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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Dimethoate solution - analytical standard, 10ug/ml in acetone , CAS No.60-51-5
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. 10ug/ml in acetone Synonyms
dimethoate|60-51-5|Phosphamide|Rogor|Phosphamid|Lurgo|Perfecthion|Perfekthion|Daphene|Dimeton|Dimevur|Fosfotox|Racusan|Sinoratox|Systoate|Cygon|Roxion|Fosfatox R|Fosfotox R|De-fend|Fostion MM|Rogor L|Rogor P|Aadimethoal|Cygon 4E|Dimethogen|Fosfamid|Rebela
Storage
Store at 2-8°C,Protected from light
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Why this grade analytical standard, 10ug/ml in acetone Patrón analítico for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light Ships Wet ice 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 103 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
dimethoate | 60-51-5 | Phosphamide | Rogor | Phosphamid | Lurgo | Perfecthion | Perfekthion | Daphene | Dimeton | Dimevur | Fosfotox | Racusan | Sinoratox | Systoate | Cygon | Roxion | Fosfatox R | Fosfotox R | De-fend | Fostion MM | Rogor L | Rogor P | Aadimethoal | Cygon 4E | Dimethogen | Fosfamid | Rebela
Especificaciones y pureza
analytical standard, 10ug/ml in acetone
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C,Protected from light
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas
CNC(=O)CSP(=S)(OC)OC
IUPAC Name
2-dimethoxyphosphinothioylsulfanyl-N-methylacetamide
InChIKey
MCWXGJITAZMZEV-UHFFFAOYSA-N
INCHI
1S/C5H12NO3PS2/c1-6-5(7)4-12-10(11,8-2)9-3/h4H2,1-3H3,(H,6,7)
Isómeros SMILES
CNC(=O)CSP(=S)(OC)OC
Número ONU
2783(solid)3018(liquid)
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1785339&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 Organic acids and derivatives Clase Organic dithiophosphoric acids and derivatives Subclass Dithiophosphate O-esters Intermediate Tree Nodes Not available Direct Parent Dithiophosphate O-esters Alternative Parents Dithiophosphate S-esters Secondary carboxylic acid amides Sulfenyl compounds Organothiophosphorus compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Dithiophosphate s-ester - Dithiophosphate o-ester - Carboxamide group - Secondary carboxylic acid amide - Sulfenyl compound - Organothiophosphorus compound - Carboxylic acid derivative - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as dithiophosphate o-esters. These are o-ester derivatives of dithiophosphates, with the general structure RSP(O)(O)=S (R = organyl group). External Descriptors Organophosphorus insecticides 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 Sensibilidad Light sensitive. Punto de inflamación (°C) 2°C Punto de ebullición (°C) 107°C Punto de fusión (°C) 52-52.5°C Peso molecular 229.300 g/mol XLogP3 0.800 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 5 Exact Mass 229 Da Monoisotopic Mass 229 Da Topological Polar Surface Area 105.000 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 191.000 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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