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Sigma-Aldrich

2-Hexyl-1-decanol

97%

Synonym(s):

2-Hexyldecanol, 2-Hexyldecyl alcohol, 2-Octyl-1-octanol, Guerbet hexadecanol, Hexyldecanol, Hexyldecyl alcohol

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About This Item

Linear Formula:
CH3(CH2)7CH[(CH2)5CH3]CH2OH
CAS Number:
2425-77-6
Molecular Weight:
242.44
EC Number:
219-370-1
MDL number:
MFCD00060903
UNSPSC Code:
12352100
PubChem Substance ID:
24870185
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.449 (lit.)

bp

193-197 °C/33 mmHg (lit.)

mp

−21-−15 °C (lit.)

density

0.836 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCC(CO)CCCCCC

InChI

1S/C16H34O/c1-3-5-7-9-10-12-14-16(15-17)13-11-8-6-4-2/h16-17H,3-15H2,1-2H3

InChI key

XULHFMYCBKQGEE-UHFFFAOYSA-N

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General description

2-Hexyl-1-decanol is a branched alcohol. It is one of the constituent of the essential oil, extracted from the roots of Adiantum flabellulatum. It is a long-chain glass forming monohydroxy alcohol and its dielectric relaxation at low temperature has been studied.

Application

2-Hexyl-1-decanol may be employed as an organic solvent to study the extraction of non-polar acidic drugs from human plasma by parallel artificial liquid membrane extraction (PALME).

Storage Class Code

10 - Combustible liquids

WGK

nwg

Flash Point(F)

318.2 °F - closed cup

Flash Point(C)

159 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mercedes Roldán-Pijuán et al.
Analytical and bioanalytical chemistry, 407(10), 2811-2819 (2015-02-16)
The new sample preparation concept "Parallel artificial liquid membrane extraction (PALME)" was evaluated for extraction of the acidic drugs ketoprofen, fenoprofen, diclofenac, flurbiprofen, ibuprofen, and gemfibrozil from human plasma samples. Plasma samples (250 μL) were loaded into individual wells in
Composition of the essential oil of Adiantum flabellulatum.
Kang WY, et al.
Chemistry of Natural Compounds, 45(4), 575-577 (2009)
Deepak Jadhav et al.
ChemSusChem, 10(11), 2527-2533 (2017-04-14)
Growing concern with the effects of CO
Yanqin Gao et al.
The Journal of chemical physics, 139(16), 164504-164504 (2013-11-05)
The dielectric relaxation of two long-chain glass forming monohydroxy alcohols, 2-butyl-1-octanol and 2-hexyl-1-decanol, is studied at low temperature. Remarkable broadening from the pure Debye relaxation is identified for the slowest dynamics, differing from the dielectric spectra of short-chain alcohols. The

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