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1. Diethylurea
1. 634-95-7
2. N,n-diethylurea
3. Asym-diethylurea
4. Diethylurea
5. Urea, N,n-diethyl-
6. Urea, 1,1-diethyl-
7. 50816-31-4
8. Einecs 211-220-3
9. Nsc 165657
10. Brn 1747730
11. Ai3-61341
12. Urea,n-diethyl-
13. Urea,1-diethyl-
14. 1,1-diethyl Urea
15. 1,1-diethylurea, 97%
16. 1,1-diethylurea (asym-)
17. Schembl24375
18. Dtxsid3060900
19. Schembl11769258
20. Zinc409175
21. Einecs 256-787-8
22. Mfcd00007960
23. Nsc165657
24. Akos000141627
25. Nsc-165657
26. As-56661
27. Db-054498
28. Cs-0181847
29. D1567
30. Ft-0606115
31. D89884
Molecular Weight | 116.16 g/mol |
---|---|
Molecular Formula | C5H12N2O |
XLogP3 | -0.2 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 2 |
Exact Mass | 116.094963011 g/mol |
Monoisotopic Mass | 116.094963011 g/mol |
Topological Polar Surface Area | 46.3 Ų |
Heavy Atom Count | 8 |
Formal Charge | 0 |
Complexity | 78.5 |
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 1,1-Diethylurea manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1,1-Diethylurea, including repackagers and relabelers. The FDA regulates 1,1-Diethylurea manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1,1-Diethylurea 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 1,1-Diethylurea supplier is an individual or a company that provides 1,1-Diethylurea active pharmaceutical ingredient (API) or 1,1-Diethylurea finished formulations upon request. The 1,1-Diethylurea suppliers may include 1,1-Diethylurea API manufacturers, exporters, distributors and traders.
1,1-Diethylurea 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 1,1-Diethylurea 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 1,1-Diethylurea GMP manufacturer or 1,1-Diethylurea GMP API supplier for your needs.
A 1,1-Diethylurea CoA (Certificate of Analysis) is a formal document that attests to 1,1-Diethylurea's compliance with 1,1-Diethylurea specifications and serves as a tool for batch-level quality control.
1,1-Diethylurea CoA mostly includes findings from lab analyses of a specific batch. For each 1,1-Diethylurea 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.
1,1-Diethylurea may be tested according to a variety of international standards, such as European Pharmacopoeia (1,1-Diethylurea EP), 1,1-Diethylurea JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1,1-Diethylurea USP).
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