Skip to Content
Merck
All Photos(1)

Key Documents

391751

Sigma-Aldrich

trans-4-Octene

technical grade, ≥90%

Sign Into View Organizational & Contract Pricing


About This Item

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

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

69.8 °F - closed cup

Flash Point(C)

21 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
A convenient, mild method for the cyclization of 3-and 4-arylalkanoic acids via their trifluoromethanesulfonic anhydride derivatives
Hulin B and Koreeda M.
The Journal of Organic Chemistry, 49(1), 207-209 (1984)
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)
Efficient hydride-assisted isomerization of alkenes via rhodium catalysis.
Morrill TC and D'Souza CA.
Organometallics, 22(8), 1626-1629 (2003)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service