Product Information
2-Amino-6-methylaminopyridine is a protonated imino compound. The protonated imino group has an interaction with the methylene group and the nitrogen atom in the 2-position, which is responsible for the UV absorption spectrum of this molecule. 2-Amino-6-methylaminopyridine has a hydrogen atom at the N atom position, which undergoes tautomerization to form a protonated amino group. The protonated amino group transfers its proton to a neighboring carboxylate ion, forming an ammonium cation that can be detected by mass spectrometry.
2-Amino-6-methylaminopyridine is synthesized by mixing hydrochloric acid and methylamine in an ice bath. This reaction produces methylammonium chloride and ammonia gas as byproducts.
Chemical properties
Technical inquiry about: 3D-ADA13546 2-Amino-6-methylaminopyridine
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