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1. Nitrosamines
1. Nitrosamide
2. Nitrous Amide
3. 35576-91-1
4. Lgb75a6poh
5. Nsc-223080
6. Nitrosamines
7. Hydroxydiazene
8. Ketohydrazine
9. Hydroxydiimine
10. Nitsoamide
11. Diazene-n-oxide
12. Hydroxydiimide
13. Nitroxylamide
14. Nsc 223080
15. N-nitrosamine
16. Unii-lgb75a6poh
17. Nitrosamine-(h2n-n=o)
18. Dtxsid2074037
19. Nitrosamine (h2n-n=0)
20. Nsc223080
21. Q26841290
| Molecular Weight | 46.029 g/mol |
|---|---|
| Molecular Formula | H2N2O |
| XLogP3 | -0.6 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 46.016712692 g/mol |
| Monoisotopic Mass | 46.016712692 g/mol |
| Topological Polar Surface Area | 55.4 Ų |
| Heavy Atom Count | 3 |
| Formal Charge | 0 |
| Complexity | 10.3 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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A Nitrosamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nitrosamine, including repackagers and relabelers. The FDA regulates Nitrosamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nitrosamine 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 Nitrosamine supplier is an individual or a company that provides Nitrosamine active pharmaceutical ingredient (API) or Nitrosamine finished formulations upon request. The Nitrosamine suppliers may include Nitrosamine API manufacturers, exporters, distributors and traders.
Nitrosamine 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 Nitrosamine 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 Nitrosamine GMP manufacturer or Nitrosamine GMP API supplier for your needs.
A Nitrosamine CoA (Certificate of Analysis) is a formal document that attests to Nitrosamine's compliance with Nitrosamine specifications and serves as a tool for batch-level quality control.
Nitrosamine CoA mostly includes findings from lab analyses of a specific batch. For each Nitrosamine 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.
Nitrosamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Nitrosamine EP), Nitrosamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Nitrosamine USP).
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