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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Picloram - ≥95% , CAS No.1918-02-1
Synonyms
WOM | 4-Amino-3,6-trichloro-2-picolinic acid | 4-Amino-3,6-trichlorpicolinsaeure | STK179674 | Picloram [ANSI:BSI:ISO] | PICLORAM [MI] | 2-Pyridinecarboxylic acid, 4-amino-3,5,6-trichloro- | 3,6-Trichloro-4-aminopicolinic acid | Tordon 22K | 4-Amino-3,5,6
Storage
Argon charged,Room temperature
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Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Argon charged,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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general Atrazine has been used as a supplement in the growth medium of embryos.
Specifications Sinónimos
WOM | 4-Amino-3, 6-trichloro-2-picolinic acid | 4-Amino-3, 6-trichlorpicolinsaeure | STK179674 | Picloram [ANSI:BSI:ISO] | PICLORAM [MI] | 2-Pyridinecarboxylic acid, 4-amino-3, 5, 6-trichloro- | 3, 6-Trichloro-4-aminopicolinic acid | Tordon 22K | 4-Amino-3, 5, 6
Especificaciones y pureza
≥95%
Mecanismos bioquímicos y fisiológicos
4-amino-3, 5, 6-trichloropyridine-2-carboxylic acid (4-amino-3, 5, 6-trichloropyridine-2-carboxylic acid) is a chlorinated herbicide widely used in the control of woody plants and broad-leaved weeds. Atrazine can induce direct somatic embryogenesis of Lilium
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Nombres e identificadores Sonrisas canónicas C1(=C(C(=NC(=C1Cl)Cl)C(=O)O)Cl)N IUPAC Name 4-amino-3,5,6-trichloropyridine-2-carboxylic acid InChIKey NQQVFXUMIDALNH-UHFFFAOYSA-N INCHI 1S/C6H3Cl3N2O2/c7-1-3(10)2(8)5(9)11-4(1)6(12)13/h(H2,10,11)(H,12,13) Isómeros SMILES C1(=C(C(=NC(=C1Cl)Cl)C(=O)O)Cl)N WGK Alemania 2 RTECS TJ7525000 Peso molecular 241.46 Beilstein 479075 Reaxy-Rn 479075 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=479075&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 Clase Pyridines and derivatives Subclass Pyridinecarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Pyridinecarboxylic acids Alternative Parents Polyhalopyridines 2-halopyridines Aminopyridines and derivatives Aryl chlorides Vinylogous halides Heteroaromatic compounds Amino acids Azacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organopnictogen compounds Primary amines Organochlorides Organic oxides Hydrocarbon derivatives Organooxygen compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents Pyridine carboxylic acid - Polyhalopyridine - Aminopyridine - 2-halopyridine - Aryl chloride - Aryl halide - Heteroaromatic compound - Vinylogous halide - Amino acid or derivatives - Amino acid - Carboxylic acid derivative - Azacycle - Carboxylic acid - Monocarboxylic acid or derivatives - Amine - Organonitrogen compound - Organochloride - Organohalogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound Descripción 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 Pyridine herbicides 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in acetone Sensibilidad Moisture sensitive Punto de fusión (°C) 200°C Peso molecular 241.500 g/mol XLogP3 2.200 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 239.926 Da Monoisotopic Mass 239.926 Da Topological Polar Surface Area 76.200 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 216.000 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
Citations of This Product Referencias 1. Zhefei Zhao, Xuyao Yao, Linlin Zhang, Minhao Chen, Xingyu Luo, Ruopeng Yu, Yinghua Xu, Youqun Chu, Xinbiao Mao, Huajun Zheng. (2024) AgCu bimetallic electrocatalyst for the selective dechlorination of 4-amino-3,5,6-trichloropyridine carboxylic acid. ELECTROCHIMICA ACTA, [PMID: [10.1016/j.electacta.2024.144722 ] 2. Jingyu Zhang, Huihui Hu, Jian Wang, Keqiang Lu, Yunyun Zhou, Lingzhi Zhao, Juanjuan Peng. (2024) Gold nanoclusters-based fluorescence sensor array for herbicides qualitative and quantitative analysis. ANALYTICA CHIMICA ACTA, [PMID:38462337 ] [10.1016/j.aca.2024.342380 ]
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