464481
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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-242-9
MDL number:
Assay:
97%
InChI key
LEACJMVNYZDSKR-UHFFFAOYSA-N
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
SMILES string
CCCCCCCCCCC(CO)CCCCCCCC
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
Quality Level
Related Categories
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
10 - Combustible liquids
wgk
nwg
flash_point_f
370.4 °F - open cup
flash_point_c
188 °C - open cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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
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)
Contact sensitivity to octyldodecanol and trometamol in an anti-itch cream.
M Singh et al.
Contact dermatitis, 56(5), 289-290 (2007-04-20)
R S Lanigan
International journal of toxicology, 20 Suppl 3, 51-59 (2002-01-05)
Octyldodecyl Stearoyl Stearate functions as an occlusive skin-conditioning agent and as a nonaqueous viscosity-increasing agent in many cosmetic formulations. Current concentrations of use are between 0.7% and 23%, although historically higher concentrations were used. The chemical is formed by a
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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