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135380

Sigma-Aldrich

Phenylacetone

99%

Sinônimo(s):

Benzyl methyl ketone, Phenyl-2-propanone

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About This Item

Fórmula linear:
C6H5CH2COCH3
Número CAS:
103-79-7
Peso molecular:
134.18
Beilstein:
742120
Número CE:
203-144-4
Número MDL:
MFCD00017249
Código UNSPSC:
12352100
ID de substância PubChem:
329750209

Ensaio

99%

forma

liquid

controle de medicamentos

USDEA Schedule II

disponibilidade

available only in EU

densidade

1.003 g/mL at 20 °C (lit.)

cadeia de caracteres SMILES

CC(=O)Cc1ccccc1

InChI

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

chave InChI

QCCDLTOVEPVEJK-UHFFFAOYSA-N

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Descrição geral

Phenylacetone is the immediate precursor for clandestine production of amphetamine and methamphetamine. Phenylacetone on anaerobic incubations with rat liver mitochondria gets reduced to phenylisopropanol.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H319

Classificações de perigo

Eye Irrit. 2

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

194.0 °F - closed cup

Ponto de fulgor (°C)

90 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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W Krawczyk et al.
Bulletin on narcotics, 57(1-2), 33-62 (2005-01-01)
1-Phenyl-2-propanone (P-2-P), also known as benzyl methyl ketone (BMK), is the main precursor used in amphetamine synthesis. In recent years, the number of seizures of P-2-P from both licit and illicit drug manufacture has increased. The present article comprises a
S Schneiders et al.
Science & justice : journal of the Forensic Science Society, 49(2), 94-101 (2009-07-18)
The isotope ratios of amphetamine type stimulants (ATS) depend as well on the precursor as the synthetic pathway. For clandestine production of amphetamine and methamphetamine, 1-phenyl-2-propanone (P2P, benzylmethylketone) is a commonly used precursor. Our aim was to determine the variation
Hassan M Badawi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 95, 435-441 (2012-05-15)
The structural stability of 1,3-diphenylurea and 1,3-diphenylacetone was investigated by the DFT-B3LYP and ab initio MP2 calculations using the 6-311G(**) basis set. From full energy optimization at the MP2 level of theory the near-planar cis-trans form of 1,3-diphenylurea was predicted
Karla I Ziegelmann-Fjeld et al.
Protein engineering, design & selection : PEDS, 20(2), 47-55 (2007-02-07)
The secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus 39E (TeSADH) is highly thermostable and solvent-stable, and it is active on a broad range of substrates. These properties make TeSADH an excellent template to engineer an industrial catalyst for chiral chemical synthesis.
Hanna M Dudek et al.
Applied microbiology and biotechnology, 88(5), 1135-1143 (2010-08-13)
Type I Baeyer-Villiger monooxygenases (BVMOs) strongly prefer NADPH over NADH as an electron donor. In order to elucidate the molecular basis for this coenzyme specificity, we have performed a site-directed mutagenesis study on phenylacetone monooxygenase (PAMO) from Thermobifida fusca. Using
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