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1. 2 Alpha,17 Alpha-dimethyldihydrotestosterone
2. 2,17-dimethyldihydrotestosterone
1. Superdrol
2. 3381-88-2
3. Methasteron
4. Methyldrostanolone
5. (2r,5s,8r,9s,10s,13s,14s,17s)-17-hydroxy-2,10,13,17-tetramethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1h-cyclopenta[a]phenanthren-3-one
6. Gh88dy98mr
7. 2alpha,17alpha-dimethyldihydrotestosterone
8. Nsc-40490
9. 17beta-hydroxy-2alpha,17-dimethyl-5alpha-androstan-3-one
10. 17a-methyl-drostanolone
11. 17-methyldrostanolone
12. 2,17-dimethyldihydrotestosterone
13. Nsc 40490
14. Unii-gh88dy98mr
15. Methasterone [who-dd]
16. Schembl4115285
17. Niosh/bv8047800
18. Chebi:79618
19. Dtxsid10187472
20. Nsc40490
21. Zinc4792120
22. Akos015902002
23. Bv80478000
24. Q15409388
25. 2-alpha,17-alpha-dimethyl-17-beta-hydroxy-5-alpha-androstan-3-one
26. 2.alpha.17.alpha.-dimethyletiocholan-3-on-17.beta.-ol
27. 5-alpha-androstan-3-one, 2-alpha,17-alpha-dimethyl-17-beta-hydroxy-
28. 17.beta.-hydroxy-2.alpha.,17.alpha.-dimethyl-5.alpha.-androstane-3-one
29. 2.alpha.,17.alpha.-dimethyl-17.beta.-hydroxy-5.alpha.-androstane-3-one
30. Androstan-3-one, 17-hydroxy-2,17-dimethyl-, (2.alpha.,5.alpha.,17.beta.)-
Molecular Weight | 318.5 g/mol |
---|---|
Molecular Formula | C21H34O2 |
XLogP3 | 4.5 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 0 |
Exact Mass | 318.255880323 g/mol |
Monoisotopic Mass | 318.255880323 g/mol |
Topological Polar Surface Area | 37.3 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 528 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 8 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Methasterone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methasterone, including repackagers and relabelers. The FDA regulates Methasterone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methasterone API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Methasterone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methasterone supplier is an individual or a company that provides Methasterone active pharmaceutical ingredient (API) or Methasterone finished formulations upon request. The Methasterone suppliers may include Methasterone API manufacturers, exporters, distributors and traders.
click here to find a list of Methasterone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Methasterone 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 Methasterone 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 Methasterone GMP manufacturer or Methasterone GMP API supplier for your needs.
A Methasterone CoA (Certificate of Analysis) is a formal document that attests to Methasterone's compliance with Methasterone specifications and serves as a tool for batch-level quality control.
Methasterone CoA mostly includes findings from lab analyses of a specific batch. For each Methasterone 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.
Methasterone may be tested according to a variety of international standards, such as European Pharmacopoeia (Methasterone EP), Methasterone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Methasterone USP).
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