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1. 6-ethyl-24-norcholane-3,7,23-triol-23 Sulfate
2. 6alpha-ethyl-24-nor-5beta-cholane-3alpha,7alpha,23-triol-23 Sulfate Sodium Salt
3. 6alpha-ethyl-3alpha,7alpha,23-trihydroxy-24-nor-5beta-cholan-23-sulfate Sodium Salt
4. Int-767
1. Int-767
2. 1000403-03-1
3. Sodium;[(3r)-3-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]butyl] Sulfate
4. Cs-5007
5. Hy-12434
6. Sulfuric Acid Sodium 3alpha,7alpha-dihydroxy-6alpha-ethyl-24-nor-5beta-cholane-23-yl Ester Salt
| Molecular Weight | 494.7 g/mol |
|---|---|
| Molecular Formula | C25H43NaO6S |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 6 |
| Exact Mass | 494.26780454 g/mol |
| Monoisotopic Mass | 494.26780454 g/mol |
| Topological Polar Surface Area | 115 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 786 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 11 |
| 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 INT 767 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 INT 767 manufacturer or INT 767 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred INT 767 manufacturer or INT 767 supplier.
PharmaCompass also assists you with knowing the INT 767 API Price utilized in the formulation of products. INT 767 API Price is not always fixed or binding as the INT 767 Price is obtained through a variety of data sources. The INT 767 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A INT 767 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INT 767, including repackagers and relabelers. The FDA regulates INT 767 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INT 767 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 INT 767 supplier is an individual or a company that provides INT 767 active pharmaceutical ingredient (API) or INT 767 finished formulations upon request. The INT 767 suppliers may include INT 767 API manufacturers, exporters, distributors and traders.
INT 767 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 INT 767 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 INT 767 GMP manufacturer or INT 767 GMP API supplier for your needs.
A INT 767 CoA (Certificate of Analysis) is a formal document that attests to INT 767's compliance with INT 767 specifications and serves as a tool for batch-level quality control.
INT 767 CoA mostly includes findings from lab analyses of a specific batch. For each INT 767 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.
INT 767 may be tested according to a variety of international standards, such as European Pharmacopoeia (INT 767 EP), INT 767 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (INT 767 USP).
