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340,000+ produits de recherche · Triple ISO certified · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock MCPA - ≥98%(T) , CAS No.94-74-6
Synonyms
MCPA [ISO]|Hormotuho|Phenoxylene 50|Empal|Linormone|Methylchlorophenoxyacetic acid|Cekherbex|Cornox-M|Anicon kombi|B-Selektonon M|Legumex db|Leuna M|Phenoxylene super|Rhonox|Rhomenc|((4-Chloro-o-tolyl)oxy)acetic acid|(4-Chloro-2-methylphenoxy)acetic acid|Dikotes|Mephanac|Acetic acid, (4-chloro-2-methylphenoxy)-|MCPA [BSI:ISO]|[(4-Chloro-o-tolyl)oxy]acetic acid|2-Methyl-4-chlorphenoxyessigsaeure [German]|MCPA|Weedone mcpa ester|Acetic acid, 2-(4-chloro-2-methylphenoxy)-|Trasan|Weedar MCPA|(4-Chloro-o-cresoxy)acetic acid|Agroxon|Chwastox|Acetic acid, [(4-chloro-o-tolyl)oxy]-|M 40|Okultin M|Chwastox 30|MCPA [Chlorophenoxy herbicides]|Netazol|4-Chloro-o-toloxyacetic acid|Cornox|Dicopur-M|Dikotex|Metaxon|Phenoxylene plus|Agritox 50|Raphone|Razol dock killer|Selektonon M|2-METHYL-4-CHLOROPHENOXYACETIC ACID|2-Methyl-4-chlorophenoxyaceticacid|Herbicide M|Acme MCPA Amine 4|Zelan|(2-Methyl-4-chlorophenoxy)acetic acid|Mecaphar|Seppic mmd|Vacate|Acetic acid, ((4-chloro-o-tolyl)oxy)-|Agricorn 500 II|Hedapur M 52|Hedarex M|Kyselina 4-chlor-2-methylfenoxyoctova|2-Methyl-4-chlorphenoxyessigsaeure|Agroxone|Kwas 4-chloro-2-metylofenoksyoctowy [Polish]|Leyspray|Ustinex|(4-Chloro-o-toloxy)acetic acid|Brominal M & plus|Kwas 4-chloro-2-metylofenoksyoctowy|2-(4-Chloro-2-methylphenoxy)acetic acid|2-(4-chloro-2-methyl-phenoxy)acetic acid|Agritox|Atlas MCPA|Hedonal M|Chwastox Extra|Rhomene|Vesakontuho mcpa|2,4-MCPA|Kilsem|Banvel M|Emcepan|(4-Chloro-2-methylphenoxy)aceticAcid-13C6|Albar-M|Bordermaster|Hornotuho|Anicon M|Chiptox|Soviet technical herbicide 2M-4C|Aceticacid, 2-(4-chloro-2-methylphenoxy)-
Spécifications Synonymes
MCPA [ISO] | Hormotuho | Phenoxylene 50 | Empal | Linormone | Methylchlorophenoxyacetic acid | Cekherbex | Cornox-M | Anicon kombi | B-Selektonon M | Legumex db | Leuna M | Phenoxylene super | Rhonox | Rhomenc | ((4-Chloro-o-tolyl)oxy)acetic acid | (4-Chloro-2-methylphenoxy)acetic acid | Dikotes | Mephanac | Acetic acid, (4-chloro-2-methy Afficher plus
Spécifications et pureté
≥98%(T)
Conditions de stockage de stockage
Room temperature
Noms et identifiants Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508808421
Sourires canoniques
CC1=C(C=CC(=C1)Cl)OCC(=O)O
IUPAC Name
2-(4-chloro-2-methylphenoxy)acetic acid
InChIKey
WHKUVVPPKQRRBV-UHFFFAOYSA-N
INCHI
1S/C9H9ClO3/c1-6-4-7(10)2-3-8(6)13-5-9(11)12/h2-4H,5H2,1H3,(H,11,12)
Isomères SMILES
CC1=C(C=CC(=C1)Cl)OCC(=O)O
Numéro ONU
3077(international)
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2051752&ln=
Données avancées Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Classe Benzene and substituted derivatives Subclass Phenoxyacetic acid derivatives Intermediate Tree Nodes Not available Direct Parent Chlorophenoxyacetates Alternative Parents Phenoxy compounds Phenol ethers Toluenes Chlorobenzenes Alkyl aryl ethers Aryl chlorides Monocarboxylic acids and derivatives Carboxylic acids Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Chlorophenoxyacetate - Phenoxy compound - Phenol ether - Alkyl aryl ether - Toluene - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organic oxide - Organochloride - Hydrocarbon derivative - Organohalogen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as chlorophenoxyacetates. These are compounds containing a phenoxyacetate that carries one or more chlorine atoms on the benzene ring. External Descriptors Phenoxy 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Solubilité Insoluble in water; Degree of Solubility in water: 630 mg/l 25 °C; Very soluble in Ethanol; Soluble in Methanol,Benzene,Toluene,Ether Point de fusion (°C) 114-118°C Poids moléculaire 200.620 g/mol XLogP3 2.600 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 3 Exact Mass 200.024 Da Monoisotopic Mass 200.024 Da Topological Polar Surface Area 46.500 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 184.000 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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