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1. P-((dimethylcarbamoylmethyl)amino)benzoic Acid Ethyl Ester
2. 92033-58-4
3. Gb-401
4. P-[(dimethylcarbamoylmethyl)amino]benzoic Acid Ethyl Ester
5. Dtxsid10238837
| Molecular Weight | 250.29 g/mol |
|---|---|
| Molecular Formula | C13H18N2O3 |
| XLogP3 | 1.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 6 |
| Exact Mass | 250.13174244 g/mol |
| Monoisotopic Mass | 250.13174244 g/mol |
| Topological Polar Surface Area | 58.6 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 284 |
| 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
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PharmaCompass offers a list of GB-401 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 GB-401 manufacturer or GB-401 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred GB-401 manufacturer or GB-401 supplier.
PharmaCompass also assists you with knowing the GB-401 API Price utilized in the formulation of products. GB-401 API Price is not always fixed or binding as the GB-401 Price is obtained through a variety of data sources. The GB-401 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A GB-401 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GB-401, including repackagers and relabelers. The FDA regulates GB-401 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GB-401 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 GB-401 supplier is an individual or a company that provides GB-401 active pharmaceutical ingredient (API) or GB-401 finished formulations upon request. The GB-401 suppliers may include GB-401 API manufacturers, exporters, distributors and traders.
GB-401 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 GB-401 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 GB-401 GMP manufacturer or GB-401 GMP API supplier for your needs.
A GB-401 CoA (Certificate of Analysis) is a formal document that attests to GB-401's compliance with GB-401 specifications and serves as a tool for batch-level quality control.
GB-401 CoA mostly includes findings from lab analyses of a specific batch. For each GB-401 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.
GB-401 may be tested according to a variety of international standards, such as European Pharmacopoeia (GB-401 EP), GB-401 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (GB-401 USP).
