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1. H-lys(tfa)-pro-oh
2. N?-trifluoroacetyl-lys-pro
3. Schembl12886523
4. N Epsilon -trifluoroacetyl-lys-pro
5. Db-015550
6. Ft-0649950
7. A800712
8. J-000926
| Molecular Weight | 339.31 g/mol |
|---|---|
| Molecular Formula | C13H20F3N3O4 |
| XLogP3 | -1.9 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 7 |
| Exact Mass | 339.14059061 g/mol |
| Monoisotopic Mass | 339.14059061 g/mol |
| Topological Polar Surface Area | 113 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 456 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A N6-Trifluoracetyl-L-Lysyl-L-Proline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N6-Trifluoracetyl-L-Lysyl-L-Proline, including repackagers and relabelers. The FDA regulates N6-Trifluoracetyl-L-Lysyl-L-Proline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N6-Trifluoracetyl-L-Lysyl-L-Proline API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A N6-Trifluoracetyl-L-Lysyl-L-Proline supplier is an individual or a company that provides N6-Trifluoracetyl-L-Lysyl-L-Proline active pharmaceutical ingredient (API) or N6-Trifluoracetyl-L-Lysyl-L-Proline finished formulations upon request. The N6-Trifluoracetyl-L-Lysyl-L-Proline suppliers may include N6-Trifluoracetyl-L-Lysyl-L-Proline API manufacturers, exporters, distributors and traders.
N6-Trifluoracetyl-L-Lysyl-L-Proline Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of N6-Trifluoracetyl-L-Lysyl-L-Proline GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right N6-Trifluoracetyl-L-Lysyl-L-Proline GMP manufacturer or N6-Trifluoracetyl-L-Lysyl-L-Proline GMP API supplier for your needs.
A N6-Trifluoracetyl-L-Lysyl-L-Proline CoA (Certificate of Analysis) is a formal document that attests to N6-Trifluoracetyl-L-Lysyl-L-Proline's compliance with N6-Trifluoracetyl-L-Lysyl-L-Proline specifications and serves as a tool for batch-level quality control.
N6-Trifluoracetyl-L-Lysyl-L-Proline CoA mostly includes findings from lab analyses of a specific batch. For each N6-Trifluoracetyl-L-Lysyl-L-Proline CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
N6-Trifluoracetyl-L-Lysyl-L-Proline may be tested according to a variety of international standards, such as European Pharmacopoeia (N6-Trifluoracetyl-L-Lysyl-L-Proline EP), N6-Trifluoracetyl-L-Lysyl-L-Proline JP (Japanese Pharmacopeia) and the US Pharmacopoeia (N6-Trifluoracetyl-L-Lysyl-L-Proline USP).
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