527408
1,3-Hexadiene, mixture of cis and trans
95%
Synonym(s):
1-Ethyl-1,3-butadiene
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About This Item
Linear Formula:
C2H5CH=CHCH=CH2
CAS Number:
Molecular Weight:
82.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-759-4
MDL number:
Assay:
95%
Product Name
1,3-Hexadiene, mixture of cis and trans, 95%
InChI key
AHAREKHAZNPPMI-UHFFFAOYSA-N
InChI
1S/C6H10/c1-3-5-6-4-2/h3,5-6H,1,4H2,2H3
SMILES string
CCC=CC=C
assay
95%
refractive index
n20/D 1.438 (lit.)
bp
72-76 °C (lit.)
density
0.714 g/mL at 25 °C (lit.)
Quality Level
Related Categories
Application
- Ethylene-alt-alpha-Olefin Copolymers by Hydrogenation of Highly Stereoregular cis-1,4 Polydienes: A study on the synthesis and structural characterization of isotactic and syndiotactic polydienes, focusing on copolymers derived from cis-1,4 poly(1,3-hexadiene) (G Ricci et al., 2024).
- Syndiotactic Alternating Ethylene/Propylene Copolymers Obtained Through Non-Catalytic Hydrogenation of Highly Stereoregular cis-1,4 Poly(1,3-diene)s: This article elaborates on the properties of ethylene/propylene copolymers derived from the hydrogenation of 1,3-diene polymers, including 1,3-hexadiene (G Ricci et al., 2017).
- Novel cobalt dichloride complexes with hindered diphenylphosphine ligands: Research on catalytic systems for the polymerization of dienes including 1,3-hexadiene (G Ricci et al., 2019).
- Synthesis and Reactivity of Pyridine (diimine) Molybdenum Olefin Complexes: A detailed look at ethylene dimerization and alkene dehydrogenation processes involving 1,3-hexadiene as an intermediate (MV Joannou et al., 2017).
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-2.2 °F - closed cup
flash_point_c
-19 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Laura Torrente-Murciano et al.
Frontiers in chemistry, 2, 37-37 (2014-07-02)
The first example of a tandem reaction involving double-bond migration in combination with telomerization is reported. Homogeneous and heterogeneous Ru catalysts were employed as isomerization catalysts, and telomerization was realized using a homogeneous Pd(0) precursor complex with a N-heterocyclic carbene
Natori et al.
Macromolecules, 31(15), 4687-4694 (1998-07-29)
The n-butyllithium (n-BuLi)/N,N,N',N'-tetramethylethylenediamine (TMEDA) system (with the molar ratio of TMEDA to n-BuLi higher than 4/4) has been found to polymerize 1,3-cyclohexadiene to produce "living" polymer having a narrow molecular weight distribution with well-controlled polymer chain length. The rate of
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