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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Amodiaquin dihydrochloride dihydrate - ≥97% , Ferriprotoporphyrin IX inhibitor, CAS No.6398-98-7, Ferriprotoporphyrin IX inhibitor
Synonyms
AMODIAQUINI HYDROCHLORIDUM [WHO-IP LATIN] | HY-B1322 | NCGC00017063-01 | NSC 755863 | SN 10751 | Tox21_110765 | NSC-755863 | 6398-98-7 (HCl hydrate) | AMODIAQUINE HYDROCHLORIDE [ORANGE BOOK] | Amodiaquini hydrochloridum | Amodiaquin HCl hydrate | Amodiaqu
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Why this grade ≥97% 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
AMODIAQUINI HYDROCHLORIDUM [WHO-IP LATIN] | HY-B1322 | NCGC00017063-01 | NSC 755863 | SN 10751 | Tox21_110765 | NSC-755863 | 6398-98-7 (HCl hydrate) | AMODIAQUINE HYDROCHLORIDE [ORANGE BOOK] | Amodiaquini hydrochloridum | Amodiaquin HCl hydrate | Amodiaqu
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Ferriprotoporphyrin IX inhibitor
Nombres e identificadores Pubchem Sid 488183633 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488183633 Sonrisas canónicas CCN(CC)CC1=C(C=CC(=C1)NC2=C3C=CC(=CC3=NC=C2)Cl)O.O.O.Cl.Cl IUPAC Name 4-[(7-chloroquinolin-4-yl)amino]-2-(diethylaminomethyl)phenol;dihydrate;dihydrochloride InChIKey YVNAYSHNIILOJS-UHFFFAOYSA-N INCHI 1S/C20H22ClN3O.2ClH.2H2O/c1-3-24(4-2)13-14-11-16(6-8-20(14)25)23-18-9-10-22-19-12-15(21)5-7-17(18)19;;;;/h5-12,25H,3-4,13H2,1-2H3,(H,22,23);2*1H;2*1H2 Isómeros SMILES CCN(CC)CC1=C(C=CC(=C1)NC2=C3C=CC(=CC3=NC=C2)Cl)O.O.O.Cl.Cl PubChem CID 64646 Peso molecular 464.81
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 Organoheterocyclic compounds Clase Quinolines and derivatives Subclass Aminoquinolines and derivatives Intermediate Tree Nodes Not available Direct Parent 4-aminoquinolines Alternative Parents Chloroquinolines p-Aminophenols Phenylmethylamines Aniline and substituted anilines Benzylamines 1-hydroxy-2-unsubstituted benzenoids Aminopyridines and derivatives Aralkylamines Aryl chlorides Heteroaromatic compounds Trialkylamines Secondary amines Azacyclic compounds Hydrocarbon derivatives Hydrochlorides Organic oxides Organochlorides Organooxygen compounds Organopnictogen compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents 4-aminoquinoline - Haloquinoline - Chloroquinoline - Aminophenol - P-aminophenol - Phenylmethylamine - Benzylamine - Aniline or substituted anilines - 1-hydroxy-2-unsubstituted benzenoid - Aminopyridine - Aralkylamine - Phenol - Pyridine - Monocyclic benzene moiety - Aryl halide - Benzenoid - Aryl chloride - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Azacycle - Secondary amine - Amine - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrochloride - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as 4-aminoquinolines. These are organic compounds containing an amino group attached to the 4-position of a quinoline ring system. External Descriptors hydrochloride 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 Soluble in water; Soluble in Methanol; Very slightly soluble in Chloroform,Benzene,Ether; Insoluble in Alcohol Peso molecular 464.800 g/mol XLogP3 Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 6 Exact Mass 463.12 Da Monoisotopic Mass 463.12 Da Topological Polar Surface Area 50.400 Ų Heavy Atom Count 29 Formal Charge 0 Complexity 406.000 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 5
Citations of This Product Referencias 1. Ying Pan, Qiongjie Ding, Baohong Li, Xiaoxiong Wang, Yiwei Liu, Junhao Chen, Fei Ke, Jianqiang Liu. (2020) Self-adjusted bimetallic zeolitic-imidazolate framework-derived hierarchical magnetic carbon composites as efficient adsorbent for optimizing drug contaminant removal. CHEMOSPHERE, [PMID:33297097 ] [10.1016/j.chemosphere.2020.128101 ]
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