O4504
2-Octanol
97%
Synonym(s):
sec-Caprylic alcohol, Capryl alcohol, Ethyl-N-amylcarbinol, Ethylpentylcarbinol
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All Photos(2)
About This Item
Linear Formula:
CH3(CH2)5CH(OH)CH3
CAS Number:
Molecular Weight:
130.23
EC Number:
MDL number:
UNSPSC Code:
12352104
PubChem Substance ID:
NACRES:
NA.21
Assay:
97%
bp:
174-181 °C (lit.)
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Quality Level
Assay
97%
form
liquid
expl. lim.
0.34-6.3 %
refractive index
n20/D 1.426 (lit.)
bp
174-181 °C (lit.)
mp
-38 °C
density
0.819 g/mL at 25 °C (lit.)
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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General description
2-Octanol is a secondary alcohol that can be oxidized by nitric acid to form 2-octanone. The performance of Al-Cu and Al-Cu-Mg mixed oxides to catalyze the dehydrogenation of 2-octanol has been investigated. The reaction kinetics of the formation of ammonium sec-octyl sulfate by reaction of 2-octanol with sulfamic acid has been reported.
Application
2-Octanol may be used as a reducer in the preparation of monodispersed nickel nanocrystals.
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
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Size-controlled monodispersed nickel nanocrystals using 2-octanol as reducing agent.
Huaman JLC, et al.
CrystEngComm, 15(4), 729-737 (2013)
The nitric acid oxidation of 2-octanol. A model reaction for multiple heterogeneous liquid-liquid reactions.
Van Woezik BAA and Westerterp KR.
Chemical Engineering and Processing, 39(6), 521-537 (2000)
A Study of the Kinetics of the Sulfation of 2-Octanol by Sulfamic Acid.
Ho WH.
J. Chin. Chem. Soc., 34(4), 257-261 (1987)
Runaway behavior and thermally safe operation of multiple liquid-liquid reactions in the semi-batch reactor: The nitric acid oxidation of 2-octanol.
Van Woezik BAA and Westerterp KR.
Chemical Engineering and Processing, 41(1), 59-77 (2002)
Characterization of Al-Cu and Al-Cu-Mg mixed oxides and their catalytic activity in dehydrogenation of 2-octanol.
Crivello M, et al.
Catalysis Today, 107, 215-222 (2005)
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