Skip to Content
Merck
CN

44095

1-Dodecanol

Selectophore, ≥98.0%

Synonym(s):

Alcohol C12, Dodecyl alcohol, Lauryl alcohol

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CH3(CH2)11OH
CAS Number:
Molecular Weight:
186.33
NACRES:
NA.05
PubChem Substance ID:
eCl@ss:
39020229
UNSPSC Code:
26111700
EC Number:
203-982-0
MDL number:
Beilstein/REAXYS Number:
1738860
Assay:
≥98.0% (GC)
≥98.0%
Bp:
260-262 °C (lit.)
Vapor pressure:
0.1 mmHg ( 20 °C)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

1-Dodecanol, Selectophore, ≥98.0%

InChI key

LQZZUXJYWNFBMV-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCCCCCCCCCO

vapor density

7.4 (vs air)

vapor pressure

0.1 mmHg ( 20 °C)

description

for ion-selective electrodes

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.)

Quality Level

Looking for similar products? Visit Product Comparison Guide

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).

General description

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

Legal Information

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

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
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
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

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