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Merck
CN

111147

3-Methyl-1-pentene

99%

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About This Item

Linear Formula:
CH3CH2CH(CH3)CH=CH2
CAS Number:
Molecular Weight:
84.16
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39010211
UNSPSC Code:
12352100
EC Number:
212-076-4
MDL number:
Beilstein/REAXYS Number:
1719110
Assay:
99%
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vapor pressure

436 mmHg ( 37.7 °C)

assay

99%

refractive index

n20/D 1.384 (lit.)

bp

54 °C (lit.)

mp

−154 °C (lit.)

density

0.67 g/mL at 25 °C (lit.)

SMILES string

CCC(C)C=C

InChI

1S/C6H12/c1-4-6(3)5-2/h4,6H,1,5H2,2-3H3

InChI key

LDTAOIUHUHHCMU-UHFFFAOYSA-N

General description

3-Methyl-1-pentene has been synthesized by the pyrolysis of ethylene –butene-2 mixtures in a static system.

Application

3-Methyl-1-pentene has been used to study the rate constant of chlorine atom.


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

-16.6 °F - closed cup

flash_point_c

-27 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

危险化学品

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Kinetics of reactions of chlorine atoms with a series of alkenes at 1 atm and 298 K: structure and reactivity.
Ezell MJ, et al.
Physical Chemistry Chemical Physics, 4(23), 5813-5820 (2002)
Ene reactions of olefins. I. The addition of ethylene to 2-butene and the decomposition of 3-methylpentene-1.
International Journal of Chemical Kinetics, 10(3), 307-324 (1978)
Peter Tieu et al.
Frontiers in chemistry, 8, 599-599 (2020-08-06)
Metal nanoparticle catalysts functionalized with small, well-defined organic ligands are important because such systems can provide a spatial control in the catalyst-substrate interactions. This article describes the synthesis, stability, and catalytic property evaluations of four different Pd nanoparticles capped with



Global Trade Item Number

SKUGTIN
111147-10G04061837322617