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Key Documents

442274

Supelco

1-Octene

analytical standard

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About This Item

Linear Formula:
CH3(CH2)5CH=CH2
CAS Number:
Molecular Weight:
112.21
Beilstein/REAXYS Number:
1734497
MDL number:
UNSPSC Code:
23151816
PubChem Substance ID:

grade

analytical standard

Quality Level

vapor density

3.9 (vs air)

vapor pressure

36 mmHg ( 38 °C)

autoignition temp.

446 °F

feature

standard type Calibration

expl. lim.

3.9 %

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.408 (lit.)
n20/D 1.409 (lit.)

bp

122-123 °C (lit.)

mp

−101 °C (lit.)

density

0.715 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care
petroleum

format

neat

storage temp.

room temp

SMILES string

CCCCCCC=C

InChI

1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3

InChI key

KWKAKUADMBZCLK-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2

supp_hazards

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

69.8 °F

flash_point_c

21 °C


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F P Guengerich
Biochemical and biophysical research communications, 138(1), 193-198 (1986-07-16)
The heme in rat liver microsomal cytochrome P-450 was labeled with 14C or 3H and the microsomes were fractionated after in vitro incubations with a variety of agents known to destroy cytochrome P-450 heme. A major fraction of the heme
I N White et al.
Biochemical pharmacology, 35(9), 1569-1575 (1986-05-01)
The enzymic activation of a model olefin oct-1-ene was studied in rat liver microsomal systems in vitro. An active metabolite was trapped using N-acetylcysteine and identified by means of capillary GLC/mass spectrometry and 360 MHz 1H NMR as S-3-oxo-octyl-N-acetylcysteine. A
Sara M Aschmann et al.
Environmental science & technology, 44(10), 3825-3831 (2010-04-28)
Products of the gas-phase reactions of OH radicals with 1-octene and 7-tetradecene have been investigated at 296 +/- 2 K and atmospheric pressure of air, using gas chromatography, direct air sampling atmospheric pressure ionization tandem mass spectrometry, and in situ
A Hempel-Jørgensen et al.
Archives of environmental health, 54(2), 86-94 (1999-03-27)
In this study, we investigated the time course effect of sensory eye irritation in 16 subjects exposed (i.e., eye only) to n-butanol and 1-octene. Half the subjects were exposed to n-butanol, and the remaining subjects were exposed to 1-octene. Each
J C Quada et al.
Bioorganic & medicinal chemistry, 9(9), 2303-2314 (2001-09-13)
The syntheses of several novel halogenated bithiazoles structurally related to the bithiazole moiety of bleomycin A(5) are described. Also described is the ability of these compounds to mediate photoactivated DNA cleavage. Chlorinated bithiazole analogues were shown to be much more

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