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Ethyl stearate | CAS:111-61-5
Ethyl stearate
  • Name:Ethyl stearate
  • CAS:111-61-5
  • Synonyms:Ethyl n-octadecanoate; Ethyl octadecanoate; KAK-ES; NSC 8919
  • Molecular Formula:C20H40O2
  • Molecular Weight:312.53
  • EINESC:203-887-4

Description

Properties

Melting point 37-38 ºC**
Density 0.862±0.06 g/cm3 (20 º

Safety

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SDS

Source SDS/MSDS Samples
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Synthetic Route
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Articles
Peer-Reviewed Papers
¹H NMR and HPLC/DAD for Cannabis sativa L. chemotype distinction, extract profiling and specification.Wieland Peschel et al.Talanta, 140, 150-165 (2015-06-07) Prenylation of olivetolate by a hemp transferase yields cannabigerolic acid, the precursor of tetrahydrocannabinol.M Fellermeier et al.FEBS letters, 427(2), 283-285 (1998-06-02) In vitro and in vivo pharmacology of synthetic olivetol- or resorcinol-derived cannabinoid receptor ligands.M G Cascio et al.British journal of pharmacology, 149(4), 431-440 (2006-09-06) 4-Methyl-5-Pentylbenzene-1,3-Diol Regulates Chemotactic Cell Aggregation and Spore Maturation Via Different Mechanisms in Dictyostelium discoideum.Anna P Kondo et al.Current microbiology, 76(3), 376-381 (2019-02-03) An Aromatic Farnesyltransferase Functions in Biosynthesis of the Anti-HIV Meroterpenoid Daurichromenic Acid.Haruna Saeki et al.Plant physiology, 178(2), 535-551 (2018-08-12) Preparation and evaluation of molecularly imprinted polymer of olivetol for solid phase extraction.Yafeng Jin et al.Se pu = Chinese journal of chromatography, 31(6), 587-595 (2013-09-26) Inhibition of the cataleptic effect of tetrahydrocannabinol by other constituents of Cannabis sativa L.E A Formukong et al.The Journal of pharmacy and pharmacology, 40(2), 132-134 (1988-02-01) Analgesic and antiinflammatory activity of constituents of Cannabis sativa L.E A Formukong et al.Inflammation, 12(4), 361-371 (1988-08-01) Analysis of olivetol in rabbit serum by high-performance liquid chromatography.D Rauls et al.Journal of chromatography, 234(2), 500-502 (1982-01-15) Structure of the Cannabis sativa olivetol-producing enzyme reveals cyclization plasticity in type III polyketide synthases.Lewis J Kearsey et al.The FEBS journal, 287(8), 1511-1524 (2019-10-13) Biotransformation of olivetol by Syncephalastrum racemosum.R H McClanahan et al.Journal of natural products, 47(5), 828-834 (1984-09-01) Quantum mechanical and experimental oxidation studies of pentadecylresorcinol, olivetol, orcinol and resorcinol.J Hładyszowski et al.Free radical research, 28(4), 359-368 (1998-07-31) Cannabidiol is a potent inhibitor of the catalytic activity of cytochrome P450 2C19.Rongrong Jiang et al.Drug metabolism and pharmacokinetics, 28(4), 332-338 (2013-01-16) Characterization of olivetol synthase, a polyketide synthase putatively involved in cannabinoid biosynthetic pathway.Futoshi Taura et al.FEBS letters, 583(12), 2061-2066 (2009-05-21)
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