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1. Ott166
2. Ott-166
3. Sf-0166
4. 1-hydroxy-2-methylpropan-2-aminium (s)-3-(6-(difluoromethoxy)pyridin-3-yl)-3-(oxo-2-3-(3-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)propyl)imidazolidin-1-yl)propanoate
| Molecular Weight | 564.6 g/mol |
|---|---|
| Molecular Formula | C27H38F2N6O5 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 11 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 154 |
| Heavy Atom Count | 40 |
| Formal Charge | 0 |
| Complexity | 745 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of OTT166 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 OTT166 manufacturer or OTT166 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred OTT166 manufacturer or OTT166 supplier.
PharmaCompass also assists you with knowing the OTT166 API Price utilized in the formulation of products. OTT166 API Price is not always fixed or binding as the OTT166 Price is obtained through a variety of data sources. The OTT166 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A OTT166 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of OTT166, including repackagers and relabelers. The FDA regulates OTT166 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. OTT166 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 OTT166 supplier is an individual or a company that provides OTT166 active pharmaceutical ingredient (API) or OTT166 finished formulations upon request. The OTT166 suppliers may include OTT166 API manufacturers, exporters, distributors and traders.
OTT166 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 OTT166 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 OTT166 GMP manufacturer or OTT166 GMP API supplier for your needs.
A OTT166 CoA (Certificate of Analysis) is a formal document that attests to OTT166's compliance with OTT166 specifications and serves as a tool for batch-level quality control.
OTT166 CoA mostly includes findings from lab analyses of a specific batch. For each OTT166 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.
OTT166 may be tested according to a variety of international standards, such as European Pharmacopoeia (OTT166 EP), OTT166 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (OTT166 USP).
