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1. 3,5,7,4'-tetrahydroxy-3',5'-dimethoxyflavylium
2. Malvidin Chloride
1. 10463-84-0
2. Chebi:6674
3. 3',5'-dimethoxy-3,4',5,7-tetrahydroxyflavylium Acid Anion
4. Brn 1691742
5. .malvidin
6. Benzopyrylium, 3 5,7-trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-, Acid Anion
7. Schembl21739
8. Chembl255753
9. Dtxsid30146622
10. 2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3,5,7-triol
11. Flavylium, 3,4',5,7-tetrahydroxy-3',5'-dimethoxy-, Acid Anion
12. Bdbm50347138
13. Benzopyrylium, 3 5,7-trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-
14. Lmpk12010004
15. C08716
16. 3,4',5,7-tetrahydroxy-3',5'-dimethoxyflavylium
17. Q137220
18. 3 4' 5 7-tetrahydroxy-3' 5'-dimethoxyflavylium Chloride
| Molecular Weight | 331.30 g/mol |
|---|---|
| Molecular Formula | C17H15O7+ |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 3 |
| Exact Mass | 331.08177781 g/mol |
| Monoisotopic Mass | 331.08177781 g/mol |
| Topological Polar Surface Area | 100 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 1 |
| Complexity | 406 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| 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 Malvidin 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 Malvidin manufacturer or Malvidin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Malvidin manufacturer or Malvidin supplier.
PharmaCompass also assists you with knowing the Malvidin API Price utilized in the formulation of products. Malvidin API Price is not always fixed or binding as the Malvidin Price is obtained through a variety of data sources. The Malvidin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Malvidin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Malvidin, including repackagers and relabelers. The FDA regulates Malvidin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Malvidin 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 Malvidin supplier is an individual or a company that provides Malvidin active pharmaceutical ingredient (API) or Malvidin finished formulations upon request. The Malvidin suppliers may include Malvidin API manufacturers, exporters, distributors and traders.
Malvidin 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 Malvidin 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 Malvidin GMP manufacturer or Malvidin GMP API supplier for your needs.
A Malvidin CoA (Certificate of Analysis) is a formal document that attests to Malvidin's compliance with Malvidin specifications and serves as a tool for batch-level quality control.
Malvidin CoA mostly includes findings from lab analyses of a specific batch. For each Malvidin 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.
Malvidin may be tested according to a variety of international standards, such as European Pharmacopoeia (Malvidin EP), Malvidin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Malvidin USP).
