[{"data":1,"prerenderedAt":21},["ShallowReactive",2],{"notifications-general-en":3,"compound-H4CBD(S)-en":4},"Due to summer holidays, the laboratory will operate on a revised schedule from July 22 to August 9, 2026. Analysis results may take 7 to 10 days from sample receipt. Thank you for your understanding.",{"name":5,"shortname":6,"synonyms":7,"cas":8,"molMass":9,"pubchemLink":10,"structure":11,"important":12,"synthetic":12,"compoundClass":13,"asociationImage":16,"summarySet":17,"compoundEffectSet":20},"S-Tetrahydrocannibidiol","H4CBD(S)",null,"4460-20-2",318.501,"https:\u002F\u002Fpubchem.ncbi.nlm.nih.gov\u002Fcompound\u002F616324","science\u002Fstructures\u002FH4CBDS-S-Tetrahydrocannibidiol_HNV61k7.png",true,{"id":14,"description":15},"2","Cannabinoids","",[18],{"summaryText":19,"language":7},"\u003Cp>Hexahydrocannabidiol, or H4CBD, is a synthesized cannabinoid created by adding four hydrogen atoms to the CBD molecule. The process used to make H4CBD is very similar to making margarine from vegetable oil. The exact properties of H4CBD remain unknown, but the limited information available on this cannabinoid indicates that it has considerably higher affinity for your brain’s CB1 neuroreceptors than conventional CBD. Since CBD normally does not typically have any affinity for CB1 receptors, it is unclear what to make of this data. Nonetheless, people who use H4CBD generally report that it feels like CBD but with considerably higher psychoactivity. The diastereomers of H4CBD can be separated by supercritical fluid cromatography, with H4CBD(S) being slightly less energetically favored.\u003Cbr>\u003C\u002Fp>",[],1785925832151]