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Merck
CN

A83407

(S)-(−)-2-Methylbutanol

99%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C5H12O
CAS Number:
Molecular Weight:
88.15
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-366-1
Beilstein/REAXYS Number:
1718809
MDL number:
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Product Name

(S)-(−)-2-Methylbutanol, 99%

InChI

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

InChI key

QPRQEDXDYOZYLA-YFKPBYRVSA-N

SMILES string

CC[C@H](C)CO

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

Quality Level

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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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

108.5 °F

flash_point_c

42.5 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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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
Synthesis and liquid crystalline investigation of chiral 6-alkoxy-2-naphathoic acid derivatives
Chothani NJ, et al.
Liq. Cryst., 43(11), 1636-1648 (2016)
Aldrichimica Acta, 13, 13-13 (1980)

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