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USP
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| Molecular Weight | 227.22 g/mol |
|---|---|
| Molecular Formula | C9H13N3O4 |
| XLogP3 | -1.8 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 227.09060590 g/mol |
| Monoisotopic Mass | 227.09060590 g/mol |
| Topological Polar Surface Area | 108 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 355 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
API SUPPLIERS
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USDMF
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ABOUT THIS PAGE
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PharmaCompass offers a list of 2-Deoxycytidine 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 2-Deoxycytidine manufacturer or 2-Deoxycytidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 2-Deoxycytidine manufacturer or 2-Deoxycytidine supplier.
PharmaCompass also assists you with knowing the 2-Deoxycytidine API Price utilized in the formulation of products. 2-Deoxycytidine API Price is not always fixed or binding as the 2-Deoxycytidine Price is obtained through a variety of data sources. The 2-Deoxycytidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2-Deoxycytidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-Deoxycytidine, including repackagers and relabelers. The FDA regulates 2-Deoxycytidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-Deoxycytidine 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 2-Deoxycytidine supplier is an individual or a company that provides 2-Deoxycytidine active pharmaceutical ingredient (API) or 2-Deoxycytidine finished formulations upon request. The 2-Deoxycytidine suppliers may include 2-Deoxycytidine API manufacturers, exporters, distributors and traders.
click here to find a list of 2-Deoxycytidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 2-Deoxycytidine DMF (Drug Master File) is a document detailing the whole manufacturing process of 2-Deoxycytidine active pharmaceutical ingredient (API) in detail. Different forms of 2-Deoxycytidine DMFs exist exist since differing nations have different regulations, such as 2-Deoxycytidine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 2-Deoxycytidine DMF submitted to regulatory agencies in the US is known as a USDMF. 2-Deoxycytidine USDMF includes data on 2-Deoxycytidine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 2-Deoxycytidine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 2-Deoxycytidine suppliers with USDMF on PharmaCompass.
2-Deoxycytidine 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-Deoxycytidine 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-Deoxycytidine GMP manufacturer or 2-Deoxycytidine GMP API supplier for your needs.
A 2-Deoxycytidine CoA (Certificate of Analysis) is a formal document that attests to 2-Deoxycytidine's compliance with 2-Deoxycytidine specifications and serves as a tool for batch-level quality control.
2-Deoxycytidine CoA mostly includes findings from lab analyses of a specific batch. For each 2-Deoxycytidine 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-Deoxycytidine may be tested according to a variety of international standards, such as European Pharmacopoeia (2-Deoxycytidine EP), 2-Deoxycytidine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2-Deoxycytidine USP).
