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1. Gc-4419 Dipropionate
2. Bis-propionato(gc4419)
3. Fw5t90vm32
4. Gc4711
5. Gc-4711
6. Rucosopasem Manganese
7. Manganese(ii), Bis-propionato((4as,13as,17as,21as)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-11,7-nitrilo-7h-dibenzo(b,h)(1,4,7,10)tetraaza-cycloheptadecine-kn5,kn13,kn18,kn21,kn22)-,
8. 2081067-45-8
9. Unii-fw5t90vm32
10. Rucosopasem Manganese [inn]
11. 2248030-85-3
12. Manganese, ((4as,13as,17as,21as)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-11,7-nitrilo-7h-dibenzo(b,h)(1,4,7,10)tetraazacycloheptadecine-.kappa.n5,.kappa.n13,.kappa.n18,.kappa.n21,.kappa.n22)bis(propanoato-.kappa.o)-, (pb-7-11-2344'3')
| Molecular Weight | 558.6 g/mol |
|---|---|
| Molecular Formula | C27H45MnN5O4 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 0 |
| Exact Mass | 558.285198 g/mol |
| Monoisotopic Mass | 558.285198 g/mol |
| Topological Polar Surface Area | 141 Ų |
| Heavy Atom Count | 37 |
| Formal Charge | 0 |
| Complexity | 416 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 4 |
ABOUT THIS PAGE
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PharmaCompass offers a list of GC4711 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 GC4711 manufacturer or GC4711 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred GC4711 manufacturer or GC4711 supplier.
PharmaCompass also assists you with knowing the GC4711 API Price utilized in the formulation of products. GC4711 API Price is not always fixed or binding as the GC4711 Price is obtained through a variety of data sources. The GC4711 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A GC4711 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GC4711, including repackagers and relabelers. The FDA regulates GC4711 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GC4711 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 GC4711 supplier is an individual or a company that provides GC4711 active pharmaceutical ingredient (API) or GC4711 finished formulations upon request. The GC4711 suppliers may include GC4711 API manufacturers, exporters, distributors and traders.
GC4711 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 GC4711 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 GC4711 GMP manufacturer or GC4711 GMP API supplier for your needs.
A GC4711 CoA (Certificate of Analysis) is a formal document that attests to GC4711's compliance with GC4711 specifications and serves as a tool for batch-level quality control.
GC4711 CoA mostly includes findings from lab analyses of a specific batch. For each GC4711 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.
GC4711 may be tested according to a variety of international standards, such as European Pharmacopoeia (GC4711 EP), GC4711 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (GC4711 USP).
