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1. 1-s-((1e)-3-phenyl-n-(sulfooxy)propanimidoyl)-1-thio-beta-d-glucopyranose
2. 2-phenylethyl Glucosinolate
3. Gluconasturtiin
4. Phenethylglucosinolate
1. Gluconasturtiin
2. 499-30-9
3. Schembl887122
4. 499-30-9 (non-salt)
| Molecular Weight | 423.5 g/mol |
|---|---|
| Molecular Formula | C15H21NO9S2 |
| XLogP3 | 0.1 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 8 |
| Exact Mass | 423.06577359 g/mol |
| Monoisotopic Mass | 423.06577359 g/mol |
| Topological Polar Surface Area | 200 Ų |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 589 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Gluconasturtiin 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 Gluconasturtiin manufacturer or Gluconasturtiin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gluconasturtiin manufacturer or Gluconasturtiin supplier.
PharmaCompass also assists you with knowing the Gluconasturtiin API Price utilized in the formulation of products. Gluconasturtiin API Price is not always fixed or binding as the Gluconasturtiin Price is obtained through a variety of data sources. The Gluconasturtiin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gluconasturtiin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gluconasturtiin, including repackagers and relabelers. The FDA regulates Gluconasturtiin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gluconasturtiin 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 Gluconasturtiin supplier is an individual or a company that provides Gluconasturtiin active pharmaceutical ingredient (API) or Gluconasturtiin finished formulations upon request. The Gluconasturtiin suppliers may include Gluconasturtiin API manufacturers, exporters, distributors and traders.
Gluconasturtiin 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 Gluconasturtiin 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 Gluconasturtiin GMP manufacturer or Gluconasturtiin GMP API supplier for your needs.
A Gluconasturtiin CoA (Certificate of Analysis) is a formal document that attests to Gluconasturtiin's compliance with Gluconasturtiin specifications and serves as a tool for batch-level quality control.
Gluconasturtiin CoA mostly includes findings from lab analyses of a specific batch. For each Gluconasturtiin 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.
Gluconasturtiin may be tested according to a variety of international standards, such as European Pharmacopoeia (Gluconasturtiin EP), Gluconasturtiin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gluconasturtiin USP).
