Synopsis
Synopsis
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USDMF
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JDMF
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KDMF
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NDC API
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VMF
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API
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FDF
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
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1. 556-02-5
2. H-d-tyr-oh
3. D-tyr
4. (r)-2-amino-3-(4-hydroxyphenyl)propanoic Acid
5. (2r)-2-amino-3-(4-hydroxyphenyl)propanoic Acid
6. 3-(4-hydroxyphenyl)-d-alanine
7. D-tyrosin
8. Chebi:28479
9. (r)-tyrosine
10. Wq5g9jq7gc
11. Chembl1076637
12. (r)-3-(p-hydroxyphenyl)alanine
13. Mfcd00063073
14. (r)-2-amino-3-(p-hydroxyphenyl)propionic Acid
15. Dty
16. D-(+)-tyrosine
17. D-p-tyrosine
18. Dtyr
19. Tyrosine, D-
20. (d)-tyrosine
21. Einecs 209-112-6
22. Unii-wq5g9jq7gc
23. Schembl20787
24. Zinc2234
25. D-4-hydroxyphenylalanine
26. Dtxsid50883441
27. Act04817
28. Cs-d1377
29. Hy-y0444
30. D-tyrosine, Reagentplus(r), 99%
31. Bdbm50463198
32. Akos015854094
33. Ac-8668
34. Am82303
35. Db03839
36. Ncgc00142608-01
37. Ncgc00142608-02
38. As-11715
39. D-tyrosine, Puriss., >=99.0% (nt)
40. D-tyrosine, Vetec(tm) Reagent Grade, 99%
41. T1141
42. C06420
43. M02937
44. T-9000
45. 556t025
46. A830718
47. J-300275
48. Q16082044
49. Q27115118
50. Z1762997038
51. (2r)-2-amino-3-(4-hydroxyphenyl)propanoic Acid;d-tyrosine
52. 1168ffd2-192c-4db4-9161-4bf71a6c98c9
53. (r)-2-amino-3-(4-hydroxyphenyl)propionic Acid, 3-(4-hydroxyphenyl)-d-alanine
| Molecular Weight | 181.19 g/mol |
|---|---|
| Molecular Formula | C9H11NO3 |
| XLogP3 | -2.3 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 181.07389321 g/mol |
| Monoisotopic Mass | 181.07389321 g/mol |
| Topological Polar Surface Area | 83.6 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 176 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
API SUPPLIERS
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| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
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ABOUT THIS PAGE
A D-Tyrosine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D-Tyrosine, including repackagers and relabelers. The FDA regulates D-Tyrosine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D-Tyrosine 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 D-Tyrosine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A D-Tyrosine supplier is an individual or a company that provides D-Tyrosine active pharmaceutical ingredient (API) or D-Tyrosine finished formulations upon request. The D-Tyrosine suppliers may include D-Tyrosine API manufacturers, exporters, distributors and traders.
click here to find a list of D-Tyrosine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
D-Tyrosine 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 D-Tyrosine 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 D-Tyrosine GMP manufacturer or D-Tyrosine GMP API supplier for your needs.
A D-Tyrosine CoA (Certificate of Analysis) is a formal document that attests to D-Tyrosine's compliance with D-Tyrosine specifications and serves as a tool for batch-level quality control.
D-Tyrosine CoA mostly includes findings from lab analyses of a specific batch. For each D-Tyrosine 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.
D-Tyrosine may be tested according to a variety of international standards, such as European Pharmacopoeia (D-Tyrosine EP), D-Tyrosine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (D-Tyrosine USP).
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