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· · COA & SDS available for every product · Same-day shipping on in-stock items 2-Amino-4,6-dimethylpyridine - ≥98% , CAS No.5407-87-4
Synonyms
4,6-Dimethyl-2-aminopyridine | 7NVZ9DW9Q5 | STL557611 | W-105678 | 2-amino-4,6-dimethyl pyridine | 2-amino-4.6-dimethylpyridine | 2-Pyridinamine 4,6-dimethyl- | BRN 0002048 | AM20070146 | BBL103801 | Z1192367241 | AKOS005145684 | 2-Pyridinamine, 4,6-dimet
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Why this grade ≥98% 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
4, 6-Dimethyl-2-aminopyridine | 7NVZ9DW9Q5 | STL557611 | W-105678 | 2-amino-4, 6-dimethyl pyridine | 2-amino-4.6-dimethylpyridine | 2-Pyridinamine 4, 6-dimethyl- | BRN 0002048 | AM20070146 | BBL103801 | Z1192367241 | AKOS005145684 | 2-Pyridinamine, 4, 6-dimet
Specifications & Purity
≥98%
Names and Identifiers Pubchem Sid 504753040 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504753040 Canonical Smiles CC1=CC(=NC(=C1)N)C IUPAC Name 4,6-dimethylpyridin-2-amine InChIKey BRBUBVKGJRPRRD-UHFFFAOYSA-N INCHI 1S/C7H10N2/c1-5-3-6(2)9-7(8)4-5/h3-4H,1-2H3,(H2,8,9) Isomeric SMILES CC1=CC(=NC(=C1)N)C WGK Germany 3 RTECS US1818000 Molecular Weight 122.17 Reaxy-Rn 2048 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2048&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 Aminopyridines and derivatives Intermediate Tree Nodes Not available Direct Parent Aminopyridines and derivatives Alternative Parents Methylpyridines Imidolactams Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Methylpyridine - Aminopyridine - Imidolactam - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as aminopyridines and derivatives. These are organic heterocyclic compounds containing an amino group attached to a pyridine ring. 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) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Boil Point(°C) 231°C Melt Point(°C) 67°C Molecular Weight 122.170 g/mol XLogP3 1.300 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 0 Exact Mass 122.084 Da Monoisotopic Mass 122.084 Da Topological Polar Surface Area 38.900 Ų Heavy Atom Count 9 Formal Charge 0 Complexity 92.900 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
Citations of This Product References 1. Li-Jing Zhu, Li-Ping Zhu, Pei-Bin Zhang, Bao-Ku Zhu, You-Yi Xu. (2016) Surface zwitterionicalization of poly(vinylidene fluoride) membranes from the entrapped reactive core–shell silica nanoparticles. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:26835581 ] [10.1016/j.jcis.2016.01.043 ] 2. Li-Jing Zhu, Li-Ping Zhu, Yi-Fan Zhao, Bao-Ku Zhu, You-Yi Xu. (2014) Anti-fouling and anti-bacterial polyethersulfone membranes quaternized from the additive of poly(2-dimethylamino ethyl methacrylate) grafted SiO2 nanoparticles. Journal of Materials Chemistry A, 2 (37): (15566-15574). [PMID: [10.1039/C4TA03199G ] 3. Li-Jing Zhu, Li-Ping Zhu, Jin-Hong Jiang, Zhuan Yi, Yi-Fan Zhao, Bao-Ku Zhu, You-Yi Xu. (2013) Hydrophilic and anti-fouling polyethersulfone ultrafiltration membranes with poly(2-hydroxyethyl methacrylate) grafted silica nanoparticles as additive. JOURNAL OF MEMBRANE SCIENCE, [PMID: [10.1016/j.memsci.2013.09.053 ] 4. Zhuan Yi, Liping Zhu, Liang Cheng, Baoku Zhu, Youyi Xu. (2011) A readily modified polyethersulfone with amino-substituted groups: Its amphiphilic copolymer synthesis and membrane application. POLYMER, [PMID: [10.1016/j.polymer.2011.11.053 ]
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