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1. 33070-32-5
2. 5-bromo-2,2-difluorobenzodioxole
3. 5-bromo-2,2-difluoro-2h-1,3-benzodioxole
4. 5-bromo-2,2-difluorobenzo[d][1,3]dioxole
5. Mfcd00236212
6. 5-bromo-2,2-difluoro-benzo[1,3]dioxole
7. 1,3-benzodioxole, 5-bromo-2,2-difluoro-
8. 4-bromo-1,2-(difluoromethylenedioxy)benzene
9. Schembl12046
10. Ambz0129
11. Dtxsid20371244
12. Bcp15764
13. Zinc2560117
14. Bbl100895
15. Stl554689
16. Akos003612230
17. Am85729
18. Cs-w001170
19. Pb24651
20. Ps-7636
21. 5-bromo2,2-difluoro-1,3-benzodioxole
22. 2,2-difluoro-5-bromo-1,3-benzodioxole
23. Sy009399
24. 5-bromo-2,2-difluoro- 1,3-benzodioxole
25. 5-bromo-2,2-difluoro-1,3-benzodioxolane
26. A5907
27. B3781
28. Bb 0300680
29. Ft-0620067
30. 199b142
31. 5-bromo-2,2-difluoro-1,3-benzodioxole, Aldrichcpr
32. Q-101060
33. Z2230863249
34. 5-bromo-2,2-difluoro-benzo[1,3]dioxole;5-bromo-2,2-difluoro-1,3-benzodioxole
| Molecular Weight | 237.00 g/mol |
|---|---|
| Molecular Formula | C7H3BrF2O2 |
| XLogP3 | 3.2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 0 |
| Exact Mass | 235.92845 g/mol |
| Monoisotopic Mass | 235.92845 g/mol |
| Topological Polar Surface Area | 18.5 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 188 |
| 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
21
PharmaCompass offers a list of 33070-32-5 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 33070-32-5 manufacturer or 33070-32-5 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 33070-32-5 manufacturer or 33070-32-5 supplier.
PharmaCompass also assists you with knowing the 33070-32-5 API Price utilized in the formulation of products. 33070-32-5 API Price is not always fixed or binding as the 33070-32-5 Price is obtained through a variety of data sources. The 33070-32-5 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 33070-32-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 33070-32-5, including repackagers and relabelers. The FDA regulates 33070-32-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 33070-32-5 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 33070-32-5 supplier is an individual or a company that provides 33070-32-5 active pharmaceutical ingredient (API) or 33070-32-5 finished formulations upon request. The 33070-32-5 suppliers may include 33070-32-5 API manufacturers, exporters, distributors and traders.
33070-32-5 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 33070-32-5 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 33070-32-5 GMP manufacturer or 33070-32-5 GMP API supplier for your needs.
A 33070-32-5 CoA (Certificate of Analysis) is a formal document that attests to 33070-32-5's compliance with 33070-32-5 specifications and serves as a tool for batch-level quality control.
33070-32-5 CoA mostly includes findings from lab analyses of a specific batch. For each 33070-32-5 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.
33070-32-5 may be tested according to a variety of international standards, such as European Pharmacopoeia (33070-32-5 EP), 33070-32-5 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (33070-32-5 USP).
