Quinine hemisulfate monohydrate, 98+%, Thermo Scientific Chemicals
Quinine hemisulfate monohydrate, 98+%, Thermo Scientific Chemicals
Quinine hemisulfate monohydrate, 98+%, Thermo Scientific Chemicals
Quinine hemisulfate monohydrate, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Quinine hemisulfate monohydrate, 98+%, Thermo Scientific Chemicals

CAS: 6119-70-6 | C40H54N4O10S | 782.95 g/mol
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Catalog number ALFA17036.09
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Chemical Identifiers
CAS5949-29-1
IUPAC Name2-hydroxypropane-1,2,3-tricarboxylic acid hydrate
Molecular FormulaC6H10O8
InChI KeyYASYEJJMZJALEJ-UHFFFAOYSA-N
SMILESO.OC(=O)CC(O)(CC(O)=O)C(O)=O
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SpecificationsSpecification SheetSpecification Sheet
Residue on ignition0.05% max
Assay (Aqueous acid-base Titration)>/= 99.5%
Moisture holding capacity
Trace Metals
Quinine hemisulfate monohydrate plays a major role in potassium channel blockers. It is also used as an antimalarial, anticholinergic, antihypertensive and a hypoglycemic agent. It inhibits mitochondrial ATP-regulated potassium channel. It is also used to study the metabolism of biocrystalized heme, hemozoin, in malarial parasites and to study the toxicity of heme (FP)-complexes.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Quinine hemisulfate monohydrate plays a major role in potassium channel blockers. It is also used as an antimalarial, anticholinergic, antihypertensive and a hypoglycemic agent. It inhibits mitochondrial ATP-regulated potassium channel. It is also used to study the metabolism of biocrystalized heme, hemozoin, in malarial parasites and to study the toxicity of heme (FP)-complexes.

Solubility
Soluble in a mixture of chloroform and absolute alcohol (2:1).

Notes
Light sensitive. Incompatible with strong oxidizing agents, alkalis, ammonia, strong bases and iodine.
RUO – Research Use Only

General References:

  1. Krzeszewski, M.; Gryko, D. T. x-Shaped Bis (areno)-1, 4-dihydropyrrolo [3, 2-b] pyrroles Generated by Oxidative Aromatic Coupling. J. Org. Chem. 2015, 80 (5), 2893-2899.
  2. Janiga, A.; Krzeszewski, M.; Gryko, D. T. Diindolo [2, 3-b: 2', 3'-f] pyrrolo [3, 2-b] pyrroles as Electron-Rich, Ladder-Type Fluorophores: Synthesis and Optical Properties. Chem. Asian J. 2015, 10 (1), 212-218.