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Merck
CN

258741

Sigma-Aldrich

1-十六烷醇

ReagentPlus®, 99%

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别名:
棕榈醇, 鲸蜡醇
线性分子式:
CH3(CH2)15OH
CAS号:
分子量:
242.44
Beilstein:
1748475
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

蒸汽密度

8.34 (vs air)

质量水平

蒸汽压

<0.01 mmHg ( 43 °C)

产品线

ReagentPlus®

检测方案

99%

形式

solid

自燃温度

483 °F

expl. lim.

8 %

bp

179-181 °C/10 mmHg (lit.)

mp

48-50 °C (lit.)

溶解性

ethanol: soluble 100 mL/mL, clear to very slightly hazy, colorless

密度

0.818 g/mL at 25 °C (lit.)

SMILES字符串

CCCCCCCCCCCCCCCCO

InChI

1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3

InChI key

BXWNKGSJHAJOGX-UHFFFAOYSA-N

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一般描述

1-十六醇是一种脂肪醇,用于表面活性剂、润滑剂、去污剂、药物和化妆品中。

应用

1-十六醇已用于制备:
  • (±)-2-甲氧基十七烷酸(脂肪酸)
  • 1-十六烷醇的高链脂肪酸酯,用于热能储存的新型有机相变材料
  • 十六烷(烷烃)存在于弗尼斯弧菌 M1 膜组分中

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Metabolic engineering of Saccharomyces cerevisiae to produce 1-hexadecanol from xylose
Guo, et al.
Microbial cell factories, 15, 1-11 (2016)
Néstor M Carballeira et al.
Pure and applied chemistry. Chimie pure et appliquee, 84(9), 1867-1875 (2012-11-03)
The fatty acids (±)-2-methoxy-6Z-heptadecenoic acid (1), (±)-2-methoxy-6-heptadecynoic acid (2) and (±)-2-methoxyheptadecanoic acid (3) were synthesized and their inhibitory activity against the Leishmania DNA topoisomerase IB enzyme (LdTopIB) determined. Acids 1 and 2 were synthesized from 4-bromo-1-pentanol, the former in ten
Metabolic engineering of Saccharomyces cerevisiae to improve 1-hexadecanol production
Feng, et al.
Metabolic engineering, 27, 10-19 (2015)
High-chain fatty acid esters of 1-hexadecanol for low temperature thermal energy storage with phase change materials.
Aydin AA and Aydin A.
Solar Energy Mat. and Solar Cells, 96, 93-100 (2012)
Myong-Ok Park
Journal of bacteriology, 187(4), 1426-1429 (2005-02-03)
Alkane biosynthesis in the bacterium Vibrio furnissii M1 involves the synthesis of long-chain alkanes via 1-alcohol. Evidence for this novel pathway are the following. (i) Both even- and odd-carbon-number n-alkanes were produced from glucose, while only even-carbon-number fatty acids were

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