hexyl alcohol

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hexyl alcohol

[′hek·səl ′al·kə‚hȯl]
(organic chemistry)
CH3(CH2)4CH2OH Colorless liquid boiling at 156°C; soluble in alcohol and ether, slightly soluble in water; used as a chemical intermediate for pharmaceuticals, perfume esters, and antiseptics.
References in periodicals archive ?
Ethyl acetate, ethyl hexanoate, ethyl octanoate, 2-methyl1-butanol, 3-methyl-1-butanol, 1-hexanol, 1-octanol, phenylethyl alcohol, and hexanoic acid were positively identified by comparing the spectra and chromatographic peak RIs of samples and analytical standards.
A conductometric study of Interaction between sodium dodecyl sulfate and 1-propanol, 1butanol, 1-pentanol and 1-hexanol at different temperatures.
6] alcohols--namely 1-hexanol, trans-2-hexenol, trans-3-hexenol, and cis-3-hexenol--were present in both free and bound form.
Structure 1 1-Hexanol 111-27-3 [FORMULA NOT REPRODUCIBLE IN ASCII] 2 1-Heptanol 111-70-6 [FORMULA NOT REPRODUCIBLE IN ASCII] Source 1-Octanol 111-87-5 [FORMULA NOT REPRODUCIBLE IN ASCII] 3 1-Nonanol 143-08-8 [FORMULA NOT REPRODUCIBLE IN ASCII] 4 1-Decanol 112-30-1 [FORMULA NOT REPRODUCIBLE IN ASCII] 5 1-Undecanol 112-42-5 [FORMULA NOT REPRODUCIBLE IN ASCII] Source 1-Dodecanol 112-53-8 [FORMULA NOT REPRODUCIBLE IN ASCII] 6 1-Tridecanol 112-70-9 [FORMULA NOT REPRODUCIBLE IN ASCII] Figure 4.
The reactivity order of alcohols was found to be methanol greater than ethanol greater than benzyl alcohol greater than 1-propanol greater than 1-butanol greater than 1-pentanol greater than 1-hexanol greater than 2-propanol.
1-hexanol 2-ethyl is produced on a massive scale as a precursor to an endocrine disrupting plasticizer DEHP.
20]) and authentic compounds including acetaldehyde, trans-2-decenal, 2-methylpropanal, 2-methylbutanal, 3-methylbutanal, pentanal, hexanal, heptanal, (E), 2-heptenal, 2-methylthiazole, benzaldehyde, octanal, benzeneacetaldehyde, nonanal, decanal, (E,E), 2,4-decadienal, ethanol, 1-propanol, 2-furanmethanol, 1-hexanol, 1-octen-3-ol, fufural, tetradecanal, 1-octanol, acetone, 2-propanone, 2,3-butanedione, 2-butanone, 2-heptanone, 3-octanone, dimethyldisulfide, pyrazine, methylpyrazine, 2,3-dimethylpyrazine etc.
To achieve this, the DOWANOL [TM] PnBGE and DOWANOL DPnP GE co-solvents present in the initial microemulsion were replaced with 1-butanol and 1-hexanol, which have lower boiling points, faster evaporation rates, and lower solubility in acrylic polymers.
The alkyl esters synthesis was evaluated as function of type of solvents used (n-hexane or t-butanol), type of alcohol used (methanol, 1-butanol, 1-hexanol, 1-octanol or ethane-1,2-diol (ethylene glycol), temperature (30, 40 and 50 [degrees]C), alcohol/RO molar ratio (1:4, unless specified otherwise) and in respect to stepwise addition of alcohol (single addition or two or three consecutive additions at different times), (Bernardes et al.
The researchers used inverse gas chromatography to assess five compounds: 1-hexanol, hexanal, (E)-2 hexenal, hexanone and hexane.