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1. 17 Beta-acetoxy-delta-(1,5)-androstadien-3-one
1. 2363-59-9
2. Boldenone 17-acetate
3. 17beta-acetoxyandrosta-1,4-dien-3-one
4. 3t5iz3hs3x
5. [(8r,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] Acetate
6. Androsta-1,4-dien-3-one, 17-(acetyloxy)-, (17b)-
7. 1-dehydrotestosterone Acetate
8. Unii-3t5iz3hs3x
9. Androsta-1,4-dien-3-one, 17-(acetyloxy)-, (17.beta.)-
10. Einecs 219-112-8
11. 17beta-acetoxy-delta-(1,5)-androstadien-3-one
12. Schembl8346843
13. Dtxsid60946450
14. 1-dehydroteststerone Acetate
15. Bcp10780
16. Zinc5166613
17. Akos015914067
18. Ds-6009
19. 17beta-acetoxy-androsta-l,4-dien-3-one
20. 1,4-androstadien-17beta-ol-3-one Acetate
21. 1,2-didehydrotestosterone 17-o-acetate
22. (17beta)-hydroxyandrosta-1,4-dien-3-one Acetate
23. 17.beta.-acetoxyandrosta-1,4-dien-3-one
24. W-107390
25. Q27258009
26. (17.beta.)-17-(acetyloxy)androsta-1,4-dien-3-one
27. Acetic Acid (8r,10r,13s,17s)-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3h-cyclopenta[a]phenanthren-17-yl Ester
| Molecular Weight | 328.4 g/mol |
|---|---|
| Molecular Formula | C21H28O3 |
| XLogP3 | 4.1 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 328.20384475 g/mol |
| Monoisotopic Mass | 328.20384475 g/mol |
| Topological Polar Surface Area | 43.4 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 646 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 6 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Boldenone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boldenone Acetate, including repackagers and relabelers. The FDA regulates Boldenone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boldenone 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 Boldenone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Boldenone Acetate supplier is an individual or a company that provides Boldenone Acetate active pharmaceutical ingredient (API) or Boldenone Acetate finished formulations upon request. The Boldenone Acetate suppliers may include Boldenone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Boldenone Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Boldenone 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 Boldenone 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 Boldenone Acetate GMP manufacturer or Boldenone Acetate GMP API supplier for your needs.
A Boldenone Acetate CoA (Certificate of Analysis) is a formal document that attests to Boldenone Acetate's compliance with Boldenone Acetate specifications and serves as a tool for batch-level quality control.
Boldenone Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Boldenone 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.
Boldenone Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Boldenone Acetate EP), Boldenone Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Boldenone Acetate USP).
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