Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

44095

Supelco

1-Dodecanol

Selectophore™, ≥98.0%

Synonym(s):

Alcohol C12, Dodecyl alcohol, Lauryl alcohol

Sign Into View Organizational & Contract Pricing
All Photos(1)

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:
26111700
eCl@ss:
39020229
PubChem Substance ID:
329756451
NACRES:
NA.05

grade

for ion-selective electrodes

Quality Level

200

vapor density

7.4 (vs air)

vapor pressure

0.1 mmHg ( 20 °C)

product line

Selectophore™

Assay

≥98.0% (GC)
≥98.0%

autoignition temp.

500 °F

expl. lim.

4 %

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

Looking for similar products? Visit Product Comparison Guide

General description

1-Dodecanol is an n-alkano organic compound.
Visit our Sensor Applications portal to learn more.

Application

It is may be used to investigate the thermal properties of caprylic acid using differential scanning calorimetry. It may also be used as extraction solvent during determination of five kinds of polycyclic aromatic hydrocarbons in water samples, using dispersive liquid-liquid microextraction based on solidification of floating organic droplet method (DLLME-SFO).

Legal Information

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCK7720
BCCF0024
BCCC1517
BCBW1615
BCBS1957V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Thermal performance of caprylic acid/1-dodecanol eutectic mixture as phase change material (PCM).
Zuo, Jianguo, Weizhong Li, and Lindong Weng
Energy and Buildings, 43.1, 207-210 (2011)
Hui Xu et al.
Analytica chimica acta, 636(1), 28-33 (2009-02-24)
A new dispersive liquid-liquid microextraction based on solidification of floating organic droplet method (DLLME-SFO) was developed for the determination of five kinds of polycyclic aromatic hydrocarbons (PAHs) in environmental water samples. In this method, no specific holder, such as the
Samuel D Banister et al.
Bioorganic & medicinal chemistry letters, 21(12), 3622-3626 (2011-05-11)
A series of N-substituted 4-azahexacyclo[5.4.1.0(2,6).0(3,10).0(5,9).0(8,11)]dodecan-3-ols incorporating the respective arylalkyl subunits from several known sigma (σ) receptor ligands were synthesized and evaluated for their affinity against σ receptors and dopamine receptors. The hybrid trishomocubane-derived ligands (4-6) showed good selectivity for σ(1)
Kun Liu et al.
Journal of chromatography. A, 1227, 96-104 (2012-01-24)
Seven crosslinking monomers, i.e., 1,3-butanediol dimethacrylate (1,3-BDDMA), 1,4-butanediol dimethacrylate (1,4-BDDMA), neopentyl glycol dimethacrylate (NPGDMA), 1,5-pentanediol dimethacrylate (1,5-PDDMA), 1,6-hexanediol dimethacrylate (1,6-HDDMA), 1,10-decanediol dimethacrylate (1,10-DDDMA), and 1,12-dodecanediol dimethacrylate (1,12-DoDDMA), were used to synthesize highly cross-linked monolithic capillary columns for reversed-phase liquid chromatography
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service