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1. 151p774
2. (2s,3s)-3,4-dimethyl-2-phenylmorpholine Bis(2,3-dihydroxysuccinate)
| Molecular Weight | 491.4 g/mol |
|---|---|
| Molecular Formula | C20H29NO13 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 7 |
| Exact Mass | 491.16388998 g/mol |
| Monoisotopic Mass | 491.16388998 g/mol |
| Topological Polar Surface Area | 243 Ų |
| Heavy Atom Count | 34 |
| Formal Charge | 0 |
| Complexity | 311 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 4 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
ABOUT THIS PAGE
A Phendimetrazine bitartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phendimetrazine bitartrate, including repackagers and relabelers. The FDA regulates Phendimetrazine bitartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phendimetrazine bitartrate 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 Phendimetrazine bitartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Phendimetrazine bitartrate supplier is an individual or a company that provides Phendimetrazine bitartrate active pharmaceutical ingredient (API) or Phendimetrazine bitartrate finished formulations upon request. The Phendimetrazine bitartrate suppliers may include Phendimetrazine bitartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Phendimetrazine bitartrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Phendimetrazine bitartrate 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 Phendimetrazine bitartrate 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 Phendimetrazine bitartrate GMP manufacturer or Phendimetrazine bitartrate GMP API supplier for your needs.
A Phendimetrazine bitartrate CoA (Certificate of Analysis) is a formal document that attests to Phendimetrazine bitartrate's compliance with Phendimetrazine bitartrate specifications and serves as a tool for batch-level quality control.
Phendimetrazine bitartrate CoA mostly includes findings from lab analyses of a specific batch. For each Phendimetrazine bitartrate 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.
Phendimetrazine bitartrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Phendimetrazine bitartrate EP), Phendimetrazine bitartrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Phendimetrazine bitartrate USP).
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