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44095

Supelco

1-Dodecanol

Selectophore™, ≥98.0%

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:
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

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General description

1-Dodecanol is an n-alkano organic compound.
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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

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.

PRTR

Class I Designated Chemical Substances

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

44095-BULK:
44095-VAR:
44095-25G:
44095-5G:
44095-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF0024
BCCC1517
BCBW1615
BCBS1957V
BCBJ5943V

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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
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
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)
Mehdi Safdarian et al.
Journal of chromatography. A, 1244, 14-19 (2012-05-23)
A new temperature controlled cold column trapping (CCT) system was developed for in-line sequestration of organic phase in dispersive liquid-liquid microextraction (DLLME) method. In the developed CCT-DLLME method, the dispersed organic extraction phase is solidified and trapped in the CCT
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