Picloram - ≥95% , CAS No.1918-02-1

CAS: 1918-02-1 Cat. No.: P141070 Formula: C6H3Cl3N2O2 Peso molecolare: 241.46 Beilstein Registry Number: 479075 Numero EC: 217-636-1
Disponibile su ordine
QUALITÀ & PUREZZA ≥95%
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
Shipped In
Normale
★
Dimensione
Germania (EU)
USA*
Prezzo
Qtà
25g
P141070-25g
—
2 Disponibile
120,53€
100g
P141070-100g
—
2 Disponibile
229,00€
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Panoramica

L'atrazina è stata utilizzata come integratore nel terreno di coltura degli embrioni.

Specifiche

Sinonimi
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
Specifiche e purezza
≥95%
Meccanismi biochimici e fisiologici
l'acido 4-amino-3,5,6-tricloropiridina-2-carbossilico (4-amino-3,5,6-tricloropiridina-2-carbossilico) è un erbicida clorurato ampiamente utilizzato nel controllo delle piante legnose e delle infestanti a foglia larga. L'atrazina può indurre l'embriogenesi
Condizioni di conservazione di stoccaggio
Argon charged,Room temperature
Spedito in
Normale
Purezza
≥95%
Nomi e identificatori
Pubchem Sid
Sorrisi canonici
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)
Isomeri SMILES
C1(=C(C(=NC(=C1Cl)Cl)C(=O)O)Cl)N
WGK Germania
2
RTECS
TJ7525000
Peso molecolare
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=

Dati avanzati

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassePyridines and derivatives
SubclassPyridinecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentPyridinecarboxylic 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 FrameworkAromatic 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
DescrizioneThis 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
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeDataOggetto
H2203571H2203571Certificate of AnalysisMay 18, 2026 P141070
L2108111L2108111Certificate of AnalysisSep 09, 2025 P141070
Proprietà chimiche e fisiche
SolubilitàSoluble in acetone
SensibilitàMoisture sensitive
Punto di fusione (°C)200°C
Peso molecolare241.500 g/mol
XLogP32.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass239.926 Da
Monoisotopic Mass239.926 Da
Topological Polar Surface Area76.200 Ų
Heavy Atom Count13
Formal Charge0
Complexity216.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Calcolatori di soluzioni
Recensioni

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