Skip to Content
Merck
All Photos(1)

Key Documents

A83407

Sigma-Aldrich

(S)-(−)-2-Methylbutanol

99%

Synonym(s):

(S)-(−)-2-Methyl-1-butanol, Active amyl alcohol

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H12O
CAS Number:
Molecular Weight:
88.15
Beilstein:
1718809
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

optical activity

[α]23/D −5.8°, neat

refractive index

n/D 1.41

bp

129-131 °C (lit.)

density

0.819 g/mL at 20 °C (lit.)
0.811 g/mL at 25 °C

SMILES string

CC[C@H](C)CO

InChI

1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3/t5-/m0/s1

InChI key

QPRQEDXDYOZYLA-YFKPBYRVSA-N

Looking for similar products? Visit Product Comparison Guide

Application

(S)-(−)-2-Methylbutanol can be used to prepare:
  • (S)-(−)-2-Methyl-1-butyloxy carbonyl amino hexyl isocyanate (MBI), which is used to synthesize isocyanate copolymers.
  • Chiral alkoxynaphathoic acid derivatives having liquid crystalline properties.
  • 3,4-Bis[(S)-2-methylbutoxy]thiophene, a key intermediate for the synthesis of polythiophenes.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Flam. Liq. 3 - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

108.5 °F

Flash Point(C)

42.5 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Synthesis and liquid crystalline investigation of chiral 6-alkoxy-2-naphathoic acid derivatives
Chothani NJ, et al.
Liq. Cryst., 43(11), 1636-1648 (2016)
On the origin of optical activity in polythiophenes
Langeveld-Voss BMW, et al.
Journal of Molecular Structure, 521(1-3), 285-301 (2000)
Anionic polymerization of isocyanates with optical functionalities.
Shin YD, et al.
Polymer, 42(19), 7979-7985 (2001)
Lawrence M Hanks et al.
Journal of economic entomology, 112(5), 2236-2252 (2019-05-29)
We present research on the chemical ecology of 14 species of longhorned beetles (Coleoptera: Cerambycidae), in four tribes of the subfamily Cerambycinae, conducted in east-central Illinois over 8 yr. Adult males produce aggregation-sex pheromones that attract both sexes. Twenty independent
Aldrichimica Acta, 13, 13-13 (1980)

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