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THC-O-acetate

Acetate ester of tetrahydrocannabinol (THC)


Acetate ester of tetrahydrocannabinol (THC)

FieldValue
Verifiedfieldschanged
verifiedrevid470476361
IUPAC_name(6a*R*,10a*R*)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6*H*-benzo[*c*]chromen-1-yl acetate
imageTHC-O-acetate.svg
image_classskin-invert-image
image2THC-O-acetate 3D BS.png
image_class2bg-transparent
legal_UKClass B
legal_USDisputed
<!--Identifiers-->CAS_number_Ref
CAS_number23132-17-4
UNIIVHV54M2AES
PubChem198013
ChemSpiderID_Ref
ChemSpiderID171383
<!--Chemical data-->C23
H32
O3
smilesO=C(Oc2cc(cc1OC([C@@H]3CC/C(=C\[C@H]3c12)C)(C)C)CCCCC)C
StdInChI_Ref
StdInChI1S/C23H32O3/c1-6-7-8-9-17-13-20(25-16(3)24)22-18-12-15(2)10-11-19(18)23(4,5)26-21(22)14-17/h12-14,18-19H,6-11H2,1-5H3/t18-,19-/m1/s1
StdInChIKey_Ref
StdInChIKeyDEWSJDIJFWQLOA-RTBURBONSA-N

THC-O-acetate (THC acetate ester, O-acetyl-THC, THC-O, AcO-THC) is the acetate ester of THC. The term THC-O-acetate is commonly used for two different isomers of this substance, dependent on which isomer of THC it is synthesized from. The difference between Δ8-THC and Δ9-THC is the location of the double bond within the cyclohexene ring system. In naming the esters of THC, the "-O-" is superfluous.

Physical data, chemistry, and properties

Esters of Δ<sup>9</sup>-THC: Top (from left); THC acetate, THC propionate, THC phosphate, THC-NE, Bottom; THC morpholinylbutyrate, THC piperidinylpropionate, THC hemisuccinate, THC hemiglutarate

THC acetate ester (THC-O or THCOA) can be synthesized from THC, or from THCA. The acetylation of THC does not change the properties of the compound to the same extent as with other acetate esters, as the parent compound (THC) is already highly lipophilic, but potency is nonetheless increased to some extent. While the acetate ester of Δ9-THC is the best studied, the acetate esters of other isomers, especially Δ8-THC but also Δ10-THC are also known, as are other esters such as THC-O-propionate, THC-O-phosphate, THC hemisuccinate, THC hemiglutarate, THC morpholinylbutyrate, THC piperidinylpropionate, THC naphthoyl ester (THC-NE), and THC-VHS, as well as the hydrogenated derivative HHC-O-acetate and the ring-expanded Abeo-HHC acetate, as well as related compounds such as THC methylcarbonate.

Pharmacology

It is a metabolic pro-drug, with its subjective effects being felt around 30 minutes after ingestion.

Psychedelic claims

In a 2023 study, anecdotal claims surrounding THC-O-acetate's supposed ability to initiate psychedelic experiences were shown to not be significant. Answers using the Mystical Experience Questionnaire (MEQ) were under the threshold of a true experience, and those who had used classical psychedelics such as LSD or psilocybin consistently scored lower on the MEQ. When asked directly, 79% of the participants said it was either "not at all" or "a little" like a psychedelic experience.

History

This substance was investigated as a possible non-lethal incapacitating agent as part of the Edgewood Arsenal experiments at some point between 1949 and 1975. It was noted to have about twice the capacity to produce ataxia (lack of voluntary coordination of muscle movements) as did THC when administered to dogs.

Author D. Gold provided synthesis instructions for this compound (calling it "THC acetate") in his 1974 book Cannabis Alchemy: Art of Modern Hashmaking, in which it is described as follows;

The U.S. DEA first encountered THC-O-acetate as an apparent controlled substance analogue of THC in 1978. It was made in an analogous manner to how aspirin (acetylsalicylic acid) was first made from willow bark extract (which is mostly salicylic acid) in the 1800s. The incident was described by Donald A. Cooper of the DEA thus:

A similar case reported in June 1995 in the United Kingdom.The description of that case appears to indicate the convicted manufacturer was using D. Gold's book Cannabis Alchemy as a guide. THC acetate was also reported to have been found by New Zealand police in 1995, again made by acetylation of purified cannabis extracts with acetic anhydride.

With passage of the 2018 United States farm bill (which eased legal restrictions on the cultivation of industrial hemp), ∆8-THC-O-acetate based vaporizers and edibles have become increasingly available in the United States and are now commonly sold at convenience stores and gas stations.

Toxicity

In 2022, researchers at Portland State University used an e-nail to vaporize CBD-acetate, CBN-acetate, and THC-O-acetate (referred to simply as "THC acetate") to screen for the presence of ketene formation when vaporizing. They reported that just like Vitamin E acetate, all three of these cannabinoid acetates produced ketene gas when heated. For this reason, the inhalation of THC-O-acetate based products could be hazardous to health.

References

References

  1. (1974). "Cannabis Alchemy: Art of Modern Hashmaking". Ronin Publishing (2010).
  2. (1990). "Marijuana Chemistry: Genetics, Processing, Potency". Ronin Publishing.
  3. (May 2023). ""Breaking bud": the effect of direct chemical modifications of phytocannabinoids on their bioavailability, physiological effects, and therapeutic potential". Organic & Biomolecular Chemistry.
  4. [https://patents.google.com/patent/US20210251947A1/en Elkarim NS. Stable formulations of dronabinol. Patent US20210251947]
  5. (1977). "Marijuana Potency". And/Or Press.
  6. (June 2023). "THC-O-Acetate: Scarce Evidence for a Psychedelic Cannabinoid". Journal of Psychoactive Drugs.
  7. "Future Synthetic Drugs of Abuse.". Drug Enforcement Administration.
  8. (2003). "Cannabis: The Genus Cannabis". Hardwood Academic Publishers.
  9. (1995). "Δ9-THC acetate from acetylation of cannabis oil.". Science and Justice.
  10. . (2019-12-20). ["President Trump Signed the Farm Bill into Law One Year Ago Today, USDA Highlights Implementation Accomplishments to Date"](https://www.usda.gov/about-usda/news/press-releases/2019/12/20/president-trump-signed-farm-bill-law-one-year-ago-today-usda-highlights-implementation). *USDA Press*.
  11. (October 2022). "∆8-THC, THC-O Acetates and CBD-di-O Acetate: Emerging Synthetic Cannabinoids Found in Commercially Sold Plant Material and Gummy Edibles". Journal of Analytical Toxicology.
  12. (July 2022). "Vaping Cannabinoid Acetates Leads to Ketene Formation". Chemical Research in Toxicology.
  13. (Oct 17, 2022). "Proceedings of the 2022 Cannabis Clinical Outcomes Research Conference (CCORC) Orlando, FL, USA, May 19-20, 2022". Medical Cannabis and Cannabinoids.
  14. "The Misuse of Drugs Act 1971 (Amendment) Order 2008". Office of Public Sector Information.
  15. (February 16, 2023). "Delta-8 And -9 THC-O Are Controlled Substances, DEA Says".
  16. "4th Circ. Sets Legal Hemp Standard In THC Firing Case - Law360".
  17. Harris, Katharine. (February 25, 2025). "A hazy legal landscape means people can get high on hemp products, even where pot is prohibited".
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