Skip to Content
Merck
All Photos(3)

Documents

721123

Sigma-Aldrich

2-Methyl-2-butanol

anhydrous, ≥99%

Synonym(s):

tert-Amyl alcohol, tert-Pentyl alcohol

Sign Into View Organizational & Contract Pricing
All Photos(3)

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

Looking for similar products? Visit Product Comparison Guide

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBS0801
SHBR2779
SHBQ0250
SHBN6892
SHBM9306

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Teai, T.; Claude-Lafontaine, A. et al.
J. Essent. Oil Res., 13, 314-314 (2001)
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)
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service