Molecular structure of Olivetol, CAS Number: 500-66-3
Olivetol (CAS 500-66-3)
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Alternate Names:
5-Pentyl-1,3-benzenediol; 3,5-Dihydroxyamylbenzene; 5-Pentylresorcinol
CAS Number:
500-66-3
Purity:
≥98%
Molecular Weight:
180.24
Molecular Formula:
C11H16O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Olivetol, an organic compound, is often utilized in synthetic chemistry as well as in biochemical research. Its structural similarity to certain natural cannabinoids makes it useful for studying the endocannabinoid system. Biochemists explore its role in biosynthetic pathways, particularly those that lead to the production of polyketides, a class of secondary metabolites with diverse biological activities. Additionally, research involving olivetol includes probing its potential as a ligand for cannabinoid receptors, helping to further understand receptor-ligand interactions and signaling pathways.
Olivetol (CAS 500-66-3) References
- Preparation and evaluation of molecularly imprinted polymer of olivetol for solid phase extraction. | Jin, Y., et al. 2013. Se Pu. 31: 587-95. PMID: 24063201
- Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol. | Yamaori, S., et al. 2014. Chem Biol Interact. 215: 62-8. PMID: 24667653
- The inhibitory effects of cannabinoids, the active constituents of Cannabis sativa L. on human and rabbit platelet aggregation. | Formukong, EA., et al. 1989. J Pharm Pharmacol. 41: 705-9. PMID: 2575149
- Novel Δ8-Tetrahydrocannabinol Vaporizers Contain Unlabeled Adulterants, Unintended Byproducts of Chemical Synthesis, and Heavy Metals. | Meehan-Atrash, J. and Rahman, I. 2022. Chem Res Toxicol. 35: 73-76. PMID: 34889611
- Stereoselective Synthesis of Nonpsychotic Natural Cannabidiol and Its Unnatural/Terpenyl/Tail-Modified Analogues. | Anand, R., et al. 2022. J Org Chem. 87: 4489-4498. PMID: 35289168
- Synthetic Strategies for Rare Cannabinoids Derived from Cannabis sativa. | Nguyen, GN., et al. 2022. J Nat Prod. 85: 1555-1568. PMID: 35648593
- Carbonyl-trapping abilities of 5-alkylresorcinols. | Zamora, R. and Hidalgo, FJ. 2022. Food Chem. 393: 133372. PMID: 35661596
- Simulated microgravity contributed to modification of callogenesis performance and secondary metabolite production in CannabisIndica. | Darigh, F., et al. 2022. Plant Physiol Biochem. 186: 157-168. PMID: 35849945
- Electrochemical Detection of Olivetol Based on Poly(L-Serine) Film Layered Copper Oxide Modified Carbon Paste Electrode (p-L-Serine/CuO/CPE). | You, Z., et al. 2022. Nanomaterials (Basel). 13: PMID: 36615980
- Malondialdehyde trapping by food phenolics. | Zamora, R., et al. 2023. Food Chem. 417: 135915. PMID: 36933433
- Analysis of olivetol in rabbit serum by high-performance liquid chromatography. | Rauls, D. and Penney, LL. 1982. J Chromatogr. 234: 500-2. PMID: 7056834
- Effects of cannabinoids on macromolecular synthesis and replication of cultured lymphocytes. | Nahas, GG., et al. 1977. Fed Proc. 36: 1748-52. PMID: 844617
- Quantum mechanical and experimental oxidation studies of pentadecylresorcinol, olivetol, orcinol and resorcinol. | Hładyszowski, J., et al. 1998. Free Radic Res. 28: 359-68. PMID: 9684980
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Olivetol, 1 g | sc-236251 | 1 g | $58.00 | |||
Olivetol, 10 g | sc-236251A | 10 g | $214.00 | |||
Olivetol, 100 g | sc-236251B | 100 g | $1047.00 | |||
Olivetol, 1 kg | sc-236251C | 1 kg | $3648.00 | |||
Olivetol, 5 kg | sc-236251D | 5 kg | $14052.00 |