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1. 28314-80-9
2. Benzoic Acid, 2,4,6-trifluoro-
3. 2,4,6-trifluorobenzoicacid
4. Mfcd00042398
5. C7h3f3o2
6. 2,4,6-trifluorobenzioc Acid
7. 2.4.6-trifluorbenzoesaeure
8. Schembl288979
9. 2,4,6-triflluorobenzoic Acid
10. Dtxsid50334327
11. 2,4,6-f3c6h2cooh
12. 2,4,6-trifluorobenzoic Acid, 98%
13. Akos000152490
14. Ac-4009
15. Benzoic Acid,2,4,6-trifluoro
16. Cs-w002210
17. Cs-11287
18. Mesoxalicacidmonohydratedisodiumsalt
19. Sy014352
20. Am20040089
21. Ft-0609862
22. T2409
23. En300-67167
24. J-507075
25. Z285150322
26. 2,3-dihydroxy Naphthalene-6-sodium Sulfonate(dihydroxy R Salt)
27. Inchi=1/c7h3f3o2/c8-3-1-4(9)6(7(11)12)5(10)2-3/h1-2h,(h,11,12
| Molecular Weight | 176.09 g/mol |
|---|---|
| Molecular Formula | C7H3F3O2 |
| XLogP3 | 1.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 37.3 |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 174 |
| 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
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PharmaCompass offers a list of Z285150322 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 Z285150322 manufacturer or Z285150322 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Z285150322 manufacturer or Z285150322 supplier.
PharmaCompass also assists you with knowing the Z285150322 API Price utilized in the formulation of products. Z285150322 API Price is not always fixed or binding as the Z285150322 Price is obtained through a variety of data sources. The Z285150322 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Z285150322 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Z285150322, including repackagers and relabelers. The FDA regulates Z285150322 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Z285150322 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 Z285150322 supplier is an individual or a company that provides Z285150322 active pharmaceutical ingredient (API) or Z285150322 finished formulations upon request. The Z285150322 suppliers may include Z285150322 API manufacturers, exporters, distributors and traders.
Z285150322 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 Z285150322 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 Z285150322 GMP manufacturer or Z285150322 GMP API supplier for your needs.
A Z285150322 CoA (Certificate of Analysis) is a formal document that attests to Z285150322's compliance with Z285150322 specifications and serves as a tool for batch-level quality control.
Z285150322 CoA mostly includes findings from lab analyses of a specific batch. For each Z285150322 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.
Z285150322 may be tested according to a variety of international standards, such as European Pharmacopoeia (Z285150322 EP), Z285150322 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Z285150322 USP).
