74858
(±)-2-Octanol
ReagentPlus®, ≥99.5% (GC)
Synonym(s):
Hexyl methyl carbinol
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About This Item
Linear Formula:
CH3(CH2)5CH(OH)CH3
CAS Number:
Molecular Weight:
130.23
Beilstein:
1719325
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
product line
ReagentPlus®
Assay
≥99.5% (GC)
form
liquid
refractive index
n20/D 1.426
density
0.819 g/mL at 20 °C (lit.)
functional group
hydroxyl
SMILES string
CCCCCCC(C)O
InChI
1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3
InChI key
SJWFXCIHNDVPSH-UHFFFAOYSA-N
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
159.8 °F - closed cup
Flash Point(C)
71 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Hiroaki Yamamoto et al.
Applied microbiology and biotechnology, 97(18), 8087-8096 (2013-01-01)
A novel enantioselective alcohol dehydrogenase, (R)-2-octanol dehydrogenase (PfODH), was discovered among methylotrophic microorganisms. The enzyme was purified from Pichia finlandica and characterized. The molecular mass of the enzyme was estimated to be 83,000 and 30,000 by gel filtration and sodium
P G Aitken et al.
Journal of neurophysiology, 80(3), 1514-1521 (1998-09-24)
Neuron membrane changes and ion redistribution during normoxic spreading depression (SD) induced, for example, by potassium injection, closely resemble those that occur during hypoxic SD-like depolarization (HSD) induced by oxygen withdrawal, but the degree to which the two phenomena are
Er-na Xun et al.
Applied biochemistry and biotechnology, 168(3), 697-707 (2012-08-01)
The lipase from Pseudomonas fluorescens (Lipase AK, AKL) was immobilized onto the magnetic Fe(3)O(4) nanoparticles via hydrophobic interaction. Enzyme loading and immobilization yield were determined as 21.4±0.5 mg/g and 49.2±1.8 %, respectively. The immobilized AKL was successfully used for resolution
Deracemization of secondary alcohols through a concurrent tandem biocatalytic oxidation and reduction.
Constance V Voss et al.
Angewandte Chemie (International ed. in English), 47(4), 741-745 (2007-12-12)
M Martinelle et al.
Biochimica et biophysica acta, 1251(2), 191-197 (1995-09-06)
The acyl transfer reactions catalysed by Candida antartica lipase B in organic media followed a bi-bi ping-pong mechanism, with competitive substrate inhibition by the alcohols used as acyl acceptors. The effect of organic solvents on Vm and Km was investigated.
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