GRADE & PURITYPharmPure™?PharmPure™ — Aladdin's line of biopharmaceutical raw and starting materials. Use for pharma manufacturing inputs needing high purity and documentation.USP?United States Pharmacopeia grade — meets USP monograph specs for pharmaceutical use. Use for drug manufacturing, QC, and applications requiring US compendial compliance.ChP?Chinese Pharmacopoeia grade — meets ChP (中国药典) monograph specifications. Use for pharmaceutical work requiring compliance with Chinese standards.JP?Japanese Pharmacopoeia grade — conforms to JP monograph standards. Use for pharmaceutical products subject to Japanese regulatory requirements.BP?British Pharmacopoeia grade — conforms to BP monograph requirements. Use for pharmaceutical products marketed under UK/BP regulatory standards.Ph.Eur.?European Pharmacopoeia grade — conforms to Ph.Eur. monographs across EU member states. Use for pharmaceutical work needing European compendial compliance.
PharmPure™, USP, ChP, JP, BP, Ph.Eur. BP,ChP,JP,Ph.Eur.,PharmPure™,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications
Specifications & Purity
PharmPure™, USP, ChP, JP, BP, Ph.Eur.
Biochemical and Physiological Mechanisms
L-L-Aspartic Acid are natural proteogen amino acids, which can be used in cell culture medium preparation, protein and polypeptide synthesis systems and experiments. L-Aspartic Acid, an NMDA receptor agonist and nonspecific glutamate receptor agonist, is
This compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors
Common amino acids - Amino acids
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
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