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1. N-ethylurea
1. 625-52-5
2. 1-ethylurea
3. N-ethylurea
4. Urea, Ethyl-
5. Polyurethane
6. Urea, 1-ethyl-
7. Ethyl Urea
8. Urea, N-ethyl-
9. 9009-54-5
10. Nsc53556
11. Nsc-53556
12. 7k14b03x18
13. Pellethane
14. Einecs 210-898-8
15. Nsc 53556
16. Ai3-52220
17. Athylisoharnstoff
18. Unii-7k14b03x18
19. N-ethylurea, 97%
20. Ethylurea, N-
21. Sorbicacidvinylester
22. Dtxsid20873854
23. Str01353
24. Zinc1684574
25. Mfcd00007953
26. Stl185700
27. Akos000120949
28. Db-054197
29. E0192
30. Ft-0626364
31. D95291
32. A833843
33. Q-201096
34. Q26840850
| Molecular Weight | 88.11 g/mol |
|---|---|
| Molecular Formula | C3H8N2O |
| XLogP3 | -0.7 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 88.063662883 g/mol |
| Monoisotopic Mass | 88.063662883 g/mol |
| Topological Polar Surface Area | 55.1 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 52.8 |
| 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 |
ABOUT THIS PAGE
A Ethylurea manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethylurea, including repackagers and relabelers. The FDA regulates Ethylurea manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethylurea 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 Ethylurea supplier is an individual or a company that provides Ethylurea active pharmaceutical ingredient (API) or Ethylurea finished formulations upon request. The Ethylurea suppliers may include Ethylurea API manufacturers, exporters, distributors and traders.
Ethylurea 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 Ethylurea 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 Ethylurea GMP manufacturer or Ethylurea GMP API supplier for your needs.
A Ethylurea CoA (Certificate of Analysis) is a formal document that attests to Ethylurea's compliance with Ethylurea specifications and serves as a tool for batch-level quality control.
Ethylurea CoA mostly includes findings from lab analyses of a specific batch. For each Ethylurea 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.
Ethylurea may be tested according to a variety of international standards, such as European Pharmacopoeia (Ethylurea EP), Ethylurea JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ethylurea USP).
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