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464481

Sigma-Aldrich

2-Octyl-1-dodecanol

97%

Synonym(s):

Octyldodecanol

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About This Item

Linear Formula:
CH3(CH2)9CH[(CH2)7CH3]CH2OH
CAS Number:
Molecular Weight:
298.55
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.453 (lit.)

bp

234-238 °C/33 mmHg (lit.)

mp

−1-1 °C (lit.)

density

0.838 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

CCCCCCCCCCC(CO)CCCCCCCC

InChI

1S/C20H42O/c1-3-5-7-9-11-12-14-16-18-20(19-21)17-15-13-10-8-6-4-2/h20-21H,3-19H2,1-2H3

InChI key

LEACJMVNYZDSKR-UHFFFAOYSA-N

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General description

2-Octyl-1-dodecanol is a branched alcohol.

Application

2-Octyl-1-dodecanol may be used to investigate its interaction with the hexameric capsules of resorcin[4]arene. It has been used as diluent in a extractant screening study for the recovery of putrescine (butylene-1,4-diamine, BDA) and cadaverine (pentylene-1,5-diamine, PDA) from aqueous solutions (fermentation broths) by liquid-liquid extraction.

Storage Class Code

10 - Combustible liquids

WGK

nwg

Flash Point(F)

370.4 °F - open cup

Flash Point(C)

188 °C - open cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Strontium removal by new alkyl phenylphosphonic acids in supported liquid membranes with strip dispersion.
Ho WSW and Wang W.
Industrial & Engineering Chemistry Research, 41(3), 381-388 (2002)
Extractive recovery of aqueous diamines for bio-based plastics production.
Krzyzaniak A, et al.
Journal of Chemical Technology and Biotechnology, 88(10), 1937-1945 (2013)
Nancy Sharma et al.
Artificial cells, nanomedicine, and biotechnology, 45(3), 409-413 (2016-03-26)
The objective of present work was to enquire the potential use of embelin-loaded nanolipid carriers for brain targeting. The average particle size and polydispersity index (PDI) of optimized formulation (F19) were found to be 152 ± 19.7 nm and 0.143 ± 0.023, respectively. Nanolipid carrier
Contact sensitivity to octyldodecanol and trometamol in an anti-itch cream.
M Singh et al.
Contact dermatitis, 56(5), 289-290 (2007-04-20)
Ikuhiro Kakubari et al.
Biological & pharmaceutical bulletin, 29(8), 1717-1722 (2006-08-02)
Skin permeation of formoterol fumarate (FF) and irritation with ethylene-vinyl acetate (EVA) copolymer matrix patches was investigated using rat and human skin in vitro and different species of experimental animal, respectively. Skin permeation of FF increased remarkably without addition of

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