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1. 154804-51-0
2. Disodium;1,3-dihydroxypropan-2-yl Phosphate;hydrate
3. 819-83-0
4. Sodium 1,3-dihydroxypropan-2-yl Phosphate Hydrate(2:1:x)
5. Sodium 1,3-dihydroxypropan-2-yl Phosphate Hydrate
6. Glycerol Phosphate Disodium Salt Hydrate, Isomeric Mixture
7. B-glycerophosphate Disodium Salt Hydrate
8. Glycerol 2-phosphate Disodium Salt Hydrate
9. Sodium Glycerophosphate (usan)
10. Akos025311014
11. Ss-glycerophosphate Disodium Salt Hydrate
12. D10489
13. Beta-glycerophosphate Disodium Salt Hydrate, <=1.0 Mol % L-alpha-isomer
14. Beta-glycerophosphate Disodium Salt Hydrate, Powder, Bioreagent, Suitable For Cell Culture
15. 305808-17-7
16. Beta-glycerophosphate Disodium Salt Hydrate, <=2.4 Mol % Alpha-isomer((based On C3h7o6pna2 With X H2o))
17. Beta-glycerophosphate Disodium Salt Hydrate, Bioultra, Suitable For Cell Culture, Suitable For Plant Cell Culture, >=99.0% (titration)
| Molecular Weight | 234.05 g/mol |
|---|---|
| Molecular Formula | C3H9Na2O7P |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 3 |
| Exact Mass | 233.98812818 g/mol |
| Monoisotopic Mass | 233.98812818 g/mol |
| Topological Polar Surface Area | 114 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 113 |
| 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 | 4 |
ABOUT THIS PAGE
A AK398595 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AK398595, including repackagers and relabelers. The FDA regulates AK398595 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AK398595 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 AK398595 supplier is an individual or a company that provides AK398595 active pharmaceutical ingredient (API) or AK398595 finished formulations upon request. The AK398595 suppliers may include AK398595 API manufacturers, exporters, distributors and traders.
AK398595 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 AK398595 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 AK398595 GMP manufacturer or AK398595 GMP API supplier for your needs.
A AK398595 CoA (Certificate of Analysis) is a formal document that attests to AK398595's compliance with AK398595 specifications and serves as a tool for batch-level quality control.
AK398595 CoA mostly includes findings from lab analyses of a specific batch. For each AK398595 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.
AK398595 may be tested according to a variety of international standards, such as European Pharmacopoeia (AK398595 EP), AK398595 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AK398595 USP).
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