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Toxicant Formation in Dabbing: The Terpene Story

[Image: see text] Inhalable, noncombustible cannabis products are playing a central role in the expansion of the medical and recreational use of cannabis. In particular, the practice of “dabbing” with butane hash oil has emerged with great popularity in states that have legalized cannabis. Despite t...

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Autores principales: Meehan-Atrash, Jiries, Luo, Wentai, Strongin, Robert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623941/
https://www.ncbi.nlm.nih.gov/pubmed/28983528
http://dx.doi.org/10.1021/acsomega.7b01130
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author Meehan-Atrash, Jiries
Luo, Wentai
Strongin, Robert M.
author_facet Meehan-Atrash, Jiries
Luo, Wentai
Strongin, Robert M.
author_sort Meehan-Atrash, Jiries
collection PubMed
description [Image: see text] Inhalable, noncombustible cannabis products are playing a central role in the expansion of the medical and recreational use of cannabis. In particular, the practice of “dabbing” with butane hash oil has emerged with great popularity in states that have legalized cannabis. Despite their growing popularity, the degradation product profiles of these new products have not been extensively investigated. The study herein focuses on the chemistry of myrcene and other common terpenes found in cannabis extracts. Methacrolein, benzene, and several other products of concern to human health were formed under the conditions that simulated real-world dabbing. The terpene degradation products observed are consistent with those reported in the atmospheric chemistry literature.
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spelling pubmed-56239412017-10-03 Toxicant Formation in Dabbing: The Terpene Story Meehan-Atrash, Jiries Luo, Wentai Strongin, Robert M. ACS Omega [Image: see text] Inhalable, noncombustible cannabis products are playing a central role in the expansion of the medical and recreational use of cannabis. In particular, the practice of “dabbing” with butane hash oil has emerged with great popularity in states that have legalized cannabis. Despite their growing popularity, the degradation product profiles of these new products have not been extensively investigated. The study herein focuses on the chemistry of myrcene and other common terpenes found in cannabis extracts. Methacrolein, benzene, and several other products of concern to human health were formed under the conditions that simulated real-world dabbing. The terpene degradation products observed are consistent with those reported in the atmospheric chemistry literature. American Chemical Society 2017-09-22 /pmc/articles/PMC5623941/ /pubmed/28983528 http://dx.doi.org/10.1021/acsomega.7b01130 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Meehan-Atrash, Jiries
Luo, Wentai
Strongin, Robert M.
Toxicant Formation in Dabbing: The Terpene Story
title Toxicant Formation in Dabbing: The Terpene Story
title_full Toxicant Formation in Dabbing: The Terpene Story
title_fullStr Toxicant Formation in Dabbing: The Terpene Story
title_full_unstemmed Toxicant Formation in Dabbing: The Terpene Story
title_short Toxicant Formation in Dabbing: The Terpene Story
title_sort toxicant formation in dabbing: the terpene story
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623941/
https://www.ncbi.nlm.nih.gov/pubmed/28983528
http://dx.doi.org/10.1021/acsomega.7b01130
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