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Merck
CN

B402

Sigma-Aldrich

鲨肝醇

99%

别名:

1-O-十八烷基-rac-甘油, rac-1-十八烷基甘油醚, DL-3-十八烷氧基-1,2-丙二醇

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关于此项目

线性分子式:
CH3(CH2)17OCH2CH(OH)CH2OH
化学文摘社编号:
分子量:
344.57
Beilstein:
1725677
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案

99%

表单

powder

mp

71-73 °C (lit.)

SMILES字符串

CCCCCCCCCCCCCCCCCCOCC(O)CO

InChI

1S/C21H44O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-24-20-21(23)19-22/h21-23H,2-20H2,1H3

InChI key

OGBUMNBNEWYMNJ-UHFFFAOYSA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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M Vanisree et al.
Journal of Asian natural products research, 3(1), 23-29 (2001-05-18)
A new ceramide, (2S,3R,4E)-1,3-dihydroxy-2-[(hexadecanoyl)amino]-nonadeca-4-ene (1), cholest-5-en-3beta,7beta,19-triol (2), identified as its, peracetyl derivative (3), and batyl alcohol (4) were isolated from Pseudopterogorgia species. 1 exhibited antibacterial activity against Gram-positive and Gram-negative bacteria.
G Schrakamp et al.
Journal of lipid research, 29(3), 325-334 (1988-03-01)
In recent years a growing number of inherited diseases have been recognized to originate from an impairment in one or more peroxisomal functions. Since it is well established that the first two steps in the biosynthesis of plasmalogens proceed in
Asymmetric synthesis of (+)- and (-)-batyl alcohol, a key synthetic intermediate for platelet-activating factor, by using biocatalysts.
H Suemune et al.
Chemical & pharmaceutical bulletin, 35(8), 3112-3118 (1987-08-01)
L Ahrné et al.
Journal of dairy science, 65(10), 1905-1911 (1982-10-01)
[Hydrogen-3] glycerol ether and [carbon-14] hexadecanol were infused into the mammary gland or jugular vein of cows in colostral or full phases of lactation to determine their relative rates of synthesis and degradation. Neutral alkylglycerols were both synthesized and cleaved
W B Rizzo et al.
Biochimica et biophysica acta, 1535(1), 1-9 (2000-12-13)
The enzyme that catalyzes the oxidation of fatty aldehyde derived from ether glycerolipid catabolism has not been identified. To determine whether microsomal fatty aldehyde dehydrogenase (FALDH) is responsible, we investigated the metabolism of 1-O-[9, 10-(3)H-octadecyl]-glycerol ([(3)H]OG) in FALDH-deficient cultured cells

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