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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:
Product Name
2-Hexanol, 99%
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
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
Quality Level
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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
Regulatory Information
危险化学品
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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 A Chaput
Physiology & behavior, 36(2), 319-324 (1986-01-01)
The "across-neuron pattern" theory of olfactory information coding states that odorants are represented by spatial patterns of activity produced across-neurons in the olfactory bulbs. The present study analyzes the different response patterns encoding olfactory information in both the inspiratory and
C G Galizia et al.
The European journal of neuroscience, 10(9), 2964-2974 (1998-10-03)
The primary olfactory neuropil, the antennal lobe (AL) in insects, is organized in glomeruli. Glomerular activity patterns are believed to represent the across-fibre pattern of the olfactory code. These patterns depend on an organized innervation from the afferent receptor cells
J K Alifimoff et al.
Anesthesiology, 66(1), 55-59 (1987-01-01)
The Meyer-Overton rule has been interpreted to mean that general anesthetics act at a nonpolar site, either in a lipid bilayer or a protein. Optical isomers, also called enantiomers, are pairs of compounds with the same molecular formula and functional
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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