B402
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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All Photos(2)
About This Item
Linear Formula:
CH3(CH2)17OCH2CH(OH)CH2OH
CAS Number:
Molecular Weight:
344.57
Beilstein:
1725677
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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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Related Categories
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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.
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
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
Treatment of peripheral leukopenia after cadaveric kidney transplantation.
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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
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