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1. Sorbitan Monohexadecanoate
2. Sorbitan Monopalmitate
3. Sorbitan Palmitate
4. Span 40
1. Sorbitan Monopalmitate
2. Sorbitan Palmitate
3. 26266-57-9
4. Sorbitan Palmitate (span 40)
5. Sr-01000883951
6. Sr-01000883951-1
| Molecular Weight | 402.6 g/mol |
|---|---|
| Molecular Formula | C22H42O6 |
| XLogP3 | 5.8 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 18 |
| Exact Mass | 402.29813906 g/mol |
| Monoisotopic Mass | 402.29813906 g/mol |
| Topological Polar Surface Area | 96.2 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 389 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Sorbitan Monopalmitate 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 Sorbitan Monopalmitate manufacturer or Sorbitan Monopalmitate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sorbitan Monopalmitate manufacturer or Sorbitan Monopalmitate supplier.
PharmaCompass also assists you with knowing the Sorbitan Monopalmitate API Price utilized in the formulation of products. Sorbitan Monopalmitate API Price is not always fixed or binding as the Sorbitan Monopalmitate Price is obtained through a variety of data sources. The Sorbitan Monopalmitate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A sorbitan palmitate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of sorbitan palmitate, including repackagers and relabelers. The FDA regulates sorbitan palmitate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. sorbitan palmitate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of sorbitan palmitate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A sorbitan palmitate supplier is an individual or a company that provides sorbitan palmitate active pharmaceutical ingredient (API) or sorbitan palmitate finished formulations upon request. The sorbitan palmitate suppliers may include sorbitan palmitate API manufacturers, exporters, distributors and traders.
click here to find a list of sorbitan palmitate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
sorbitan palmitate 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 sorbitan palmitate 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 sorbitan palmitate GMP manufacturer or sorbitan palmitate GMP API supplier for your needs.
A sorbitan palmitate CoA (Certificate of Analysis) is a formal document that attests to sorbitan palmitate's compliance with sorbitan palmitate specifications and serves as a tool for batch-level quality control.
sorbitan palmitate CoA mostly includes findings from lab analyses of a specific batch. For each sorbitan palmitate 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.
sorbitan palmitate may be tested according to a variety of international standards, such as European Pharmacopoeia (sorbitan palmitate EP), sorbitan palmitate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (sorbitan palmitate USP).
