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1. 1-(3-fluoro-4-(trifluoromethoxy)phenyl)-3-(1-((2s)-2-methylbutanoyl)-4-piperidinyl)urea
2. Ec5026
3. Urea, N-(3-fluoro-4-(trifluoromethoxy)phenyl)-n'-(1-((2s)-2-methyl-1-oxobutyl)-4-piperidinyl)-
1. 1809885-32-2
2. Ec5026
3. D5x8a5hwl0
4. Ec-5026
5. Ec-5062
6. 1-[3-fluoro-4-(trifluoromethoxy)phenyl]-3-[1-[(2s)-2-methylbutanoyl]piperidin-4-yl]urea
7. N-[3-fluoro-4-(trifluoromethoxy)phenyl]-n'-[1-[(2s)-2-methyl-1-oxobutyl]-4-piperidinyl]urea
8. Urea, N-(3-fluoro-4-(trifluoromethoxy)phenyl)-n'-(1-((2s)-2-methyl-1-oxobutyl)-4-piperidinyl)-
9. Mfcd32667032
10. Unii-d5x8a5hwl0
11. Chembl4752759
12. Schembl17114596
13. Bdbm409005
14. Ex-a3264
15. Bpn-19186
16. Akos037648812
17. At14069
18. Us10377744, Compound No. 26
19. Bpn-19186bpn-19186
20. Ac-36370
21. Bs-15699
22. Hy-135653
23. Cs-0113694
24. Q66977824
| Molecular Weight | 405.4 g/mol |
|---|---|
| Molecular Formula | C18H23F4N3O3 |
| XLogP3 | 3.7 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 5 |
| Exact Mass | 405.16755425 g/mol |
| Monoisotopic Mass | 405.16755425 g/mol |
| Topological Polar Surface Area | 70.7 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 539 |
| 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 | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of EC5026 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right EC5026 manufacturer or EC5026 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred EC5026 manufacturer or EC5026 supplier.
PharmaCompass also assists you with knowing the EC5026 API Price utilized in the formulation of products. EC5026 API Price is not always fixed or binding as the EC5026 Price is obtained through a variety of data sources. The EC5026 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EC5026 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EC5026, including repackagers and relabelers. The FDA regulates EC5026 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EC5026 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 EC5026 supplier is an individual or a company that provides EC5026 active pharmaceutical ingredient (API) or EC5026 finished formulations upon request. The EC5026 suppliers may include EC5026 API manufacturers, exporters, distributors and traders.
EC5026 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 EC5026 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 EC5026 GMP manufacturer or EC5026 GMP API supplier for your needs.
A EC5026 CoA (Certificate of Analysis) is a formal document that attests to EC5026's compliance with EC5026 specifications and serves as a tool for batch-level quality control.
EC5026 CoA mostly includes findings from lab analyses of a specific batch. For each EC5026 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.
EC5026 may be tested according to a variety of international standards, such as European Pharmacopoeia (EC5026 EP), EC5026 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (EC5026 USP).
