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1. Phenythilone
2. Thimorlone
3. 115-55-9
4. 2-ethyl-2-phenylthiomorpholine-3,5-dione
5. Dl-thimorlone
6. Phenythilone [inn]
7. 2-ethyl-2-phenyl-3,5-thiamorpholinedione
8. Nsc-18713
9. V8350f4a37
10. 3,5-thiomorpholinedione, 2-ethyl-2-phenyl-
11. Unii-v8350f4a37
12. Nsc18713
13. 3,5-thiomorpholinedione,2-ethyl-2-phenyl-
14. 3, 2-ethyl-2-phenyl-
15. Schembl719266
16. Chembl2106881
17. Dtxsid50861744
18. Nsc 18713
19. Ds-013969
20. 2-ethyl-2-phenyl-3,5-thiomorpholinedione #
21. 2-ethyl-2-phenyl-1,4-thiazine-3,5(4h,6h)-dione
22. Q27291654
| Molecular Weight | 235.30 g/mol |
|---|---|
| Molecular Formula | C12H13NO2S |
| XLogP3 | 2.2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 235.06669983 g/mol |
| Monoisotopic Mass | 235.06669983 g/mol |
| Topological Polar Surface Area | 71.5 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 299 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Phenylthilone 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 Phenylthilone manufacturer or Phenylthilone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenylthilone manufacturer or Phenylthilone supplier.
PharmaCompass also assists you with knowing the Phenylthilone API Price utilized in the formulation of products. Phenylthilone API Price is not always fixed or binding as the Phenylthilone Price is obtained through a variety of data sources. The Phenylthilone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PHENYLPROPANOLAMINE POLISTIREX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PHENYLPROPANOLAMINE POLISTIREX, including repackagers and relabelers. The FDA regulates PHENYLPROPANOLAMINE POLISTIREX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PHENYLPROPANOLAMINE POLISTIREX 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 PHENYLPROPANOLAMINE POLISTIREX supplier is an individual or a company that provides PHENYLPROPANOLAMINE POLISTIREX active pharmaceutical ingredient (API) or PHENYLPROPANOLAMINE POLISTIREX finished formulations upon request. The PHENYLPROPANOLAMINE POLISTIREX suppliers may include PHENYLPROPANOLAMINE POLISTIREX API manufacturers, exporters, distributors and traders.
PHENYLPROPANOLAMINE POLISTIREX 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 PHENYLPROPANOLAMINE POLISTIREX 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 PHENYLPROPANOLAMINE POLISTIREX GMP manufacturer or PHENYLPROPANOLAMINE POLISTIREX GMP API supplier for your needs.
A PHENYLPROPANOLAMINE POLISTIREX CoA (Certificate of Analysis) is a formal document that attests to PHENYLPROPANOLAMINE POLISTIREX's compliance with PHENYLPROPANOLAMINE POLISTIREX specifications and serves as a tool for batch-level quality control.
PHENYLPROPANOLAMINE POLISTIREX CoA mostly includes findings from lab analyses of a specific batch. For each PHENYLPROPANOLAMINE POLISTIREX 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.
PHENYLPROPANOLAMINE POLISTIREX may be tested according to a variety of international standards, such as European Pharmacopoeia (PHENYLPROPANOLAMINE POLISTIREX EP), PHENYLPROPANOLAMINE POLISTIREX JP (Japanese Pharmacopeia) and the US Pharmacopoeia (PHENYLPROPANOLAMINE POLISTIREX USP).
