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82119

Sigma-Aldrich

Propylbenzene

≥99.0% (GC)

Synonym(s):

1-Phenylpropane

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About This Item

Linear Formula:
C6H5CH2CH2CH3
CAS Number:
103-65-1
Molecular Weight:
120.19
Beilstein:
1903006
EC Number:
203-132-9
MDL number:
MFCD00009377
UNSPSC Code:
12352100
PubChem Substance ID:
57652905
NACRES:
NA.22

vapor density

4.14 (vs air)

vapor pressure

2 mmHg ( 20 °C)

Assay

≥99.0% (GC)

form

liquid

autoignition temp.

842 °F

expl. lim.

6 %

refractive index

n20/D 1.491 (lit.)
n20/D 1.491

bp

159 °C (lit.)

mp

−99 °C (lit.)

density

0.862 g/mL at 25 °C (lit.)

SMILES string

CCCc1ccccc1

InChI

1S/C9H12/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3

InChI key

ODLMAHJVESYWTB-UHFFFAOYSA-N

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Related Categories

Signal Word

Danger

Hazard Statements

H226,H304,H335,H411

Precautionary Statements

P210 - P273 - P301 + P310 + P331

Hazard Classifications

Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 3 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

107.6 °F - closed cup

Flash Point(C)

42.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Q S Li et al.
FEBS letters, 508(2), 249-252 (2001-11-24)
We report here oxidation of propylbenzene and 3-chlorostyrene by wild-type cytochrome P450 BM-3 with high turnover (479 nmol 1-phenyl-1-propanol/min/nmol P450 and 300 nmol 3-chlorostyrene oxide/min/nmol P450). Furthermore, the residue size at position 87 of P450 BM-3 was found to play
J Schuberth
Journal of chromatographic science, 34(7), 314-319 (1996-07-01)
The full evaporation technique (FET), which is a variant of headspace analysis used to overcome matrix effects, was combined with capillary gas chromatography (GC) and ion-trap detection (ITD). The aim was to enable quantitative tests of volatile organic compounds (VOCs)
W L Backes et al.
Xenobiotica; the fate of foreign compounds in biological systems, 23(12), 1353-1366 (1993-12-01)
1. Treatment of male rat with the small aromatic hydrocarbons, benzene, toluene, ethylbenzene, n-propylbenzene, m-xylene, and p-xylene increased several P450-dependent activities, with ethylbenzene, m-xylene, and n-propylbenzene producing the greatest response. Hydrocarbon treatment differentially affected toluene metabolism, producing a response dependent
R Rabus et al.
Archives of microbiology, 163(2), 96-103 (1995-02-01)
Anaerobic degradation of alkylbenzenes with side chains longer than that of toluene was studied in freshwater mud samples in the presence of nitrate. Two new denitrifying strains, EbN1 and PbN1, were isolated on ethylbenzene and n-propylbenzene, respectively. For comparison, two
M J Huertas et al.
Applied and environmental microbiology, 64(1), 38-42 (1998-01-22)
We assayed the tolerance to solvents of three toluene-degrading Pseudomonas putida strains and Pseudomonas mendocina KR1 in liquid and soil systems. P. putida DOT-T1 tolerated concentrations of heptane, propylbenzene, octanol, and toluene of at least 10% (vol/vol), while P. putida
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