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1. 21973-56-8
2. [(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 5-methylsulfanyl-n-sulfooxypentanimidothioate
3. N2xe2b8fyy
4. 4-methylthiobutyl Glucosinolate
5. Unii-n2xe2b8fyy
6. Ccris 9054
7. Dtxsid50944561
8. Einecs 244-689-8
9. Mfcd00049366
10. C08409
11. 1-s-[5-(methylsulfanyl)-n-(sulfooxy)pentanimidoyl]-1-thiohexopyranose
12. 1-thio-beta-d-glucopyranose 1-(5-(methylthio)-n-(sulphooxy)valerimidate)
13. [(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl] 5-methylsulfanyl-n-sulfooxy-pentanimidothioate
14. 5-(methylthio)-n-sulfoxy-thiovalerimidic Acid [(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl] Ester
| Molecular Weight | 421.5 g/mol |
|---|---|
| Molecular Formula | C12H23NO9S3 |
| XLogP3 | -0.5 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 10 |
| Exact Mass | 421.05349483 g/mol |
| Monoisotopic Mass | 421.05349483 g/mol |
| Topological Polar Surface Area | 225 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 524 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 1 |
| Covalently Bonded Unit Count | 1 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Glucoerucin 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 Glucoerucin manufacturer or Glucoerucin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glucoerucin manufacturer or Glucoerucin supplier.
PharmaCompass also assists you with knowing the Glucoerucin API Price utilized in the formulation of products. Glucoerucin API Price is not always fixed or binding as the Glucoerucin Price is obtained through a variety of data sources. The Glucoerucin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glucoerucin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucoerucin, including repackagers and relabelers. The FDA regulates Glucoerucin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucoerucin 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 Glucoerucin supplier is an individual or a company that provides Glucoerucin active pharmaceutical ingredient (API) or Glucoerucin finished formulations upon request. The Glucoerucin suppliers may include Glucoerucin API manufacturers, exporters, distributors and traders.
Glucoerucin 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 Glucoerucin 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 Glucoerucin GMP manufacturer or Glucoerucin GMP API supplier for your needs.
A Glucoerucin CoA (Certificate of Analysis) is a formal document that attests to Glucoerucin's compliance with Glucoerucin specifications and serves as a tool for batch-level quality control.
Glucoerucin CoA mostly includes findings from lab analyses of a specific batch. For each Glucoerucin 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.
Glucoerucin may be tested according to a variety of international standards, such as European Pharmacopoeia (Glucoerucin EP), Glucoerucin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Glucoerucin USP).
