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1. Akos005898435
2. K40128a63i
3. N-(phenyloxycarbonyl)-dl-valine Methyl Ester
4. 2-[(phenoxycarbonyl)amino]-3-methylbutyric Acid Methyl Ester
Molecular Weight | 251.28 g/mol |
---|---|
Molecular Formula | C13H17NO4 |
XLogP3 | 2.8 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 6 |
Exact Mass | 251.11575802 g/mol |
Monoisotopic Mass | 251.11575802 g/mol |
Topological Polar Surface Area | 64.6 Ų |
Heavy Atom Count | 18 |
Formal Charge | 0 |
Complexity | 285 |
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 | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Methyl N-Phenoxycarbonyl-L-Valinate 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 Methyl N-Phenoxycarbonyl-L-Valinate manufacturer or Methyl N-Phenoxycarbonyl-L-Valinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methyl N-Phenoxycarbonyl-L-Valinate manufacturer or Methyl N-Phenoxycarbonyl-L-Valinate supplier.
PharmaCompass also assists you with knowing the Methyl N-Phenoxycarbonyl-L-Valinate API Price utilized in the formulation of products. Methyl N-Phenoxycarbonyl-L-Valinate API Price is not always fixed or binding as the Methyl N-Phenoxycarbonyl-L-Valinate Price is obtained through a variety of data sources. The Methyl N-Phenoxycarbonyl-L-Valinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Methyl N-Phenoxycarbonyl-L-Valinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyl N-Phenoxycarbonyl-L-Valinate, including repackagers and relabelers. The FDA regulates Methyl N-Phenoxycarbonyl-L-Valinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyl N-Phenoxycarbonyl-L-Valinate 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 Methyl N-Phenoxycarbonyl-L-Valinate supplier is an individual or a company that provides Methyl N-Phenoxycarbonyl-L-Valinate active pharmaceutical ingredient (API) or Methyl N-Phenoxycarbonyl-L-Valinate finished formulations upon request. The Methyl N-Phenoxycarbonyl-L-Valinate suppliers may include Methyl N-Phenoxycarbonyl-L-Valinate API manufacturers, exporters, distributors and traders.
click here to find a list of Methyl N-Phenoxycarbonyl-L-Valinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Methyl N-Phenoxycarbonyl-L-Valinate DMF (Drug Master File) is a document detailing the whole manufacturing process of Methyl N-Phenoxycarbonyl-L-Valinate active pharmaceutical ingredient (API) in detail. Different forms of Methyl N-Phenoxycarbonyl-L-Valinate DMFs exist exist since differing nations have different regulations, such as Methyl N-Phenoxycarbonyl-L-Valinate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Methyl N-Phenoxycarbonyl-L-Valinate DMF submitted to regulatory agencies in the US is known as a USDMF. Methyl N-Phenoxycarbonyl-L-Valinate USDMF includes data on Methyl N-Phenoxycarbonyl-L-Valinate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Methyl N-Phenoxycarbonyl-L-Valinate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Methyl N-Phenoxycarbonyl-L-Valinate suppliers with USDMF on PharmaCompass.
Methyl N-Phenoxycarbonyl-L-Valinate 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 Methyl N-Phenoxycarbonyl-L-Valinate 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 Methyl N-Phenoxycarbonyl-L-Valinate GMP manufacturer or Methyl N-Phenoxycarbonyl-L-Valinate GMP API supplier for your needs.
A Methyl N-Phenoxycarbonyl-L-Valinate CoA (Certificate of Analysis) is a formal document that attests to Methyl N-Phenoxycarbonyl-L-Valinate's compliance with Methyl N-Phenoxycarbonyl-L-Valinate specifications and serves as a tool for batch-level quality control.
Methyl N-Phenoxycarbonyl-L-Valinate CoA mostly includes findings from lab analyses of a specific batch. For each Methyl N-Phenoxycarbonyl-L-Valinate 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.
Methyl N-Phenoxycarbonyl-L-Valinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Methyl N-Phenoxycarbonyl-L-Valinate EP), Methyl N-Phenoxycarbonyl-L-Valinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Methyl N-Phenoxycarbonyl-L-Valinate USP).