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Key Documents

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B402

Sigma-Aldrich

Batyl alcohol

99%

Sinónimos:

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

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About This Item

Fórmula lineal:
CH3(CH2)17OCH2CH(OH)CH2OH
Número de CAS:
544-62-7
Peso molecular:
344.57
Beilstein/REAXYS Number:
1725677
EC Number:
208-874-7
MDL number:
MFCD00004720
UNSPSC Code:
12352100
PubChem Substance ID:
24891746
NACRES:
NA.22

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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Categorías relacionadas

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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Certificados de análisis (COA)

Lot/Batch Number
18496LJV
MKBV9078V
18496LJ
18825JD
10830CN

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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
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
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