 | |
| Names | |
|---|---|
| Preferred IUPAC name (1′R,2′R)-2,6-Dihydroxy-5′-methyl-4-pentyl-2′-(prop-1-en-2-yl)-1′,2′,3′,4′-tetrahydro[1,1′-biphenyl]-3-carboxylic acid | |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| KEGG | |
| UNII | |
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| Properties | |
| C22H30O4 | |
| Molar mass | 358.478 g·mol−1 |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Cannabidiolic acid (CBDA), is acannabinoid produced incannabis plants.[1] It is theprecursor tocannabidiol (CBD). It is most abundant in the glandulartrichomes on the female seedless flowers or more accuratelyinfructescence often colloquially referred to as buds or flowers.[2]
Cannabidiolic acid is a natural productsesquiterpene biosynthesized incannabis viaCannabidiolic acid synthase from the conjugation ofolivetolic acid andcannabigerolic acid.[3]
CBDA is the chemical precursor tocannabidiol (CBD). Through the process ofdecarboxylation, cannabidiol is derived through loss of the carbon and two oxygen atoms that make up the carboxylic acid moeity on the aromatic ring.