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1. Glycerophosphoethanolamine
2. Glycerylphosphorylethanolamine
3. Sn-glycerol-3-phosphoethanolamine
1. 1190-00-7
2. 2-aminoethyl (2,3-dihydroxypropyl) Hydrogen Phosphate
3. Sn-glycerol-3-phosphoethanolamine
4. 2-aminoethyl 2,3-dihydroxypropyl Hydrogen Phosphate
5. Glycerophosphoethanolamine
6. Glycerylphosphoethanolamine
7. Glycerophosphoryethanolamine
8. Glycerol 3-phosphoethanolamine
9. Glyceryl-3-phosphorylethanolamine
10. 240i539pwq
11. (2-aminoethoxy)(2,3-dihydroxypropoxy)phosphinic Acid
12. Phosphoric Acid, Mono(2-aminoethyl) Mono(2,3-dihydroxypropyl) Ester
13. Glycerophosphatidylethanolamine
14. Unii-240i539pwq
15. Gpea
16. A-glycerophosphorylethanolamine
17. Schembl692470
18. Chebi:52330
19. Glycerol 3-phosphorylethanolamine
20. Dtxsid20862586
21. Alpha-glycerophosphorylethanolamine
22. (+/-)-alpha-glycerophosphorylethanolamine
23. Glycerophosphoethanolamine [who-dd]
24. .alpha.-glycerophosphorylethanolamine
25. 2-aminoethyl Ester 1-glycerophosphoric Acid
26. Ft-0688264
27. Ft-0699527
28. 2-aminoethyl(2,3-dihydroxypropyl)hydrogenphosphate
29. A936512
30. .alpha.-glycerophosphorylethanolamine, (rs)-
31. .alpha.-glycerophosphorylethanolamine, (+/-)-
32. 2-aminoethyl (2,3-dihydroxypropyl)hydrogen Phosphate
33. L-a-glycerophosphorylethanolamine*from E Coli
34. Q27123382
| Molecular Weight | 215.14 g/mol |
|---|---|
| Molecular Formula | C5H14NO6P |
| XLogP3 | -5.5 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 7 |
| Exact Mass | 215.05587416 g/mol |
| Monoisotopic Mass | 215.05587416 g/mol |
| Topological Polar Surface Area | 122 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 176 |
| 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
A Glycerophosphorylethanolamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glycerophosphorylethanolamine, including repackagers and relabelers. The FDA regulates Glycerophosphorylethanolamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glycerophosphorylethanolamine 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 Glycerophosphorylethanolamine supplier is an individual or a company that provides Glycerophosphorylethanolamine active pharmaceutical ingredient (API) or Glycerophosphorylethanolamine finished formulations upon request. The Glycerophosphorylethanolamine suppliers may include Glycerophosphorylethanolamine API manufacturers, exporters, distributors and traders.
Glycerophosphorylethanolamine 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 Glycerophosphorylethanolamine 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 Glycerophosphorylethanolamine GMP manufacturer or Glycerophosphorylethanolamine GMP API supplier for your needs.
A Glycerophosphorylethanolamine CoA (Certificate of Analysis) is a formal document that attests to Glycerophosphorylethanolamine's compliance with Glycerophosphorylethanolamine specifications and serves as a tool for batch-level quality control.
Glycerophosphorylethanolamine CoA mostly includes findings from lab analyses of a specific batch. For each Glycerophosphorylethanolamine 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.
Glycerophosphorylethanolamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Glycerophosphorylethanolamine EP), Glycerophosphorylethanolamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Glycerophosphorylethanolamine USP).
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