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1. Retinol Propanoate
1. 7069-42-3
2. Retinol Propionate
3. Retinol, Propanoate
4. Vitamin A Propionate
5. [(2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenyl] Propanoate
6. 32jk994wmc
7. Ec 230-363-2
8. Unii-32jk994wmc
9. Propionic Acid, Retinol Ester
10. (2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-yl Propionate
11. Einecs 230-363-2
12. Retinol, 15-propanoate
13. Retinyl Propionate [inci]
14. Dtxsid701019851
15. Microvit A Dlc [veterinary] (tn)
16. Retinol Propionate [who-dd]
17. Zinc16609980
18. Akos024386409
19. Retinol, Propionate, All-trans-
20. Ac-34856
21. Ls-15018
22. Vitamin A Propionate 2.5 Mio Iu/g
23. All-(e)-retinol Propionate [who-ip]
24. D08477
25. Retinyl Propionate (stabilized With Bht) 90%
26. W-110194
27. Q27256177
28. Retinyl Propionate (stabilized With Bht) 90per Cent
29. Retinyl Propionate, >=98.0% (sum Of Isomers, Hplc), ~2500 U/mg
30. Retinyl Propionate, Pharmaceutical Secondary Standard; Certified Reference Material
31. (2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ylpropionate
32. (2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetraenyl Propionate
| Molecular Weight | 342.5 g/mol |
|---|---|
| Molecular Formula | C23H34O2 |
| XLogP3 | 6.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 8 |
| Exact Mass | 342.255880323 g/mol |
| Monoisotopic Mass | 342.255880323 g/mol |
| Topological Polar Surface Area | 26.3 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 610 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 4 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Vitamin A Propionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vitamin A Propionate, including repackagers and relabelers. The FDA regulates Vitamin A Propionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vitamin A Propionate 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 Vitamin A Propionate supplier is an individual or a company that provides Vitamin A Propionate active pharmaceutical ingredient (API) or Vitamin A Propionate finished formulations upon request. The Vitamin A Propionate suppliers may include Vitamin A Propionate API manufacturers, exporters, distributors and traders.
Vitamin A Propionate 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 Vitamin A Propionate 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 Vitamin A Propionate GMP manufacturer or Vitamin A Propionate GMP API supplier for your needs.
A Vitamin A Propionate CoA (Certificate of Analysis) is a formal document that attests to Vitamin A Propionate's compliance with Vitamin A Propionate specifications and serves as a tool for batch-level quality control.
Vitamin A Propionate CoA mostly includes findings from lab analyses of a specific batch. For each Vitamin A Propionate 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.
Vitamin A Propionate may be tested according to a variety of international standards, such as European Pharmacopoeia (Vitamin A Propionate EP), Vitamin A Propionate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vitamin A Propionate USP).
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