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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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
H O Herrmann et al.
Molecular and biochemical parasitology, 5(2), 65-76 (1982-02-01)
A long-chain 0-alkylglycerol, 1-0-[1'-14C]octadecyl-sn-glycerol, was taken up and metabolized extensively in Leishmania donovani promastigotes grown on a lipid-free, semi-defined medium as well as on a lipid-free, synthetic medium in nearly identical ways. Cleavage of the ether bond was the main
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
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
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
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