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1. 4-(n-maleimidomethyl)cyclohexane-1-carboxylic Acid 3-sulfo-n-hydroxysuccinimide Ester Sodium Salt
2. Schembl2810989
3. Akos030255406
4. 921s249
| Molecular Weight | 437.4 g/mol |
|---|---|
| Molecular Formula | C16H18N2NaO9S |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 6 |
| Exact Mass | 437.06307061 g/mol |
| Monoisotopic Mass | 437.06307061 g/mol |
| Topological Polar Surface Area | 164 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 847 |
| 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 | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of CAS 618-887-3 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 CAS 618-887-3 manufacturer or CAS 618-887-3 supplier for your needs.
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A CAS 618-887-3 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS 618-887-3, including repackagers and relabelers. The FDA regulates CAS 618-887-3 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS 618-887-3 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 CAS 618-887-3 supplier is an individual or a company that provides CAS 618-887-3 active pharmaceutical ingredient (API) or CAS 618-887-3 finished formulations upon request. The CAS 618-887-3 suppliers may include CAS 618-887-3 API manufacturers, exporters, distributors and traders.
CAS 618-887-3 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 CAS 618-887-3 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 CAS 618-887-3 GMP manufacturer or CAS 618-887-3 GMP API supplier for your needs.
A CAS 618-887-3 CoA (Certificate of Analysis) is a formal document that attests to CAS 618-887-3's compliance with CAS 618-887-3 specifications and serves as a tool for batch-level quality control.
CAS 618-887-3 CoA mostly includes findings from lab analyses of a specific batch. For each CAS 618-887-3 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.
CAS 618-887-3 may be tested according to a variety of international standards, such as European Pharmacopoeia (CAS 618-887-3 EP), CAS 618-887-3 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (CAS 618-887-3 USP).
