Technical Parameters
Description
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Good Quality Diphenylamine-d10丨CAS 37055-51-9
Chemical Identifiers
| InChI | InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H/i1D,2D,3D,4D,5D,6D,7D,8D,9D,10D |
| InChI Key | DMBHHRLKUKUOEG-LHNTUAQVSA-N |
| Smiles | [2H]C1=C(C(=C(C(=C1[2H])[2H])NC2=C(C(=C(C(=C2[2H])[2H])[2H])[2H])[2H])[2H])[2H] |
| EC No. | |
| MDL No. | MFCD00144154 |
| PubChem CID | 87087746 |
Applications
Analytical Chemistry and Mass Spectrometry
Deuterated compounds are valuable tools in analytical method development and isotope-labeling research. Diphenylamine-d10 may be used as a reference material or as a precursor for preparing labeled compounds in suitable analytical workflows, including mass spectrometry studies, depending on the method requirements.
Pharmaceutical Research and Drug Discovery
Diphenylamine-d10 can serve as a starting material for preparing deuterium-labeled aromatic compounds in pharmaceutical research. Isotopic labeling can help researchers investigate molecular transformations, reaction pathways, and the behavior of labeled compounds during drug discovery and development.
Organic Synthesis and Chemical Research
The nitrogen atom in the diphenylamine structure provides opportunities for chemical modification and derivatization. Diphenylamine-d10 can be incorporated into synthetic pathways for preparing deuterated aromatic amines and other specialized organic compounds for research purposes.
Materials Science
Diphenylamine-based structures are used in the research and development of functional organic materials, including compounds investigated for electronic and optoelectronic applications. Diphenylamine-d10 may support the synthesis of deuterated derivatives for studying molecular properties and material performance, depending on the target structure.

