4'-(METHYLTHIO)ACETOPHENONE

PRODUCT IDENTIFICATION

CAS NO. 1778-09-2

4'-(METHYLTHIO)ACETOPHENONE

EINECS NO.

FORMULA (CH3S)C6H4COCH3
MOL WT. 166.24

H.S. CODE

TOXICITY

SYNONYMS 4'-methylthioacetophenone; MTA;
SMILES

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE pale yllow crystals
MELTING POINT 80 - 82 C
BOLING POINT

 

SPECIFIC GRAVITY

 

SOLUBILITY IN WATER  
pH  
VAPOR DENSITY

 

REFRACTIVE INDEX

 

NFPA RATINGS

 

AUTOIGNITION

 

FLASH POINT

 

STABILITY Stable under normal conditions

GENERAL DESCRIPTION & APPLICATIONS

Acetophenone, the simplest aromatic ketone, is a clear liquid or crystals; melting point 19 - 20 C; boiling point 202 C; very slightly soluble in water. Commercial acetophenone can be obtained from benzene with acetic anhydride or acetyl chloride by Friedel-Crafts process. It can be also obtained by air oxidation of ethylbenzene, as a by-product of cumene or from acrylonitrile. It is used as a polymerization catalyst for the manufacture of olefins. It is used as an intermediate for pharmaceuticals, agrochemicals and other organic compounds. It also has been used as a drug to induce sleep. Its is used in tear gas (especially as the form of chloro acetophenone) and warfare. It is used as an solvent for plastics, resins, cellulose ethers, and esters. The dimer (dipnone) is used as a plasticizer. Actophenone and its derivatives, having additionally substituted saturated alkyls, oxygenated alkyl groups, thio groups, additional aromatic groups, unsaturated aliphatic side chains, and other functional groups, are ingredients of flavor & fragrance for in soaps, detergents, cosmetics, and perfumes as well as in foods, beverages, and tobacco.

Intermediate for pharmaceuticals (especially osteoarthritis and rheumatoid arthritis drugs) and pesticides

SALES SPECIFICATION

APPEARANCE

pale yllow crystals

ASSAY

99.0% min

MELTING POINT

80 - 82 C
TRANSPORTATION
PACKING  
HAZARD CLASS  
UN NO.  
OTHER INFORMATION
Hazard Symbols: XN, Risk Phrases: 36/37/38, Safety Phrases: 26-36