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· · COA & SDS available for every product · Same-day shipping on in-stock items 5-Methoxynicotinic acid - ≥97% , CAS No.20826-03-3
Synonyms
VDZUWTLBWRZRTR-UHFFFAOYSA-N | 3-PYRIDINECARBOXYLIC ACID, 5-METHOXY- | AM20070161 | SY101244 | DTXSID101313471 | 5-methoxypyridine-3-carboxylic Acid | MFCD01603648 | 5-Methoxypyridine-3-carboxylic acid, 97% | FT-0678833 | 5-Methoxynicotinic acid | 5-Methox
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
VDZUWTLBWRZRTR-UHFFFAOYSA-N | 3-PYRIDINECARBOXYLIC ACID, 5-METHOXY- | AM20070161 | SY101244 | DTXSID101313471 | 5-methoxypyridine-3-carboxylic Acid | MFCD01603648 | 5-Methoxypyridine-3-carboxylic acid, 97% | FT-0678833 | 5-Methoxynicotinic acid | 5-Methox
Specifications & Purity
≥97%
Names and Identifiers Pubchem Sid 488194983 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488194983 Canonical Smiles COC1=CN=CC(=C1)C(=O)O IUPAC Name 5-methoxypyridine-3-carboxylic acid InChIKey VDZUWTLBWRZRTR-UHFFFAOYSA-N INCHI 1S/C7H7NO3/c1-11-6-2-5(7(9)10)3-8-4-6/h2-4H,1H3,(H,9,10) Isomeric SMILES COC1=CN=CC(=C1)C(=O)O WGK Germany 3 Molecular Weight 153.14 Reaxy-Rn 387440 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=387440&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Pyridines and derivatives Subclass Pyridinecarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Pyridinecarboxylic acids Alternative Parents Alkyl aryl ethers Heteroaromatic compounds Carboxylic acids Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Pyridine carboxylic acid - Alkyl aryl ether - Heteroaromatic compound - Azacycle - Ether - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as pyridinecarboxylic acids. These are compounds containing a pyridine ring bearing a carboxylic acid group. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 153.140 g/mol XLogP3 0.300 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 2 Exact Mass 153.043 Da Monoisotopic Mass 153.043 Da Topological Polar Surface Area 59.400 Ų Heavy Atom Count 11 Formal Charge 0 Complexity 149.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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