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Merck
CN

44095

Supelco

1-十二烷醇

Selectophore, ≥98.0%

别名:

十二碳醇, 十二醇, 月桂醇

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About This Item

线性分子式:
CH3(CH2)11OH
CAS号:
分子量:
186.33
Beilstein:
1738860
EC 号:
MDL编号:
UNSPSC代码:
26111700
eCl@ss:
39020229
PubChem化学物质编号:
NACRES:
NA.05
等级:
for ion-selective electrodes
方案:
≥98.0% (GC)
≥98.0%
沸点:
260-262 °C (lit.)
蒸汽压:
0.1 mmHg ( 20 °C)

等级

for ion-selective electrodes

质量水平

蒸汽密度

7.4 (vs air)

蒸汽压

0.1 mmHg ( 20 °C)

产品线

Selectophore

方案

≥98.0% (GC)
≥98.0%

自燃温度

500 °F

expl. lim.

4 %

折射率

n20/D 1.442 (lit.)

沸点

260-262 °C (lit.)

mp

22-26 °C (lit.)

密度

0.833 g/mL at 25 °C (lit.)

SMILES字符串

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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一般描述

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

应用

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).

法律信息

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

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

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

249.8 °F - closed cup

闪点(°C)

121 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

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)
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

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