CBG (cannabigerol)

CBDV (cannabidivarin)

THCA (tetrahydrocannabinolic acid)

Humulene

Caryophyllene

CBDA (cannabidiolic acid)

Pinene

THC (tetrahydrocannabinol)

Myrcene

Limonene

CBD (cannabidiol)

CBN (cannabinol)

Terpinolene

Linalool

CBC (cannabichromene)

THCV (tetrahydrocannabivarin)

Terpineol

Combustion

52°C | 126°F

65°C | 149°F

90°C | 194°F

107°C | 225°F

129°C | 264°F

130°C | 266°F

155°C | 311°F

157°C | 315°F

167°C | 333°F

176°C | 349°F

180°C | 356°F

185°C | 365°F

187°C | 369°F

198°C | 388°F

220°C | 428°F

220°C | 428°F

221°C | 430°F

230°C | 451°F

 

REFERENCES:

  • US National Library of Medicine, National Center for Biotechnology Information, PubChem Open Chemistry database. https://pubchem.ncbi.nlm.nih.gov/

  • McPartland, John & Russo, Ethan. (2001). Cannabis and cannabis extracts: Greater than the sum of their parts?. J Cannabis Therapeutics. 1. 103-132. 10.1300/J175v01n03_08. 

  • Wikipedia. https://en.wikipedia.org/

  • Project CBD. www.projectcbd.org

  • Cerilliant Analytical Reference Standards. www.cerilliant.com

  • Kerstin Iffland, Michael Carus and Dr. med. Franjo Grotenhermen, nova-Institut GmbH. Decarboxylation of Tetrahydrocannabinolic acid (THCA) to active THC. http://eiha.org/media/2014/08/16-10-25-Decarboxylation-of-THCA-to-active-THC.pdf