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B402

Sigma-Aldrich

Batyl alcohol

99%

Synonym(s):

1-O-Octadecyl-rac-glycerol, rac-Glycerol 1-octadecyl ether, DL-3-Octadecyloxy-1,2-propanediol

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About This Item

Linear Formula:
CH3(CH2)17OCH2CH(OH)CH2OH
CAS Number:
Molecular Weight:
344.57
Beilstein/REAXYS Number:
1725677
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

$80.94

List Price$85.20Save 5%
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Available to ship onApril 29, 2025Details


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assay

99%

form

powder

mp

71-73 °C (lit.)

SMILES string

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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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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.
D Meusel et al.
Chemistry and physics of lipids, 61(2), 193-198 (1992-04-01)
Stereoselectivity of several triacylglycerol lipases (EC 3.1.1.3) has been investigated in the enzymatic esterification of rac-1-O-octadecylglycerol with oleic acid in the presence of organic solvents, such as hexane. X-1(3)-O-Octadecylmonooleoylglycerols were the only products formed with most lipases; considerable proportions of
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
Treatment of peripheral leukopenia after cadaveric kidney transplantation.
B Xiwen et al.
Transplantation proceedings, 28(3), 1631-1632 (1996-06-01)

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