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1. Y4f5odm66l
2. Magnesium Aspartate Dihydrate, (+)-
3. Magnesium Aspartate Dihydrate [who-dd]
4. L-aspartic Acid, Magnesium Salt (2:1), Dihydrate
5. L-aspartic Acid, Magnesium Salt, Hydrate (2:1:2)
6. Magnesium L-aspartate Dihydrate
7. 215533-00-9
8. Unii-y4f5odm66l
9. Magnesium Aspartate Dihydrate [ep Monograph]
| Molecular Weight | 324.53 g/mol |
|---|---|
| Molecular Formula | C8H16MgN2O10 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 2 |
| Exact Mass | 324.0655364 g/mol |
| Monoisotopic Mass | 324.0655364 g/mol |
| Topological Polar Surface Area | 215 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 122 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 7 |
ABOUT THIS PAGE
A Magnesium Aspartate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magnesium Aspartate Dihydrate, including repackagers and relabelers. The FDA regulates Magnesium Aspartate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magnesium Aspartate Dihydrate 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 Magnesium Aspartate Dihydrate supplier is an individual or a company that provides Magnesium Aspartate Dihydrate active pharmaceutical ingredient (API) or Magnesium Aspartate Dihydrate finished formulations upon request. The Magnesium Aspartate Dihydrate suppliers may include Magnesium Aspartate Dihydrate API manufacturers, exporters, distributors and traders.
Magnesium Aspartate Dihydrate 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 Magnesium Aspartate Dihydrate 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 Magnesium Aspartate Dihydrate GMP manufacturer or Magnesium Aspartate Dihydrate GMP API supplier for your needs.
A Magnesium Aspartate Dihydrate CoA (Certificate of Analysis) is a formal document that attests to Magnesium Aspartate Dihydrate's compliance with Magnesium Aspartate Dihydrate specifications and serves as a tool for batch-level quality control.
Magnesium Aspartate Dihydrate CoA mostly includes findings from lab analyses of a specific batch. For each Magnesium Aspartate Dihydrate 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.
Magnesium Aspartate Dihydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Magnesium Aspartate Dihydrate EP), Magnesium Aspartate Dihydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Magnesium Aspartate Dihydrate USP).
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