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135380

Sigma-Aldrich

Phenylacetone

99%

Sinonimo/i:

Benzyl methyl ketone, Phenyl-2-propanone

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About This Item

Formula condensata:
C6H5CH2COCH3
Numero CAS:
103-79-7
Peso molecolare:
134.18
Beilstein:
742120
Numero CE:
203-144-4
Numero MDL:
MFCD00017249
Codice UNSPSC:
12352100
ID PubChem:
329750209

Saggio

99%

Stato

liquid

Controllo stupefacenti

USDEA Schedule II

Disponibilità

available only in EU

Densità

1.003 g/mL at 20 °C (lit.)

Stringa SMILE

CC(=O)Cc1ccccc1

InChI

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

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Descrizione generale

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H319

Classi di pericolo

Eye Irrit. 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

194.0 °F - closed cup

Punto d’infiammabilità (°C)

90 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBD9315V
STBC4467V
S55474V
STBC1781V
STBB2773

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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
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.
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
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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