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1. N-maleimide
2. 1-(2-methylnaphthyl)-1h-pyrrole-2,5-dione
3. 70017-56-0
4. N-(2-methyl-naphth-1-yl)maleimide
5. 1h-pyrrole-2,5-dione, 1-(2-methyl-1-naphthalenyl)-
6. 24y91vgr7n
7. Caswell No. 902aa
8. Atv 129
9. Einecs 274-255-3
10. Epa Pesticide Chemical Code 113701
11. Unii-24y91vgr7n
12. Schembl397529
13. N-(2-methylnaphthyl)maleinimide
14. Dtxsid4042179
15. Atv-129
16. Ft-0701152
17. Q27253885
| Molecular Weight | 237.25 g/mol |
|---|---|
| Molecular Formula | C15H11NO2 |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 237.078978594 g/mol |
| Monoisotopic Mass | 237.078978594 g/mol |
| Topological Polar Surface Area | 37.4 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 383 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A N-Maleimide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N-Maleimide, including repackagers and relabelers. The FDA regulates N-Maleimide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N-Maleimide 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 N-Maleimide supplier is an individual or a company that provides N-Maleimide active pharmaceutical ingredient (API) or N-Maleimide finished formulations upon request. The N-Maleimide suppliers may include N-Maleimide API manufacturers, exporters, distributors and traders.
click here to find a list of N-Maleimide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A N-Maleimide DMF (Drug Master File) is a document detailing the whole manufacturing process of N-Maleimide active pharmaceutical ingredient (API) in detail. Different forms of N-Maleimide DMFs exist exist since differing nations have different regulations, such as N-Maleimide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A N-Maleimide DMF submitted to regulatory agencies in the US is known as a USDMF. N-Maleimide USDMF includes data on N-Maleimide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The N-Maleimide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of N-Maleimide suppliers with USDMF on PharmaCompass.
N-Maleimide 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 N-Maleimide 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 N-Maleimide GMP manufacturer or N-Maleimide GMP API supplier for your needs.
A N-Maleimide CoA (Certificate of Analysis) is a formal document that attests to N-Maleimide's compliance with N-Maleimide specifications and serves as a tool for batch-level quality control.
N-Maleimide CoA mostly includes findings from lab analyses of a specific batch. For each N-Maleimide 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.
N-Maleimide may be tested according to a variety of international standards, such as European Pharmacopoeia (N-Maleimide EP), N-Maleimide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (N-Maleimide USP).
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