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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Melperone hydrochloride - ≥99%(HPLC) , CAS No.1622-79-3
Synonyms
C16H23ClFNO | J-009916 | metylperon hydrochloride | NC00426 | MELPERONE HYDROCHLORIDE [MI] | Melperone HCl | MELPERONE HYDROCHLORIDE [WHO-DD] | CCG-101176 | 1-(4-Fluorophenyl)-4-(4-methylpiperidin-1-yl)butan-1-onehydrochloride | AS-77510 | SMR000468736 |
Storage
Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
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Why this grade ≥99%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Desiccated 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
C16H23ClFNO | J-009916 | metylperon hydrochloride | NC00426 | MELPERONE HYDROCHLORIDE [MI] | Melperone HCl | MELPERONE HYDROCHLORIDE [WHO-DD] | CCG-101176 | 1-(4-Fluorophenyl)-4-(4-methylpiperidin-1-yl)butan-1-onehydrochloride | AS-77510 | SMR000468736 |
Especificaciones y pureza
≥99%(HPLC)
Mecanismos bioquímicos y fisiológicos
Atypical neuroleptic; 5-HT2A/D2receptor antagonist (Kivalues are 120 and 180 nM respectively). Causes an increase in dopamine levels in the medial prefrontal cortex (mPFC) and nucleus accumbens and an increase in ACh in the mPFC. Also binds adrenergicα1an
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Desiccated
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 488196438 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488196438 Sonrisas canónicas CC1CCN(CC1)CCCC(=O)C2=CC=C(C=C2)F.Cl IUPAC Name 1-(4-fluorophenyl)-4-(4-methylpiperidin-1-yl)butan-1-one;hydrochloride InChIKey MQHYXXIJLKFQGY-UHFFFAOYSA-N INCHI 1S/C16H22FNO.ClH/c1-13-8-11-18(12-9-13)10-2-3-16(19)14-4-6-15(17)7-5-14;/h4-7,13H,2-3,8-12H2,1H3;1H Isómeros SMILES CC1CCN(CC1)CCCC(=O)C2=CC=C(C=C2)F.Cl PubChem CID 9926325 Peso molecular 299.81
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 oxygen compounds Clase Organooxygen compounds Subclass Carbonyl compounds Intermediate Tree Nodes Ketones - Aryl ketones - Phenylketones Direct Parent Alkyl-phenylketones Alternative Parents Phenylbutylamines Butyrophenones Aryl alkyl ketones Benzoyl derivatives Fluorobenzenes Piperidines Aryl fluorides Gamma-amino ketones Trialkylamines Azacyclic compounds Hydrocarbon derivatives Organic chloride salts Organic oxides Organic zwitterions Organofluorides Organopnictogen compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents Alkyl-phenylketone - Butyrophenone - Phenylbutylamine - Benzoyl - Aryl alkyl ketone - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Gamma-aminoketone - Piperidine - Benzenoid - Tertiary amine - Tertiary aliphatic amine - Azacycle - Organoheterocyclic compound - Amine - Organonitrogen compound - Organofluoride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic zwitterion - Organic nitrogen compound - Organic chloride salt - Organic salt - Aromatic heteromonocyclic compound Descripción 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.
Estructura 3D Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:water, Max Conc. mg/mL: 29.98, Max Conc. mM: 100; Solvent:DMSO, Max Conc. mg/mL: 29.98, Max Conc. mM: 100 Peso molecular 299.810 g/mol XLogP3 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 5 Exact Mass 299.145 Da Monoisotopic Mass 299.145 Da Topological Polar Surface Area 20.300 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 278.000 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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