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Key Documents

18-0320

Sigma-Aldrich

1-Dodecanol

SAJ special grade, ≥97.0%

Synonym(s):

Alcohol C12, Dodecyl alcohol, Lauryl alcohol

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About This Item

Linear Formula:
CH3(CH2)11OH
CAS Number:
Molecular Weight:
186.33
Beilstein/REAXYS Number:
1738860
EC Number:
MDL number:
UNSPSC Code:
12352104
PubChem Substance ID:

grade

SAJ special grade

vapor density

7.4 (vs air)

vapor pressure

0.1 mmHg ( 20 °C)

assay

≥97.0%

form

solid

autoignition temp.

500 °F

expl. lim.

4 %

availability

available only in Japan

refractive index

n20/D 1.442 (lit.)

bp

260-262 °C (lit.)

mp

22-26 °C (lit.)

density

0.833 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCO

InChI

1S/C12H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-12H2,1H3

InChI key

LQZZUXJYWNFBMV-UHFFFAOYSA-N

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pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

249.8 °F - closed cup

flash_point_c

121 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Chris Grant et al.
Biotechnology and bioengineering, 109(9), 2179-2189 (2012-04-05)
This article describes the first reported microwell whole-cell bioconversion using a water immiscible substrate that matches the specific activity and yield achieved in a 1.2 L stirred tank bioreactor. Maximum yields of 0.6 g/L(total) 1-dodecanol achieved in 24 h compare
Norbert V Heeb et al.
Chemosphere, 88(5), 655-662 (2012-04-24)
Pentabromocyclododecanols (PBCDOHs) are potential environmental transformation products of hexabromocyclododecanes (HBCDs). They are also potential stage one metabolites of biological HBCD transformations. Herein, we present analytical evidence that PBCDOHs are also constituents of technical HBCDs and flame-proofed polystyrenes (FP-PSs). PBCDOHs are
Shigemitsu Tanaka et al.
Bioresource technology, 116, 448-452 (2012-05-12)
A polytetrafluoroethylene (PTFE) membrane was used in membrane-assisted extractive (MAE) fermentation of acetone-butanol-ethanol (ABE) by Clostridium saccharoperbutylacetonicum N1-4. The growth inhibition effects of 1-dodecanol, which has a high partition coefficient for butanol, can be prevented by employing 1-dodecanol as an
Rebecca A Hall et al.
Eukaryotic cell, 10(8), 1034-1042 (2011-06-15)
Living as a commensal, Candida albicans must adapt and respond to environmental cues generated by the mammalian host and by microbes comprising the natural flora. These signals have opposing effects on C. albicans, with host cues promoting the yeast-to-hyphal transition
Kateřina Vávrová et al.
Pharmaceutical research, 28(12), 3105-3115 (2011-06-15)
Acyclic nucleoside phosphonates possess unique antiviral and antineoplastic activities; however, their polar phosphonate moiety is associated with low ability to cross biological membranes. We explored the potential of transdermal and topical delivery of 2,6-diaminopurine derivative cPr-PMEDAP. In vitro diffusion of

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