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240486

Sigma-Aldrich

2-Methyl-2-butanol

ReagentPlus®, ≥99%

Synonym(s):

tert-Amyl alcohol, tert-Pentyl alcohol

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About This Item

Linear Formula:
CH3CH2C(CH3)2OH
CAS Number:
75-85-4
Molecular Weight:
88.15
Beilstein:
1361351
EC Number:
200-908-9
MDL number:
MFCD00004478
UNSPSC Code:
12352100
PubChem Substance ID:
24854418
NACRES:
NA.21

vapor density

3 (vs air)

Quality Level

100

vapor pressure

12 mmHg ( 20 °C)

product line

ReagentPlus®

Assay

≥99%

form

liquid

autoignition temp.

819 °F

expl. lim.

9 %

refractive index

n20/D 1.405 (lit.)

bp

102 °C (lit.)

mp

−12 °C (lit.)

density

0.805 g/mL at 25 °C (lit.)

SMILES string

CCC(C)(C)O

InChI

1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3

InChI key

MSXVEPNJUHWQHW-UHFFFAOYSA-N

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General description

2-Methyl-2-butanol is a sterically hindered alcohol.

Application

2-Methyl-2-butanol may be used as a solvent in the following processes:
  • Palladium (II)-catalyzed ortho-C–H olefination of phenylacetic acids.
  • Rhodium-catalyzed direct C-H functionalization at the C7 position of N-pivaloylindoles.

It may also be used in the preparation of 2-chloro-2-methylbutane by reacting with concentrated hydrochloric acid.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Central nervous system, Respiratory system

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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General kinetic modeling of the selective hydrogenation of 2-methyl-3-butyn-2-ol over a commercial palladium-based catalyst.
Vernuccio S, et al.
Industrial & Engineering Chemistry Research, 54(46), 11543-11551 (2015)
Yoon Ju Cho et al.
Laboratory animal research, 27(3), 197-203 (2011-10-15)
Tribromoethanol (2,2,2-tribromoethanol, TBE) is a popular injectable anesthetic agent used in mice in Korea. Our goal was to assess the risks associated with side effects (lesions) in the abdominal cavity, especially at high doses. To understand the underlying pathophysiological changes
?-tert-alkylation of ketones: 2-tert-pentylcyclopentanone
Organic Syntheses, 62, 95-95 (1984)
Rhodium?Catalyzed Regioselective C7?Functionalization of N?Pivaloylindoles.
Xu L, et al.
Angewandte Chemie (International Edition in English), 55(1), 321-325 (2016)
Ternary and Binary LLE Measurements for Solvent (4-Methyl-2-pentanone and 2-Methyl-2-butanol)+ Furfural+ Water between 298 and 401K.
Ma?nnisto? M, et al.
Journal of Chemical and Engineering Data, 61(2), 903-911 (2016)
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