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721123

Sigma-Aldrich

2-Methyl-2-butanol

anhydrous, ≥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:
12352001
PubChem Substance ID:
329763822
NACRES:
NA.21

grade

anhydrous

Quality Level

100

vapor density

3 (vs air)

Assay

≥99%

form

liquid

autoignition temp.

819 °F

expl. lim.

9 %

impurities

≤0.003% water (Karl Fischer, all unit sizes greater than 100 mL)
≤0.005% water (100 mL pkg)

evapn. residue

≤0.0005%

refractive index

n20/D 1.405 (lit.)

pH

6.0 (20 °C, 118 g/L)

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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Application

tert-Amyl alcohol is useful as organic solvent chemical intermediates for gasoline fuel additives, food flavor, pharmaceutical peroxy esters, ink composition, and stabilizer in rubber productions.

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

68.9 °F - closed cup

Flash Point(C)

20.5 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS0801
SHBR2779
SHBQ0250
SHBN6892
SHBM9306

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Torsten Weil et al.
Organic letters, 10(8), 1513-1516 (2008-03-28)
We present a mild and efficient method for the completely regioselective alcoholysis of styrene oxides utilizing a cooperative Brønsted acid-type organocatalytic system comprised of mandelic acid (1 mol %) and N,N'-bis-[3,5-bis-(trifluoromethyl)phenyl]-thiourea (1 mol %). Various styrene oxides are readily transformed
Funk, R.L.; Daily, W.J.; Parvez, D.M.
The Journal of Organic Chemistry, 53, 4143-4143 (1998)
Teai, T.; Claude-Lafontaine, A. et al.
J. Essent. Oil Res., 13, 314-314 (2001)
Chen, C.-X., Wu, Q.
Enz. Microbiol. Technol., 42, 601-601 (2008)
Wouter F Slotema et al.
Biotechnology and bioengineering, 82(6), 664-669 (2003-04-04)
An economically pertinent process for the lipase-catalyzed synthesis of amides was developed. A continuous plug flow reactor was used. The model reaction was the production of oleamide, a lubricant and anti-slip agent, via direct Candida antarctica lipase B-catalyzed amidation of
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