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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
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
Signal Word
Danger
Hazard Statements
Precautionary 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
Regulatory Information
危险化学品
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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)
Efficient hydride-assisted isomerization of alkenes via rhodium catalysis.
Morrill TC and D'Souza CA.
Organometallics, 22(8), 1626-1629 (2003)
Friedel-Crafts alkylation of alkenes: ethylaluminum sesquichloride induced alkylations with alkyl chloroformates.
Biermann U and Metzger JO.
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 38(24), 3675-3677 (1999)
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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