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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items N-Acetylprocainamide hydrochloride - ≥98%(HPLC) , CAS No.34118-92-8
Synonyms
A20512 | Acecainide hydrochloride | NCGC00015072-10 | Tox21_500009 | Benzylpenicillin G | J-019456 | SCHEMBL122991 | SMR000059132 | SPECTRUM2300154 | AS-75674 | N16908 | Benzamide, 4-(acetylamino)-N-(2-(diethylamino)ethyl)-, monohydrochloride | Riboazaura
Shipped In
Ice chest + Ice pads
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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 Sinónimos
A20512 | Acecainide hydrochloride | NCGC00015072-10 | Tox21_500009 | Benzylpenicillin G | J-019456 | SCHEMBL122991 | SMR000059132 | SPECTRUM2300154 | AS-75674 | N16908 | Benzamide, 4-(acetylamino)-N-(2-(diethylamino)ethyl)-, monohydrochloride | Riboazaura
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Class III antiarrhythmic. Increases the duration of the action potential by decreasing the delayed outward potassium current, slightly decreasing the calcium current, and slightly depressing the inward rectifier potassium current. This is the active metab
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 504754624 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504754624 Sonrisas canónicas CCN(CC)CCNC(=O)C1=CC=C(C=C1)NC(=O)C.Cl IUPAC Name 4-acetamido-N-[2-(diethylamino)ethyl]benzamide;hydrochloride InChIKey IYEWBJUCJHKLHD-UHFFFAOYSA-N INCHI 1S/C15H23N3O2.ClH/c1-4-18(5-2)11-10-16-15(20)13-6-8-14(9-7-13)17-12(3)19;/h6-9H,4-5,10-11H2,1-3H3,(H,16,20)(H,17,19);1H Isómeros SMILES CCN(CC)CCNC(=O)C1=CC=C(C=C1)NC(=O)C.Cl WGK Alemania 3 Peso molecular 313.82 Reaxy-Rn 6548563 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6548563&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 Clase Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Acylaminobenzoic acid and derivatives Alternative Parents Acetanilides N-acetylarylamines Benzamides Benzoyl derivatives Acetamides Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Organopnictogen compounds Organic oxides Hydrochlorides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Acylaminobenzoic acid or derivatives - Acetanilide - Benzamide - N-acetylarylamine - Anilide - Benzoyl - N-arylamide - Acetamide - Amino acid or derivatives - Carboxamide group - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carboxylic acid derivative - Amine - Organooxygen compound - Organonitrogen compound - Hydrochloride - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated. 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 H2O: 50 mg/mL Sensibilidad Moisture sensitive. Punto de fusión (°C) 184-186 °C Peso molecular 313.820 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 7 Exact Mass 313.156 Da Monoisotopic Mass 313.156 Da Topological Polar Surface Area 61.400 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 308.000 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 2
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