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447153

Sigma-Aldrich

trans-3-Hexene

≥99%

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About This Item

Linear Formula:
C2H5CH=CHC2H5
CAS Number:
13269-52-8
Molecular Weight:
84.16
Beilstein:
1718859
EC Number:
236-261-4
MDL number:
MFCD00009386
UNSPSC Code:
12352100
PubChem Substance ID:
24868321
NACRES:
NA.22

Assay

≥99%

refractive index

n20/D 1.394 (lit.)

bp

67 °C (lit.)

density

0.677 g/mL at 25 °C (lit.)

SMILES string

CC\C=C\CC

InChI

1S/C6H12/c1-3-5-6-4-2/h5-6H,3-4H2,1-2H3/b6-5+

InChI key

ZQDPJFUHLCOCRG-AATRIKPKSA-N

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accessory

Product No.
Description
Pricing

Pictograms

FlameHealth hazard
GHS02,GHS08

Signal Word

Danger

Hazard Statements

H225,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-13.0 °F - closed cup

Flash Point(C)

-25 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

JAN Code

447153-BULK:
447153-VAR:
447153-1G:
447153-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP5985
MKCL9691
MKCK7764
MKCG4653
MKBZ9803V

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Electronic effects of bis (2-aryl-4, 5, 6, 7-tetrahydroindenyl) titanocene dichlorides on the catalytic epoxidation of trans-3-hexene.
Halterman RL and Ramsey TM.
Journal of Organometallic Chemistry, 465(1), 175-179 (1994)
Synthesis and ene reactions of di-(-)-menthyl diazenedicarboxylate.
Brimble MA, et al.
Tetrahedron Asymmetry, 7(7), 2007-2016 (1996)
Study on the separation of 1-hexene and trans-3-hexene using ionic liquids.
Jiqin Z, et al.
Fluid Phase Equilibria, 247(1), 102-106 (2006)
Oligomers from the ozonolyses of cis-and trans-3-hexene and cis-and trans-2, 5-dimethyl-3-hexene
Murray RW and Su JS.
The Journal of Organic Chemistry, 48(6), 817-822 (1983)
Alla Zelenyuk et al.
Faraday discussions, 200, 143-164 (2017-06-06)
When secondary organic aerosol (SOA) particles are formed by ozonolysis in the presence of gas-phase polycyclic aromatic hydrocarbons (PAHs), their formation and properties are significantly different from SOA particles formed without PAHs. For all SOA precursors and all PAHs, discussed
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