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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Bisoprolol hemifumarate salt - ≥98%(HPLC) , Beta-1 adrenergic receptor antagonist, CAS No.104344-23-2, Beta-1 adrenergic receptor antagonist
Synonyms
BB164256 | Maintate | Godal | BISOPROLOL FUMARATE [VANDF] | EMD 33512 | BISOPROLOL FUMARATE [USP MONOGRAPH] | BISOPROLOL FUMARATE [USP-RS] | EMD-33512 | EMD-33-512 | 2-Propanol, 1-(4-((2-(1-methylethoxy)ethoxy)methyl)phenoxy)-3-((1-methylethyl)amino)-, (+
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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 Room temperature Ships Normal 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
BB164256 | Maintate | Godal | BISOPROLOL FUMARATE [VANDF] | EMD 33512 | BISOPROLOL FUMARATE [USP MONOGRAPH] | BISOPROLOL FUMARATE [USP-RS] | EMD-33512 | EMD-33-512 | 2-Propanol, 1-(4-((2-(1-methylethoxy)ethoxy)methyl)phenoxy)-3-((1-methylethyl)amino)-, (+
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Selective β 1 antagonist (K i = 22.4 nM). Antihypertensive agent.
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Beta-1 adrenergic receptor antagonist
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Nombres e identificadores Pubchem Sid 488195222 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488195222 Sonrisas canónicas CC(C)NCC(COC1=CC=C(C=C1)COCCOC(C)C)O.CC(C)NCC(COC1=CC=C(C=C1)COCCOC(C)C)O.C(=CC(=O)O)C(=O)O IUPAC Name (E)-but-2-enedioic acid;1-(propan-2-ylamino)-3-[4-(2-propan-2-yloxyethoxymethyl)phenoxy]propan-2-ol InChIKey VMDFASMUILANOL-WXXKFALUSA-N INCHI 1S/2C18H31NO4.C4H4O4/c2*1-14(2)19-11-17(20)13-23-18-7-5-16(6-8-18)12-21-9-10-22-15(3)4;5-3(6)1-2-4(7)8/h2*5-8,14-15,17,19-20H,9-13H2,1-4H3;1-2H,(H,5,6)(H,7,8)/b;;2-1+ Isómeros SMILES CC(C)NCC(COC1=CC=C(C=C1)COCCOC(C)C)O.CC(C)NCC(COC1=CC=C(C=C1)COCCOC(C)C)O.C(=C/C(=O)O)\C(=O)O WGK Alemania 3 RTECS UB8390000 PubChem CID 5281064 Peso molecular 383.48
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 Clase Carboxylic acids and derivatives Subclass Dicarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Dicarboxylic acids and derivatives Alternative Parents Unsaturated fatty acids Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Not available Substituents Fatty acyl - Fatty acid - Unsaturated fatty acid - Dicarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. External Descriptors fumarate 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 Peso molecular 767.000 g/mol XLogP3 Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 14 Rotatable Bond Count 26 Exact Mass 766.462 Da Monoisotopic Mass 766.462 Da Topological Polar Surface Area 195.000 Ų Heavy Atom Count 54 Formal Charge 0 Complexity 397.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 2 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 3
Citations of This Product Referencias 1. Qinghao Cao, Chao Chen, Jun Huang, Dantong Shen, Haolin Chen, Huiqing Zhong, Zhiming Liu, Zhouyi Guo. (2022) Mussel-inspired hydrogels for fast fabrication of flexible SERS tape for point-of-care testing of β-blockers. ANALYST, 147 (16): (3652-3661). [PMID:35839093 ] [10.1039/D2AN00688J ]
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