128570
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:
Molecular Weight:
102.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-971-4
Beilstein/REAXYS Number:
1718996
MDL number:
Assay:
99%
Form:
liquid
InChI key
QNVRIHYSUZMSGM-UHFFFAOYSA-N
InChI
1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3
SMILES string
CCCCC(C)O
assay
99%
form
liquid
Quality Level
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
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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).
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
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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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
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.
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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