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| Molecular Weight | 2784.1 g/mol |
|---|---|
| Molecular Formula | C114H179N39O37S3 |
| Hydrogen Bond Donor Count | 47 |
| Hydrogen Bond Acceptor Count | 45 |
| Rotatable Bond Count | 61 |
| Exact Mass | 2783.2519761 g/mol |
| Monoisotopic Mass | 2782.2486213 g/mol |
| Topological Polar Surface Area | 1350 Ų |
| Heavy Atom Count | 193 |
| Formal Charge | 0 |
| Complexity | 6050 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 21 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Anaritide Acetate 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 Anaritide Acetate manufacturer or Anaritide Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Anaritide Acetate manufacturer or Anaritide Acetate supplier.
PharmaCompass also assists you with knowing the Anaritide Acetate API Price utilized in the formulation of products. Anaritide Acetate API Price is not always fixed or binding as the Anaritide Acetate Price is obtained through a variety of data sources. The Anaritide Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anaritide Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anaritide Acetate, including repackagers and relabelers. The FDA regulates Anaritide Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anaritide 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.
A Anaritide Acetate supplier is an individual or a company that provides Anaritide Acetate active pharmaceutical ingredient (API) or Anaritide Acetate finished formulations upon request. The Anaritide Acetate suppliers may include Anaritide Acetate API manufacturers, exporters, distributors and traders.
Anaritide 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 Anaritide 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 Anaritide Acetate GMP manufacturer or Anaritide Acetate GMP API supplier for your needs.
A Anaritide Acetate CoA (Certificate of Analysis) is a formal document that attests to Anaritide Acetate's compliance with Anaritide Acetate specifications and serves as a tool for batch-level quality control.
Anaritide Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Anaritide 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.
Anaritide Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Anaritide Acetate EP), Anaritide Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Anaritide Acetate USP).