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· · COA & SDS available for every product · Same-day shipping on in-stock items Triflumuron - analytical standard , CAS No.64628-44-0
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Synonyms
Triflumuron|64628-44-0|Trifluron|Triflumuron [ISO]|SIR 8514|2-Chloro-N-(((4-(trifluoromethoxy)phenyl)amino)carbonyl)benzamide|Alsystin|3FT64DYG8K|1-(o-chlorobenzoyl)-3-(p-(trifluoromethoxy)phenyl)urea|2-chloro-N-[[4-(trifluoromethoxy)phenyl]carbamoyl]benz
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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 Room temperature Ships Normal 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 43 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Triflumuron is a chitin biosynthesis inhibitor capable of preventing the incorporation of uridine into RNA.
Specifications Synonyms
Triflumuron | 64628-44-0 | Trifluron | Triflumuron [ISO] | SIR 8514 | 2-Chloro-N-(((4-(trifluoromethoxy)phenyl)amino)carbonyl)benzamide | Alsystin | 3FT64DYG8K | 1-(o-chlorobenzoyl)-3-(p-(trifluoromethoxy)phenyl)urea | 2-chloro-N-[[4-(trifluoromethoxy)phenyl]carbamoyl]benz
Specifications & Purity
analytical standard
Names and Identifiers Pubchem Sid 528772119 Canonical Smiles C1=CC=C(C(=C1)C(=O)NC(=O)NC2=CC=C(C=C2)OC(F)(F)F)Cl IUPAC Name 2-chloro-N-[[4-(trifluoromethoxy)phenyl]carbamoyl]benzamide InChIKey XAIPTRIXGHTTNT-UHFFFAOYSA-N INCHI 1S/C15H10ClF3N2O3/c16-12-4-2-1-3-11(12)13(22)21-14(23)20-9-5-7-10(8-6-9)24-15(17,18)19/h1-8H,(H2,20,21,22,23) Isomeric SMILES C1=CC=C(C(=C1)C(=O)NC(=O)NC2=CC=C(C=C2)OC(F)(F)F)Cl WGK Germany 2 RTECS CV2474000 Molecular Weight 358.7 Beilstein 2776684 Reaxy-Rn 2776684 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2776684&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 Class Benzene and substituted derivatives Subclass N-phenylureas Intermediate Tree Nodes N-acyl-phenylureas Direct Parent N-benzoyl-N'-phenylureas Alternative Parents 2-halobenzoic acids and derivatives Phenoxy compounds Phenol ethers Benzoyl derivatives Chlorobenzenes Aryl chlorides Vinylogous halides Ureas Trihalomethanes Carboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Organochlorides Carbonyl compounds Organofluorides Organonitrogen compounds Alkyl fluorides Organopnictogen compounds Molecular Framework Aromatic homomonocyclic compounds Substituents N-benzoyl-n'-phenylurea - Halobenzoic acid or derivatives - 2-halobenzoic acid or derivatives - Benzoic acid or derivatives - Phenoxy compound - Benzoyl - Phenol ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Vinylogous halide - Trihalomethane - Urea - Carbonic acid derivative - Carboxylic acid derivative - Alkyl fluoride - Organofluoride - Organochloride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Halomethane - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as n-benzoyl-n'-phenylureas. These are n-acyl-phenylureas that have the acyl group substituted by a phenyl group. External Descriptors Pesticides 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 Molecular Weight 358.700 g/mol XLogP3 5.600 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 3 Exact Mass 358.033 Da Monoisotopic Mass 358.033 Da Topological Polar Surface Area 67.400 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 454.000 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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