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128570

Sigma-Aldrich

2-Hexanol

99%

Sinónimos:

(±)-2-Hexanol, Butyl methyl carbinol

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About This Item

Fórmula lineal:
CH3(CH2)3CH(OH)CH3
Número de CAS:
626-93-7
Peso molecular:
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.)

functional group

hydroxyl

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

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Certificados de análisis (COA)

Lot/Batch Number
SHBS2056
SHBR1754
SHBR1753
SHBN1139
SHBH9898

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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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
C P Granvil et al.
Toxicology letters, 70(3), 263-267 (1994-02-15)
The metabolic fate of methyl n-butyl ketone (MnBK) and its isomer methyl isobutyl ketone (MiBK) was studied in mice. The concentrations of both ketones and their metabolites in blood and brain were measured at different time intervals after their administration.
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