On apomorphine detection by colour reactions

In this communication the reaction routs of the Grimbert/Leclrc and Helch tests for apomorphine have been established.In the first assay an acid-base reaction occurs first between a phenol group in apomorphine and the acetate anion from the sodium salt.The resulting phenoxide displaces a chloride ion from HgCl2, the reagent.The mixed mercury oxychloride is labile and splits off in a phenoxyl radical and HgCl.The same process is repeated with the other hydroxyl group.A biradical is formed in the apomorphine molecule which reacts with the intermediate carbon-carbon double bond.A 1,2-benzoquinone and Cl-Hg-Hg-Cl are formed.In the Helch test the dichromate anion reacts with hydrochloric acid from morphine hydrochloride.Protonation of dichromic acid yields chromic acid and chromium trioxide.The latter reacts with a phenolic group by acid catalysis yielding a mixed chromate.Protonation of this ester affords chromous acid and an ortho-quinone.

Publication Details

Journal
Journal of Chemical Biological and Physical Sciences
Published
2025-02-10
DOI
https://doi.org/10.24214/jcbps.a.15.1.00105
Citations
5
Primary Topic
Forensic Toxicology and Drug Analysis
Type
article
Field-Weighted Citation Impact
6.54
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article

On apomorphine detection by colour reactions

5 citations
Journal of Chemical Biological and Physical Sciences
Forensic Toxicology and Drug Analysis
6.54
article

On apomorphine detection by colour reactions

article en
5 citations

Abstract

In this communication the reaction routs of the Grimbert/Leclrc and Helch tests for apomorphine have been established.In the first assay an acid-base reaction occurs first between a phenol group in apomorphine and the acetate anion from the sodium salt.The resulting phenoxide displaces a chloride ion from HgCl2, the reagent.The mixed mercury oxychloride is labile and splits off in a phenoxyl radical and HgCl.The same process is repeated with the other hydroxyl group.A biradical is formed in the apomorphine molecule which reacts with the intermediate carbon-carbon double bond.A 1,2-benzoquinone and Cl-Hg-Hg-Cl are formed.In the Helch test the dichromate anion reacts with hydrochloric acid from morphine hydrochloride.Protonation of dichromic acid yields chromic acid and chromium trioxide.The latter reacts with a phenolic group by acid catalysis yielding a mixed chromate.Protonation of this ester affords chromous acid and an ortho-quinone.

Journal of Chemical Biological and Physical SciencesVol. 15(1)
Openalex Percentile: Top 4%
Forensic Toxicology and Drug Analysis
6.54
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