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Canagliflozin impurity F

Also known as: Canagliflozin Impurities or impurities of Canagliflozin
Chemical Name Canagliflozin impurity F
CAT No. CS-AQ-00195
CAS Registry# 1071929-08-2
Status Prompt Dispatch
Category Impurities
Mol. Wt. 422.26 g/mol
Mol. For. C₁₈H₁₂FIOS
Hazardous This is a Hazardous Compound
COA View Sample COA

Additional Information

Controlled No
Parent API Canagliflozin
Purity >98%
Therapeutic Anti-Diabetic
Smileys O=C(C(C=C(I)C=C1)=C1C)C2=CC=C(C3=CC=C(F)C=C3)S2
Canonical Smiles CC1=C(C=C(C=C1)I)C(=O)C2=CC=C(S2)C3=CC=C(C=C3)F
Inchl InChI=1S/C18H12FIOS/c1-11-2-7-14(20)10-15(11)18(21)17-9-8-16(22-17)12-3-5-13(19)6-4-12/h2-10H,1H3
IUPAC [5-(4-fluorophenyl)thiophen-2-yl]-(5-iodo-2-methylphenyl)methanone
Hazardous Yes

Usage and description

Canagliflozin impurity F is a chemical compound that is commonly used in the pharmaceutical industry as an impurity in the production of Canagliflozin, which is a drug used to treat type 2 diabetes. Canagliflozin impurity F is also known as (2S,3R,4S,5S,6R)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. The chemical formula of Canagliflozin impurity F is C21H25ClO7 and it has a molecular weight of 436.88 g/mol. It is a white to off-white powder with a melting point of 132-136°C. This impurity is known to be a potential genotoxic impurity and thus, its presence in the final drug product should be less than the acceptable limits set by regulatory bodies. Canagliflozin impurity F is used in the production of Canagliflozin as a starting material or intermediate. The impurity is introduced during the synthesis process and is subsequently removed through various purification steps to obtain the final drug product. In conclusion, Canagliflozin impurity F is an important intermediate in the production of Canagliflozin, a drug used to treat type 2 diabetes. Its usage is strictly regulated, and its presence in the final drug product should be minimized.

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