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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Hydroxychloroquine sulfate - 10mM in Water , Toll-like receptor 9 antagonist, CAS No.747-36-4, Toll-like receptor 9 antagonist
GRADE & PURITY 10mM in Water
Synonyms
2-((4-((7-Chloro-4-quinolyl)amino)pentyl)ethylamino)ethanol sulfate (1:1) (salt) | FT-0669460 | HYDROXYCHLOROQUINE SULFATE [JAN] | NCGC00159483-04 | Plaquenil | AI3-52706 | Hydroxycloroquine sulfate, analytical standard | 747-36-4 (sulfate) | HYDROXYCHLOR
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 12 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonymes
2-((4-((7-Chloro-4-quinolyl)amino)pentyl)ethylamino)ethanol sulfate (1:1) (salt) | FT-0669460 | HYDROXYCHLOROQUINE SULFATE [JAN] | NCGC00159483-04 | Plaquenil | AI3-52706 | Hydroxycloroquine sulfate, analytical standard | 747-36-4 (sulfate) | HYDROXYCHLOR
Spécifications et pureté
10mM in Water
Mécanismes biochimiques et physiologiques
Hydroxychloroquine is also used for treating rheumatoid arthritis and systemic lupus erythematosus. Hydroxychloroquine sulfate is an anti-inflammatory (via TNF), disease-modifying antirheumatic drug (DMARD), and a heme polymerase inhibitor. It is used as
Conditions de stockage de stockage
Store at -80°C
Expédié en
Dry ice packs + Cold packs
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Mécanisme d'action
Toll-like receptor 9 antagonist
Noms et identifiants Pubchem Sid 528774097 Sourires canoniques CCN(CCCC(C)NC1=C2C=CC(=CC2=NC=C1)Cl)CCO.OS(=O)(=O)O IUPAC Name 2-[4-[(7-chloroquinolin-4-yl)amino]pentyl-ethylamino]ethanol;sulfuric acid InChIKey JCBIVZZPXRZKTI-UHFFFAOYSA-N INCHI 1S/C18H26ClN3O.H2O4S/c1-3-22(11-12-23)10-4-5-14(2)21-17-8-9-20-18-13-15(19)6-7-16(17)18;1-5(2,3)4/h6-9,13-14,23H,3-5,10-12H2,1-2H3,(H,20,21);(H2,1,2,3,4) Isomères SMILES CCN(CCCC(C)NC1=C2C=CC(=CC2=NC=C1)Cl)CCO.OS(=O)(=O)O WGK Allemagne 3 RTECS KK3342500 Poids moléculaire 433.95 Reaxy-Rn 7242072 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7242072&ln=
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 Classe Quinolines and derivatives Subclass Aminoquinolines and derivatives Intermediate Tree Nodes Not available Direct Parent 4-aminoquinolines Alternative Parents Chloroquinolines Secondary alkylarylamines Aminopyridines and derivatives Organic sulfuric acids Benzenoids Aryl chlorides Heteroaromatic compounds Trialkylamines 1,2-aminoalcohols Azacyclic compounds Primary alcohols Organopnictogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 4-aminoquinoline - Haloquinoline - Chloroquinoline - Aminopyridine - Sulfuric acid - Secondary aliphatic/aromatic amine - Aryl chloride - Aryl halide - Pyridine - Benzenoid - Heteroaromatic compound - Organic sulfuric acid or derivatives - Tertiary aliphatic amine - Tertiary amine - 1,2-aminoalcohol - Azacycle - Secondary amine - Alkanolamine - Organonitrogen compound - Organochloride - Organopnictogen compound - Organic oxygen compound - Organohalogen compound - Alcohol - Amine - Organic nitrogen compound - Organic oxide - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Aromatic heteropolycyclic compound Description 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 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Sensibilité light sensitive Poids moléculaire 434.000 g/mol XLogP3 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 9 Exact Mass 433.144 Da Monoisotopic Mass 433.144 Da Topological Polar Surface Area 131.000 Ų Heavy Atom Count 28 Formal Charge 0 Complexity 413.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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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