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| Molecular Weight | 151.13 g/mol |
|---|---|
| Molecular Formula | C5H5N5O |
| XLogP3 | -1 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 151.04940980 g/mol |
| Monoisotopic Mass | 151.04940980 g/mol |
| Topological Polar Surface Area | 96.2 A^2 |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 225 |
| 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 |
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PharmaCompass offers a list of Guanine 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 Guanine manufacturer or Guanine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Guanine manufacturer or Guanine supplier.
PharmaCompass also assists you with knowing the Guanine API Price utilized in the formulation of products. Guanine API Price is not always fixed or binding as the Guanine Price is obtained through a variety of data sources. The Guanine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2-amino-6-oxopurine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-amino-6-oxopurine, including repackagers and relabelers. The FDA regulates 2-amino-6-oxopurine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-amino-6-oxopurine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of 2-amino-6-oxopurine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 2-amino-6-oxopurine supplier is an individual or a company that provides 2-amino-6-oxopurine active pharmaceutical ingredient (API) or 2-amino-6-oxopurine finished formulations upon request. The 2-amino-6-oxopurine suppliers may include 2-amino-6-oxopurine API manufacturers, exporters, distributors and traders.
click here to find a list of 2-amino-6-oxopurine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
2-amino-6-oxopurine 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 2-amino-6-oxopurine 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 2-amino-6-oxopurine GMP manufacturer or 2-amino-6-oxopurine GMP API supplier for your needs.
A 2-amino-6-oxopurine CoA (Certificate of Analysis) is a formal document that attests to 2-amino-6-oxopurine's compliance with 2-amino-6-oxopurine specifications and serves as a tool for batch-level quality control.
2-amino-6-oxopurine CoA mostly includes findings from lab analyses of a specific batch. For each 2-amino-6-oxopurine 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.
2-amino-6-oxopurine may be tested according to a variety of international standards, such as European Pharmacopoeia (2-amino-6-oxopurine EP), 2-amino-6-oxopurine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2-amino-6-oxopurine USP).
