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A propos de cet article
grade
pharmaceutical primary standard
agency
USP
API family
oligosaccharide sst mixture
form
solid
manufacturer/tradename
USP
application(s)
USP Biologics
pharmaceutical (small molecule)
pharmaceutical
pharmaceutical
format
mixture
General description
Oligosaccharide System Suitability Mixture C contains a series of saccharide fragments to test the suitability and reproducibility of chromatographic methods. It is used in the analysis of carbohydrate-based therapeutics and vaccines.
The USP biologics carbohydrates category includes a variety of carbohydrate-based substances that are essential in the development and manufacturing of therapeutic products. These carbohydrates play crucial roles in biological processes and are often utilized as excipients, stabilizers, or active ingredients in pharmaceuticals. The USP provides comprehensive standards, reference materials, and analytical procedures to ensure the identity, quality, purity, and consistency of carbohydrate therapeutics throughout their lifecycle.
The United States Pharmacopeia (USP) provides quality standards for biologics to ensure their safety, efficacy, and quality throughout the manufacturing process. These standards assist manufacturers in adhering to regulatory requirements and help safeguard public health by reducing risks associated with biologics.
Application
Also used to prepare AB-labeled standard solutions for liquid chromatographic separation.
Additionally, used to separate Bi-, tri-, and tetra-antennary N-linked oligosaccharides with variable sialylation.
Analysis Note
Other Notes
Classe de stockage
11 - Combustible Solids
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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