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100% Original Canagliflozin Hemihydrate - Cinchonidine CAS 485-71-2 Assay 98.5%~101.0% API High Purity – Ruifu Featured Image
  • 100% Original Canagliflozin Hemihydrate - Cinchonidine CAS 485-71-2 Assay 98.5%~101.0% API High Purity – Ruifu

100% Original Canagliflozin Hemihydrate - Cinchonidine CAS 485-71-2 Assay 98.5%~101.0% API High Purity – Ruifu

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100% Original Canagliflozin Hemihydrate - Cinchonidine CAS 485-71-2 Assay 98.5%~101.0% API High Purity – Ruifu Detail:

Manufacturer with High Purity and Stable Quality
Chemical Name: Cinchonidine  
CAS: 485-71-2 
Cinchonidine is a Cinchona Alkaloid with Antimalarial Activity
API High Quality, Commercial Production

Chemical Name Cinchonidine
Synonyms (−)-Cinchonidine
CAS Number 485-71-2
CAT Number RF-API33
Stock Status In Stock, Production Scale Up to Hundreds of Kilograms
Molecular Formula C19H22N2O
Molecular Weight 294.39
Brand Ruifu Chemical
Item Specifications
Appearance White Crystals, Crystalline or Granular Powder, Bitter
Identification To Past Tests
Solubility Soluble in Chloroform, Soluble in Alcohol, Practically Insoluble in Water
Acidity of a 1% Suspension pH 7.0~9.0
Chloroform-Alcohol-Insoluble Substance ≤0.10%
Loss on Drying ≤0.20%
Specific Optical Rotation -105° to -115°
Other Cinchona Alkaloids Quinine+hydroquinine ≤5.0%
Assay 99.0%~101.0% (By non-aqueous titration, Calculated on the dried basis)
Sulphated Ash ≤0.10%
Heavy Metals ≤10 ppm
Chloride ≤200 ppm
Sulphate ≤500 ppm
Melting Point 200.0℃~207.0℃
Residul Solvents Meets the Pharmacopoeial Requirements
Test Standard United States Pharmacopoeia (USP)
Usage Cinchonidine is an Cinchona Alkaloid with Antimalarial Activity

Package: Bottle, Aluminum foil bag, Cardboard drum, 25kg/Drum, or according to customer’s requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

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Cinchonidine (CAS 485-71-2) is an cinchona alkaloid with antimalarial activity. Cinchonidine is an alkaloid found in Cinchona officinalis. It is used in asymmetric synthesis in organic chemistry. It is a stereoisomer and pseudo-enantiomer of cinchonine.

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