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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino Buflomedil HCl - ≥98% , CAS No.35543-24-9
Synonyms
Bufedil | Buflomedil (hydrochloride) | Buflomedil HCl | Loftyl | MLS006010627 | BCP13305 | AB03021 | NCGC00256242-01 | SY102086 | CAS-35543-24-9 | DTXCID902511 | Fonzylane | LL 1656 | Buflocit | SW196920-4 | NC00128 | NSC 759291 | Buflomedil hydrochloride
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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 2-8°C Ships Wet ice 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.
Panoramica Buflomedil HCl is a vasodilator used to treat claudication or the symptoms of peripheral arterial disease.
Specifications Sinonimi
Bufedil | Buflomedil (hydrochloride) | Buflomedil HCl | Loftyl | MLS006010627 | BCP13305 | AB03021 | NCGC00256242-01 | SY102086 | CAS-35543-24-9 | DTXCID902511 | Fonzylane | LL 1656 | Buflocit | SW196920-4 | NC00128 | NSC 759291 | Buflomedil hydrochloride
Condizioni di conservazione di stoccaggio
Store at 2-8°C
Spedito in
Wet ice
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488195747
Sorrisi canonici
COC1=CC(=C(C(=C1)OC)C(=O)CCCN2CCCC2)OC.Cl
IUPAC Name
4-pyrrolidin-1-yl-1-(2,4,6-trimethoxyphenyl)butan-1-one;hydrochloride
InChIKey
ZDPACSAHMZADFZ-UHFFFAOYSA-N
INCHI
1S/C17H25NO4.ClH/c1-20-13-11-15(21-2)17(16(12-13)22-3)14(19)7-6-10-18-8-4-5-9-18;/h11-12H,4-10H2,1-3H3;1H
Isomeri SMILES
COC1=CC(=C(C(=C1)OC)C(=O)CCCN2CCCC2)OC.Cl
CAS alternativo
55837-25-7；35543-24-9
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6023423&ln=
Documentazione 📋 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 oxygen compounds Classe Organooxygen compounds Subclass Carbonyl compounds Intermediate Tree Nodes Ketones - Aryl ketones - Phenylketones Direct Parent Alkyl-phenylketones Alternative Parents Butyrophenones Phenylbutylamines Anisoles Aryl alkyl ketones Benzoyl derivatives Methoxybenzenes Phenoxy compounds Alkyl aryl ethers N-alkylpyrrolidines Gamma-amino ketones Trialkylamines Azacyclic compounds Hydrocarbon derivatives Organic chloride salts Organic oxides Organic zwitterions Organopnictogen compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents Alkyl-phenylketone - Butyrophenone - Phenylbutylamine - Phenoxy compound - Anisole - Benzoyl - Phenol ether - Methoxybenzene - Aryl alkyl ketone - Alkyl aryl ether - Monocyclic benzene moiety - Gamma-aminoketone - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Ether - Organoheterocyclic compound - Organopnictogen compound - Organic chloride salt - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic zwitterion - Organic salt - Aromatic heteromonocyclic compound Descrizione This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. 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.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Solubilità DMSO 31 mg/mL Water 69 mg/mL Ethanol 7 mg/mL Punto di fusione (°C) 193°C Peso molecolare 343.800 g/mol XLogP3 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 8 Exact Mass 343.155 Da Monoisotopic Mass 343.155 Da Topological Polar Surface Area 48.000 Ų Heavy Atom Count 23 Formal Charge 0 Complexity 330.000 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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