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224,000+ research products · Triple ISO certified · COA & SDS available for every product · Same-day shipping on in-stock items Fipexide hydrochloride - ≥97% , CAS No.34161-23-4
Synonyms
SR-01000806671-4 | Fipexide hydrochloride, analytical standard | SC 998 | Fipexide hydrochloride | UNII-NQ702L425I | SPECTRUM1503222 | BP 662 | HMS1922K07 | J-019471 | Pharmakon1600-01503222 | Water-soluble menthol | Fipexidum hydrochloride | Prestwick_60
Storage
Protected from light,Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Store at -20°C,Argon charged 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.
Overview Application:
Fipexide Hydrochloride is one of five potential drug candidates to overcome the melphalan-induced vascular toxicity.
Specifications Synonyms
SR-01000806671-4 | Fipexide hydrochloride, analytical standard | SC 998 | Fipexide hydrochloride | UNII-NQ702L425I | SPECTRUM1503222 | BP 662 | HMS1922K07 | J-019471 | Pharmakon1600-01503222 | Water-soluble menthol | Fipexidum hydrochloride | Prestwick_60
Specifications & Purity
≥97%
Biochemical and Physiological Mechanisms
Fipexide hydrochloride, a parachloro-phenossiacetic acid derivative, is a nootropic agent. Fipexide hydrochloride reduces striatal adenylate cyclase activity. Fipexide hydrochloride has positive effect on cognitive performance by dopaminergic neurotransmi
Storage
Protected from light, Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles C1CN(CCN1CC2=CC3=C(C=C2)OCO3)C(=O)COC4=CC=C(C=C4)Cl.Cl IUPAC Name 1-[4-(1,3-benzodioxol-5-ylmethyl)piperazin-1-yl]-2-(4-chlorophenoxy)ethanone;hydrochloride InChIKey MVOWQBJZZKOQNU-UHFFFAOYSA-N INCHI 1S/C20H21ClN2O4.ClH/c21-16-2-4-17(5-3-16)25-13-20(24)23-9-7-22(8-10-23)12-15-1-6-18-19(11-15)27-14-26-18;/h1-6,11H,7-10,12-14H2;1H Isomeric SMILES C1CN(CCN1CC2=CC3=C(C=C2)OCO3)C(=O)COC4=CC=C(C=C4)Cl.Cl WGK Germany 3 PubChem CID 161803 Molecular Weight 425.31
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 Class Benzodioxoles Subclass Not available Intermediate Tree Nodes Not available Direct Parent Benzodioxoles Alternative Parents Phenoxy compounds Phenol ethers Alkyl aryl ethers N-alkylpiperazines Aralkylamines Chlorobenzenes Aryl chlorides Tertiary carboxylic acid amides Trialkylamines Amino acids and derivatives Oxacyclic compounds Acetals Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Hydrochlorides Organic oxides Organochlorides Organopnictogen compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Benzodioxole - Phenoxy compound - Phenol ether - Halobenzene - Chlorobenzene - Alkyl aryl ether - N-alkylpiperazine - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Piperazine - 1,4-diazinane - Aryl halide - Aryl chloride - Tertiary carboxylic acid amide - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Amino acid or derivatives - Carboxylic acid derivative - Ether - Acetal - Azacycle - Oxacycle - Organic nitrogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrochloride - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates(CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility DMSO (Slightly), Methanol (Slightly, Heated) Sensitivity Light sensitive Melt Point(°C) 219-221°C Molecular Weight 425.300 g/mol XLogP3 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 5 Exact Mass 424.096 Da Monoisotopic Mass 424.096 Da Topological Polar Surface Area 51.200 Ų Heavy Atom Count 28 Formal Charge 0 Complexity 492.000 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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