Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. Cyanidin-3-o-arabinoside
2. 111613-04-8
3. Cyanidin Arabinoside
4. Cyanidin 3-arabinoside Chloride
5. Cyanidin 3-monoarabinoside
6. (2s,3r,4s,5s)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxyoxane-3,4,5-triol;chloride
7. 7c8yz321e8
8. Cyanidin-3-o-arabinoside Chloride
9. Cyanidin, 3-alpha-l-arabinoside
10. Cyanidin 3-alpha-l-arabinopyranoside
11. Cyanidin 3-o-alpha-l-arabinopyranoside
12. Unii-7c8yz321e8
13. Chebi:189019
14. Glxc-13688
15. 1-benzopyrylium, 3-(alpha-l-arabinopyranosyloxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-, Chloride (1:1)
16. Cyanidin, 3-.alpha.-l-arabinoside
17. Hy-129139
18. Cs-0103762
19. Cyanidin 3-.alpha.-l-arabinopyranoside
20. E89001
21. Cyanidin 3-o-.alpha.-l-arabinopyranoside
22. Cyanidin 3-o-alpha-l-arabinoside Chloride
23. Q27268061
24. Cyanidin 3-o-alpha-l-arabinoside Chloride, Analytical Standard
25. 1-benzopyrylium, 3-(.alpha.-l-arabinopyranosyloxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-, Chloride (1:1)
| Molecular Weight | 454.8 g/mol |
|---|---|
| Molecular Formula | C20H19ClO10 |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 3 |
| Exact Mass | 454.0666745 g/mol |
| Monoisotopic Mass | 454.0666745 g/mol |
| Topological Polar Surface Area | 161 Ų |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 578 |
| 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 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
15
PharmaCompass offers a list of UNII-7C8YZ321E8 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-7C8YZ321E8 manufacturer or UNII-7C8YZ321E8 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred UNII-7C8YZ321E8 manufacturer or UNII-7C8YZ321E8 supplier.
PharmaCompass also assists you with knowing the UNII-7C8YZ321E8 API Price utilized in the formulation of products. UNII-7C8YZ321E8 API Price is not always fixed or binding as the UNII-7C8YZ321E8 Price is obtained through a variety of data sources. The UNII-7C8YZ321E8 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A UNII-7C8YZ321E8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-7C8YZ321E8, including repackagers and relabelers. The FDA regulates UNII-7C8YZ321E8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-7C8YZ321E8 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-7C8YZ321E8 supplier is an individual or a company that provides UNII-7C8YZ321E8 active pharmaceutical ingredient (API) or UNII-7C8YZ321E8 finished formulations upon request. The UNII-7C8YZ321E8 suppliers may include UNII-7C8YZ321E8 API manufacturers, exporters, distributors and traders.
UNII-7C8YZ321E8 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-7C8YZ321E8 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-7C8YZ321E8 GMP manufacturer or UNII-7C8YZ321E8 GMP API supplier for your needs.
A UNII-7C8YZ321E8 CoA (Certificate of Analysis) is a formal document that attests to UNII-7C8YZ321E8's compliance with UNII-7C8YZ321E8 specifications and serves as a tool for batch-level quality control.
UNII-7C8YZ321E8 CoA mostly includes findings from lab analyses of a specific batch. For each UNII-7C8YZ321E8 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-7C8YZ321E8 may be tested according to a variety of international standards, such as European Pharmacopoeia (UNII-7C8YZ321E8 EP), UNII-7C8YZ321E8 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (UNII-7C8YZ321E8 USP).
