Synopsis
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NDC API
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FDA Orange Book
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1. Schembl145070
| Molecular Weight | 982.8 g/mol |
|---|---|
| Molecular Formula | C12H22O35S8 |
| XLogP3 | -8.6 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 35 |
| Rotatable Bond Count | 21 |
| Exact Mass | 981.7707318 g/mol |
| Monoisotopic Mass | 981.7707318 g/mol |
| Topological Polar Surface Area | 604 Ų |
| Heavy Atom Count | 55 |
| Formal Charge | 0 |
| Complexity | 2230 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 9 |
| Undefined Atom Stereocenter Count | 0 |
| 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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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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PharmaCompass offers a list of Sucrose Octasulfate 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 Sucrose Octasulfate manufacturer or Sucrose Octasulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sucrose Octasulfate manufacturer or Sucrose Octasulfate supplier.
PharmaCompass also assists you with knowing the Sucrose Octasulfate API Price utilized in the formulation of products. Sucrose Octasulfate API Price is not always fixed or binding as the Sucrose Octasulfate Price is obtained through a variety of data sources. The Sucrose Octasulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sucrose Octasulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sucrose Octasulfate, including repackagers and relabelers. The FDA regulates Sucrose Octasulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sucrose Octasulfate 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 Sucrose Octasulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sucrose Octasulfate supplier is an individual or a company that provides Sucrose Octasulfate active pharmaceutical ingredient (API) or Sucrose Octasulfate finished formulations upon request. The Sucrose Octasulfate suppliers may include Sucrose Octasulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Sucrose Octasulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sucrose Octasulfate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sucrose Octasulfate active pharmaceutical ingredient (API) in detail. Different forms of Sucrose Octasulfate DMFs exist exist since differing nations have different regulations, such as Sucrose Octasulfate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sucrose Octasulfate DMF submitted to regulatory agencies in the US is known as a USDMF. Sucrose Octasulfate USDMF includes data on Sucrose Octasulfate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sucrose Octasulfate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sucrose Octasulfate suppliers with USDMF on PharmaCompass.
Sucrose Octasulfate 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 Sucrose Octasulfate 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 Sucrose Octasulfate GMP manufacturer or Sucrose Octasulfate GMP API supplier for your needs.
A Sucrose Octasulfate CoA (Certificate of Analysis) is a formal document that attests to Sucrose Octasulfate's compliance with Sucrose Octasulfate specifications and serves as a tool for batch-level quality control.
Sucrose Octasulfate CoA mostly includes findings from lab analyses of a specific batch. For each Sucrose Octasulfate 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.
Sucrose Octasulfate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sucrose Octasulfate EP), Sucrose Octasulfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sucrose Octasulfate USP).
