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Safety Information

111147

Sigma-Aldrich

3-Methyl-1-pentene

99%

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About This Item

Linear Formula:
CH3CH2CH(CH3)CH=CH2
CAS Number:
Molecular Weight:
84.16
Beilstein:
1719110
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39010211
PubChem Substance ID:
NACRES:
NA.22

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

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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

Signal Word

Danger

Hazard Statements

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-16.6 °F - closed cup

Flash Point(C)

-27 °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

111147-1G:
111147-VAR:
111147-10G:
111147-BULK:
111147-5G:


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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

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