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1. 171370-55-1
2. 8kie206xha
3. (2s,3r,4s,5s)-2-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol;chloride
4. Delphinidin-3-o-arabinoside Chloride
5. Unii-8kie206xha
6. Delphinidin 3-alpha-l-arabinopyranoside
7. Delphinidin 3-o-alpha-l-arabinopyranoside
8. Chebi:169736
9. Dtxsid101341478
10. 1-benzopyrylium, 3-(alpha-l-arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-, Chloride (1:1)
11. Delphinidin 3-.alpha.-l-arabinopyranoside
12. Delphinidin 3-o-.alpha.-l-arabinopyranoside
13. Q27270673
14. 5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3-chromeniumyl Alpha-l-arabinopyranoside Chloride
15. 1-benzopyrylium, 3-(.alpha.-l-arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-, Chloride (1:1)
| Molecular Weight | 470.8 g/mol |
|---|---|
| Molecular Formula | C20H19ClO11 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 3 |
| Exact Mass | 470.0615891 g/mol |
| Monoisotopic Mass | 470.0615891 g/mol |
| Topological Polar Surface Area | 181 Ų |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 596 |
| 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 | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of UNII-8KIE206XHA 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 UNII-8KIE206XHA manufacturer or UNII-8KIE206XHA supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred UNII-8KIE206XHA manufacturer or UNII-8KIE206XHA supplier.
PharmaCompass also assists you with knowing the UNII-8KIE206XHA API Price utilized in the formulation of products. UNII-8KIE206XHA API Price is not always fixed or binding as the UNII-8KIE206XHA Price is obtained through a variety of data sources. The UNII-8KIE206XHA Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A UNII-8KIE206XHA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-8KIE206XHA, including repackagers and relabelers. The FDA regulates UNII-8KIE206XHA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-8KIE206XHA 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 UNII-8KIE206XHA supplier is an individual or a company that provides UNII-8KIE206XHA active pharmaceutical ingredient (API) or UNII-8KIE206XHA finished formulations upon request. The UNII-8KIE206XHA suppliers may include UNII-8KIE206XHA API manufacturers, exporters, distributors and traders.
UNII-8KIE206XHA 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 UNII-8KIE206XHA 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 UNII-8KIE206XHA GMP manufacturer or UNII-8KIE206XHA GMP API supplier for your needs.
A UNII-8KIE206XHA CoA (Certificate of Analysis) is a formal document that attests to UNII-8KIE206XHA's compliance with UNII-8KIE206XHA specifications and serves as a tool for batch-level quality control.
UNII-8KIE206XHA CoA mostly includes findings from lab analyses of a specific batch. For each UNII-8KIE206XHA 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.
UNII-8KIE206XHA may be tested according to a variety of international standards, such as European Pharmacopoeia (UNII-8KIE206XHA EP), UNII-8KIE206XHA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (UNII-8KIE206XHA USP).
