Description

2-Amino-3-methyl-5-nitropyridine (CAS No. 18344-51-9) is a high-purity nitropyridine derivative with the molecular formula C₆H₇N₃O₂. This compound, also known by its IUPAC name 3-methyl-5-nitropyridin-2-amine, is a versatile intermediate in organic synthesis and pharmaceutical research. Its unique structure, featuring an amino group and a nitro group on a pyridine ring, makes it valuable for heterocyclic chemistry applications. Our product is rigorously tested for purity and consistency, ensuring reliable performance in sensitive reactions. Available in various quantities, it is ideal for researchers requiring a stable, well-characterized building block for drug discovery, agrochemical development, and material science applications.

Properties

• CAS Number: 18344-51-9
• Complexity: 156
• IUPAC Name: 3-methyl-5-nitro-pyridin-2-amine
• InChI: InChI=1S/C6H7N3O2/c1-4-2-5(9(10)11)3-8-6(4)7/h2-3H,1H3,(H2,7,8)
• InChI Key: JLPYUDJJBGYXEZ-UHFFFAOYSA-N
• Exact Mass: 153.053826475
• Molecular Formula: C6H7N3O2
• Molecular Weight: 153.14
• SMILES: CC1=CC(=CN=C1N)[N+](=O)[O-]
• Topological: 84.7
• Monoisotopic Mass: 153.053826475
• Synonyms: 2-Amino-3-methyl-5-nitropyridine, 18344-51-9, DTXSID80370314, DTXCID60321349, 623-204-7, 2-Amino-5-nitro-3-picoline, 3-methyl-5-nitropyridin-2-amine, MFCD03095060, 2-Amino-5-nitro-3-methylpyridine, 2-PYRIDINAMINE, 3-METHYL-5-NITRO-, 3-methyl-5-nitro-2-pyridylamine, SCHEMBL913434, SCHEMBL4711982, 3-methyl-5nitro-2-aminopyridine, JLPYUDJJBGYXEZ-UHFFFAOYSA-, BCP22231, 3-methyl-5-nitro-pyridin-2-ylamine, SBB005535, AKOS005257701, pyridine, 2-amino-3-methyl-5-nitro-, AB13441, 2-Amino-3-methyl-5-nitropyridine, 97%, AC-27507, DS-10925, SY014360, DB-020397, A1891, CS-0059204, ST51040187, EN300-123243, O10648, 2-Amino-5-nitro-3-picoline (2-Amino-3-methyl-5-nitropyridine), InChI=1/C6H7N3O2/c1-4-2-5(9(10)11)3-8-6(4)7/h2-3H,1H3,(H2,7,8)

Application

2-Amino-3-methyl-5-nitropyridine serves as a key intermediate in the synthesis of pharmaceutical compounds and agrochemicals. Its reactive nitro and amino groups enable facile functionalization for creating diverse heterocyclic structures. Researchers utilize this compound in medicinal chemistry for developing potential drug candidates targeting various diseases. It also finds application in material science as a precursor for specialty chemicals and dyes.

Safety and Hazards

GHS Hazard Statements

• H302 (89.1%): Harmful if swallowed [Warning Acute toxicity, oral]
• H315 (15.2%): Causes skin irritation [Warning Skin corrosion/irritation]
• H318 (84.8%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
• H319 (15.2%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (13%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (89.1%)
• Skin Irrit. 2 (15.2%)
• Eye Dam. 1 (84.8%)
• Eye Irrit. 2A (15.2%)
• STOT SE 3 (13%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.