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1. Polyoxypropylene 15 Stearyl Ether
2. Polypropylene Glycol Stearyl Ether 15
3. Ppg-15
1. 25231-21-4
2. Polyoxypropylene 15 Stearyl Ether
3. Ppg-15 Stearyl Ether
4. Polypropylene Glycol Monostearyl Ether
5. Schembl1091934
6. Dtxsid60865197
7. 1-(octadecyloxy)propan-2-ol
Molecular Weight | 328.6 g/mol |
---|---|
Molecular Formula | C21H44O2 |
XLogP3 | 8.7 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 19 |
Exact Mass | 328.334130642 g/mol |
Monoisotopic Mass | 328.334130642 g/mol |
Topological Polar Surface Area | 29.5 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 206 |
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 1-Octadecoxypropan-2-Ol 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 1-Octadecoxypropan-2-Ol manufacturer or 1-Octadecoxypropan-2-Ol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 1-Octadecoxypropan-2-Ol manufacturer or 1-Octadecoxypropan-2-Ol supplier.
PharmaCompass also assists you with knowing the 1-Octadecoxypropan-2-Ol API Price utilized in the formulation of products. 1-Octadecoxypropan-2-Ol API Price is not always fixed or binding as the 1-Octadecoxypropan-2-Ol Price is obtained through a variety of data sources. The 1-Octadecoxypropan-2-Ol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A polyoxypropylene 15 stearyl ether manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of polyoxypropylene 15 stearyl ether, including repackagers and relabelers. The FDA regulates polyoxypropylene 15 stearyl ether manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. polyoxypropylene 15 stearyl ether 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 polyoxypropylene 15 stearyl ether supplier is an individual or a company that provides polyoxypropylene 15 stearyl ether active pharmaceutical ingredient (API) or polyoxypropylene 15 stearyl ether finished formulations upon request. The polyoxypropylene 15 stearyl ether suppliers may include polyoxypropylene 15 stearyl ether API manufacturers, exporters, distributors and traders.
polyoxypropylene 15 stearyl ether 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 polyoxypropylene 15 stearyl ether 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 polyoxypropylene 15 stearyl ether GMP manufacturer or polyoxypropylene 15 stearyl ether GMP API supplier for your needs.
A polyoxypropylene 15 stearyl ether CoA (Certificate of Analysis) is a formal document that attests to polyoxypropylene 15 stearyl ether's compliance with polyoxypropylene 15 stearyl ether specifications and serves as a tool for batch-level quality control.
polyoxypropylene 15 stearyl ether CoA mostly includes findings from lab analyses of a specific batch. For each polyoxypropylene 15 stearyl ether 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.
polyoxypropylene 15 stearyl ether may be tested according to a variety of international standards, such as European Pharmacopoeia (polyoxypropylene 15 stearyl ether EP), polyoxypropylene 15 stearyl ether JP (Japanese Pharmacopeia) and the US Pharmacopoeia (polyoxypropylene 15 stearyl ether USP).