2-Hexanol

2-Hexanol Structure
2-Hexanol structure
Common Name 2-Hexanol
CAS Number 626-93-7 Molecular Weight 102.175
Density 0.8±0.1 g/cm3 Boiling Point 139.7±3.0 °C at 760 mmHg
Molecular Formula C6H14O Melting Point -23ºC
MSDS Chinese USA Flash Point 46.1±0.0 °C
Symbol GHS02 GHS07
GHS02, GHS07
Signal Word Warning

Convenient QSAR model for predicting the complexation of structurally diverse compounds with β-cyclodextrins

Bioorg. Med. Chem. 17 , 896-904, (2009)

This paper reports a QSAR study for predicting the complexation of a large and heterogeneous variety of substances (233 organic compounds) with beta-cyclodextrins (beta-CDs). Several different theoretical molecular descriptors, calculated solely from the mole...

Changes of n-hexane metabolites in urine of rats exposed to various concentrations of n-hexane and to its mixture with toluene or MEK.

Int. Arch. Occup. Environ. Health 53(1) , 1-8, (1983)

It is well known that n-hexane produces peripheral neuropathy, and 2,5-hexanedione, one of the metabolites of n-hexane, is thought to be the main causative agent. Recently, the metabolites of n-hexane in urine have been measured by gas chromatography, and 2,5...

Two-chiral-component microemulsion electrokinetic chromatography-chiral surfactant and chiral oil: part 1. dibutyl tartrate.

Electrophoresis 28(11) , 1723-34, (2007)

The first simultaneous use of a chiral surfactant and a chiral oil for microemulsion EKC (MEEKC) is reported. Six stereochemical combinations of dodecoxycarbonylvaline (DDCV: R, S, or racemic, 2.00% w/v), racemic 2-hexanol (1.65% v/v), and dibutyl tartrate (D...

Chiral microemulsion electrokinetic chromatography with two chiral components: Improved separations via synergies between a chiral surfactant and a chiral cosurfactant.

Electrophoresis 27(4) , 896-904, (2006)

In this study, the combination of two chiral components in a microemulsion formulation for the separation of enantiomers via microemulsion EKC (MEEKC) was successfully accomplished. Previous publications of chiral microemulsions have utilized only one chiral ...

[An experimental study on the neurotoxicity of 2-octanone and 2-hexanol, a metabolite of n-hexane].

Sangyo. Igaku. 24(5) , 475-84, (1982)

An electrophysiological study of the neurotoxicity of 2-octanone (an analogue of methyl n-butyl ketone) and 2-hexanol (a metabolite of n-hexane) was conducted on rats as a part of the study to determine the specific molecular arrangement required for the deve...

Differential involvement of glutamate-gated chloride channel splice variants in the olfactory memory processes of the honeybee Apis mellifera.

Pharmacol. Biochem. Behav. 124 , 137-44, (2014)

Glutamate-gated chloride channels (GluCl) belong to the cys-loop ligand-gated ion channel superfamily and their expression had been described in several invertebrate nervous systems. In the honeybee, a unique gene amel_glucl encodes two alternatively spliced ...

Effects of n-hexane and its metabolites on cloned voltage-operated neuronal potassium channels.

Arch. Toxicol. 71(4) , 238-42, (1997)

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 w...

Metabolism of n-hexane by rat liver and extrahepatic tissues and the effect of cytochrome P-450 inducers.

Hum. Exp. Toxicol. 16(3) , 131-7, (1997)

1. The in vitro metabolism of n-hexane was studied in rat liver, lung, brain and skeletal muscle microsomes and in microsomes prepared from cell lines expressing human cytochrome P-450 2E1 or 2B6. The hydroxylated metabolites of n-hexane were quantified by ga...

An investigation into the role of rat skeletal muscle as a site for xenobiotic metabolism using microsomes and isolated cells.

Hum. Exp. Toxicol. 16(3) , 138-45, (1997)

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 fra...

Olfactory discrimination of structurally similar alcohols by cockroaches.

J. Comp. Physiol. A. Neuroethol. Sens. Neural. Behav. Physiol. 188(10) , 787-97, (2002)

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 sucros...