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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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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
Treatment of peripheral leukopenia after cadaveric kidney transplantation.
B Xiwen et al.
Transplantation proceedings, 28(3), 1631-1632 (1996-06-01)
N Yamamoto et al.
Cancer research, 48(21), 6044-6049 (1988-11-01)
Alkylglycerols, inflammation products of lipids in cancerous tissues, are potent macrophage stimulating agents. Administration of small amounts (10-100 ng) of alkylglycerols to mice greatly enhanced macrophage activation for Fc-mediated ingestion activity at the 5th day posttreatment. Dose effect analysis revealed
A K Das et al.
Lipids, 27(6), 401-405 (1992-06-01)
Chronic feeding of 1-O-octadecyl-sn-glycerol (batyl alcohol) to patients suffering from congenital deficiency in tissue ether glycerolipids showed an increase in the plasmalogens content of their erythrocytes. However, nothing is known about the ether lipid content of other tissues in these
Xiao-Feng Sun et al.
Biotechnology letters, 27(2), 113-117 (2005-02-11)
Novel mutual pro-drugs in which 2',3'-dideoxyinosine anti-HIV (human immunodeficiency virus) drug and 3-octadecyloxy-propane-1,2-diol anti-inflammatory drug were attached to the same molecule via different biodegradable linkages, were synthesized through two-step enzymatic transesterification by a commercial lipase in acetone.

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