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Merck
CN

447153

trans-3-Hexene

≥99%

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About This Item

Linear Formula:
C2H5CH=CHC2H5
CAS Number:
Molecular Weight:
84.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
236-261-4
Beilstein/REAXYS Number:
1718859
MDL number:
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Product Name

trans-3-Hexene, ≥99%

InChI key

ZQDPJFUHLCOCRG-AATRIKPKSA-N

InChI

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

SMILES string

CC\C=C\CC

assay

≥99%

refractive index

n20/D 1.394 (lit.)

bp

67 °C (lit.)

density

0.677 g/mL at 25 °C (lit.)

Quality Level

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pictograms

FlameHealth hazard

signalword

Danger

hcodes

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-13.0 °F - closed cup

flash_point_c

-25 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Synthesis and ene reactions of di-(-)-menthyl diazenedicarboxylate.
Brimble MA, et al.
Tetrahedron Asymmetry, 7(7), 2007-2016 (1996)
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)
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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