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1. 6132-05-4
2. Sodium Hydrogencitrate Sesquihydrate, Reagentplus(r), 99%
| Molecular Weight | 526.22 g/mol |
|---|---|
| Molecular Formula | C12H18Na4O17 |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 17 |
| Rotatable Bond Count | 6 |
| Exact Mass | 526.01347623 g/mol |
| Monoisotopic Mass | 526.01347623 g/mol |
| Topological Polar Surface Area | 279 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 216 |
| 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 | 9 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Disodium Citrate Sesquihydrate 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 Disodium Citrate Sesquihydrate manufacturer or Disodium Citrate Sesquihydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Disodium Citrate Sesquihydrate manufacturer or Disodium Citrate Sesquihydrate supplier.
PharmaCompass also assists you with knowing the Disodium Citrate Sesquihydrate API Price utilized in the formulation of products. Disodium Citrate Sesquihydrate API Price is not always fixed or binding as the Disodium Citrate Sesquihydrate Price is obtained through a variety of data sources. The Disodium Citrate Sesquihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Disodium Citrate 1,5-hydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disodium Citrate 1,5-hydrate, including repackagers and relabelers. The FDA regulates Disodium Citrate 1,5-hydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disodium Citrate 1,5-hydrate 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 Disodium Citrate 1,5-hydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disodium Citrate 1,5-hydrate supplier is an individual or a company that provides Disodium Citrate 1,5-hydrate active pharmaceutical ingredient (API) or Disodium Citrate 1,5-hydrate finished formulations upon request. The Disodium Citrate 1,5-hydrate suppliers may include Disodium Citrate 1,5-hydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Disodium Citrate 1,5-hydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Disodium Citrate 1,5-hydrate 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 Disodium Citrate 1,5-hydrate 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 Disodium Citrate 1,5-hydrate GMP manufacturer or Disodium Citrate 1,5-hydrate GMP API supplier for your needs.
A Disodium Citrate 1,5-hydrate CoA (Certificate of Analysis) is a formal document that attests to Disodium Citrate 1,5-hydrate's compliance with Disodium Citrate 1,5-hydrate specifications and serves as a tool for batch-level quality control.
Disodium Citrate 1,5-hydrate CoA mostly includes findings from lab analyses of a specific batch. For each Disodium Citrate 1,5-hydrate 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.
Disodium Citrate 1,5-hydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Disodium Citrate 1,5-hydrate EP), Disodium Citrate 1,5-hydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Disodium Citrate 1,5-hydrate USP).
