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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Boron trifluoride acetic acid complex - ≥98% , CAS No.373-61-5
Disponível para encomenda
Synonyms
MFCD00036359 | A874127 | acetic acid;trifluoroborane | Borate(1-), bis(acetato-.kappa.O)difluoro-, hydrogen fluoride (1:2:1), (T-4)- | AKOS015903322 | SCHEMBL734341 | FT-0623181 | Borate(1-), bis(acetato-O)difluoro-, dihydrogen fluoride, (T-4)-
Storage
Room temperature,Argon charged,Desiccated
Shipped In
FedEx DG Service
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Argon charged,Desiccated 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
MFCD00036359 | A874127 | acetic acid;trifluoroborane | Borate(1-), bis(acetato-.kappa.O)difluoro-, hydrogen fluoride (1:2:1), (T-4)- | AKOS015903322 | SCHEMBL734341 | FT-0623181 | Borate(1-), bis(acetato-O)difluoro-, dihydrogen fluoride, (T-4)-
Especificações e pureza
≥98%
Condições de armazenamento de armazenamento
Room temperature,Argon charged,Desiccated
Enviado em
FedEx DG Service
Nomes e identificadores Pubchem Sid 528769058 Sorrisos canónicos B(F)(F)F.CC(=O)O.CC(=O)O IUPAC Name acetic acid;trifluoroborane InChIKey COTMJGCQSLZICX-UHFFFAOYSA-N INCHI 1S/2C2H4O2.BF3/c2*1-2(3)4;2-1(3)4/h2*1H3,(H,3,4); SMILES isoméricas B(F)(F)F.CC(=O)O.CC(=O)O WGK Alemanha 3 PubChem CID 11116786 Número UN 1742 Grupo de embalagem II Peso molecular 187.91 Beilstein 3686517
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 Classe Carboxylic acids and derivatives Subclass Carboxylic acids Intermediate Tree Nodes Not available Direct Parent Carboxylic acids Alternative Parents Organic metalloid salts Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Not available Substituents Organic metalloid salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound Descrição This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH. 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.
Estrutura 3D Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade Moisture sensitive. Índice de refração 1.368 Ponto de inflamação (°F) 181.4 °F Ponto de inflamação (°C) 83 °C Peso molecular 187.910 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 0 Exact Mass 188.047 Da Monoisotopic Mass 188.047 Da Topological Polar Surface Area 74.600 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 39.000 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 3
Citations of This Product Referências 1. Jiajun Gao, Wenyan Ma, Linpo Yuan, Yafen Dai, Chunxi Li. (2013) Catalytic oxidative desulfurization mechanism in Lewis–Brønsted complex acid. APPLIED CATALYSIS A-GENERAL, [PMID: [10.1016/j.apcata.2013.07.023 ]
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