Technical Parameters
Description
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Chemical Identifiers
| InChI | InChI=1S/CH5N.ClH/c1-2;/h2H2,1H3;1H/i1D3; |
| InChI Key | NQMRYBIKMRVZLB-NIIDSAIPSA-N |
| Smiles | [2H]C([2H])([2H])N.Cl |
| EC No. | |
| MDL No. | |
| PubChem CID | 2723974 |
Applications
Isotope Effect and Mechanistic Studies
Replacing hydrogen with deuterium allows researchers to investigate kinetic isotope effects and reaction mechanisms. Methyl-d3-amine monohydrochloride offers a defined isotopic source for studying reactions involving methylamine-derived groups and evaluating how isotopic substitution influences chemical transformations.
Pharmaceutical Research and Drug Discovery
Deuterium-labeled building blocks are valuable in medicinal chemistry for preparing isotopically modified molecules and investigating their chemical and metabolic properties. Methyl-d3-amine monohydrochloride can serve as a starting material for introducing a deuterated methylamino group into pharmaceutical intermediates and research compounds, depending on the synthetic route.
Organic Synthesis and Labeled Building Blocks
The compound provides a convenient source of deuterated methylamine for suitable synthetic reactions. Its primary amine functionality can participate in reactions such as amination and other nitrogen-functionalization processes under appropriate conditions, supporting the preparation of deuterium-labeled amines, amides, and related compounds.
Analytical Chemistry and Mass Spectrometry Research
Deuterium-labeled compounds can support analytical method development and isotope-related investigations. Methyl-d3-amine monohydrochloride may be used to prepare labeled reference compounds or other analytical research materials when a deuterated methylamino unit is required. Its suitability depends on the target compound and analytical workflow.

