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· · COA & SDS available for every product · 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
Overview Atrazine has been used as a supplement in the growth medium of embryos.
Specifications 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
Specifications & Purity
≥95%
Biochemical and Physiological Mechanisms
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
Storage
Argon charged,Room temperature
Names and Identifiers Canonical Smiles
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)
Isomeric SMILES
C1(=C(C(=NC(=C1Cl)Cl)C(=O)O)Cl)N
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=479075&ln=
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 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 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 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.
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 acetone Sensitivity Moisture sensitive x_melt_point_char 200°C Molecular Weight 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
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