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B16003

Sigma-Aldrich

4-Phenyl-2-butanone

98%

Synonym(s):

Benzylacetone, Methyl 2-phenethyl ketone, NSC 44829, NSC 813

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About This Item

Linear Formula:
C6H5CH2CH2COCH3
CAS Number:
2550-26-7
Molecular Weight:
148.20
Beilstein/REAXYS Number:
1907123
EC Number:
219-847-4
MDL number:
MFCD00008790
UNSPSC Code:
12352100
PubChem Substance ID:
24891600
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.512 (lit.)

bp

235 °C (lit.)

density

0.989 g/mL at 25 °C (lit.)

SMILES string

CC(=O)CCc1ccccc1

InChI

1S/C10H12O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3

InChI key

AKGGYBADQZYZPD-UHFFFAOYSA-N

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Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

221.0 °F - closed cup

flash_point_c

105 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Gilles Brackman et al.
PloS one, 6(1), e16084-e16084 (2011-01-21)
Many bacteria, including Vibrio spp., regulate virulence gene expression in a cell-density dependent way through a communication process termed quorum sensing (QS). Hence, interfering with QS could be a valuable novel antipathogenic strategy. Cinnamaldehyde has previously been shown to inhibit
Cheanyeh Cheng et al.
Journal of chromatography. A, 1380, 1-10 (2015-01-08)
An online solid-phase microextraction coupled liquid chromatography-electrospray ionization-ion trap mass spectrometry was developed for the analysis of trace R- and S-4-phenyl-2-butanol (R- and S-pbol) in salt rich cell culture of Saccharomyces cerevisiae catalyzed stereoselective reduction of 4-pheny-2-butanone (pbone). A Supel-Q

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