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About This Item
Linear Formula:
HOCH2CH(OH)CH2O(CH2)15CH3
CAS Number:
Molecular Weight:
316.52
EC Number:
228-149-9
UNSPSC Code:
12352211
PubChem Substance ID:
Beilstein/REAXYS Number:
1724514
MDL number:
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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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
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
S Reynolds et al.
Clinical & experimental metastasis, 18(4), 309-312 (2001-07-13)
The ability of the naturally occurring ether lipid, 1-O (2 methoxy) hexadecyl glycerol (MHG), and phenylbutyrate (BP) to inhibit cellular proliferation, anchorage-independent growth and cellular invasion in the human prostate cancer LnCap and DU145 cells was determined. Both MHG and
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