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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:
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

Signal Word

Warning

Hazard Statements

H226

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

114.8 °F - closed cup

Flash Point(C)

46 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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
Kenji Gomi et al.
Plant molecular biology, 53(1-2), 189-199 (2004-02-06)
An expression profile of genes induced by non-pathogenic Alternaria alternata on rough lemon leaves was obtained by sequencing 500 subtractive PCR clones generated from mRNA of leaves inoculated with the fungus after subtraction with that of non-inoculated leaves. About 6%
Zhi-Xia Zheng et al.
Electrophoresis, 25(18-19), 3263-3269 (2004-10-09)
A novel chiral microemulsion, which involved the use of chiral alcohols as cosurfactants, was demonstrated for the enantiomeric separation of a number of pharmaceutical drugs in microemulsion electrokinetic chromatography (MEEKC). The chiral alcohols investigated were optically active 2-alkanols, with the
S J Crosbie et al.
Human & experimental toxicology, 16(3), 131-137 (1997-03-01)
1. The in vitro metabolism of n-hexane was studied in rat liver, lung, brain and skeletal muscle microsomes and in microsomes prepared from cell lines expressing human cytochrome P-450 2E1 or 2B6. The hydroxylated metabolites of n-hexane were quantified by
B Mortensen et al.
Pharmacology & toxicology, 81(1), 35-41 (1997-07-01)
In vitro systems of high biological organization, e.g. containing intact hepatocytes, have been considered as more reliable for metabolic studies and in vivo predictions of toxicokinetics than subcellular systems. For this reason, the kinetics and metabolism of low-molecular-weight volatile chemicals
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