Cas no 88482-17-1 (5-amino-2-methylpyridine-4-carboxylic acid)

5-Amino-2-methylpyridine-4-carboxylic acid is a heterocyclic organic compound featuring both amino and carboxylic acid functional groups on a pyridine backbone. This structure makes it a valuable intermediate in pharmaceutical and agrochemical synthesis, particularly for developing active ingredients with enhanced bioactivity. The methyl group at the 2-position and the amino group at the 5-position contribute to its steric and electronic properties, facilitating selective reactions in medicinal chemistry. Its carboxylic acid moiety allows for further derivatization, enabling the formation of amides, esters, or coordination complexes. The compound exhibits high purity and stability under standard conditions, ensuring reliable performance in research and industrial applications. Its versatility in heterocyclic chemistry underscores its importance as a building block for drug discovery and specialty chemical development.
5-amino-2-methylpyridine-4-carboxylic acid structure
88482-17-1 structure
Product Name:5-amino-2-methylpyridine-4-carboxylic acid
CAS No:88482-17-1
MF:C7H8N2O2
MW:152.150621414185
MDL:MFCD15143307
CID:709497
Update Time:2025-11-01

5-amino-2-methylpyridine-4-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 5-Amino-2-methylisonicotinic acid
    • 4-Pyridinecarboxylicacid, 5-amino-2-methyl-
    • 5-ami-2-methylisonicotinic acid
    • 5-AMINO-2-METHYLPYRIDINE-4-CARBOXYLIC ACID
    • 5-Amino-2-methylpyridine-4-carboxylic acid hydrochloride
    • 4-Pyridinecarboxylicacid,5-amino-2-methyl
    • 5-Amino-2-methyl-4pyridinecarboxylic acid
    • 5-amino-2-methyl-isonicotinic acid
    • 5-Amino-2-methyl-isonicotinsaeure
    • 4-Pyridinecarboxylicacid,5-amino-2-methyl-(9CI)
    • 4-PYRIDINECARBOXYLIC ACID, 5-AMINO-2-METHYL-
    • ZB0105
    • 4148AC
    • FCH1176078
    • PB22731
    • OR345039
    • AX8216556
    • 5-amino-2-methyl-4-pyridinecarboxylic acid
    • 5-azanyl-2-methyl-pyridine-4-carboxylic acid
    • A84261
    • 5-Amino-2-methyl-4-pyridinecarboxylic acid (ACI)
    • 5-amino-2-methylpyridine-4-carboxylic acid
    • MDL: MFCD15143307
    • Inchi: 1S/C7H8N2O2/c1-4-2-5(7(10)11)6(8)3-9-4/h2-3H,8H2,1H3,(H,10,11)
    • InChI Key: BXOBZGPEZABVEA-UHFFFAOYSA-N
    • SMILES: O=C(C1C(N)=CN=C(C)C=1)O

Computed Properties

  • Exact Mass: 152.05900
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 161
  • Topological Polar Surface Area: 76.2

Experimental Properties

  • PSA: 76.21000
  • LogP: 1.25160

5-amino-2-methylpyridine-4-carboxylic acid Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

5-amino-2-methylpyridine-4-carboxylic acid Pricemore >>

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Additional information on 5-amino-2-methylpyridine-4-carboxylic acid

Comprehensive Overview of 5-amino-2-methylpyridine-4-carboxylic acid (CAS No. 88482-17-1)

5-amino-2-methylpyridine-4-carboxylic acid (CAS No. 88482-17-1) is a specialized organic compound widely recognized for its versatile applications in pharmaceutical synthesis, agrochemical research, and material science. This heterocyclic derivative, featuring an amino group and a carboxylic acid moiety, has garnered significant attention due to its unique structural properties and reactivity. Researchers and industries increasingly seek this compound for its role in developing novel drug intermediates, biologically active molecules, and catalysts.

The growing demand for 5-amino-2-methylpyridine-4-carboxylic acid is driven by its relevance in medicinal chemistry, particularly in the design of small-molecule inhibitors and antibacterial agents. Recent studies highlight its potential in targeting enzyme pathways and receptor modulation, aligning with trends in personalized medicine and targeted therapy. Its CAS No. 88482-17-1 serves as a critical identifier for regulatory compliance and procurement in global markets.

From a synthetic perspective, 5-amino-2-methylpyridine-4-carboxylic acid is valued for its chemo-selectivity and compatibility with cross-coupling reactions, making it a staple in organocatalysis and green chemistry initiatives. Environmental concerns and the push for sustainable synthesis have further amplified interest in this compound, as it can be derived from eco-friendly protocols with minimal waste generation.

In the agrochemical sector, 5-amino-2-methylpyridine-4-carboxylic acid is explored for formulating crop protection agents and growth regulators. Its structural motifs are pivotal in enhancing the efficacy of pesticide formulations while reducing ecological toxicity—a priority for modern agriculture. Searches for CAS 88482-17-1 suppliers often correlate with queries about high-purity intermediates and custom synthesis services, reflecting its niche industrial demand.

Analytical techniques such as HPLC, NMR, and mass spectrometry are routinely employed to verify the purity and identity of 5-amino-2-methylpyridine-4-carboxylic acid. Quality control remains paramount, especially for applications in GMP-compliant production and preclinical research. The compound’s stability under varying pH and temperature conditions also makes it suitable for formulation studies and drug delivery systems.

Emerging trends in AI-driven drug discovery and computational chemistry have further spotlighted 5-amino-2-methylpyridine-4-carboxylic acid as a scaffold for virtual screening and molecular docking. Its pharmacophore features are frequently queried in databases like PubChem and Reaxys, underscoring its interdisciplinary utility. FAQs around 88482-17-1 solubility, synthetic routes, and patent literature dominate academic and industrial forums.

In summary, 5-amino-2-methylpyridine-4-carboxylic acid (CAS No. 88482-17-1) exemplifies innovation at the intersection of chemistry and life sciences. Its adaptability across biopharmaceuticals, agrochemicals, and advanced materials ensures sustained relevance in research and commercial pipelines. As industries prioritize efficient synthesis and functional diversity, this compound will continue to be a cornerstone of modern chemical development.

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