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Merck
CN

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:
5333-42-6
Molecular Weight:
298.55
NACRES:
NA.22
PubChem Substance ID:
24870186
UNSPSC Code:
12352100
EC Number:
226-242-9
MDL number:
MFCD01310428
Assay:
97%

Key Documents

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Product Name

2-Octyl-1-dodecanol, 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

100

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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.

General description

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

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCX8095
MKCC3645
MKBX5301V
MKBS8301V
MKBS0287V

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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)
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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)
Adriana Gámbaro et al.
Journal of cosmetic science, 57(6), 455-463 (2007-01-27)
Nine formulations to be used as stick bases were manufactured using sodium stearate, propyleneglycol, and water, adding different concentrations of the following conditioning agents: octyldodecanol, PPG-5-ceteth-20, and PPG-15-stearyl ether. Free-choice-profile methodology was used to select the most adequate concentration of
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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