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1. Ag 66.18
2. Duroliopaque
3. Ethyl Iodostearate
1. 6k4rsm9b6p
2. Octadecanoic Acid, 10-iodo-, Ethyl Ester
3. 18672-39-4
4. Ethyl Iodostearate
5. Unii-6k4rsm9b6p
6. Unii-10l756ed3y
7. 10l756ed3y
8. Dtxsid101043189
9. Ethyl 9(or 10)-iodooctadecanoate
10. Einecs 249-728-2
11. 9(or 10)-iodooctadecanoic Acid, Ethyl Ester
12. Q27265032
13. 29611-66-3
| Molecular Weight | 438.4 g/mol |
|---|---|
| Molecular Formula | C20H39IO2 |
| XLogP3 | 9.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 18 |
| Exact Mass | 438.19948 g/mol |
| Monoisotopic Mass | 438.19948 g/mol |
| Topological Polar Surface Area | 26.3 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 256 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| 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 Ethyl 10-iodostearate 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 Ethyl 10-iodostearate manufacturer or Ethyl 10-iodostearate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethyl 10-iodostearate manufacturer or Ethyl 10-iodostearate supplier.
PharmaCompass also assists you with knowing the Ethyl 10-iodostearate API Price utilized in the formulation of products. Ethyl 10-iodostearate API Price is not always fixed or binding as the Ethyl 10-iodostearate Price is obtained through a variety of data sources. The Ethyl 10-iodostearate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ethyl 10-iodostearate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethyl 10-iodostearate, including repackagers and relabelers. The FDA regulates Ethyl 10-iodostearate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethyl 10-iodostearate 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 Ethyl 10-iodostearate supplier is an individual or a company that provides Ethyl 10-iodostearate active pharmaceutical ingredient (API) or Ethyl 10-iodostearate finished formulations upon request. The Ethyl 10-iodostearate suppliers may include Ethyl 10-iodostearate API manufacturers, exporters, distributors and traders.
Ethyl 10-iodostearate 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 Ethyl 10-iodostearate 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 Ethyl 10-iodostearate GMP manufacturer or Ethyl 10-iodostearate GMP API supplier for your needs.
A Ethyl 10-iodostearate CoA (Certificate of Analysis) is a formal document that attests to Ethyl 10-iodostearate's compliance with Ethyl 10-iodostearate specifications and serves as a tool for batch-level quality control.
Ethyl 10-iodostearate CoA mostly includes findings from lab analyses of a specific batch. For each Ethyl 10-iodostearate 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.
Ethyl 10-iodostearate may be tested according to a variety of international standards, such as European Pharmacopoeia (Ethyl 10-iodostearate EP), Ethyl 10-iodostearate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ethyl 10-iodostearate USP).
