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1. 1916-07-0
2. Trimethylgallic Acid Methyl Ester
3. Methyl Tri-o-methylgallate
4. Benzoic Acid, 3,4,5-trimethoxy-, Methyl Ester
5. 3,4,5-trimethoxybenzoic Acid Methyl Ester
6. Methyl Eudesmate
7. 3,4,5-trimethoxybenzoic Acid, Methyl Ester
8. Methyl 3,4,5-trimethoxy Benzoate
9. Qfp1lsc7tk
10. Methyl Gallate Trimethyl Ether
11. Nsc-16955
12. Unii-qfp1lsc7tk
13. Einecs 217-629-3
14. Nsc 16955
15. Brn 2218156
16. Ai3-21154
17. Trimethoprim Ep Impurity H
18. Trimethylgallicacidmethylester
19. 4-10-00-01999 (beilstein Handbook Reference)
20. Methyl 3,5-trimethoxybenzoate
21. Schembl211747
22. Chembl1651039
23. Dtxsid0062058
24. Zinc57165
25. Chebi:192678
26. Amy22196
27. Bcp18705
28. Hy-n2044
29. Nsc16955
30. 3,4,5-trimethoxybenzoic Acid Methyl
31. Bbl009653
32. Mfcd00008431
33. S3863
34. Stk401656
35. Akos003283901
36. Ccg-266765
37. 3,5-trimethoxybenzoic Acid Methyl Ester
38. Methyl 3,4,5-trimethoxybenzoate, 98%
39. 3,5-trimethoxybenzoic Acid, Methyl Ester
40. Ac-11227
41. Ac-34705
42. As-60488
43. Benzoic Acid,4,5-trimethoxy-, Methyl Ester
44. Cs-0018534
45. Ft-0614163
46. T1092
47. Trimethoprim Impurity H [ep Impurity]
48. D70529
49. Ac-907/25014289
50. 3,4,5-trimethoxy Benzoic Acid Methyl Ester
51. Trimebutine Maleate Impurity C [ep Impurity]
52. W-107730
53. Q27287238
54. F0001-0689
55. 3,4,5-trimethoxybenzoic Acid Methyl Ester; Methyl Eudesmate; Methyl Gallate Trimethyl Ether; Methyl Tri-o-methylgallatemethyl 3,4,5-trimethoxybenzoate; Trimethylgallic Acid Methyl Ester
| Molecular Weight | 226.23 g/mol |
|---|---|
| Molecular Formula | C11H14O5 |
| XLogP3 | 1.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 5 |
| Exact Mass | 226.08412354 g/mol |
| Monoisotopic Mass | 226.08412354 g/mol |
| Topological Polar Surface Area | 54 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 216 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Methyl EudesMate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyl EudesMate, including repackagers and relabelers. The FDA regulates Methyl EudesMate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyl EudesMate 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 Methyl EudesMate supplier is an individual or a company that provides Methyl EudesMate active pharmaceutical ingredient (API) or Methyl EudesMate finished formulations upon request. The Methyl EudesMate suppliers may include Methyl EudesMate API manufacturers, exporters, distributors and traders.
Methyl EudesMate 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 Methyl EudesMate 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 Methyl EudesMate GMP manufacturer or Methyl EudesMate GMP API supplier for your needs.
A Methyl EudesMate CoA (Certificate of Analysis) is a formal document that attests to Methyl EudesMate's compliance with Methyl EudesMate specifications and serves as a tool for batch-level quality control.
Methyl EudesMate CoA mostly includes findings from lab analyses of a specific batch. For each Methyl EudesMate 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.
Methyl EudesMate may be tested according to a variety of international standards, such as European Pharmacopoeia (Methyl EudesMate EP), Methyl EudesMate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Methyl EudesMate USP).
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