Name | Phenylacetone |
Synonyms | Phenylacetone 1-phenylacetone 1-PHENYLACETONE Phenyl-2-propanone Benaylmethyldetone alpha-Phenylacetone 3-Phenyl-2-propanone 1-phenylpropan-2-one Benzyl methyl ketone 1-PHENYL-2-PROPANONE 2-Propanone,1-phenyl- 2-Propanone, 1-phenyl- Fenproporex-M (desamino-oxo-) |
CAS | 103-79-7 |
EINECS | 203-144-4 |
InChI | InChI=1/C9H10O/c1-8(10)7-9-5-3-2-4-6-9/h2-6H,7H2,1H3 |
Molecular Formula | C9H10O |
Molar Mass | 134.18 |
Density | 1.003g/mLat 20°C(lit.) |
Melting Point | -15 °C |
Boling Point | 216 °C |
Flash Point | 83°C |
Water Solubility | Insoluble |
Vapor Presure | 0.159mmHg at 25°C |
BRN | 742120 |
Storage Condition | Controlled Substance, -20°C Freezer |
Refractive Index | 1.5155-1.5175 |
Physical and Chemical Properties | Density 1.015 melting point -15°C boiling point 216°C refractive index 1.5155-1.5175 flash point 83°C water-soluble Insoluble |
Use | Used as an organic intermediate for the synthesis of the enemy rat sodium salt; Pharmaceutical intermediates for the synthesis of amphetamine, phenylisopropylamine, etc |
Safety Description | 24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
RTECS | UC3500100 |
HS Code | 29143910 |
Toxicity | LD50 intraperitoneal in mouse: 540mg/kg |
Raw Materials | Phenylacetic acid |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Use | 1-phenyl-2-acetone is an intermediate of rodenticide diphthine and chlororone. used as an organic intermediate, used for the synthesis of sodium diphrenic salt; pharmaceutical intermediate, used for the synthesis of amphetamine, phenylisopropylamine, etc. used for the synthesis of pesticide intermediates such as sodium diphrenic salt, Amphetamine, phenylisopropylamine and other pharmaceutical intermediates This product is an organic synthetic intermediate, used for the production of rodenticide sodium diphrenic. |
Production method | It is obtained by the reaction of phenylacetic acid and acetic anhydride. the preparation method is to react benzaldehyde with methyl 2-chloropropionate, then hydrolyze and decarboxylate to obtain crude product, adjust pH = 6 in aqueous solution, extract with ethyl acetate, treat the aqueous phase with 25% K2CO3 solution to pH = 6, then treat with ethyl acetate, and then distill the crude product to obtain the product. |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |