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1. 20545-92-0
2. N-(2-hydroxyethyl)undec-10-enamide
3. Undecylenamide Mea
4. Undecylenoyl Monoethanolamide
5. N-(2-hydroxyethyl)-10-undecenamide
6. Undecylenic Acid Monoethanolamide
7. 9870n09i68
8. N-(2-hydroxyethyl)undecenamide
9. N-(2-hydroxyethyl)undecylenamide
10. Unii-9870n09i68
11. Einecs 243-870-9
12. Mayfung
13. Metanid
14. Fungicid Uma
15. Undecylenic Monoethanolamide
16. Steinazid U 185
17. Steinazid U-185
18. Rewocid U 185
19. Rewocid U-185
20. Schembl3967869
21. Dtxsid4066624
22. Undecylenamide Mea [inci]
23. Undecenamide, N-(2-hydroxyethyl)-
24. Mfcd18967756
25. 10-undecenamide,n-(2-hydroxyethyl)-
26. Akos028110914
27. As-62522
28. Undecylenic Acid Monoethanolamide (mea)
29. Undecylenic Acid Monoethanolamide [who-dd]
30. Q27272090
| Molecular Weight | 227.34 g/mol |
|---|---|
| Molecular Formula | C13H25NO2 |
| XLogP3 | 2.9 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 11 |
| Exact Mass | 227.188529040 g/mol |
| Monoisotopic Mass | 227.188529040 g/mol |
| Topological Polar Surface Area | 49.3 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 181 |
| 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 Undecylenic acid monoethanolamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Undecylenic acid monoethanolamide, including repackagers and relabelers. The FDA regulates Undecylenic acid monoethanolamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Undecylenic acid monoethanolamide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Undecylenic acid monoethanolamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Undecylenic acid monoethanolamide supplier is an individual or a company that provides Undecylenic acid monoethanolamide active pharmaceutical ingredient (API) or Undecylenic acid monoethanolamide finished formulations upon request. The Undecylenic acid monoethanolamide suppliers may include Undecylenic acid monoethanolamide API manufacturers, exporters, distributors and traders.
click here to find a list of Undecylenic acid monoethanolamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Undecylenic acid monoethanolamide 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 Undecylenic acid monoethanolamide 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 Undecylenic acid monoethanolamide GMP manufacturer or Undecylenic acid monoethanolamide GMP API supplier for your needs.
A Undecylenic acid monoethanolamide CoA (Certificate of Analysis) is a formal document that attests to Undecylenic acid monoethanolamide's compliance with Undecylenic acid monoethanolamide specifications and serves as a tool for batch-level quality control.
Undecylenic acid monoethanolamide CoA mostly includes findings from lab analyses of a specific batch. For each Undecylenic acid monoethanolamide 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.
Undecylenic acid monoethanolamide may be tested according to a variety of international standards, such as European Pharmacopoeia (Undecylenic acid monoethanolamide EP), Undecylenic acid monoethanolamide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Undecylenic acid monoethanolamide USP).
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