Technical Parameters
Description
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Real Dimethyl-d6-amine hydrochloride丨CAS 53170-19-7 Manufacturer
Chemical Identifiers
| InChI | InChI=1S/C2H7N.ClH/c1-3-2;/h3H,1-2H3;1H/i1D3,2D3; |
| InChI Key | IQDGSYLLQPDQDV-TXHXQZCNSA-N |
| Smiles | [2H]C([2H])([2H])NC([2H])([2H])[2H].Cl |
| EC No. | |
| MDL No. | |
| PubChem CID | 12199012 |
Applications
Isotope Effect and Mechanistic Studies
Replacing hydrogen with deuterium can help researchers investigate kinetic isotope effects and reaction mechanisms. Dimethyl-d6-amine hydrochloride offers a defined isotopic source for studying transformations involving dimethylamine groups and examining how isotopic substitution may influence chemical behavior.
Pharmaceutical Research and Drug Discovery
Deuterium-labeled building blocks are useful in medicinal chemistry for preparing isotopically modified compounds and investigating their chemical and biological properties. Dimethyl-d6-amine hydrochloride can serve as a source of deuterated dimethylamine for synthesizing labeled pharmaceutical intermediates and target molecules, depending on the reaction design.
Organic Synthesis and Deuterated Building Blocks
The compound provides a deuterated dimethylamine unit for selected synthetic applications. Researchers can use it in suitable reactions to introduce a fully deuterated dimethylamino group into target molecules, supporting the preparation of labeled amines and other nitrogen-containing compounds.
Analytical Chemistry and Mass Spectrometry Research
Deuterated compounds can be useful in developing analytical methods and studying isotope-dependent behavior. Dimethyl-d6-amine hydrochloride may support the preparation of labeled reference compounds or analytical research materials when a deuterated dimethylamine moiety is required. Suitability depends on the target analyte and analytical method.

