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Merck
CN

111236

trans-2-Octene

97%

Synonym(s):

β-trans-Octene, (2E)-2-Octene, (E)-2-Octene

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About This Item

Linear Formula:
CH3(CH2)4CH=CHCH3
CAS Number:
13389-42-9
Molecular Weight:
112.21
NACRES:
NA.22
PubChem Substance ID:
24847016
eCl@ss:
39010220
UNSPSC Code:
12352100
EC Number:
236-463-2
MDL number:
MFCD00009532
Beilstein/REAXYS Number:
1719497

Key Documents

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Product Name

trans-2-Octene, 97%

InChI key

ILPBINAXDRFYPL-HWKANZROSA-N

InChI

1S/C8H16/c1-3-5-7-8-6-4-2/h3,5H,4,6-8H2,1-2H3/b5-3+

SMILES string

CCCCC\C=C\C

vapor pressure

31 mmHg ( 37.7 °C)

assay

97%

refractive index

n20/D 1.413 (lit.)

bp

123 °C (lit.)

density

0.718 g/mL at 25 °C (lit.)

Quality Level

100

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General description

trans-2-Octene undergoes epoxidation with two manganese(III) porphyrin complexes by meta-chloroperbenzoic acid under catalytic reaction conditions in various solvents.

pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Danger

hcodes

H225,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

69.8 °F - closed cup

flash_point_c

21 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
MKCS2658
MKCT7739
MKCG1697
MKBS2659V
MKBP2395V

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Min Young Hyun et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(5), 1810-1818 (2012-11-28)
The participation of multiple active oxidants generated from the reactions of two manganese(III) porphyrin complexes containing electron-withdrawing and -donating substituents with peroxyphenylacetic acid (PPAA) as a mechanistic probe was studied by carrying out catalytic oxidations of cyclohexene, 1-octene, and ethylbenzene
Aleksandr Fridlyand et al.
The journal of physical chemistry. A, 119(28), 7559-7577 (2015-02-25)
The high pressure and temperature oxidation of methyl trans-2-nonenoate, methyl trans-3-nonenoate, 1-octene, and trans-2-octene are investigated experimentally to probe the influence of the double bond position on the chemical kinetics of long esters and alkenes. Single pulse shock tube experiments

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