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1. Dl-theanine
2. 34271-54-0
3. N-ethylglutamine
4. Mfcd08460601
5. L-glutamic Acid Gamma-ethyl Amide;ngamma-ethyl-l-glutamine
6. Mfcd00059653
7. L-theanin
8. Nsc21308
9. L-theanine (synthetic)
10. 2-amino-5-(ethylamino)-5-oxopentanoicacid
11. Schembl290430
12. (2s)-2-azaniumyl-5-(ethylamino)-5-oxopentanoate
13. Chembl4303298
14. Dtxsid20863098
15. Dl-theanine (h-dl-gln(et)-oh)
16. Ac9268
17. Akos006230087
18. Am82647
19. Ncgc00095702-01
20. Ac-23977
21. Ls-13325
22. Sy006013
23. Sy250932
24. Db-047911
25. Ft-0628022
26. Ft-0656318
27. Ft-0695774
28. 271t540
29. A822145
Molecular Weight | 174.20 g/mol |
---|---|
Molecular Formula | C7H14N2O3 |
XLogP3 | -3.6 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 5 |
Exact Mass | 174.10044231 g/mol |
Monoisotopic Mass | 174.10044231 g/mol |
Topological Polar Surface Area | 92.4 Ų |
Heavy Atom Count | 12 |
Formal Charge | 0 |
Complexity | 170 |
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 Dl-Theanine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dl-Theanine, including repackagers and relabelers. The FDA regulates Dl-Theanine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dl-Theanine 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 Dl-Theanine supplier is an individual or a company that provides Dl-Theanine active pharmaceutical ingredient (API) or Dl-Theanine finished formulations upon request. The Dl-Theanine suppliers may include Dl-Theanine API manufacturers, exporters, distributors and traders.
Dl-Theanine 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 Dl-Theanine 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 Dl-Theanine GMP manufacturer or Dl-Theanine GMP API supplier for your needs.
A Dl-Theanine CoA (Certificate of Analysis) is a formal document that attests to Dl-Theanine's compliance with Dl-Theanine specifications and serves as a tool for batch-level quality control.
Dl-Theanine CoA mostly includes findings from lab analyses of a specific batch. For each Dl-Theanine 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.
Dl-Theanine may be tested according to a variety of international standards, such as European Pharmacopoeia (Dl-Theanine EP), Dl-Theanine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dl-Theanine USP).
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