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· · COA & SDS available for every product · Same-day shipping on in-stock items Binapacryl - analytical standard , CAS No.485-31-4
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Synonyms
BINAPACRYL|485-31-4|Endosan|Dinapacryl|Acricid|Dapacryl|Morocide|Morrocid|Ambox|Dinoseb methacrylate|Niagara 9044|HOE 2784 OA|Dinoseb, 3,3-dimethylacryl ester|2-(1-Methylpropyl)-4,6-dinitrophenyl 3-methyl-2-butenoate|FMC 9044|HOE 2784|NIA 9044|ENT 25,793|
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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 FedEx DG Service 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 Synonyms
BINAPACRYL | 485-31-4 | Endosan | Dinapacryl | Acricid | Dapacryl | Morocide | Morrocid | Ambox | Dinoseb methacrylate | Niagara 9044 | HOE 2784 OA | Dinoseb, 3, 3-dimethylacryl ester | 2-(1-Methylpropyl)-4, 6-dinitrophenyl 3-methyl-2-butenoate | FMC 9044 | HOE 2784 | NIA 9044 | ENT 25, 793 |
Specifications & Purity
analytical standard
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This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CCC(C)C1=C(C(=CC(=C1)[N+](=O)[O-])[N+](=O)[O-])OC(=O)C=C(C)C IUPAC Name (2-butan-2-yl-4,6-dinitrophenyl) 3-methylbut-2-enoate InChIKey ZRDUSMYWDRPZRM-UHFFFAOYSA-N INCHI 1S/C15H18N2O6/c1-5-10(4)12-7-11(16(19)20)8-13(17(21)22)15(12)23-14(18)6-9(2)3/h6-8,10H,5H2,1-4H3 Isomeric SMILES CCC(C)C1=C(C(=CC(=C1)[N+](=O)[O-])[N+](=O)[O-])OC(=O)C=C(C)C WGK Germany 3 RTECS GQ5600000 UN Number 2811 Packing Group III Molecular Weight 322.31 Beilstein 2013712 Reaxy-Rn 2013712 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2013712&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 Phenol esters Subclass Not available Intermediate Tree Nodes Not available Direct Parent Phenol esters Alternative Parents Phenylpropanes Nitrobenzenes Phenoxy compounds Nitroaromatic compounds Fatty acid esters Enoate esters Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Monocarboxylic acids and derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Phenol ester - Nitrobenzene - Phenylpropane - Phenoxy compound - Nitroaromatic compound - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Organic oxoazanium - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group. External Descriptors Acaricides 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 Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Melt Point(°C) 65-69°C Molecular Weight 322.310 g/mol XLogP3 4.600 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 5 Exact Mass 322.116 Da Monoisotopic Mass 322.116 Da Topological Polar Surface Area 118.000 Ų Heavy Atom Count 23 Formal Charge 0 Complexity 489.000 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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