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
Beilstein:
1718996
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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).
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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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
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
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
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
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