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· · COA & SDS available for every product · Same-day shipping on in-stock items 2-Amino-4-picoline - Moligand™, ≥98% , Inhibitor of Inducible NOS, CAS No.695-34-1, Inhibitor of Inducible NOS
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% Synonyms
A0402 | BRD-K74039237-001-01-7 | WLN: T6NJ BZ D1 | AKOS000119085 | FT-0661940 | Tocris-1020 | W-45 | 4-methylpyridyl amine | STK385035 | 4M2AP | DTXCID9024720 | Ascensil | DTXSID1044720 | Methyl-4 amino-2-pyridine | NSC-176165 | 4-METHYLPYRIDIN-2-AMINE, 6
Storage
Store at 2-8°C,Argon charged
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Why this grade Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Argon charged Ships Wet ice 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Product Description：
2-Amino-4-methylpyridine acts as ligand and forms methoxo-bridged copper(II) complexes.
Product Application：
2-Amino-4-methylpyridine has been used in the synthesis of 2-amino-4-methyl-pyridinium 2-hy¬droxy¬benzoate.
Specifications Synonyms
A0402 | BRD-K74039237-001-01-7 | WLN: T6NJ BZ D1 | AKOS000119085 | FT-0661940 | Tocris-1020 | W-45 | 4-methylpyridyl amine | STK385035 | 4M2AP | DTXCID9024720 | Ascensil | DTXSID1044720 | Methyl-4 amino-2-pyridine | NSC-176165 | 4-METHYLPYRIDIN-2-AMINE, 6
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
2-Amino-4-methylpyridine inhibits the activity of inducible NO synthase isolated from mouse RAW 264.7 cells in vitro.
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Inhibitor of Inducible NOS
Names and Identifiers Canonical Smiles CC1=CC(=NC=C1)N IUPAC Name 4-methylpyridin-2-amine InChIKey ORLGLBZRQYOWNA-UHFFFAOYSA-N INCHI 1S/C6H8N2/c1-5-2-3-8-6(7)4-5/h2-4H,1H3,(H2,7,8) Isomeric SMILES CC1=CC(=NC=C1)N WGK Germany 3 RTECS TJ5150000 UN Number 2811 Molecular Weight 108.14 Beilstein 107066 Reaxy-Rn 107066 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=107066&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 Solubility Soluble in water (41 mg/ml at 20 °C), lower alcohols (slightly), chloroform, ethyl acetate, and DMF. Sensitivity Moisture sensitive Flash Point(°F) 244.4 °F Flash Point(°C) 118 °C Boil Point(°C) 230°C Melt Point(°C) 96-101°C Molecular Weight 108.140 g/mol XLogP3 0.600 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 0 Exact Mass 108.069 Da Monoisotopic Mass 108.069 Da Topological Polar Surface Area 38.900 Ų Heavy Atom Count 8 Formal Charge 0 Complexity 72.900 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. Xiaopeng Wei, Shuang Chen, Guoyuan Zheng, Qiule Zhao, Shuyi Mo, Jilin Wang, Disheng Yao, Nan Tian, Fei Long. (2024) Synthesis, crystal structure, thermal stability, and photovoltaic properties of organic-inorganic hybridized copper-based perovskite single crystals modulated by organics. JOURNAL OF MOLECULAR STRUCTURE, [PMID: [10.1016/j.molstruc.2024.137634 ]
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