Related Experiment Video
Updated: Nov 9, 2025

A General Method for Detecting Nitrosamide Formation in the In Vitro Metabolism of Nitrosamines by Cytochrome P450s
Published on: September 25, 2017
Nitrosamine formation from the reaction of methamphetamine with gaseous nitrous acid
Alexandra Mayer1, Joel Rindelaub1, Gordon M Miskelly1
1School of Chemical Sciences, University of Auckland, Auckland, New Zealand.
Abstract:
Methamphetamine is the most commonly seized amphetamine-type stimulant (ATS) worldwide. Chemical residues associated with the use or manufacture of methamphetamine can persist in the air and surfaces in a property for over 5 years and potentially pose risks to the health and safety of the public. When a house is tested for contamination, the test focuses on the presence of surface methamphetamine residue; however, other hazardous chemicals may also be present, including methamphetamine precursors and reaction products. As little has been reported about the ageing of the methamphetamine inside dwellings, there is currently large uncertainty regarding its fate and/or degradation products in such environments. If the indoor reactivity of methamphetamine is similar to that of nicotine-derived third-hand smoke, the production of a carcinogenic nitrosamine is an expected result. Thus, this proof-of-concept study investigated the reaction of methamphetamine with the common gaseous indoor oxidant nitrous acid (HONO) and monitored the fate of the resulting reaction products in simulated laboratory experiments to further understand the potential health risks associated with contaminated properties. Surface methamphetamine residue was observed to decrease with an exponential decay with an upper limit of 2.38 ± 0.5 × 10-3 min-1 upon exposure to HONO gas (5.7 ppmv, 0.25 L min-1 ). N-nitrosomethamphetamine (NMA), a suspected human mutagen and carcinogen, was detected to have a steady-state formation over the sampling time frame, with a surface area concentration of 0.87 μg/100 cm2 , suggesting that the risks to public health for properties contaminated with methamphetamine may be currently underestimated.
Insights
Methamphetamine residue in homes can form carcinogenic N-nitrosomethamphetamine (NMA) when reacting with indoor nitrous acid. This study shows NMA formation, indicating underestimated public health risks from contaminated properties.
Area of Science:
- Environmental Chemistry
- Toxicology
- Public Health
Background:
- Methamphetamine residues persist in properties for years, posing health risks.
- Limited data exists on methamphetamine degradation and byproducts in indoor environments.
- Indoor chemical reactions may generate hazardous substances from methamphetamine.
Purpose of the Study:
- To investigate the reaction of methamphetamine with nitrous acid (HONO), a common indoor oxidant.
- To identify and quantify degradation and reaction products of methamphetamine.
- To assess potential public health risks from methamphetamine-contaminated properties.
Main Methods:
- Simulated laboratory experiments exposed surface methamphetamine residue to HONO gas.
- Monitored the decay of methamphetamine residue.
- Analyzed for the formation of reaction products, specifically N-nitrosomethamphetamine (NMA).
Main Results:
- Surface methamphetamine residue decreased exponentially upon HONO exposure (decay rate: 2.38 × 10⁻³ min⁻¹).
- N-nitrosomethamphetamine (NMA), a suspected carcinogen, was detected.
- NMA reached a steady-state surface concentration of 0.87 μg/100 cm².
Conclusions:
- Methamphetamine reacts with indoor nitrous acid to form carcinogenic NMA.
- The presence of NMA suggests that health risks in contaminated properties may be underestimated.
- Further research is needed to understand the long-term fate and risks of methamphetamine byproducts.
More Related Videos
08:05Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O
Published on: October 7, 2020
07:30A Direct, Regioselective and Atom-Economical Synthesis of 3-Aroyl-N-hydroxy-5-nitroindoles by Cycloaddition of 4-Nitronitrosobenzene with Alkynones
Published on: January 21, 2020
Related Concept Videos
2° Amines to N-Nitrosamines: Reaction with NaNO2
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
Preparation of Amines: Alkylation of Ammonia and Amines
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Carboxylic Acids to Methylesters: Alkylation using Diazomethane