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Molecular Weight | 236.23 g/mol |
---|---|
Molecular Formula | C10H12N4O3 |
XLogP3 | -1.6 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 1 |
Exact Mass | 236.09094026 g/mol |
Monoisotopic Mass | 236.09094026 g/mol |
Topological Polar Surface Area | 108 A^2 |
Heavy Atom Count | 17 |
Formal Charge | 0 |
Complexity | 478 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Carbazochrome 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 Carbazochrome manufacturer or Carbazochrome supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carbazochrome manufacturer or Carbazochrome supplier.
PharmaCompass also assists you with knowing the Carbazochrome API Price utilized in the formulation of products. Carbazochrome API Price is not always fixed or binding as the Carbazochrome Price is obtained through a variety of data sources. The Carbazochrome Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Adrenochrome monosemicarbazone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adrenochrome monosemicarbazone, including repackagers and relabelers. The FDA regulates Adrenochrome monosemicarbazone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adrenochrome monosemicarbazone 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 Adrenochrome monosemicarbazone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Adrenochrome monosemicarbazone supplier is an individual or a company that provides Adrenochrome monosemicarbazone active pharmaceutical ingredient (API) or Adrenochrome monosemicarbazone finished formulations upon request. The Adrenochrome monosemicarbazone suppliers may include Adrenochrome monosemicarbazone API manufacturers, exporters, distributors and traders.
click here to find a list of Adrenochrome monosemicarbazone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Adrenochrome monosemicarbazone Drug Master File in Japan (Adrenochrome monosemicarbazone JDMF) empowers Adrenochrome monosemicarbazone API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Adrenochrome monosemicarbazone JDMF during the approval evaluation for pharmaceutical products. At the time of Adrenochrome monosemicarbazone JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Adrenochrome monosemicarbazone suppliers with JDMF on PharmaCompass.
Adrenochrome monosemicarbazone 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 Adrenochrome monosemicarbazone 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 Adrenochrome monosemicarbazone GMP manufacturer or Adrenochrome monosemicarbazone GMP API supplier for your needs.
A Adrenochrome monosemicarbazone CoA (Certificate of Analysis) is a formal document that attests to Adrenochrome monosemicarbazone's compliance with Adrenochrome monosemicarbazone specifications and serves as a tool for batch-level quality control.
Adrenochrome monosemicarbazone CoA mostly includes findings from lab analyses of a specific batch. For each Adrenochrome monosemicarbazone 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.
Adrenochrome monosemicarbazone may be tested according to a variety of international standards, such as European Pharmacopoeia (Adrenochrome monosemicarbazone EP), Adrenochrome monosemicarbazone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Adrenochrome monosemicarbazone USP).