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Molecular Weight | 305.4 g/mol |
---|---|
Molecular Formula | C11H15NO5S2 |
XLogP3 | 0.8 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 2 |
Exact Mass | 305.03916493 g/mol |
Monoisotopic Mass | 305.03916493 g/mol |
Topological Polar Surface Area | 103 Ų |
Heavy Atom Count | 19 |
Formal Charge | 0 |
Complexity | 676 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 1 |
Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone, including repackagers and relabelers. The FDA regulates 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone 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 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone supplier is an individual or a company that provides 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone active pharmaceutical ingredient (API) or 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone finished formulations upon request. The 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone suppliers may include 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone API manufacturers, exporters, distributors and traders.
2,4-disulfonyl alpha-phenyl tertiary butyl nitrone 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 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone 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 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone GMP manufacturer or 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone GMP API supplier for your needs.
A 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone CoA (Certificate of Analysis) is a formal document that attests to 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone's compliance with 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone specifications and serves as a tool for batch-level quality control.
2,4-disulfonyl alpha-phenyl tertiary butyl nitrone CoA mostly includes findings from lab analyses of a specific batch. For each 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone 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.
2,4-disulfonyl alpha-phenyl tertiary butyl nitrone may be tested according to a variety of international standards, such as European Pharmacopoeia (2,4-disulfonyl alpha-phenyl tertiary butyl nitrone EP), 2,4-disulfonyl alpha-phenyl tertiary butyl nitrone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2,4-disulfonyl alpha-phenyl tertiary butyl nitrone USP).
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