802.

J. T. Baker NEUTRASORB(R) or TEAM(R) 'Low Na+' acid neutralizers are recommended for spills of this product.

7. Handling and Storage

Store in a cool, dry, ventilated storage area with acid resistant floors and good drainage. Protect from physical damage. Keep out of direct sunlight and away from heat, water, and incompatible materials. Do not wash out container and use it for other purposes. When diluting, the acid should always be added slowly to water and in small amounts. Never use hot water and never add water to the acid. Water added to acid can cause uncontrolled boiling and splashing. When opening metal containers, use non-sparking tools because of the possibility of hydrogen gas being present. Containers of this material may be hazardous when empty since they retain product residues (vapors, liquid); observe all warnings and precautions listed for the product.

8. Exposure Controls/Personal Protection

Airborne Exposure Limits:
For Hydrochloric acid:
- OSHA Permissible Exposure Limit (PEL):
5 ppm (Ceiling)
- ACGIH Threshold Limit Value (TLV):
5 ppm (STEL/Ceiling)


Ventilation System:

A system of local and/or general exhaust is recommended to keep employee exposures below the Airborne Exposure Limits. Local exhaust ventilation is generally preferred because it can control the emissions of the contaminant at its source, preventing dispersion of it into the general work area. Please refer to the ACGIH document, Industrial Ventilation, A Manual of Recommended Practices, most recent edition, for details.

Personal Respirators (NIOSH Approved):

If the exposure limit is exceeded, a full facepiece respirator with an acid gas cartridge may be worn up to 50 times the exposure limit or the maximum use concentration specified by the appropriate regulatory agency or respirator supplier, whichever is lowest. For emergencies or instances where the exposure levels are not known, use a full-facepiece positive-pressure, air-supplied respirator. WARNING: Air purifying respirators do not protect workers in oxygen-deficient atmospheres.

Skin Protection:

Rubber or neoprene gloves and additional protection including impervious boots, apron, or coveralls, as needed in areas of unusual exposure to prevent skin contact.

Eye Protection:

Use chemical safety goggles and/or a full face shield where splashing is possible. Maintain eye wash fountain and quick-drench facilities in work area.

9. Physical and Chemical Properties

Appearance:
Clear, colorless liquid.
Odor:
Pungent odor.
Solubility:
Infinitely soluble.
Density:
1.05 @ 15C (59F)
pH:
For HCL solutions: 0.1 (1.0 N), 1.1 (0.1 N), 2.02 (0.01 N)
% Volatiles by volume @ 21C (70F):
100
Boiling Point:
101 - 103C (214 - 217F)
Melting Point:
No information found.
Vapor Density (Air=1):
No information found.
Vapor Pressure (mm Hg):
No information found.
Evaporation Rate (BuAc=1):
No information found.

10. Stability and Reactivity

Stability:
Stable under ordinary conditions of use and storage.
Hazardous Decomposition Products:
When heated to decomposition, emits toxic hydrogen chloride fumes and will react with water or steam to produce heat and toxic and corrosive fumes. Thermal oxidative decomposition produces toxic chlorine fumes and explosive hydrogen gas.
Hazardous Polymerization:
Will not occur.
Incompatibilities:
A strong mineral acid, concentrated hydrochloric acid is highly reactive with strong bases, metals, metal oxides, hydroxides, amines, carbonates and other alkaline materials. Incompatible with materials such as cyanides, sulfides, sulfites, and formaldehyde.
Conditions to Avoid:
Heat, direct sunlight.

11. Toxicological Information

Hydrochloric acid: Inhalation rat LC50: 3124 ppm/1H; Oral rabbit LD50: 900 mg/kg. Investigated as a tumorigen, mutagen, reproductive effector.
--------\Cancer Lists\------------------------------------------------------
---NTP Carcinogen---
Ingredient Known Anticipated IARC Category
------------------------------------ ----- ----------- -------------
Hydrogen Chloride (7647-01-0) No No 3
Water (7732-18-5) No No None

12. Ecological Information

Environmental Fate:
When released into the soil, this material is not expected to biodegrade. When released into the soil, this material may leach into groundwater.
Environmental Toxicity:
This material is expected to be toxic to aquatic life.

13. Disposal Considerations

Whatever cannot be saved for recovery or recycling should be handled as hazardous waste and sent to a RCRA approved waste facility. Processing, use or contamination of this product may change the waste management options. State and local disposal regulations may differ from federal disposal regulations. Dispose of container and unused contents in accordance with federal, state and local requirements.

14. Transport Information

Domestic (Land, D.O.T.)
-----------------------
Proper Shipping Name: HYDROCHLORIC ACID
Hazard Class: 8
UN/NA: UN1789
Packing Group: II
Information reported for product/size: 200L

International (Water, I.M.O.)
-----------------------------
Proper Shipping Name: HYDROCHLORIC ACID
Hazard Class: 8
UN/NA: UN1789
Packing Group: II
Information reported for product/size: 200L

15. Regulatory Information

--------\Chemical Inventory Status - Part 1\---------------------------------
Ingredient TSCA EC Japan Australia
----------------------------------------------- ---- --- ----- ---------
Hydrogen Chloride (7647-01-0) Yes Yes Yes Yes
Water (7732-18-5) Yes Yes Yes Yes

--------\Chemical Inventory Status - Part 2\---------------------------------
--Canada--
Ingredient Korea DSL NDSL Phil.
----------------------------------------------- ----- --- ---- -----
Hydrogen Chloride (7647-01-0) Yes Yes No Yes
Water (7732-18-5) Yes Yes No Yes

--------\Federal, State & International Regulations - Part 1\----------------
-SARA 302- ------SARA 313------
Ingredient RQ TPQ List Chemical Catg.
----------------------------------------- --- ----- ---- --------------
Hydrogen Chloride (7647-01-0) 5000 500* Yes No
Water (7732-18-5) No No No No

--------\Federal, State & International Regulations - Part 2\----------------
-RCRA- -TSCA-
Ingredient CERCLA 261.33 8(d)
----------------------------------------- ------ ------ ------
Hydrogen Chloride (7647-01-0) 5000 No No
Water (7732-18-5) No No No


Chemical Weapons Convention: No TSCA 12(b): No CDTA: Yes
SARA 311/312: Acute: Yes Chronic: Yes Fire: No Pressure: No
Reactivity: No (Mixture / Liquid)


Australian Hazchem Code: 2R
Poison Schedule: No information found.
WHMIS:
This MSDS has been prepared according to the hazard criteria of the Controlled Products Regulations (CPR) and the MSDS contains all of the information required by the CPR.

16. Other Information

NFPA Ratings: Health: 3 Flammability: 0 Reactivity: 0
Label Hazard Warning:
POISON! DANGER! CORROSIVE. LIQUID AND MIST CAUSE SEVERE BURNS TO ALL BODY TISSUE. MAY BE FATAL IF SWALLOWED OR INHALED.
Label Precautions:
Do not get in eyes, on skin, or on clothing.
Avoid breathing vapor or mist.
Keep container closed.
Use with adequate ventilation.
Wash thoroughly after handling.
Label First Aid:
If swallowed, DO NOT INDUCE VOMITING. Give large quantities of water. Never give anything by mouth to an unconscious person. If inhaled, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. In case of contact, immediately flush eyes or skin with plenty of water for at least 15 minutes. Remove contaminated clothing and shoes. Wash clothing before reuse. In all cases call a physician.
Product Use:
Laboratory Reagent.
Revision Information:
No changes.
Disclaimer:
************************************************************************************************
Mallinckrodt Baker, Inc. provides the information contained herein in good faith but makes no representation as to its comprehensiveness or accuracy. This document is intended only as a guide to the appropriate precautionary handling of the material by a properly trained person using this product. Individuals receiving the information must exercise their independent judgment in determining its appropriateness for a particular purpose. MALLINCKRODT BAKER, INC. MAKES NO REPRESENTATIONS OR WARRANTIES, EITHER EXPRESS OR IMPLIED, INCLUDING WITHOUT LIMITATION ANY WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE WITH RESPECT TO THE INFORMATION SET FORTH HEREIN OR THE PRODUCT TO WHICH THE INFORMATION REFERS. ACCORDINGLY, MALLINCKRODT BAKER, INC. WILL NOT BE RESPONSIBLE FOR DAMAGES RESULTING FROM USE OF OR RELIANCE UPON THIS INFORMATION.
************************************************************************************************
Prepared by: Strategic Services Division

Sodium Bisulfite test, MSDS







Procedure:

Place 1 mL of sodium bisulfite reagent in a test tube and add 0.3 mL or 300 mg of unknown. Stopper the test tube and shake vigorously.
Sodium bisulfite reagent: Add 1 mL of ethanol to 4 mL of a 40% aqueous solution of sodium bisulfite. Decant or filter the solution prior to use.

Positive Test

Formation of a precipitate is a positive test.

Complications

Aryl methyl ketones form the precipitate slowly or not at all.
Addition complex stable only in neutral solution.


MSDS FOR SODIUM BISULFITE

________________________________________
1. Product Identification
Synonyms: Sodium acid sulfite; Sulfurous acid, monosodium salt; Sodium hydrogen sulfite, solid
CAS No.: 7631-90-5
Molecular Weight: 104.06
Chemical Formula: A mixture of NaHSO3 (sodium bisulfite) and Na2S2O5 (sodium metabisulfite)
Product Codes: 3556, 3557
________________________________________
2. Composition/Information on Ingredients

Ingredient CAS No Percent Hazardous
--------------------------------------- ------------ ------------ ---------

Sodium Bisulfite 7631-90-5 58 - 99% Yes
Sodium Metabisulfite 7681-57-4 1 - 42% Yes

________________________________________
3. Hazards Identification
Emergency Overview
--------------------------
WARNING
!
HARMFUL IF SWALLOWED OR INHALED. MAY CAUSE ALLERGIC RESPIRATORY REACTION. CAUSES IRRITATION TO SKIN, EYES AND RESPIRATORY TRACT. REACTS WITH ACIDS AND WATER RELEASING TOXIC SULFUR DIOXIDE GAS.

SAF-T-DATA(tm) Ratings (Provided here for your convenience)
-----------------------------------------------------------------------------------------------------------
Health Rating: 2 - Moderate (Life)

Flammability Rating: 0 - None
Reactivity Rating: 2 - Moderate
Contact Rating: 3 - Severe
Lab Protective Equip: GOGGLES & SHIELD; LAB COAT & APRON; VENT HOOD; PROPER GLOVES
Storage Color Code: Green (General Storage)
-----------------------------------------------------------------------------------------------------------

Potential Health Effects
----------------------------------

Inhalation:

Causes irritation to the respiratory tract. Symptoms may include coughing, shortness of breath. May cause allergic reaction in sensitive individuals.

Ingestion:

May cause gastric irritation by the liberation of sulfurous acid. An asthmatic reaction may occur after ingestion. Large doses may result in nausea, vomiting, diarrhea, abdominal pains, circulatory disturbance, and central nervous system depression. Estimated fatal dose is 10 gm.
Skin Contact:

Causes irritation to skin. Symptoms include redness, itching, and pain.

Eye Contact:
Causes irritation, redness, and pain. Contact may cause irreversible eye damage. Symptoms may include stinging, tearing, redness, swelling, corneal damage and blindness.

Chronic Exposure:
No information found.
Aggravation of Pre-existing Conditions:
Some individuals are said to be dangerously sensitive to minute amounts of sulfites in foods. Symptoms may include broncho constriction, shock, gastrointestinal disturbances, angio edema, flushing, and tingling sensations. Once allergy develops, future exposures can cause asthma attacks with shortness of breath, wheezing, and cough.
________________________________________
4. First Aid Measures

Inhalation:
Remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical attention.
Ingestion:
Induce vomiting immediately as directed by medical personnel. Never give anything by mouth to an unconscious person. Get medical attention.
Skin Contact:
Wipe off excess material from skin then immediately flush skin with plenty of water for at least 15 minutes. Remove contaminated clothing and shoes. Get medical attention. Wash clothing before reuse. Thoroughly clean shoes before reuse.
Eye Contact:
Immediately flush eyes with plenty of water for at least 15 minutes, lifting lower and upper eyelids occasionally. Get medical attention immediately.
________________________________________
5. Fire Fighting Measures
Fire:
Not considered to be a fire hazard.
Explosion:
Not considered to be an explosion hazard.
Fire Extinguishing Media:
Use any means suitable for extinguishing surrounding fire. Do not allow water runoff to enter sewers or waterways.
Special Information:
In the event of a fire, wear full protective clothing and NIOSH-approved self-contained breathing apparatus with full facepiece operated in the pressure demand or other positive pressure mode.
________________________________________
6. Accidental Release Measures

Ventilate area of leak or spill. Wear appropriate personal protective equipment as specified in Section 8. Spills: Pick up and place in a suitable container for reclamation or disposal, using a method that does not generate dust. Cautiously spray residue with plenty of water, providing ventilation to clear sulfur dioxide fumes generated from water contact. US Regulations (CERCLA) require reporting spills and releases to soil, water and air in excess of reportable quantities. The toll free number for the US Coast Guard National Response Center is (800) 424-8802.

________________________________________
7. Handling and Storage

Keep in a tightly closed container. Protect from physical damage. Store in a cool, dry, ventilated area away from sources of heat, moisture and incompatibilities. Releases toxic sulfur dioxide gas when in contact with water, ice. Containers of this material may be hazardous when empty since they retain product residues (dust, solids); observe all warnings and precautions listed for the product.
________________________________________
8. Exposure Controls/Personal Protection
Airborne Exposure Limits:
-ACGIH Threshold Limit Value (TLV):
5mg/m3 (TWA) for sodium bisulfite & for sodium metabisulfite, A4 Not classifiable as a human carcinogen.
Ventilation System:
A system of local and/or general exhaust is recommended to keep employee exposures below the Airborne Exposure Limits. Local exhaust ventilation is generally preferred because it can control the emissions of the contaminant at its source, preventing dispersion of it into the general work area. Please refer to the ACGIH document, Industrial Ventilation, A Manual of Recommended Practices, most recent edition, for details.

Personal Respirators (NIOSH Approved):
If the exposure limit is exceeded and engineering controls are not feasible, a half-face respirator with an acid gas cartridge may be worn for up to ten times the exposure limit or the maximum use concentration specified by the appropriate regulatory agency or respirator supplier, whichever is lowest. A full-face piece respirator with an acid gas cartridge may be worn up to 50 times the exposure limit, or the maximum use concentration specified by the appropriate regulatory agency, or respirator supplier, whichever is lowest. For emergencies or instances where the exposure levels are not known, use a full-facepiece positive-pressure, air-supplied respirator. WARNING: Air-purifying respirators do not protect workers in oxygen-deficient atmospheres.

Skin Protection:
Wear impervious protective clothing, including boots, gloves, lab coat, apron or coveralls, as appropriate, to prevent skin contact.

Eye Protection:
Use chemical safety goggles. Maintain eye wash fountain and quick-drench facilities in work area.
________________________________________
9. Physical and Chemical Properties
Appearance:
Coarse white granules.
Odor:
Slight odor of sulfur dioxide.
Solubility:
Very soluble in water, insoluble in alcohol.
Specific Gravity:
1.48
pH:
No information found.
% Volatiles by volume @ 21C (70F):
No information found.
Boiling Point:
Not applicable.
Melting Point:
150C (302F)
Vapor Density (Air=1):
No information found.
Vapor Pressure (mm Hg):
No information found.
Evaporation Rate (BuAc=1):
No information found.
________________________________________
10. Stability and Reactivity
Stability:
Strength diminishes somewhat with age. Gradually decomposes in air to sulfate, generating sulfurous acid gas. Contact with moisture (water, wet ice, etc.), will release toxic sulfur dioxide gas.
Hazardous Decomposition Products:
Burning may produce sulfur oxides.
Hazardous Polymerization:
Will not occur.
Incompatibilities:
Water, acids, alkalis, sodium nitrite, oxidizers, aluminum powder.
Conditions to Avoid:
Moisture, heat, flames, ignition sources and incompatibles.
________________________________________
11. Toxicological Information

Sodium Metabisulfite [7681-57-4]: No LD50/LC50 information found relating to normal routes of occupational exposure. Investigated as a tumorigen, mutagen and reproductive effector. Sodium Bisulfite [7631-90-5]: Oral rat LD50: 2000 mg/kg. Investigated as a tumorigen and mutagen.
--------\Cancer Lists\------------------------------------------------------
---NTP Carcinogen---
Ingredient Known Anticipated IARC Category
------------------------------------ ----- ----------- -------------
Sodium Bisulfite (7631-90-5) No No 3
Sodium Metabisulfite (7681-57-4) No No 3
________________________________________
12. Ecological Information
Environmental Fate:
No information found.
Environmental Toxicity:
No information found.
________________________________________
13. Disposal Considerations


Whatever cannot be saved for recovery or recycling should be managed in an appropriate and approved waste disposal facility. Processing, use or contamination of this product may change the waste management options. State and local disposal regulations may differ from federal disposal regulations. Dispose of container and unused contents in accordance with federal, state and local requirements.
________________________________________
14. Transport Information
Not regulated.
________________________________________
15. Regulatory Information
--------\Chemical Inventory Status - Part 1\---------------------------------
Ingredient TSCA EC Japan Australia
----------------------------------------------- ---- --- ----- ---------
Sodium Bisulfite (7631-90-5) Yes Yes Yes Yes
Sodium Metabisulfite (7681-57-4) Yes Yes Yes Yes

--------\Chemical Inventory Status - Part 2\---------------------------------
--Canada--
Ingredient Korea DSL NDSL Phil.
----------------------------------------------- ----- --- ---- -----
Sodium Bisulfite (7631-90-5) Yes Yes No Yes
Sodium Metabisulfite (7681-57-4) Yes Yes No Yes

--------\Federal, State & International Regulations - Part 1\----------------
-SARA 302- ------SARA 313------
Ingredient RQ TPQ List Chemical Catg.
----------------------------------------- --- ----- ---- --------------
Sodium Bisulfite (7631-90-5) No No No No
Sodium Metabisulfite (7681-57-4) No No No No

--------\Federal, State & International Regulations - Part 2\----------------
-RCRA- -TSCA-
Ingredient CERCLA 261.33 8(d)
----------------------------------------- ------ ------ ------
Sodium Bisulfite (7631-90-5) 5000 No Yes
Sodium Metabisulfite (7681-57-4) No No Yes


Chemical Weapons Convention: No TSCA 12(b): No CDTA: No
SARA 311/312: Acute: Yes Chronic: No Fire: No Pressure: No
Reactivity: No (Mixture / Solid)


Australian Hazchem Code: None allocated.
Poison Schedule: None allocated.
WHMIS:
This MSDS has been prepared according to the hazard criteria of the Controlled Products Regulations (CPR) and the MSDS contains all of the information required by the CPR.
________________________________________
16. Other Information
NFPA Ratings: Health: 1 Flammability: 0 Reactivity: 1
Label Hazard Warning:
WARNING! HARMFUL IF SWALLOWED OR INHALED. MAY CAUSE ALLERGIC RESPIRATORY REACTION. CAUSES IRRITATION TO SKIN, EYES AND RESPIRATORY TRACT. REACTS WITH ACIDS AND WATER RELEASING TOXIC SULFUR DIOXIDE GAS.
Label Precautions:
Avoid breathing dust.
Avoid contact with eyes, skin and clothing.
Keep container closed.
Use only with adequate ventilation.
Wash thoroughly after handling.
For Reagent and Technical Grades: Not For Food Use.For TAC Grades: Do not use in meats or in foods recognized as a source of Vitamin B-1, nor in fruits or vegetables to be served or sold raw to consumers or to be presented to consumers as fresh.

If swallowed, induce vomiting immediately as directed by medical personnel. Never give anything by mouth to an unconscious person. If inhaled, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. In case of contact, wipe off excess material from skin then immediately flush eyes or skin with plenty of water for at least 15 minutes. Remove contaminated clothing and shoes. Wash clothing before reuse. In all cases, get medical attention.
Product Use:
Laboratory Reagent.
Revision Information:
No Changes.
Disclaimer:
************************************************************************************************
Mallinckrodt Baker, Inc. provides the information contained herein in good faith but makes no representation as to its comprehensiveness or accuracy. This document is intended only as a guide to the appropriate precautionary handling of the material by a properly trained person using this product. Individuals receiving the information must exercise their independent judgment in determining its appropriateness for a particular purpose. MALLINCKRODT BAKER, INC. MAKES NO REPRESENTATIONS OR WARRANTIES, EITHER EXPRESS OR IMPLIED, INCLUDING WITHOUT LIMITATION ANY WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE WITH RESPECT TO THE INFORMATION SET FORTH HEREIN OR THE PRODUCT TO WHICH THE INFORMATION REFERS. ACCORDINGLY, MALLINCKRODT BAKER, INC. WILL NOT BE RESPONSIBLE FOR DAMAGES RESULTING FROM USE OF OR RELIANCE UPON THIS INFORMATION.
************************************************************************************************
Prepared by: Environmental Health & Safety
Phone Number: (314) 654-1600 (U.S.A.)

2,4-Dinitrophenylhydrazine test, MSDS







2,4-Dinitrophenylhydrazine
_______________________________________________________________________________
2,4-Dinitrophenylhydrazine can be used to qualitatively detect the carbonyl functionality of a ketone or aldehyde functional group. A positive test is signaled by a yellow or red precipitate (known as a dinitrophenylhydrazone):
RR'C=O + C6H3(NO2)2NHNH2 → C6H3(NO2)2NHNCRR' + H2O
This reaction can be described as a condensation reaction, with two molecules joining together with loss of water. It is also considered an addition-elimination

reaction:
nucleophilic addition of the -NH2 group to the C=O carbonyl group, followed by the removal of a H2O molecule.
The mechanism for the reaction between 2,4-dinitrophenylhydrazine and an aldehyde or ketone is shown:
Crystals of different hydrazones have characteristic melting and boiling points, allowing the identity of a substance to be determined in a method known as derivatization. In particular, the use of 2,4-dinitrophenylhydrazine was developed by Brady and Elsmie.[3] Modern spectroscopic and spectrometric techniques have since superseded these techniques.

2,4-DNP reacting with 2-heptanone

Dinitrophenylhydrazine does not react with other carbonyl-containing functional groups such as carboxylic acids, amides, and esters. For carboxylic acids, amides and esters, there is resonance associated stability as a lone-pair of electrons interacts with the p-orbital of the carbonyl carbon resulting in increased delocalisation in the molecule. This stability would be lost by addition of a reagent to the carbonyl group. Hence, these compounds are more resistant to addition reactions.


Procedure


Add a solution of 1 or 2 drops or 30 mg of unknown in 2 mL of 95% ethanol to 3 mL of 2,4-dinitrophenylhydrazine reagent. Shake vigorously, and, if no precipitate forms immediately, allow the solution to stand for 15 minutes.
2,4-Dinitrophenylhydrazine reagent: Dissolve 3 g of 2,4-Dinitrophenylhydrazine in 15 mL of conc. sulfuric acid. This solution is then added with stirring to 20 mL of water and 70 mL of 95% ethanol. This solution is mixed thoroughly and filtered.

Positive Test

Formation of a precipitate is a positive test.

Complications
Some ketones give oils which will not solidify.
Some allylic alcohols are oxidized by the reagent to aldehydes and give a positive test.
Some alcohols, if not purified, may contain aldehyde or ketone impurities.


Safety data for 2,4-dinitrophenylhydrazineGeneral
Synonyms: 2,4-DNPH, (2,4-dinitrophenyl)hydrazine, 1-hydrazino-2,4-dinitrobenzene, DNPH, DNP-hydrazine
Use:
Molecular formula: C6H6N4O4
CAS No: 119-26-6
EINECS No: 204-309-3
Physical data
Appearance: red powder
Melting point: 200 - 202 C
Boiling point:
Vapour density:
Vapour pressure:
Density (g cm-3):
Flash point:
Explosion limits:
Autoignition temperature:
Water solubility:

Stability
Stable when wet, but explosive when dry. May be shock sensitive when dry. Highly flammable. Incompatible with strong oxidizing agents.

Toxicology
Harmful if swallowed.

Toxicity data

(The meaning of any toxicological abbreviations which appear in this section is given here.)
ORL-RAT LD50 500 mg kg-1
IPR-RAT LD50 450 mg kg-1
Risk phrases
(The meaning of any risk phrases which appear in this section is given here.)
R1 R11 R22.

Transport information

(The meaning of any UN hazard codes which appear in this section is given here.)
UN No 1325. Hazard class 4.1. Packing group II.
Personal protection
Safety glasses, adequate ventilation. Do not dry or heat this material.
Safety phrases
(The meaning of any safety phrases which appear in this section is given here.)

Ketone









Ketone:

In organic chemistry, a ketone (pronounced /ˈkiːtoʊn/ KEE-toan) is a type of compound that features one carbonyl group (C=O) bonded to two other carbon atoms, i.e., R3CCO-CR3 where R can be a variety of atoms and groups of atoms.[1] With carbonyl carbon bonded to two carbon atoms, ketones are distinct from many other functional groups, such as carboxylic acids, aldehydes, esters, amides, and other oxygen-containing compounds. The double-bond of the carbonyl group distinguishes ketones from alcohols and ethers.
A carbon atom adjacent to a carbonyl group is called an α-carbon. Hydrogen atoms attached to these α-carbon centers are called α-hydrogens. Ketones with α-hydrogen centers participate in a so-called keto-enol tautomerism. The reaction with a strong base gives the corresponding enolate, often by deprotonation of the enol.

Nomenclature:

According to the rules of IUPAC nomenclature, ketones are named by changing the suffix -e of the parent alkane to -one. For the most important ketones, however, traditional nonsystematic names are used virtually exclusively, e.g. acetone and benzophenone. These nonsystematic names are considered retained IUPAC names.[2], although some introductory chemistry textbooks use names such as 2-propanone instead of acetone, the simplest ketone (CH3-CO-CH3). The position of the carbonyl group is usually denoted by a number.
Oxo is the IUPAC nomenclature for a ketone functional group. Other prefixes, however, are also used. For some common chemicals (mainly in biochemistry), "keto" or "oxo" is the term that describes the ketone functional group. The term "oxo" is used widely through chemistry, for example it also refers to a single oxygen atom coordinated to a transition metal (a metal oxo).

Structure and properties:

Representative ketones, from the left: acetone, a common solvent; oxaloacetate, an intermediate in the metabolism of sugars; acetylacetone in its (mono) enol form (the enol highlighted in blue); cyclohexanone, precursor to Nylon; muscone, an animal scent; and tetracycline, an antibiotic.
The ketone carbon is often described as "sp2 hybridized," terminology that describes both their electronic and molecular structure. Ketones are trigonal planar about the ketonic carbon, with C-C-O and C-C-C bond angles of approximately 120°.
The carbonyl group is polar as a consequence of the fact that the electronegativity of the oxygen center is greater than that for carbonyl carbon. Thus, ketones are nucleophilic at oxygen and electrophilic at carbon. Because the carbonyl group interacts with water by hydrogen bonding, ketones are typically more soluble in water than the related methylene compounds. Ketones are a hydrogen-bond acceptors. Ketones are not usually hydrogen-bond donors and cannot hydrogen-bond to itself. Because of their inability to serve both as hydrogen-bond donors and acceptors, ketones tend not to "self-associate" and are more volatile than alcohols and carboxylic acids of comparable molecular weights. These factors relate to pervasiveness of ketones in perfumery and as solvents.

Classes of ketones:

Ketones are classified on the basis of their substituents. One broad classification subdivides ketones into symmetrical and unsymmetrical derivatives, depending on the equivalency of the two organic substituents attached to the carbonyl center. Acetone and benzophenone are symmetrical ketones. Acetophenone (C6H5C(O)CH3) is an unsymmetrical ketone. In the area of stereochemistry, unsymmetrical ketones are known for being prochiral.

Diketones:

Many kinds of diketones are known, some with unusual properties. The simplest is biacetyl (CH3C(O)C(O)CH3), once used as butter-flavoring in popcorn. Acetylacetone (pentane-2,4-dione) is virtually a misnomer (inappropriate name) because this species exists mainly as the monoenol CH3C(O)CH=C(OH)CH3. Its enolate is a common ligand in coordination chemistry.

Unsaturated ketones:

Ketones containing alkene and alkyne units are often called unsaturated ketones. The most widely used member of this class of compounds is methyl vinyl ketone, CH3C(O)CH=CH2, which is useful in Robinson annulation reaction. Lest there be confusion, a ketone itself is a site of unsaturation, that is it can be hydrogenated.

Cyclic ketones:

Many ketones are cyclic. The simplest class have the formula (CH2)nCO where n varies from 3 for cyclopropanone to the teens. Larger derivatives exist. Cyclohexanone, a symmetrical cyclic ketone, is an important intermediate in the production of nylon. Isophorone, derived from acetone, is an unsaturated, unsymmetrical ketone that is the precursor to other polymers. Muscone, 3-methylpentadecanone, is a animal pheromone.

Keto-enol tautomerization

Keto-enol tautomerism. 1 is the keto form; 2 is the enol.
Ketones that have at least one Éø-hydrogen center, undergo keto-enol tautomerization; the tautomer is an enol. Tautomerization may be catalyzed by both acids and bases. Usually, the keto form is more stable than the enol. This equilibrium allows ketones to be prepared via the hydration of alkynes.

Acidity of ketones:

Ketones are far more acidic (pKa ≈ 20) than a regular alkane (pKa ≈ 50). This difference reflects resonance stabilization of the enolate ion that is formed through dissociation. The relative acidity of the α-hydrogen is important in the enolization reactions of ketones and other carbonyl compounds. The acidity of the α-hydrogen also allows ketones and other carbonyl compounds to undergo nucleophilic reactions at that position, with either stoichiometric or catalytic base.

Characterization:
Spectroscopy:

Ketones and aldehydes display an intense absorption in infra-red spectrum near 1700 cm−1. The peak can occur at slightly higher or lower energies, depending on the substituents.
Whereas 1H NMR spectroscopy is generally not useful for establishing the presence of a ketone, 13C NMR spectra exhibit signals somewhat downfield of 200 ppm depending on structure. Such signals are typically weak due to the absence of NoE effects. Since aldehydes resonate at similar chemical shifts, multiple resonance experiments are employed to definitively distinguish aldehydes and ketones.

Qualitative organic tests:

Ketones give positive results in Brady's test, the reaction with 2,4-dinitrophenylhydrazine to give the corresponding hydrazone. Ketones may be distinguished from aldehydes by giving a negative result with Tollens' reagent. Methyl ketones give positive results for the iodoform test.

Synthesis:

Many methods exist for the preparation of ketones in industrial scale, biology, and in academic laboratories. In industry, the most important method probably involves oxidation of hydrocarbons. For example, billion kilograms of cyclohexanone are produced annually by aerobic oxidation of cyclohexane. The oxidation of secondary alcohols is also common:
H3C-CH(OH)-CH3 + O → H3C-CO-CH3 + H2O
Typically, such oxidations employ air or oxygen for industrial processes. For specialized applications, such reactions rely on a strong oxidant such as potassium permanganate or a Cr(VI) compound. Milder conditions such as use of the Dess-Martin periodinane or the Moffatt-Swern oxidation are commonly employed in organic synthesis.

Many other methods have been developed including:• Ketones can be prepared by geminal halide hydrolysis.
• Alkynes can be converted to enols through a hydration reaction in the presence of an acid and HgSO4, and subsequent enol-keto tautomerization gives a ketone. This reaction always produces a ketone, even with a terminal alkyne.
• Aromatic ketones can be prepared in the Friedel-Crafts acylation, the related Houben-Hoesch reaction and the Fries rearrangement.
• Ozonolysis, and related dihydroxylation/oxidative sequences, cleave alkenes to give aldehydes and/or ketones, depending on alkene substitution pattern.
• In the Kornblum–DeLaMare rearrangement ketones are prepared from peroxides and base.
• In the Ruzicka cyclization, cyclic ketones are prepared from dicarboxylic acids.
• In the Nef reaction, ketones form by hydrolysis of salts of secondary nitro compounds.
• In the Fukuyama coupling, ketones form from a thioester and an organozinc compound.
• Ketones can be prepared by the reaction of an acid chloride with organocadmium compounds or organocopper compounds.
• The Dakin-West reaction provides an efficient method for preparation of certain methyl ketones from carboxylic acids.
• Ketones can also be prepared by the reaction of grignard reagents with nitriles which following hydrolysis produce the appropriate ketone in high yield.

Reactions

Ketones engage in many organic reactions but the most important reactions follow from the susceptibility of the carbonyl carbon toward nucleophilic addition and the tendency for the enolates to add to electrophiles. Nucleophilic additions include in approximate order of their generality:
• reaction with water (hydration) gives geminal diols
• the reaction with the anion of a terminal alkyne gives a hydroxyalkyne
• the reaction with ammonia or a primary amine gives an imine + water
• the reaction with secondary amine gives an enamine + water
• the reaction with a Grignard reagent or organolithium reagent to give, after aqueous workup, a tertiary alcohol
• the reaction with an alcohol, an acid or base gives a hemiketal and water and further reaction with an alcohol gives the ketal + water. This is a carbonyl-protecting reaction.
• reaction of RCOR' with sodium amide results in cleavage with formation of the amide RCONH2 and the alkane R'H, a reaction called the Haller-Bauer reaction.[3]
• Electrophilic addition, reaction with an electrophile gives a resonance stabilized cation.
• the reaction with phosphonium ylides in the Wittig reaction gives alkenes
• reaction with thiols gives a thioacetal
• reaction with hydrazine or derivatives of hydrazine gives hydrazones
• reaction with a metal hydride gives a metal alkoxide salt and then with water an alcohol
• reaction of an enol with halogens to form α-haloketone
• a reaction at an α-carbon is the reaction of a ketone with heavy water to give a deuterated ketone-d.
• fragmentation in photochemical Norrish reaction
• reaction with halogens and base of methyl ketones in the Haloform reaction
• reaction of 1,4-aminodiketones to oxazoles by dehydration in the Robinson-Gabriel synthesis
• reaction of aryl alkyl ketones with sulfur and an amine to amides in the Willgerodt reaction
• reaction of ketones with hydroxylamine produces oximes

Biochemistry:

Acetone, acetoacetate and beta-hydroxybutyrate are ketones (or ketone bodies) generated from carbohydrates, fatty acids and amino acids in humans and most vertebrates. Ketones are elevated in blood after fasting including a night of sleep, and in both blood and urine in starvation, hypoglycemia due to causes other than hyperinsulinism, various inborn errors of metabolism, and ketoacidosis (usually due to diabetes mellitus). Although ketoacidosis is characteristic of decompensated or untreated type 1 diabetes, ketosis or even ketoacidosis can occur in type 2 diabetes in some circumstances as well. Acetoacetate and beta-hydroxybutyrate are an important fuel for many tissues, especially during fasting and starvation. The brain, in particular, relies heavily on ketone bodies as a substrate for lipid synthesis and for energy during times of reduced food intake. Ketones have been described as "magic" in their ability to increase metabolic efficiency, while decreasing production of free radicals, the damaging byproducts of normal metabolism. Ketone bodies are relevant to neurological diseases such as Alzheimer's and Parkinson's disease,[4] and the heart and brain operate 25% more efficiently using ketones as a source of energy.[5] Research has also shown ketones play a role in reducing epileptic seizures with the so-called high-fat, near-zero carbohydrate Ketogenic Diet.

Applications:

Ketones are produced on massive scales in industry as solvents, polymer precursors, and pharmaceuticals. In terms of scale, the most important ketones are acetone, methylethyl ketone, and cyclohexanone. They are also common in biochemistry, but less so than in organic chemistry in general. The combustion of hydrocarbons is an uncontrolled oxidation process that give ketones as well as many other types of compounds.

Toxicity:

Although it is difficult to generalize on the toxicity of such a broad class of compounds, simple ketones are generally not highly toxic (for instance, the sugar fructose is a ketone). This characteristic is one reason for their popularity as solvents. Exceptions to this rule are the unsaturated ketones such as methyl vinyl ketone with LD50 of 7 mg/kg (oral).


References:

1. ^ International Union of Pure and Applied Chemistry. "ketones". Compendium of Chemical Terminology Internet edition.
2. ^ List of retained IUPAC names retained IUPAC names Link
3. ^ Haller-Bauer Reaction
4. ^ Y. Kashiwaya, T. Takeshima, N. Mori, K. Nakashima, K. Clarke and R. L. Veech (2000). "D-beta -Hydroxybutyrate protects neurons in models of Alzheimer's and Parkinson's disease". PNAS 97 (10): 5440–5444. doi:10.1073/pnas.97.10.5440. PMID 10805800.
5. ^ Y. Kashiwaya, K. Sato, N. Tsuchiya, S. Thomas, D. A. Fell, R. L. Veech and J. V. Passonneau (1994). "Control of glucose utilization in working perfused rat heart". J. Biol. Chem. 269 (41): 25502–25514. PMID 7929251. http://www.jbc.org/cgi/content/abstract/269/41/25502.

Aldehyde






Aldehyde:
An aldehyde is an organic compound containing a formyl group. This functional group consists of a carbonyl centre bonded to hydrogen, O=CH-. This group is called the aldehyde group or formyl group. Compounds containing this group are called aldehydes. Aldehydes are common in organic chemistry. Many fragrances are aldehydes.

Nomenclature:

IUPAC names for aldehydes:
The common names for aldehydes do not strictly follow official guidelines, such as those recommended by IUPAC but these rules are useful. IUPAC prescribes the following nomenclature for aldehydes.
1. Acyclic aliphatic aldehydes are named as derivatives of the longest carbon chain containing the aldehyde group. Thus, HCHO is named as a derivative of methane, and CH3CH2CH2CHO is named as a derivative of butane. The name is formed by changing the suffix -e of the parent alkane to -al, so that HCHO is named methanal, and CH3CH2CH2CHO is named butanal.
2. In other cases, such as when a -CHO group is attached to a ring, the suffix -carbaldehyde may be used. Thus, C6H11CHO is known as cyclohexanecarbaldehyde. If the presence of another functional group demands the use of a suffix, the aldehyde group is named with the prefix formyl-. This prefix is preferred to methanoyl-.
3. If the compound is a natural product or a carboxylic acid, the prefix oxo- may be used to indicate which carbon atom is part of the aldehyde group; for example, CHOCH2COOH is named 3-oxopropanoic acid.
4. If replacing the aldehyde group with a carboxyl group (-COOH) would yield a carboxylic acid with a trivial name, the aldehyde may be named by replacing the suffix -ic acid or -oic acid in this trivial name by -aldehyde.
Etymology:
The word aldehyde seems to have arisen from alcohol dehydrogenated. In the past, aldehydes were sometimes named after the corresponding alcohols, for example, vinous aldehyde for acetaldehyde. (Vinous is from Latin vinum = wine (the traditional source of ethanol), cognate with vinyl.
)
Structure and bonding:

Owing to resonance stabilization of the conjugate base, an α-hydrogen in an aldehyde is far more acidic with a pKa near 17, than a C-H bond in a typical alkane, with a pKa in the 30's. This acidification is attributed to (i) the electron-withdrawing quality of the formyl center and (ii) the fact that the conjugate base, an enolate anion, delocalizes its negative charge. Related to (i), the aldehyde group is somewhat polar. The -CHO center is non-acidic.
Aldehydes (except formaldehyde) can exist in either the keto or enol tautomers. Keto-enol tautomerism is catalyzed by either acid or base. Usually the enol is the minority tautomer, but it is more reactive.

Physical properties and characterization:

Aldehydes have properties that are diverse and which depend on the remainder of the molecule. Smaller aldehydes are more soluble in water, formaldehyde and acetaldehyde completely so. The volatile aldehydes have pungent odors. Aldehydes degrade in air via the process of autoxidation.
Both of the small industrially important aldehydes, formaldehyde and acetaldehyde, have complicated behavior because of their tendency to oligomerize or polymerize. They also tend to hydrate in the presence of water, forming the geminal diol. These properties are often not appreciated because the oligomers/polymers and the hydrates exist in equilibrium with the parent aldehyde.
Aldehydes are readily identified by spectroscopic methods. Using IR spectroscopy, they display a strong νCO band near 1700 cm-1. In their 1H NMR spectra, the formyl hydrogen centre absorbs near δ9, which is a distinctive part of the spectrum. This signal characteristically shows coupling to any protons on the alpha carbon.

Applications and occurrence:

Important aldehydes and related compounds. From the left: formaldehyde and its trimer, acetaldehyde and its enol, glucose (pyranose form), the flavorant cinnamaldehyde, the visual pigment retinal, and the vitamin pyridoxal.
Aldehydes are important precursors to commercially useful plasticizers and detergents. Millions of tons of aldehydes are produced industrially each year.

Naturally occurring aldehydes:

Traces of many aldehydes are found in essential oils and often contribute to their favorable odors, e.g. cinnamaldehyde and vanillin. Possibly because of the high reactivity of the formyl group, aldehydes are not common in several of the natural building blocks - amino acids, nucleic acids, lipids. Most sugars, however, are derivatives of aldehydes. Thse "aldoses" exist as hemiacetals, a sort of masked form of the parent aldehyde. For example, in aqueous solution only a tiny fraction of glucose exists as the aldehyde.

Synthesis:

There are several methods for preparing aldehydes,[4]" but the dominant technology is hydroformylation.[5] Illustrative is the generation of butyraldehyde by hydroformylation of propene:
H2 + CO + CH3CH=CH2 → CH3CH2CH2CHO
The method is attractive because the carbon-chain length is extended by one atom.

Oxidative routes:
Aldehydes are commonly generated by alcohol oxidation. In industry, formaldehyde is produced on a large scale by oxidation of methanol. Oxygen is the reagent of choice, being "green" and cheap. In the laboratory, more specialized oxidizing agents are used, but chromium(VI) reagents are popular. Oxidation can be achieved by heating the alcohol with an acidified solution of potassium dichromate. In this case, excess dichromate will further oxidize the aldehyde to a carboxylic acid, so either the aldehyde is distilled out as it forms (if volatile) or milder reagents such as PCC are used.[6]
"O" + CH3(CH2)9OH → CH3(CH2)8CHO + H2O
Oxidation of primary alcohols to form aldehydes and can be achieved under milder, chromium-free conditions by employing methods or reagents such as IBX acid, Dess-Martin periodinane, Swern oxidation, TEMPO, or the Oppenauer oxidation.
Another industrially significant oxidation route is the Wacker process whereby ethylene is oxidized to acetaldehyde in the presence of copper and palladium catalysts (acetaldehyde is also produced on a large scale by the hydration of acetylene).

Common reactions:

Aldehydes are highly reactive and participate in many reactions.[4]" From the industrial perspective, important reactions are condensations, e.g. to prepare plasticizers and polyols, and reduction to produce alcohols, especially "oxo-alcohols." From the biological perspective, the key reactions involve addition of nucleophiles to the formyl carbon in the formation of imines (oxidative deamination) and hemiacetals (structures of aldose sugars).

Reduction:

The" formyl group can be readily reduced to a primary alcohol (-CH2OH). Typically this conversion is accomplished by catalytic hydrogenation either directly or by transfer hydrogenation. Stoichiometric reductions are also popular, as can be effected with sodium borohydride.

Oxidation:

The formyl group readily oxidizes to the corresponding carboxylic acid (-COOH). The preferred oxidant in industry is oxygen or air. In the laboratory, popular oxidizing agents include potassium permanganate, nitric acid, chromium(VI) oxide, and chromic acid. The combination of manganese dioxide, acetic acid and methanol will convert the aldehyde to a methyl ester.
Another oxidation reaction is the basis of the silver mirror test. In this test, an aldehyde is treated with Tollens' reagent, which is prepared by adding a drop of sodium hydroxide solution into silver nitrate solution to give a precipitate of silver(I) oxide, and then adding just enough dilute ammonia solution to redissolve the precipitate in aqueous ammonia to produce [Ag(NH3)2]+ complex. This reagent will convert aldehydes to carboxylic acids without attacking carbon-carbon double-bonds. The name silver mirror test arises because this reaction will produce a precipitate of silver whose presence can be used to test for the presence of an aldehyde.
If the aldehyde can not form an enolate (e.g. benzaldehyde), addition of strong base induces the Cannizzaro reaction. This reaction results in disproportionation, producing a mixture of alcohol and carboxylic acid


References:
1. ^ Short Summary of IUPAC Nomenclature of Organic Compounds, web page, University of Wisconsin Colleges, accessed on line August 4, 2007.
2. ^ §R-5.6.1, Aldehydes, thioaldehydes, and their analogues, A Guide to IUPAC Nomenclature of Organic Compounds: recommendations 1993, IUPAC, Commission on Nomenclature of Organic Chemistry, Blackwell Scientific, 1993.
3. ^ §R-5.7.1, Carboxylic acids, A Guide to IUPAC Nomenclature of Organic Compounds: recommendations 1993, IUPAC, Commission on Nomenclature of Organic Chemistry, Blackwell Scientific, 1993.
4. ^ a b c Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 0-471-72091-7
5. ^ W." Bertleff, M. Roeper, X. Sava, “Carbonylation” in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH: Weinheim, 2003. doi: 10.1002/14356007.a05_217.pub2
6. ^ R. W. Ratcliffe (1988), "Oxidation with the Chromium Trioxide-Pyridine Complex Prepared in situ: 1-Decanal", Org. Synth., http://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=cv6p0373; Coll. Vol. 6: 373
7. ^ New methods for the oxidation of aldehydes to carboxylic acids and esters Elias J. Corey, Norman W. Gilman, and B. E. Ganem J. Am. Chem. Soc. 1968; 90(20) pp 5616 - 5617; doi:10.1021/ja01022a059.

Ferric Chloride - Pyridine Test , MSDS







Ferric Chloride - Pyridine Test:

The ferric chloride test is used to determine the presence or absence of phenols in a given sample. Enols give positive results as well. The bromine test is useful to confirm the result, although modern spectroscopic techniques (e.g. NMR and IR spectroscopy) are far superior in determining the identity of the unknown. The quantity of total phenols may be spectroscopically determined by the Folin-Ciocalteau assay.

Technique

The sample is dissolved in water, or a mixture of water and ethanol, and a few drops of dilute ferric chloride solution is added. The formation of a red, blue, green, or purple coloration indicates the presence of phenols. Where the sample is insoluble in water, it may be dissolved in dichloromethane with a small amount of pyridine.

Chemistry:

Phenols form a complex with Fe(III), which is intensely colored. This is the basis for the test.

Ferric Chloride test for Phenols.:

Just as enols can form colored complexes with ferric ion, phenolate ions can as well. Therefore, this test is designed to convert the weakly acidic phenols to their conjugate base which can then complex with ferric ion. If the phenol is water soluble, add a few drops of 2.5% aqueous ferric chloride solution to a 3% aqueous solution of the phenol. A deep red, green, or blue color is positive. If the phenol is not water soluble, dissolve 20 mg of the solid (or 1 drop of the liquid) in 1 mL of methylene chloride and add 1 drop of pyridine. Add 3 drops of 1% ferric chloride in methylene chloride. An intense color is a positive test. Use phenol as a known. Not all phenols will give a positive test.

Procedure:

In hood: Add 4 or 5 drops or 30 - 50 mg of unknown to 2 mL of pure chloroform in a clean, dry test tube. Stir the solution. If the unknown does not dissolve, even partially, add 2 - 3 mL more chloroform and warm gently. Cool to 25oC and add 2 drops of 1% solution of anhydrous ferric chloride in chlorofrom followed by 3 drops of pyridine. Shake the test tube and note the color produced immediately.

Positive Test:

The appearance of blue, violet, purple, green, or red-brown color is a positive test.

Complications:

Not all phenols or enols give positive results
Most oximes, hydroxamic acids, and sulfinic acids give a positive

Iron (III) Chloride Test for Water-Soluble Phenol Standard
Phenol

Procedure (for water-soluble phenols)
The iron (III) chloride test for phenols is not completely reliable for acidic phenols, but can be administered by dissolving 15 mg of the unknown compound in 0.5 mL of water or water-alcohol mixture and add 1 to 2 drops of 1% aqueous iron (III) chloride solution.

Positive Test

A red, blue, green, or purple color is a positive test.

Cleaning up

Since the quantity of material is extremely small, the test solution can be diluted with water and flushed down the drain.

Iron(III) Chloride - Pyridine Test for Water-Insoluble Phenols

Standard
Phenol
Procedure
(for water-insoluble phenols or less reactive phenols)
A more sensitive test for phenols consists of dissolving or suspending 15 mg of the unknown in 0.5 mL of methylene chloride and adding 3-5 drops of a 1% solution ferric chloride in methylene chloride. Add a drop of pyridine and stir.

Positive Test (b)

Addition of pyridine and stirring will produce a color if phenols or enols are present.


Why phenols give ferric chloride test?


We use Ferric Chloride (FeCl3) in the lab to test for the presence (or in some case absence) of phenols, although some enols will also yield positive results. The OH (hydroxy group) which is attached directly to an aromatic nucleus (Benzene, for example) is detected by the Ferric chloride. It is important to note that alcohols do not undergo the reaction. Phenols will typically yield dramatic purple,blue,red or green color as an indication of a positive test. FeCl3 will also indicate the presence of aliphatic acids (that is, non-aromatic organic acids, such as Acetic acid) turning the solution a yellow color. Aromatic acids will test as a beige-tan color. Enols will also show a characteristic yellow color. It is also important to understand that not all phenols will test positively in the presence of the FeCl3 reagent. A good example of this is in highly hindered phenols which do not yield positive tests. However, a negative test is not completely conclusive, so other tests can be preformed to verify the absence of a phenol (such as NMR and IR spectroscopy)
We use Ferric Chloride (FeCl3) in the lab to test for the presence (or in some case absence) of phenols, although some enols will also yield positive results. The OH (hydroxy group) which is attached directly to an aromatic nucleus (Benzene, for example) is detected by the Ferric chloride. It is important to note that alcohols do not undergo the reaction. Phenols will typically yield dramatic purple,blue,red or green color as an indication of a positive test. FeCl3 will also indicate the presence of aliphatic acids (that is, non-aromatic organic acids, such as Acetic acid) turning the solution a yellow color. Aromatic acids will test as a beige-tan color. Enols will also show a characteristic yellow color. It is also important to understand that not all phenols will test positively in the presence of the FeCl3 reagent. A good example of this is in highly hindered phenols which do not yield positive tests. However, a negative test is not completely conclusive, so other tests can be preformed to verify the absence of a phenol (such as NMR and IR spectroscopy)



Material Safety Data SheetFerric Chloride TS MSDS

Section 1: Chemical Product and Company Identification
Product Name: Ferric Chloride TS
Catalog Codes: SLF1045
CAS#: Mixture.
RTECS: Not applicable.
TSCA: TSCA 8(b) inventory: Water; Ferric chloride
hexahydrate
CI#: Not available.
Synonym: Ferric Chloride Test Solution
Chemical Name: Not applicable.
Chemical Formula: Not applicable.
Contact Information:
Sciencelab.com, Inc.
14025 Smith Rd.
Houston, Texas 77396
US Sales: 1-800-901-7247
International Sales: 1-281-441-4400
Order Online: ScienceLab.com
CHEMTREC (24HR Emergency Telephone), call:
1-800-424-9300
International CHEMTREC, call: 1-703-527-3887
For non-emergency assistance, call: 1-281-441-4400
Section 2: Composition and Information on Ingredients
Composition:
Name CAS # % by Weight
Water 7732-18-5 91
Ferric chloride hexahydrate 10025-77-1 9
Toxicological Data on Ingredients: Ferric chloride hexahydrate LD50: Not available. LC50: Not available.
Section 3: Hazards Identification
Potential Acute Health Effects:
Very hazardous in case of skin contact (irritant), of eye contact (irritant), of ingestion, . Hazardous in case of skin
contact (corrosive, permeator), of eye contact (corrosive). Slightly hazardous in case of inhalation (lung
sensitizer). Non-corrosive for lungs. Liquid or spray mist may produce tissue damage particularly on mucous
membranes of eyes, mouth and respiratory tract. Skin contact may produce burns. Inhalation of the spray mist
may produce severe irritation of respiratory tract, characterized by coughing, choking, or shortness of breath.
Severe over-exposure can result in death. Inflammation of the eye is characterized by redness, watering, and
itching. Skin inflammation is characterized by itching, scaling, reddening, or, occasionally, blistering.
Potential Chronic Health Effects:
CARCINOGENIC EFFECTS: Not available.
MUTAGENIC EFFECTS: Mutagenic for mammalian somatic cells. [Ferric chloride hexahydrate].
p. 1
TERATOGENIC EFFECTS: Not available.
DEVELOPMENTAL TOXICITY: Not available.
The substance may be toxic to kidneys, liver, spleen, cardiovascular system, central nervous system (CNS).
Repeated or prolonged exposure to the substance can produce target organs damage. Repeated or prolonged
contact with spray mist may produce chronic eye irritation and severe skin irritation. Repeated or prolonged
exposure to spray mist may produce respiratory tract irritation leading to frequent attacks of bronchial infection.
Repeated exposure to a highly toxic material may produce general deterioration of health by an accumulation in
one or many human organs.
Section 4: First Aid Measures
Eye Contact:
Check for and remove any contact lenses. In case of contact, immediately flush eyes with plenty of water for at
least 15 minutes. Cold water may be used. Get medical attention immediately.
Skin Contact:
In case of contact, immediately flush skin with plenty of water for at least 15 minutes while removing contaminated
clothing and shoes. Cover the irritated skin with an emollient. Cold water may be used.Wash clothing before
reuse. Thoroughly clean shoes before reuse. Get medical attention immediately.
Serious Skin Contact:
Wash with a disinfectant soap and cover the contaminated skin with an anti-bacterial cream. Seek immediate
medical attention.
Inhalation:
If inhaled, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get
medical attention immediately.
Serious Inhalation:
Evacuate the victim to a safe area as soon as possible. Loosen tight clothing such as a collar, tie, belt or
waistband. If breathing is difficult, administer oxygen. If the victim is not breathing, perform mouth-to-mouth
resuscitation. Seek medical attention.
Ingestion:
If swallowed, do not induce vomiting unless directed to do so by medical personnel. Never give anything by
mouth to an unconscious person. Loosen tight clothing such as a collar, tie, belt or waistband. Get medical
attention immediately.
Serious Ingestion: Not available.
Section 5: Fire and Explosion Data
Flammability of the Product: Non-flammable.
Auto-Ignition Temperature: Not applicable.
Flash Points: Not applicable.
Flammable Limits: Not applicable.
Products of Combustion: Not available.
Fire Hazards in Presence of Various Substances: Not applicable.
Explosion Hazards in Presence of Various Substances: Non-explosive in presence of open flames and sparks, of shocks.
Fire Fighting Media and Instructions: Not applicable.
Special Remarks on Fire Hazards: Not available.
p. 2
Special Remarks on Explosion Hazards: Not available.
Section 6: Accidental Release Measures
Small Spill:
Dilute with water and mop up, or absorb with an inert dry material and place in an appropriate waste disposal
container.
Large Spill:
Corrosive liquid. Poisonous liquid.
Stop leak if without risk. Absorb with DRY earth, sand or other non-combustible material. Do not get water inside
container. Do not touch spilled material. Use water spray curtain to divert vapor drift. Use water spray to reduce
vapors. Prevent entry into sewers, basements or confined areas; dike if needed. Call for assistance on disposal.
Be careful that the product is not present at a concentration level above TLV. Check TLV on the MSDS and with
local authorities.
Section 7: Handling and Storage
Precautions:
Keep locked up.. Keep container dry. Do not ingest. Do not breathe gas/fumes/ vapor/spray. Never add water
to this product. In case of insufficient ventilation, wear suitable respiratory equipment. If ingested, seek medical
advice immediately and show the container or the label. Avoid contact with skin and eyes.
Storage: Keep container tightly closed. Keep container in a cool, well-ventilated area. Do not store above 24°C (75.2°F).
Section 8: Exposure Controls/Personal Protection
Engineering Controls:
Provide exhaust ventilation or other engineering controls to keep the airborne concentrations of vapors below their
respective threshold limit value.
Personal Protection:
Face shield. Full suit. Vapor respirator. Be sure to use an approved/certified respirator or equivalent. Gloves.
Boots.
Personal Protection in Case of a Large Spill:
Splash goggles. Full suit. Vapor respirator. Boots. Gloves. A self contained breathing apparatus should be
used to avoid inhalation of the product. Suggested protective clothing might not be sufficient; consult a specialist
BEFORE handling this product.
Exposure Limits:
Ferric chloride hexahydrate
TWA: 1 (mg/m3) from ACGIH (TLV) [United States]
TWA: 1 (mg/m3) from NIOSH
Consult local authorities for acceptable exposure limits.
Section 9: Physical and Chemical Properties
Physical state and appearance: Liquid.
Odor: Not available.
Taste: Not available.
Molecular Weight: Not applicable.
Color: Not available.
p. 3
pH (1% soln/water): Neutral.
Boiling Point: The lowest known value is 100°C (212°F) (Water).
Melting Point: Not available.
Critical Temperature: Not available.
Specific Gravity: Weighted average: 1.04 (Water = 1)
Vapor Pressure: The highest known value is 2.3 kPa (@ 20°C) (Water).
Vapor Density: The highest known value is 0.62 (Air = 1) (Water).
Volatility: Not available.
Odor Threshold: Not available.
Water/Oil Dist. Coeff.: Not available.
Ionicity (in Water): Not available.
Dispersion Properties: See solubility in water.
Solubility: Easily soluble in cold water, hot water.
Section 10: Stability and Reactivity Data
Stability: The product is stable.
Instability Temperature: Not available.
Conditions of Instability: Incompatible materials
Incompatibility with various substances: Not available.
Corrosivity: Non-corrosive in presence of glass.
Special Remarks on Reactivity: Hygroscopic (Ferric chloride hexahydrate)
Special Remarks on Corrosivity: Not available.
Polymerization: Will not occur.
Section 11: Toxicological Information
Routes of Entry: Absorbed through skin. Dermal contact. Eye contact.
Toxicity to Animals:
LD50: Not available.
LC50: Not available.
Chronic Effects on Humans:
MUTAGENIC EFFECTS: Mutagenic for mammalian somatic cells. [Ferric chloride hexahydrate].
Contains material which may cause damage to the following organs: kidneys, liver, spleen, cardiovascular system,
, central nervous system (CNS).
Other Toxic Effects on Humans:
Very hazardous in case of skin contact (irritant), of ingestion, .
p. 4
Hazardous in case of skin contact (corrosive, permeator), of eye contact (corrosive).
Slightly hazardous in case of inhalation (lung sensitizer, lung corrosive).
Special Remarks on Toxicity to Animals: LDL [Rat] - Route: Oral; Dose: 900 mg/kg (Ferric chloride hexahydrate)
Special Remarks on Chronic Effects on Humans: May affect genetic material (mutagen) (Ferric chloride hexahydrate)
Special Remarks on other Toxic Effects on Humans:
Acute Potential Health Effects:
Skin: Causes irritation and burns of the skin.
Eyes: Causes eye irritation and burns. Higher exposures may lead to corneal or conjunctival ulceration.
Ingestion: Harmful if swallowed. Causes irritation of the gastrointestinal (digestive) tract with nausea, vomiting,
diarrhea and hemorrage and possible burns. May cause severe and permanent damage to the digestive tract.
Delayed effects may include cardiovascular disturbances, liver/kidney damage, cerebral coma and possible death.
Inhalation: Causes irritation of the respiratory tract with possible burns.
Chronic Potential Health Effects:
May affect genetic material
Ingestion: May affect liver, spleen Kidneys, ureter, bladder), central nervous system, and cardiovascular system.
Section 12: Ecological Information
Ecotoxicity: Not available.
BOD5 and COD: Not available.
Products of Biodegradation:
Possibly hazardous short term degradation products are not likely. However, long term degradation products may
arise.
Toxicity of the Products of Biodegradation: The products of degradation are less toxic than the product itself.
Special Remarks on the Products of Biodegradation: Not available.
Section 13: Disposal Considerations
Waste Disposal:
Waste must be disposed of in accordance with federal, state and local environmental
control regulations.
Section 14: Transport Information
DOT Classification: Class 8: Corrosive material
Identification: : Ferric Chloride Solution (Ferric chloride hexahydrate) UNNA: 2582 PG: III
Special Provisions for Transport: Not available.
Section 15: Other Regulatory Information
Federal and State Regulations:
Pennsylvania RTK: Ferric chloride hexahydrate
Minnesota: Ferric chloride hexahydrate
TSCA 8(b) inventory: Water; Ferric chloride hexahydrate
Other Regulations: OSHA: Hazardous by definition of Hazard Communication Standard (29 CFR 1910.1200).
Other Classifications:
p. 5
WHMIS (Canada):
CLASS D-2B: Material causing other toxic effects (TOXIC).
CLASS E: Corrosive liquid.
DSCL (EEC):
R25- Toxic if swallowed.
R36/38- Irritating to eyes and skin.
S1/2- Keep locked up and out of the reach of
children.
S45- In case of accident or if you feel unwell,
seek medical advice immediately (show the
label where possible).
S46- If swallowed, seek medical advice
immediately and show this container or label.
HMIS (U.S.A.):
Health Hazard: 3
Fire Hazard: 0
Reactivity: 0
Personal Protection:
National Fire Protection Association (U.S.A.):
Health: 2
Flammability: 0
Reactivity: 0
Specific hazard:
Protective Equipment:
Gloves.
Full suit.
Vapor respirator. Be sure to use an
approved/certified respirator or
equivalent. Wear appropriate respirator
when ventilation is inadequate.
Face shield.
Section 16: Other Information
References: Not available.
Other Special Considerations: Not available.
Created: 10/10/2005 10:12 AM
Last Updated: 11/06/2008 12:00 PM
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make no warranty of merchantability or any other warranty, express or implied, with respect to such information, and we
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information for their particular purposes. In no event shall ScienceLab.com be liable for any claims, losses, or damages of any
third party or for lost profits or any special, indirect, incidental, consequential or exemplary damages, howsoever arising, even
if ScienceLab.com has been advised of the possibility of such damages.
p. 6



Safety data for pyridine:

General

Synonyms: azabenzene, pyridin
Molecular formula: C5H5N
CAS No: 110-86-1
EINECS No: 203-809-9
Annex I Index No: 613-002-00-7
Physical data
Appearance: colourless liquid with a very unpleasant odour
Melting point: -42 C
Boiling point: 115 C
Vapour density: 2.7 (air = 1)
Vapour pressure: 16 mm Hg at 20 C
Density (g cm-3):
Flash point: 17 C (closed cup)
Explosion limits: 1.8 % - 12.4 %
Autoignition temperature:
Water solubility:

Stability

Stable. Flammable. Incompatible with strong oxidizing agents, strong acids.

Toxicology
Harmful by ingestion, inhalation and if absorbed through skin. May affect fertility. May cause irreversible effects. Severe eye and skin irritant - may cause burns. Long-term exposure may cause liver, kidney or CNS damage. Typical STEL 10 ppm. Typical PEL 15 ppm.

Toxicity data
(The meaning of any toxicological abbreviations which appear in this section is given here.)
ORL-RAT LD50 891 mg kg-1
IPR-RAT LD50 866 mg kg-1
SCU-RAT LD50 1000 mg kg-1
SKN-RBT LD50 1121 mg kg-1
Risk phrases
(The meaning of any risk phrases which appear in this section is given here.)
R11 R20 R21 R22.

Transport information
(The meaning of any UN hazard codes which appear in this section is given here.)
UN No 1282. Hazard class 3. Packing group II.
Personal protection
Safety glasses, gloves, good ventilation.


Refrence:

1.www.chemicalinfo.com
2. http://msds.chem.ox.ac.uk
3. http://www.inchem.com.ph
4. http:www.hvchemical.com
5. http://en.wikipedia.org
6. http://www.osha.gov
7. http://chemfinder.cumbridgesoft.com
8. http://www.sciencelab.com
9. www.wellesley.edu/.../phenol_amine_nitro.html