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Safety Information

129402

Sigma-Aldrich

3-Methyl-3-buten-1-ol

97%

Synonym(s):

3-Isopentenyl alcohol, Isoprenol

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About This Item

Linear Formula:
CH2=C(CH3)CH2CH2OH
CAS Number:
Molecular Weight:
86.13
Beilstein:
1071239
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.433 (lit.)

bp

130-132 °C (lit.)

density

0.853 g/mL at 25 °C (lit.)

SMILES string

CC(=C)CCO

InChI

1S/C5H10O/c1-5(2)3-4-6/h6H,1,3-4H2,2H3

InChI key

CPJRRXSHAYUTGL-UHFFFAOYSA-N

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Application

3-Methyl-3-buten-1-ol was used to study the rate coefficient for the gas-phase reaction of OH radical with 3-methyl-3-buten-1-ol.

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

107.6 °F - closed cup

Flash Point(C)

42 °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 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

129402-5ML:
129402-BULK:
129402-VAR:
129402-100ML:
129402-500ML:


Certificates of Analysis (COA)

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Pablo M Cometto et al.
The journal of physical chemistry. A, 112(19), 4444-4450 (2008-04-25)
Rate coefficients for the gas-phase reactions of OH radicals with four unsaturated alcohols, 3-methyl-3-buten-1-ol (k1), 2-buten-1-ol (k2), 2-methyl-2-propen-1-ol (k3) and 3-buten-1-ol (k4), were measured using two different techniques, a conventional relative rate method and the pulsed laser photolysis-laser induced fluorescence
Tian-He Wang et al.
Huan jing ke xue= Huanjing kexue, 32(12), 3599-3605 (2012-04-04)
Multiphase acid-catalyzed oxidation with hydrogen peroxide (H2O2) has been suggested recently to be a potential route to SOA formation, but the kinetics and chemical mechanism of this process have not been well-known yet. In this work, the uptake of 3-methyl-3-buten-1-ol
[Penetration of primary and tertiary alcohol isomers through rubber and isolated skin].
A L Mikhaleva et al.
Gigiena truda i professional'nye zabolevaniia, (11)(11), 46-47 (1982-01-01)

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