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Lisdexamfetamine Dimesylate impurity G

Also known as: Lisdexamfetamine Impurities or impurities of Lisdexamfetamine
Chemical Name Lisdexamfetamine Dimesylate impurity G
CAT No. CS-O-37997
CAS Registry# 849605-16-9
Status Prompt Dispatch
Category Impurities
Mol. Wt. 363.49 g/mol
Mol. For. C₂₀H₃₃N₃O₃
Hazardous This is not a Hazardous Compound
COA View Sample COA

Additional Information


Controlled No
Parent API Lisdexamfetamine
Smileys C[C@H](NC([C@@H](NC(OC(C)(C)C)=O)CCCCN)=O)CC1=CC=CC=C1
Hazardous No


Usage and description


Lisdexamfetamine Dimesylate impurity G is a chemical compound that is used in the pharmaceutical industry as an impurity reference standard for the analysis and quantification of impurities in Lisdexamfetamine Dimesylate. Lisdexamfetamine Dimesylate, also known as Vyvanse, is a central nervous system stimulant medication used to treat attention deficit hyperactivity disorder (ADHD) and binge eating disorder (BED). As an impurity reference standard, Lisdexamfetamine Dimesylate impurity G is used to ensure the purity and quality of Lisdexamfetamine Dimesylate. It is important to monitor impurities in pharmaceuticals as they can affect the efficacy and safety of the medication. Impurities can be formed during the manufacturing process or during storage, and the presence of impurities can affect the stability and shelf life of the medication. Chemically, Lisdexamfetamine Dimesylate impurity G is a derivative of Lisdexamfetamine Dimesylate, which is an amphetamine prodrug. The impurity G compound contains a methyl group and a hydroxyl group, which are both important functional groups in organic chemistry. The molecular formula of Lisdexamfetamine Dimesylate impurity G is C15H23N2O2S.CH3SO3H, and its molecular weight is 408.5 g/mol. In conclusion, Lisdexamfetamine Dimesylate impurity G is a critical reference standard used in the pharmaceutical industry to ensure the quality and purity of Lisdexamfetamine Dimesylate. Its chemical properties and molecular structure are important for the analysis and quantification of impurities in the medication.

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