Synopsis
Synopsis
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USDMF
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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Others
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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News #PharmaBuzz
1. 17 Beta-hydroxy-7 Alpha-methylestr-4-en-3-one Acetate
2. 7 Alpha-methyl-19-nortestosterone Acetate
3. U 15614
4. U-15,614
1. 6157-87-5
2. Orgasteron Acetate
3. Trestolone Acetate [usan]
4. U-15,614
5. 52xdf4n1xl
6. U-15614
7. 17beta-hydroxy-7alpha-methylestr-4-en-3-one Acetate
8. Nsc-69948
9. Trestolone Acetate (usan)
10. Cdb 903
11. Nsc 69948
12. Unii-52xdf4n1xl
13. 17.beta.-hydroxy-7.alpha.-methylestr-4-en-3-one Acetate
14. 7.alpha.-methyl-19-nortestosterone Acetate
15. Ment Acetate
16. 19-nortestosterone, 7alpha-methyl-, Acetate
17. Chembl452329
18. Schembl2787569
19. Estr-4-en-3-one, 17-(acetyloxy)-7-methyl-, (7.alpha.,17.beta.)-
20. Cdb-903
21. Dtxsid80977160
22. Db13958
23. 7alpha-methyl-19-nortestosterone Acetate
24. D06214
25. 7alpha-methyl-19-nortestosterone 17beta-acetate
26. Q27261025
27. Estr-4-en-3-one, 17beta-hydroxy-7alpha-methyl-, Acetate
28. Estr-4-en-3-one, 17-(acetyloxy)-7-methyl-, (7alpha,17beta)-
29. [(7r,8r,9s,10r,13s,14s,17s)-7,13-dimethyl-3-oxo-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-17-yl] Acetate
Molecular Weight | 330.5 g/mol |
---|---|
Molecular Formula | C21H30O3 |
XLogP3 | 3.4 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 2 |
Exact Mass | 330.21949481 g/mol |
Monoisotopic Mass | 330.21949481 g/mol |
Topological Polar Surface Area | 43.4 Ų |
Heavy Atom Count | 24 |
Formal Charge | 0 |
Complexity | 592 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 7 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
36
PharmaCompass offers a list of Trestolone Acetate 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 Trestolone Acetate manufacturer or Trestolone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trestolone Acetate manufacturer or Trestolone Acetate supplier.
PharmaCompass also assists you with knowing the Trestolone Acetate API Price utilized in the formulation of products. Trestolone Acetate API Price is not always fixed or binding as the Trestolone Acetate Price is obtained through a variety of data sources. The Trestolone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MENT ACETATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MENT ACETATE, including repackagers and relabelers. The FDA regulates MENT ACETATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MENT ACETATE 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 MENT ACETATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MENT ACETATE supplier is an individual or a company that provides MENT ACETATE active pharmaceutical ingredient (API) or MENT ACETATE finished formulations upon request. The MENT ACETATE suppliers may include MENT ACETATE API manufacturers, exporters, distributors and traders.
click here to find a list of MENT ACETATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
MENT ACETATE 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 MENT ACETATE 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 MENT ACETATE GMP manufacturer or MENT ACETATE GMP API supplier for your needs.
A MENT ACETATE CoA (Certificate of Analysis) is a formal document that attests to MENT ACETATE's compliance with MENT ACETATE specifications and serves as a tool for batch-level quality control.
MENT ACETATE CoA mostly includes findings from lab analyses of a specific batch. For each MENT ACETATE 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.
MENT ACETATE may be tested according to a variety of international standards, such as European Pharmacopoeia (MENT ACETATE EP), MENT ACETATE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MENT ACETATE USP).