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Merck
CN

464473

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
NACRES:
NA.22
PubChem Substance ID:
24870185
UNSPSC Code:
12352100
EC Number:
219-370-1
MDL number:
MFCD00060903

Key Documents

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Product Name

2-Hexyl-1-decanol, 97%

InChI key

XULHFMYCBKQGEE-UHFFFAOYSA-N

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

SMILES string

CCCCCCCCC(CO)CCCCCC

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.)

functional group

hydroxyl

Quality Level

100

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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).

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.

Storage Class

10 - Combustible liquids

wgk

nwg

flash_point_f

318.2 °F - closed cup

flash_point_c

159 °C - closed cup

ppe

Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBP1687V
12123BU
09421KQ

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Deepak Jadhav et al.
ChemSusChem, 10(11), 2527-2533 (2017-04-14)
Growing concern with the effects of CO
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)
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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