258741
1-十六烷醇
ReagentPlus®, 99%
别名:
棕榈醇, 鲸蜡醇
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线性分子式:
CH3(CH2)15OH
化学文摘社编号:
分子量:
242.44
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
253-149-0
Beilstein/REAXYS Number:
1748475
MDL number:
Assay:
99%
Bp:
179-181 °C/10 mmHg (lit.)
Vapor pressure:
<0.01 mmHg ( 43 °C)
产品名称
1-十六烷醇, ReagentPlus®, 99%
InChI key
BXWNKGSJHAJOGX-UHFFFAOYSA-N
InChI
1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3
SMILES string
CCCCCCCCCCCCCCCCO
vapor density
8.34 (vs air)
vapor pressure
<0.01 mmHg ( 43 °C)
product line
ReagentPlus®
assay
99%
form
solid
autoignition temp.
483 °F
expl. lim.
8 %
dilution
(for general lab use)
bp
179-181 °C/10 mmHg (lit.)
mp
48-50 °C (lit.)
solubility
ethanol: soluble 100 mL/mL, clear to very slightly hazy, colorless
density
0.818 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
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Application
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
General description
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。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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 produce 1-hexadecanol from xylose
Guo, et al.
Microbial cell factories, 15, 1-11 (2016)
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)
Metabolic engineering of Saccharomyces cerevisiae to improve 1-hexadecanol production
Feng, et al.
Metabolic engineering, 27, 10-19 (2015)
S Karen Gomez et al.
BMC plant biology, 9, 10-10 (2009-01-24)
Most vascular flowering plants have the capacity to form symbiotic associations with arbuscular mycorrhizal (AM) fungi. The symbiosis develops in the roots where AM fungi colonize the root cortex and form arbuscules within the cortical cells. Arbuscules are enveloped in
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