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391751

Sigma-Aldrich

trans-4-Octene

technical grade, ≥90%

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Linear Formula:
CH3CH2CH2CH=CHCH2CH2CH3
CAS Number:
Molecular Weight:
112.21
Beilstein:
1719104
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Quality Level

Assay

≥90%

form

liquid

refractive index

n20/D 1.412 (lit.)

bp

122-123 °C (lit.)

solubility

water: insoluble

density

0.715 g/mL at 25 °C (lit.)

SMILES string

[H]\C(CCC)=C(\[H])CCC

InChI

1S/C8H16/c1-3-5-7-8-6-4-2/h7-8H,3-6H2,1-2H3/b8-7+

InChI key

IRUCBBFNLDIMIK-BQYQJAHWSA-N

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General description

trans-4-Octene is an acyclic olefin. Its synthesis has been reported. Its Raman spectra has been reported. Rate constant of the gas-phase reactions of trans-4-octene with hydroxyl radicals and ozone has been investigated. Its enantiomeric epoxidation has been studied. Its isomerization into isomeric octenes has been studied.

Application

trans-4-Octene may be used in the synthesis of the following:
  • n-nonanal
  • aliphatic unsaturated polyesters
  • 4-isopropyloctane
  • diasterioisomeric 4-(difluoroiodomethyl)-5-iodooctane
  • siliranes
  • m-dioxanes

Pictograms

FlameHealth hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 2

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The Stereochemistry of the Debromination of Vicinal Dibromides by Metals1.
Schubert WM, et al.
Journal of the American Chemical Society, 74(18), 4590-4592 (1952)
Raman Spectra of Hydrocarbons I. 1-Octene, cis+ trans 2-Octene, trans-3-Octene, trans-4-Octene, 4-Octyne, and 1-Octyne.
Cleveland FF.
J. Chem. Phys. , 11(1), 1-6 (1943)
Rate constants for the gas-phase reaction of ozone with 1, 2-disubstituted alkenes.
Grosjean E and Grosjean D.
International Journal of Chemical Kinetics, 28(6), 461-466 (1996)
Synthesis and characterization of aliphatic unsaturated polyesters from trans-4-octene-1, 8-dioic and trans-3-hexene-1, 6-dioic acids.
Maglio G et al.
Eur. Polymer J., 15(7), 695-699 (1979)
Synthesis, physicochemical studies and aerobic enantioselective epoxidation of non functionalized olefins catalyzed by new Co (II) chiral salen complexes.
Kureshy RI et al.
J. Mol. Catal. A: Chem., 121(1), 25-31 (1997)

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