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Safety Information

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:
112-53-8
Molecular Weight:
186.33
Beilstein:
1738860
EC Number:
203-982-0
MDL number:
MFCD00004753
UNSPSC Code:
12352104
PubChem Substance ID:
329751611

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
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H319,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

249.8 °F - closed cup

Flash Point(C)

121 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

18-0320-5-500G-J:

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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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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