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128570

Sigma-Aldrich

2-Hexanol

99%

Synonym(s):

(±)-2-Hexanol, Butyl methyl carbinol

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About This Item

Linear Formula:
CH3(CH2)3CH(OH)CH3
CAS Number:
626-93-7
Molecular Weight:
102.17
Beilstein/REAXYS Number:
1718996
EC Number:
210-971-4
MDL number:
MFCD00004585
UNSPSC Code:
12352100
PubChem Substance ID:
24847868
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.414 (lit.)

bp

136 °C (lit.)

density

0.814 g/mL at 20 °C
0.81 g/mL at 25 °C (lit.)

SMILES string

CCCCC(C)O

InChI

1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3

InChI key

QNVRIHYSUZMSGM-UHFFFAOYSA-N

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General description

2-Hexanol is one of the constituent of Porella arboris-vitae extracts which has been determined by solid phase microextraction, gas chromatography-mass spectrometry (SPME GC-MS).

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

114.8 °F - closed cup

flash_point_c

46 °C - closed cup

ppe

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

Certificates of Analysis (COA)

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Amit Kumar Tyagi et al.
Evidence-based complementary and alternative medicine : eCAM, 2013, 382927-382927 (2013-02-01)
The chemical composition of Porella arboris-vitae extracts was determined by solid phase microextraction, gas chromatography-mass spectrometry (SPME GC-MS), and 66 constituents were identified. The dominant compounds in methanol extract of P. arboris-vitae were β-caryophyllene (14.7%), α-gurjunene (10.9%), α-selinene (10.8%), β-elemene
M Sakura et al.
Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 188(10), 787-797 (2002-12-06)
The capability of the cockroach Periplaneta americana to discriminate odors of structurally similar aliphatic alcohols was studied by using an operant conditioning paradigm. Cockroaches were trained to discriminate three odors: one odor associated with sucrose solution (reward) and two odors
P Manini et al.
Toxicology letters, 108(2-3), 225-231 (1999-10-08)
Since n-hexane metabolites are excreted as glucuronide conjugates, most conventional analytical procedures require preliminary hydrolysis, yielding to the 'total' 2,5-hexanedione (2,5-HD), but also giving rise to a number of artifacts. The whole pattern of n-hexane metabolites, both conjugated and unconjugated
M Madeja et al.
Archives of toxicology, 71(4), 238-242 (1997-01-01)
In order to study the mechanisms of acute n-hexane intoxication, the effects of n-hexane and its metabolites 2-hexanol, methyl-n-butyl ketone, 2,5-hexanediol and 2,5-hexanedione on the cloned voltage-operated potassium channels Kv1.1, Kv1.4, Kv2.1 and Kv3.4 were investigated with electrophysiological techniques in
S J Crosbie et al.
Human & experimental toxicology, 16(3), 138-145 (1997-03-01)
1. The role of skeletal muscle microsomes as a site of extrahepatic xenobiotic metabolism using n-hexane as a model substrate was investigated. The observed cytochrome P450-dependent metabolism was compared with that found with liver, and brain microsomal fractions. 2. Rat
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