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H2510

Sigma-Aldrich

1-O-Palmityl-rac-glycerol

~99%

Synonym(s):

rac-1-Hexadecyl-glycerol, rac-Glycerol-1-hexadecyl ether, DL-α-Hexadecylglycerol

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About This Item

Linear Formula:
HOCH2CH(OH)CH2O(CH2)15CH3
CAS Number:
Molecular Weight:
316.52
Beilstein/REAXYS Number:
1724514
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:

assay

~99%

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCCOCC(O)CO

InChI

1S/C19H40O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-22-18-19(21)17-20/h19-21H,2-18H2,1H3

InChI key

OOWQBDFWEXAXPB-UHFFFAOYSA-N

Gene Information

rat ... Cnr1(25248)

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 4

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Shann Ménard et al.
Physiology & behavior, 208, 112577-112577 (2019-06-14)
The neuropeptides oxytocin (OT) and vasopressin (AVP) are critical in the formation of pair bonding in the vole, and potentially in other species. The finding that normally promiscuous male rats display a conditioned ejaculatory preference (CEP) for females that bear
S Umeki et al.
Biochimica et biophysica acta, 793(1), 123-128 (1984-03-27)
Exposure of Tetrahymena pyriformis NT-1 to chimyl alcohol (1-O-hexadecyl glycerol) produced a reproducible enhancement in unsaturated fatty acids and a great decrease in order parameter (S), which result from the 2-fold increases of stearoyl-CoA and oleoyl-CoA desaturase activities in microsomes.
L E Bertello et al.
Lipids, 32(8), 907-911 (1997-08-01)
A simple method is presented to esterify 1-O-hexadecyl-rac-glycerol using lipases in different organic solvents. The following fatty acids were used: C14:0, C16:0, C18:0, C18:1, and C18:2. Monoesterification was achieved by using a limiting amount of fatty acid. Both the 1-O-hexadecyl-3-O-acylglycerol
T Ishibashi et al.
Journal of lipid research, 26(3), 393-395 (1985-03-01)
Alkylglycerol monooxygenase of rat liver microsomes was purified approximately to 97-fold with a 30% yield by procedures including affinity chromatography on chimyl alcohol-Sepharose 4B. Chimyl alcohol (1-O-hexadecylglycerol) was converted to the p-aminobenzylidene derivative and then coupled to 6-carboxyhexyl-Sepharose. The final
N Maulik et al.
Journal of cardiovascular pharmacology, 24(3), 486-492 (1994-09-01)
A recent study demonstrated biochemical and structural alterations of peroxisomes in rat kidney after ischemia/reperfusion. We examined whether peroxisomes play any role in the pathophysiology of myocardial ischemia/reperfusion injury. Isolated perfused rat heart was made ischemic for 30 min by

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