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1. C70 Fullerene
2. Fullerene 70
1. 115383-22-7
2. C70 Fullerene
3. Fullerene 70
4. (c70-d5h(6))[5,6]fullerene
5. [5,6]-fullerene-c70
6. Mfcd31654066
7. Rugbyballene
8. [5,6]fullerene-c70-d5h(6)
9. Fullerene C-70
10. Carbon C70
11. Fullerene - C70
12. [70-d5h]fullerene
13. Buckminsterfullerene C70
14. Chebi:33195
15. Dtxsid90151050
16. [5,6]fullerene-c70-d5h(6
17. (5,6)fullerene-c70-d5h (6)
18. Zinc96068395
19. Akos037648485
20. Bs-14126
21. F1233
22. Ft-0626557
23. D82998
24. Q3885009
25. Fullerene C70 (purified By Sublimation) [for Organic Electronics]
Molecular Weight | 840.7 g/mol |
---|---|
Molecular Formula | C70 |
XLogP3 | 10.1 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 0 |
Rotatable Bond Count | 0 |
Exact Mass | 840 g/mol |
Monoisotopic Mass | 840 g/mol |
Topological Polar Surface Area | 0 Ų |
Heavy Atom Count | 70 |
Formal Charge | 0 |
Complexity | 4760 |
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 Fullerene C70 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fullerene C70, including repackagers and relabelers. The FDA regulates Fullerene C70 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fullerene C70 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 Fullerene C70 supplier is an individual or a company that provides Fullerene C70 active pharmaceutical ingredient (API) or Fullerene C70 finished formulations upon request. The Fullerene C70 suppliers may include Fullerene C70 API manufacturers, exporters, distributors and traders.
Fullerene C70 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 Fullerene C70 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 Fullerene C70 GMP manufacturer or Fullerene C70 GMP API supplier for your needs.
A Fullerene C70 CoA (Certificate of Analysis) is a formal document that attests to Fullerene C70's compliance with Fullerene C70 specifications and serves as a tool for batch-level quality control.
Fullerene C70 CoA mostly includes findings from lab analyses of a specific batch. For each Fullerene C70 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.
Fullerene C70 may be tested according to a variety of international standards, such as European Pharmacopoeia (Fullerene C70 EP), Fullerene C70 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fullerene C70 USP).
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