THCVa
C20H26O4 acid form non-psychoactive
THCVa is the raw acid form of THCV. Heat removes one CO2 and turns THCVa into THCV, so a gram of THCVa can yield at most 0.867 g of THCV.
Turn THCVa into THCV with heat
Raw flower holds THCVa, the acid form. Drag the heat up: past 220 °F the COOH group leaves as CO2 and what stays behind is THCV.
70 °F: raw, the acid still carries its COOH group
0.4% THCVa × 0.867 = 0.35% THCV, plus 0.02% THCV already there, equals 0.37% Total THCV.
Worked example. 0.4% THCVa × 0.867 = 0.35% THCV, plus 0.02% THCV already there, equals 0.37% Total THCV. Example numbers, for illustration only. The 0.867 is the molar-mass ratio of THCV to THCVa: the CO2 that leaves weighs about 13.3% of the acid.
What is THCVa?
THCVA (tetrahydrocannabivarinic acid) is the raw acidic form of THCV, and the easiest way to picture it is as a shorter-tailed sibling of THCA. The two share the same three-ring core. What differs is the carbon chain on one side of the molecule: five carbons long in THCA, three in THCVA. That two-carbon difference is enough to put THCVA in its own family, the varins.
The living plant stores its cannabinoids as acids like this one, and heat, or time, strips the acid group away to leave the neutral form, THCV in this case. In most modern cultivars THCVA is present only at low levels, when it shows up at all.
Commonly associated effects
THCVa is commonly associated with the following qualities. These reflect general research and community reports, not guaranteed or medical outcomes.
A shorter tail from a different starter
Cannabinoids begin as a small ring-shaped building block with a tail attached. For the familiar five-carbon family that block is olivetolic acid, built starting from a fatty acid called hexanoic acid, and an enzyme then attaches a geranyl group to it to make CBGA. The varins are expected to follow the same route from a shorter fatty acid, butanoic acid, which would give divarinic acid and then CBGVA, the varin counterpart of CBGA. Researchers writing in 2018 noted that where the plant gets either fatty acid was unknown. Researchers also believe the synthases that close CBGA into THCA or CBDA act on CBGVA, which is how a plant can make THCVA or CBDVA.
Where it turns up
Varins are not spread evenly across cannabis. Researchers report that they can make up a significant share of the cannabinoids in some ecotypes, the locally adapted populations, of Asian and African origin, while contemporary domesticated lines usually carry them at low levels. Individual plants can be extreme: in a 2018 Australian study of a diverse germplasm collection, one plant from a proprietary breeding line carried THCVA as 75.1 percent of its total cannabinoids. How tail length passes from parent to seedling was also unresolved at the time. A breeding study from the same group that followed 210 second-generation offspring found patterns that did not fit simple Mendelian ratios, pointing to more than one gene and to genes that influence each other.
Reading THCVA on a lab report
Because the plant makes the acid, fresh or carefully stored material holds this varin mostly as THCVA, with only a little THCV beside it. One 2024 study of an air-dried, CBD-rich hemp variety measured roughly one part THCV to twenty parts THCVA after about two weeks of drying in the dark at room temperature, with THCVA at 0.3 percent of the total cannabinoids. Heating shifts that balance toward THCV. When a certificate lists both, reading them together, rather than either one alone, gives the fuller picture of this varin in the sample.
Frequently asked questions
Is THCVA psychoactive?
What is the difference between THCVA and THCA?
How does THCVA become THCV?
Why might a lab report not list THCVA?
Other cannabinoids
Where THCVa sits in the Heat Row: acids on top, the forms heat makes below, then the rest.
Sources
- PubChem: Tetrahydrocannabivarinic acid (CID 59444416)
- PubChem: Tetrahydrocannabinolic acid (CID 3082459)
- Welling et al. (2018), Frontiers in Plant Science: Developmental Plasticity of the Major Alkyl Cannabinoid Chemotypes in a Diverse Cannabis Genetic Resource Collection (PMC)
- Welling et al. (2019), Scientific Reports: Complex Patterns of Cannabinoid Alkyl Side-Chain Inheritance in Cannabis (PubMed)
- Kim et al. (2024), Scientific Reports: Comparison of decarboxylation rates of acidic cannabinoids between secretory cavity contents and air-dried inflorescence extracts in Cannabis sativa cv. 'Cherry Wine' (PubMed)
- Wang et al. (2016), Cannabis and Cannabinoid Research: Decarboxylation Study of Acidic Cannabinoids (PubMed)
Educational information only, not medical advice. Terpene and cannabinoid effects are an active area of research and vary by person, product, and dose. Cannabis is for adults 21+ where legal.
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