CAS 103-79-7

Phenylacetone

Description:

Phenylacetone, also known as 1-phenylpropan-2-one, is an organic compound with the chemical formula C9H10O. It is characterized by a ketone functional group, specifically a carbonyl group (C=O) adjacent to a phenyl group (C6H5) and an alkyl chain. This colorless to pale yellow liquid has a sweet, floral odor and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water. Phenylacetone is primarily used in the synthesis of various pharmaceuticals and fragrances, and it serves as an intermediate in the production of other organic compounds. It is also known for its role in the illicit synthesis of certain drugs, which has led to regulatory scrutiny. The compound has a moderate boiling point and exhibits typical reactivity associated with ketones, including nucleophilic addition reactions. Safety precautions are necessary when handling phenylacetone, as it can be harmful if inhaled or ingested, and may cause skin and eye irritation.

Formula: C₉H₁₀O

InChI: InChI=1S/C9H10O/c1-8(10)7-9-5-3-2-4-6-9/h2-6H,7H2,1H3

InChI key: InChIKey=QCCDLTOVEPVEJK-UHFFFAOYSA-N

SMILES: C(C(C)=O)C1=CC=CC=C1

Synonyms:

• 1-Phenylacetone
• 2-Propanone, 1-phenyl-
• 2-Propanone, phenyl-
• 3-Phenyl-2-propanone
• Benzyl methyl ketone
• Fenilacetona
• Methyl benzyl ketone
• Nsc 9827
• Phenyl acetone
• Phenyl-2-propanone
• Phenylaceton
• Phenylacetone,
• Phenylmethyl methyl ketone
• α-Phenylacetone

Phenylaceton

Controlled Product

CAS: 103-79-7

Color and Shape: Neat

Ref: LP-PNA-1073-10

Phenylacetone Drug Precursor

Controlled Product

CAS: 103-79-7

Formula: C₉H₁₀O

Color and Shape: Neat

Molecular weight: 134.18

Ref: 86-MM0741.04

Phenylacetone

Controlled Product

CAS: 103-79-7

Phenylacetone is a compound that is used in the synthesis of various drugs, including amphetamine and methamphetamine. It is also used as an analytical reagent to measure the concentration of dinucleotide phosphate in wastewater. Phenylacetone can be synthesized by reacting phenylacetic acid with either sodium or methyl ethyl ketone. The reaction mechanism for this reaction includes the formation of a nitro group from sodium nitrite, which then reacts with phenylacetic acid to form an intermediate. This intermediate reacts with methyl ethyl ketone to form phenylacetone, which is then hydrolyzed to produce methamphetamine. Phenylacetone also has the ability to react with hydrogen peroxide and form 3-hydroxybenzaldehyde and benzene.

Formula: C₉H₁₀O

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 134.18 g/mol

Ref: 3D-FP26929

Dextroamphetamine Related Compound B CII (Phenyl acetone)

Controlled Product

CAS: 103-79-7

Phenylacetone (phenylpropan-2-one)

Formula: C₉H₁₀O

Color and Shape: Clear Pale Yellow Liquid

Molecular weight: 134.07316

Ref: 45-1180026