Synopsis
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1. Schembl30549301
2. Bdbm722436
3. Hsk39004
4. Ex-a16444
5. Us20250059186, Compound 7
6. 2939748-69-1
| Molecular Weight | 480.6 g/mol |
|---|---|
| Molecular Formula | C26H31N5O4 |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 6 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 109 |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 849 |
| Isotope Atom Count | 3 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| 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 HSK39004 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right HSK39004 manufacturer or HSK39004 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred HSK39004 manufacturer or HSK39004 supplier.
A HSK39004 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HSK39004, including repackagers and relabelers. The FDA regulates HSK39004 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HSK39004 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 HSK39004 supplier is an individual or a company that provides HSK39004 active pharmaceutical ingredient (API) or HSK39004 finished formulations upon request. The HSK39004 suppliers may include HSK39004 API manufacturers, exporters, distributors and traders.
HSK39004 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 HSK39004 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right HSK39004 GMP manufacturer or HSK39004 GMP API supplier for your needs.
A HSK39004 CoA (Certificate of Analysis) is a formal document that attests to HSK39004's compliance with HSK39004 specifications and serves as a tool for batch-level quality control.
HSK39004 CoA mostly includes findings from lab analyses of a specific batch. For each HSK39004 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.
HSK39004 may be tested according to a variety of international standards, such as European Pharmacopoeia (HSK39004 EP), HSK39004 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (HSK39004 USP).
