2',4',6'-TRIHYDROXYACETOPHENONE MONOHYDRATE

PRODUCT IDENTIFICATION
CAS NO. 480-66-0

2',4',6'-TRIHYDROXYACETOPHENONE

EINECS NO. 207-556-5
FORMULA (HO)3C6H2COCH3·H2O
MOL WT. 186.16

H.S. CODE

 2914.50.3000

TOXICITY

 
SYNONYMS Phloroacetophenone monohydrate; THAP;  Acetophloroglucine;
2',4',6'-Trihidroxiacetofenona; 2',4',6'-Trihydroxyacétophénone; 1-(2,4,6-Trihydroxyphenyl)ethanone; 2',4',6'-Trihydroxyacetophenone; Acetylphloroglucinol; 1-(2,4,6-Trihydroxyphenyl)ethane;
SMILES O=C(c1c(O)cc(O)cc1O)C

CLASSIFICATION

 

EXTRA NOTES

 

PHYSICAL AND CHEMICAL PROPERTIES
PHYSICAL STATE

yellowish crystals

MELTING POINT

 219 - 221 C
BOILING POINT  
SPECIFIC GRAVITY  

SOLUBILITY IN WATER

  
pH  
VISCOSITY  
AUTOIGNITION

 

REFRACTIVE INDEX

 

NFPA RATINGS  
FLASH POINT

 

STABILITY Stable under ordinary conditions

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking

Google Scholar Search

PubChem Compound Summary - 2,4,6-Trihydroxyacetophenone

KEGG (Kyoto Encyclopedia of Genes and Genomes) -  2,4,6-Trihydroxyacetophenone

http://www.ebi.ac.uk/ -  2,4,6-Trihydroxyacetophenone

http://www.ncbi.nlm.nih.gov/ -  2,4,6-Trihydroxyacetophenone

Material Safety Data Sheet

Local:
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.

Trihydroxyacetophenone is used as building block for the synthesis of target compounds.
SALES SPECIFICATION

APPEARANCE

 clear  to yellow liquid

ASSAY

99.0% min

MELTING POINT

219 - 221 C

TRANSPORTATION
PACKING  
HAZARD CLASS  
UN NO.  
SAFETY INFORMATION

HAZARD OVERVIEW

 Irritating to eyes, respiratory system and skin. OSHA Hazards: Target Organ Effect, Irritant. Target Organs: Damage to the eyes.

GHS

 
SIGNAL WORD Warning

PICTOGRAMS

HAZARD STATEMENTS

H315-H319-H335

P STATEMENTS

P261-P305 + P351 + P338
EC DIRECTIVES

 
HAZARD CODES

RISK PHRASES

36/37/38

SAFETY PHRASES

24/25

PRICE INFORMATION