At 25 °C pyridine has a viscosity of 0.88 mPa/s and thermal conductivity of 0.166 W·m−1·K−1. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. The enthalpy of vaporization is 35.09 kJ·mol−1 at the boiling point and normal pressure.The enthalpy of fusion is 8.28 kJ·mol−1 at the melting point. Electric Literature of 1603-41-4.
Nithya, S.;Chandar Shekar, B.;Aranganayagam, K. R.;Boopathi, K. research published 《 Growth and characterization of 2-amino-5-methylpyridinium phosphate crystals》, the research content is summarized as follows. Good-quality single crystals of 2- Amino-5-methylpyridinium phosphate (2A5MPP) have been grown by slow evaporation technique. The cell parameters of the grown crystals were studied and the crystal belongs to monoclinic structure with the space group P21/n. FTIR spectral analyses were carried out in order to determine the functional groups. The UV-visible absorption spectra were recorded for the grown crystal. The nonlinear refractive index and third order susceptibility values of 2A5MPP crystal are estimated using a Z-scan technique.
1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, Electric Literature of 1603-41-4