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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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
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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
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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Treatment of peripheral leukopenia after cadaveric kidney transplantation.
B Xiwen et al.
Transplantation proceedings, 28(3), 1631-1632 (1996-06-01)
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
Nancy E Braverman et al.
Biochimica et biophysica acta, 1822(9), 1442-1452 (2012-05-26)
Plasmalogens are a unique class of membrane glycerophospholipids containing a fatty alcohol with a vinyl-ether bond at the sn-1 position, and enriched in polyunsaturated fatty acids at the sn-2 position of the glycerol backbone. These two features provide novel properties
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)
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