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1. 7-acetylintermedine
2. 74243-01-9
3. [(7r,8r)-7-acetyloxy-5,6,7,8-tetrahydro-3h-pyrrolizin-1-yl]methyl (2s)-2-hydroxy-2-[(1r)-1-hydroxyethyl]-3-methylbutanoate
4. Chebi:80702
5. Dtxsid201019870
6. 7-o-acetylintermedine , Hplc Grade
7. Mfcd31631254
8. Butanoic Acid, 2,3-dihydroxy-2-(1-methylethyl)-, (1-(acetyloxy)-2,3,5,7a-tetrahydro-1h-pyrrolizin-7-yl)methyl Ester, (1r-(1alpha,7(2s*,3r*),7abeta))-
9. Hy-127011
10. Cs-0091352
11. Q27149735
12. ((1r,7ar)-1-acetoxy-2,3,5,7a-tetrahydro-1h-pyrrolizin-7-yl)methyl (2s,3r)-2,3-dihydroxy-2-isopropylbutanoate
13. Butanoic Acid, 2,3-dihydroxy-2-(1-methylethyl)-, ((1r,7ar)-1-(acetyloxy)-2,3,5,7a-tetrahydro-1h-pyrrolizin-7-yl)methyl Ester, (2s,3r)-
| Molecular Weight | 341.4 g/mol |
|---|---|
| Molecular Formula | C17H27NO6 |
| XLogP3 | 0.1 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 8 |
| Exact Mass | 341.18383758 g/mol |
| Monoisotopic Mass | 341.18383758 g/mol |
| Topological Polar Surface Area | 96.3 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 531 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Acetylintermedine 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 Acetylintermedine manufacturer or Acetylintermedine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acetylintermedine manufacturer or Acetylintermedine supplier.
PharmaCompass also assists you with knowing the Acetylintermedine API Price utilized in the formulation of products. Acetylintermedine API Price is not always fixed or binding as the Acetylintermedine Price is obtained through a variety of data sources. The Acetylintermedine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acetylintermedine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetylintermedine, including repackagers and relabelers. The FDA regulates Acetylintermedine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetylintermedine 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 Acetylintermedine supplier is an individual or a company that provides Acetylintermedine active pharmaceutical ingredient (API) or Acetylintermedine finished formulations upon request. The Acetylintermedine suppliers may include Acetylintermedine API manufacturers, exporters, distributors and traders.
Acetylintermedine 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 Acetylintermedine 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 Acetylintermedine GMP manufacturer or Acetylintermedine GMP API supplier for your needs.
A Acetylintermedine CoA (Certificate of Analysis) is a formal document that attests to Acetylintermedine's compliance with Acetylintermedine specifications and serves as a tool for batch-level quality control.
Acetylintermedine CoA mostly includes findings from lab analyses of a specific batch. For each Acetylintermedine 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.
Acetylintermedine may be tested according to a variety of international standards, such as European Pharmacopoeia (Acetylintermedine EP), Acetylintermedine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Acetylintermedine USP).
