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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items (±)-Diclofop - analytical standard , CAS No.40843-25-2
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Synonyms
2-[4-(2,4-Dichlorophenoxy)phenoxy]propanoic acid | 2-(4-(2',4'-DICHLOROPHENOXY)PHENOXY)PROPIONIC ACID | 2-(4-(2,4-dichlorophenoxy)phenoxy)propionic acid | HOE-021079 | NCGC00164481-01 | Diclofop | UNII-3LN56779KT | Diclofop [ANSI:BSI:ISO] | (+/-)-Diclofop
Shipped In
Ice chest + Ice pads
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Why this grade analytical standard Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
2-[4-(2, 4-Dichlorophenoxy)phenoxy]propanoic acid | 2-(4-(2', 4'-DICHLOROPHENOXY)PHENOXY)PROPIONIC ACID | 2-(4-(2, 4-dichlorophenoxy)phenoxy)propionic acid | HOE-021079 | NCGC00164481-01 | Diclofop | UNII-3LN56779KT | Diclofop [ANSI:BSI:ISO] | (+/-)-Diclofop
Especificaciones y pureza
analytical standard
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas CC(C(=O)O)OC1=CC=C(C=C1)OC2=C(C=C(C=C2)Cl)Cl IUPAC Name 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid InChIKey OOLBCHYXZDXLDS-UHFFFAOYSA-N INCHI 1S/C15H12Cl2O4/c1-9(15(18)19)20-11-3-5-12(6-4-11)21-14-7-2-10(16)8-13(14)17/h2-9H,1H3,(H,18,19) Isómeros SMILES CC(C(=O)O)OC1=CC=C(C=C1)OC2=C(C=C(C=C2)Cl)Cl Peso molecular 327.16 Reaxy-Rn 2338390 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2338390&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 Benzenoids Clase Benzene and substituted derivatives Subclass 2-phenoxypropionic acids Intermediate Tree Nodes Not available Direct Parent Aryloxyphenoxypropionic acids Alternative Parents Diphenylethers Phenoxyacetic acid derivatives Diarylethers Phenoxy compounds Phenol ethers Dichlorobenzenes Alkyl aryl ethers Aryl chlorides Monocarboxylic acids and derivatives Carboxylic acids Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Aryloxyphenoxypropionic acid - Diphenylether - Phenoxyacetate - Diaryl ether - Phenoxy compound - Phenol ether - 1,3-dichlorobenzene - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organochloride - Organohalogen compound - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as aryloxyphenoxypropionic acids. These are aromatic compounds containing a phenoxypropionic acid that is para-substituted with an aryl group. 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.
Estructura 3D Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad DMSO (Slightly), Methanol (Slightly) Punto de fusión (°C) 99-107°C Peso molecular 327.200 g/mol XLogP3 5.000 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 5 Exact Mass 326.011 Da Monoisotopic Mass 326.011 Da Topological Polar Surface Area 55.800 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 345.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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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