Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

product name	Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)
CAS	N/A
Product Code	REF-T13017
MF	N/A
MW	N/A
Purity	93.10%
Product nature	Customer customization
Unit	mg
Min. Order	5mg
Supply Ability	1000
Location	china
color/storage temp	Store at -20℃
Related Names	Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification),Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)Standard,Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)Reference

 

TOSUN PHARM was established in 1999. In China, it is a collection of drugs, APIs, reference listed drugs, impurities, excipients, intermediates import and export, import registration services, generic drug research and development services, innovative drugs and high-end FDF technology transfer, A group company integrating marketing, academic promotion and cooperative production. With a global procurement, R&D and marketing network, it can quickly meet the needs of product R&D, production and market sales of Chinese and global pharmaceutical companies.

 

Synthesis of Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

Complex Impurity Of Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

Chemical Standards of Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)，

Characterization Of Unknown Impurities of Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

Structure Profiling of Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

Identification of Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

Isolation & Purification of Impurity of Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

Reference Standards  Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)
Research Chemical Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)
Drug substance Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)
Impurity Standards Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)
Reference Standards Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)
Work Standards Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

 

Complex Impurity Of Chemical Standards of Triamcinolone Impurity G(RRT approximately 0.37)(Separation and purification)

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