| Chemical Properties | Back Directory | [Boiling point ]
488.1±45.0 °C(Predicted) | [density ]
1.008±0.06 g/cm3(Predicted) | [storage temp. ]
-80°C | [solubility ]
DMF: 50 mg/ml; DMSO: 60 mg/ml; DMSO:PBS (pH 7.2) (1:3): 0.25 mg/ml; Ethanol: 35 mg/ml | [form ]
A solution in acetonitrile | [pka]
9.63±0.45(Predicted) | [InChI]
InChI=1S/C23H34O2/c1-5-6-7-8-9-10-18-14-21(24)23(22(25)15-18)20-13-17(4)11-12-19(20)16(2)3/h13-15,19-20,24-25H,2,5-12H2,1,3-4H3/t19-,20+/m0/s1 | [InChIKey]
GGHRHCGOMWNLCE-VQTJNVASSA-N | [SMILES]
C1(O)=CC(CCCCCCC)=CC(O)=C1[C@H]1[C@H](C(C)=C)CCC(C)=C1 |
| Hazard Information | Back Directory | [Description]
CBDP (Item No. 30169) is an analytical reference standard categorized as a phytocannabinoid. It is a bis-homolog of cannabidiol (Item Nos. 90080 | ISO60156) that has been found in certain strains of Cannabis. This product is intended for research and forensic applications. | [Uses]
Cannabidiphorol (CBDP) is a phytocannabinoid that increases the production of reactive oxygen species (ROS) and activates cellular pathways related to ROS signaling. Cannabidiphorol inhibits cell viability of breast cancer cells[1]. | [References]
1. Crombie, L., and Crombie, W.M.L. Cannabinoid bis-homologues: Miniaturised synthesis and GLC study. Phytochemistry 14, 213-220 (1975). DOI:10.1016/0031-9422(75)85042-4
2. Citti, C., Linciano, P., Russo, F., et al. A novel phytocannabinoid isolated from Cannabis sativa L. with an in vivo cannabimimetic activity higher than Δ9-tetrahydrocannabinol: Δ9-Tetrahydrocannabiphorol. Sci. Rep. 9(1), 20335 (2019). DOI:10.1038/s41598-019-56785-1 |
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| Company Name: |
Merck KGaA
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| Tel: |
21-20338288 |
| Website: |
www.sigmaaldrich.cn |
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