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1. L-op
2. Ocr-002
3. Ornithine Phenylacetate [usan]
4. 952154-79-9
5. 9d6yz105sn
6. Op
7. Ornithine Phenylacetate (usan)
8. L-ornithine Phenylacetate
9. Unii-9d6yz105sn
10. Op [ammonia Detoxifying Agent]
11. L-ornithine Phenyl Acetate
12. Schembl1702338
13. Chembl4297204
14. Dtxsid90241788
15. Mnk-6105
16. At24078
17. Ornithine Phenylacetate [who-dd]
18. L-ornithine, Benzeneacetate (1:1)
19. D09942
20. Q27272385
21. (2s)-2,5-diaminopentanoic Acid Phenylacetate (1:1)
| Molecular Weight | 268.31 g/mol |
|---|---|
| Molecular Formula | C13H20N2O4 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 6 |
| Exact Mass | 268.14230712 g/mol |
| Monoisotopic Mass | 268.14230712 g/mol |
| Topological Polar Surface Area | 127 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 209 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A Ornithine Phenylacetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ornithine Phenylacetate, including repackagers and relabelers. The FDA regulates Ornithine Phenylacetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ornithine Phenylacetate 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 Ornithine Phenylacetate supplier is an individual or a company that provides Ornithine Phenylacetate active pharmaceutical ingredient (API) or Ornithine Phenylacetate finished formulations upon request. The Ornithine Phenylacetate suppliers may include Ornithine Phenylacetate API manufacturers, exporters, distributors and traders.
Ornithine Phenylacetate 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 Ornithine Phenylacetate 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 Ornithine Phenylacetate GMP manufacturer or Ornithine Phenylacetate GMP API supplier for your needs.
A Ornithine Phenylacetate CoA (Certificate of Analysis) is a formal document that attests to Ornithine Phenylacetate's compliance with Ornithine Phenylacetate specifications and serves as a tool for batch-level quality control.
Ornithine Phenylacetate CoA mostly includes findings from lab analyses of a specific batch. For each Ornithine Phenylacetate 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.
Ornithine Phenylacetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Ornithine Phenylacetate EP), Ornithine Phenylacetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ornithine Phenylacetate USP).
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