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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Brompheniramine hydrogen maleate - ≥98% , Histamine H1 receptor antagonist, CAS No.980-71-2, Histamine H1 receptor antagonist
Synonyms
Brompheniramine Maleate (1:1) | Dimotane | 2-Pyridinepropanamine, gamma-(4-bromophenyl)-N,N-dimethyl-, (Z)-butenedioate (1:1) | BROMPHENIRAMINE MALEATE (MART.) | Gammistin | NCGC00093676-01 | NCGC00093676-02 | 2-Pyridinepropanamine, gamma-(4-bromophenyl)-
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% 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.
Descripción general Brompheniramine hydrogen maleate is a histamine H1 receptors antagonist.
Specifications Sinónimos
Brompheniramine Maleate (1:1) | Dimotane | 2-Pyridinepropanamine, gamma-(4-bromophenyl)-N, N-dimethyl-, (Z)-butenedioate (1:1) | BROMPHENIRAMINE MALEATE (MART.) | Gammistin | NCGC00093676-01 | NCGC00093676-02 | 2-Pyridinepropanamine, gamma-(4-bromophenyl)-
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Brompheniramine Maleate is a histamine H1 receptors antagonist. Brompheniramine Maleate also functions as a moderately effective anticholinergic agent, and is likely an antimuscarinic agent similar to other common antihistamines such as diphenhydramine. B
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.
Mecanismo de acción
Histamine H1 receptor antagonist
Nombres e identificadores Pubchem Sid 488195225 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488195225 Sonrisas canónicas CN(C)CCC(C1=CC=C(C=C1)Br)C2=CC=CC=N2.C(=CC(=O)O)C(=O)O IUPAC Name 3-(4-bromophenyl)-N,N-dimethyl-3-pyridin-2-ylpropan-1-amine;(Z)-but-2-enedioic acid InChIKey SRGKFVAASLQVBO-BTJKTKAUSA-N INCHI 1S/C16H19BrN2.C4H4O4/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13;5-3(6)1-2-4(7)8/h3-9,11,15H,10,12H2,1-2H3;1-2H,(H,5,6)(H,7,8)/b;2-1- Isómeros SMILES CN(C)CCC(C1=CC=C(C=C1)Br)C2=CC=CC=N2.C(=C\C(=O)O)\C(=O)O WGK Alemania 1 Peso molecular 435.31 Reaxy-Rn 34821314 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=34821314&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 Pyridines and derivatives Subclass Pheniramines Intermediate Tree Nodes Not available Direct Parent Pheniramines Alternative Parents Bromobenzenes Aralkylamines Unsaturated fatty acids Dicarboxylic acids and derivatives Aryl bromides Heteroaromatic compounds Trialkylamines Carboxylic acids Azacyclic compounds Organopnictogen compounds Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Not available Substituents Pheniramine - Bromobenzene - Halobenzene - Aralkylamine - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Unsaturated fatty acid - Benzenoid - Fatty acid - Fatty acyl - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Azacycle - Carboxylic acid derivative - Carboxylic acid - Hydrocarbon derivative - Organohalogen compound - Organic oxygen compound - Organobromide - Amine - Organic nitrogen compound - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as pheniramines. These are compounds containing a pheniramine moiety, which is structurally characterized by the presence of a 2-benzylpyridine linked to an dimethyl(propyl)amine to form a dimethyl[3-phenyl-3-(pyridin-2-yl)propyl]amine skeleton. External Descriptors maleate salt 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 DMSO mg/mL Water mg/mL Ethanol mg/mL Punto de fusión (°C) 136 °C Peso molecular 435.300 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 7 Exact Mass 434.084 Da Monoisotopic Mass 434.084 Da Topological Polar Surface Area 90.700 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 368.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 2
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