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| Molecular Weight | 504.4 g/mol |
|---|---|
| Molecular Formula | C30H16O8 |
| XLogP3 | 6.9 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 0 |
| Exact Mass | 504.08451746 g/mol |
| Monoisotopic Mass | 504.08451746 g/mol |
| Topological Polar Surface Area | 156 A^2 |
| Heavy Atom Count | 38 |
| Formal Charge | 0 |
| Complexity | 981 |
| Isotope Atom Count | 0 |
| 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 |
Drugs in Development
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REF. STANDARDS & IMPURITIES
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CAS Number : 548-04-9
Quantity Per Vial : 5 MG
Sale Unit :
Price : Euro 300
Details : Purity > 98.0 %
Monograph :
Storage :
Code/Batch No : 7501278
CAS Number : 548-04-9
Quantity Per Vial : 10 MG
Sale Unit :
Price : Euro 510
Details : Purity > 98.0 %
Monograph :
Storage :
Code/Batch No : 7501278
CAS Number : 548-04-9
Quantity Per Vial : 20 MG
Sale Unit :
Price : Euro 690
Details : Purity > 98.0 %
Monograph :
Storage :
Code/Batch No : 7501278
CAS Number :
Quantity Per Vial : 5 MG
Sale Unit :
Price : Euro 320
Details : Purity > 98.0 %
Monograph :
Storage :
Code/Batch No : 7500026
CAS Number :
Quantity Per Vial : 10 MG
Sale Unit :
Price : Euro 520
Details : Purity > 98.0 %
Monograph :
Storage :
Code/Batch No : 7500026
CAS Number :
Quantity Per Vial : 20 MG
Sale Unit :
Price : Euro 710
Details : Purity > 98.0 %
Monograph :
Storage :
Code/Batch No : 7500026
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
A Hypericin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hypericin, including repackagers and relabelers. The FDA regulates Hypericin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hypericin 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 Hypericin supplier is an individual or a company that provides Hypericin active pharmaceutical ingredient (API) or Hypericin finished formulations upon request. The Hypericin suppliers may include Hypericin API manufacturers, exporters, distributors and traders.
Hypericin 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 Hypericin 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 Hypericin GMP manufacturer or Hypericin GMP API supplier for your needs.
A Hypericin CoA (Certificate of Analysis) is a formal document that attests to Hypericin's compliance with Hypericin specifications and serves as a tool for batch-level quality control.
Hypericin CoA mostly includes findings from lab analyses of a specific batch. For each Hypericin 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.
Hypericin may be tested according to a variety of international standards, such as European Pharmacopoeia (Hypericin EP), Hypericin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Hypericin USP).
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