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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:
5333-42-6
Molecular Weight:
298.55
EC Number:
226-242-9
MDL number:
MFCD01310428
UNSPSC Code:
12352100
PubChem Substance ID:
24870186
NACRES:
NA.22

Quality Level

100

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.)

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.

WGK

nwg

Flash Point(F)

370.4 °F

Flash Point(C)

188 °C

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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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
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
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)
Contact sensitivity to octyldodecanol and trometamol in an anti-itch cream.
M Singh et al.
Contact dermatitis, 56(5), 289-290 (2007-04-20)
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