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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items (1,3,4,5,6,7-Hexahydro-1,3-dioxo-2H-isoindol-2-yl)methyl (1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate - analytical standard , CAS No.1166-46-7
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Synonyms
1166-46-7|d-Tetramethrin|D-trans-Tetramethrin|(+)-trans-Tetramethrin|(1R)-trans-Tetramethrin|Tetramethrin, D-trans-|trans-Tetramethrin|(1,3,4,5,6,7-Hexahydro-1,3-dioxo-2H-isoindol-2-yl)methyl (1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarb
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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 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
1166-46-7 | d-Tetramethrin | D-trans-Tetramethrin | (+)-trans-Tetramethrin | (1R)-trans-Tetramethrin | Tetramethrin, D-trans- | trans-Tetramethrin | (1, 3, 4, 5, 6, 7-Hexahydro-1, 3-dioxo-2H-isoindol-2-yl)methyl (1R-trans)-2, 2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarb
Especificaciones y pureza
analytical standard
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Sonrisas canónicas CC(=CC1C(C1(C)C)C(=O)OCN2C(=O)C3=C(C2=O)CCCC3)C IUPAC Name (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate InChIKey CXBMCYHAMVGWJQ-CABCVRRESA-N INCHI 1S/C19H25NO4/c1-11(2)9-14-15(19(14,3)4)18(23)24-10-20-16(21)12-7-5-6-8-13(12)17(20)22/h9,14-15H,5-8,10H2,1-4H3/t14-,15+/m1/s1 Isómeros SMILES CC(=C[C@@H]1[C@H](C1(C)C)C(=O)OCN2C(=O)C3=C(C2=O)CCCC3)C Peso molecular 331.406 Reaxy-Rn 1547171 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1547171&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 Organoheterocyclic compounds Clase Isoindoles and derivatives Subclass Isoindolines Intermediate Tree Nodes Not available Direct Parent Isoindolones Alternative Parents Bicyclic monoterpenoids Isoindoles Maleimides Cyclopropanecarboxylic acids and derivatives N-substituted carboxylic acid imides Pyrrolines Dicarboximides Carboxylic acid esters Lactams Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Organonitrogen compounds Carbonyl compounds Organopnictogen compounds Molecular Framework Aliphatic heteropolycyclic compounds Substituents Bicyclic monoterpenoid - Isoindolone - Monoterpenoid - Isoindole - Maleimide - Cyclopropanecarboxylic acid or derivatives - Carboxylic acid imide, n-substituted - Pyrroline - Carboxylic acid imide - Dicarboximide - Carboxylic acid ester - Lactam - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Aliphatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone. External Descriptors Not available 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 Solubilidad Insoluble in water, soluble in hexane, methanol, xylene and other organic solvents. Punto de inflamación (°C) 200ºC Punto de fusión (°C) 68-70ºC Peso molecular 331.400 g/mol XLogP3 4.700 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 5 Exact Mass 331.178 Da Monoisotopic Mass 331.178 Da Topological Polar Surface Area 63.700 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 639.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 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
Citations of This Product Referencias 1. Yang Li, Mijia Li, Shiyi Duan, Sijie Zhang, Huiqiang Lu, Xinchun Guo, Keyuan Zhong. (2024) d-Tetramethrin causes zebrafish hepatotoxicity by inducing oxidative stress and inhibiting cell proliferation. TOXICOLOGY AND APPLIED PHARMACOLOGY, [PMID:38215995 ] [10.1016/j.taap.2024.116817 ] 2. Xinhao Ye, Mijia Li, YunLong Meng, Shiyi Duan, Sijie Zhang, Keyuan Zhong. (2025) D-tetramethrin induces cardiac looping failure in zebrafish during embryonic development. COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, [PMID:40086682 ] [10.1016/j.cbpc.2025.110193 ] 3. Yang Li, Keyuan Zhong, Sijie Zhang, Shiyi Duan, Kaijie Huang, Xiaofang Che, Xinchun Guo, Huiqiang Lu. (2025) Effects of D-Tetramethrin on Zebrafish Development and Immune System. ENVIRONMENTAL TOXICOLOGY, [PMID:39960059 ] [10.1002/tox.24487 ]
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