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1. 3',5-dihydroxy-4',6,7-trimethoxyflavone
1. 855-96-9
2. 3',5-dihydroxy-4',6,7-trimethoxyflavone
3. Eupatorine
4. 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,7-dimethoxy-4h-chromen-4-one
5. Eupatorin - 94%
6. 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,7-dimethoxychromen-4-one
7. 5,3'-dihydroxy-6,7,4'-trimethoxyflavone
8. 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,7-dimethoxy-4h-1-benzopyran-4-one
9. Flavone, 3',5-dihydroxy-4',6,7-trimethoxy-
10. 6-methoxyluteolin 4',7-dimethyl Ether
11. 4h-1-benzopyran-4-one, 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,7-dimethoxy-
12. 3j474av6my
13. Chembl487402
14. Nsc-106402
15. Nsc 106402
16. Unii-3j474av6my
17. Mfcd00016929
18. Kinome_3214
19. Spectrum_001037
20. Specplus_000923
21. Eupatorin [mi]
22. Spectrum2_000456
23. Spectrum4_001833
24. Spectrum5_000625
25. 3',6,7-trimethoxyflavone
26. Kbiogr_002532
27. Kbioss_001517
28. Divk1c_007019
29. Eupatorin, Analytical Standard
30. Schembl555597
31. Spbio_000532
32. Zinc1412
33. Eupatorin, >=97% (hplc)
34. Acon1_001351
35. Kbio1_001963
36. Kbio2_001517
37. Kbio2_004085
38. Kbio2_006653
39. Dtxsid20234704
40. Chebi:136666
41. Hms3262o20
42. Hy-n2374
43. Tox21_500799
44. Bdbm50344054
45. Ccg-38698
46. Lmpk12111239
47. Nsc106402
48. 4h-1-benzopyran-4-one,7-dimethoxy-
49. Akos015856247
50. 6-methoxyluteolin-4'',7-dimethyl Ether
51. Ncgc00180598-01
52. Ncgc00180598-03
53. Ncgc00261484-01
54. Ac-34037
55. As-75882
56. Flavone,5-dihydroxy-4',6,7-trimethoxy-
57. Xe165300
58. Cs-0022554
59. Ft-0614615
60. 3'',5-dihydroxy-4'',6,7-trimethoxy Flavone
61. Q3060386
62. 3'',5-dihydroxy-4'',6,7-trimethoxyflavone
63. 5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-6,7-dimethoxy-chromen-4-one
Molecular Weight | 344.3 g/mol |
---|---|
Molecular Formula | C18H16O7 |
XLogP3 | 2.9 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 7 |
Rotatable Bond Count | 4 |
Exact Mass | 344.08960285 g/mol |
Monoisotopic Mass | 344.08960285 g/mol |
Topological Polar Surface Area | 94.4 Ų |
Heavy Atom Count | 25 |
Formal Charge | 0 |
Complexity | 520 |
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 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Eupatorin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eupatorin, including repackagers and relabelers. The FDA regulates Eupatorin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eupatorin 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 Eupatorin supplier is an individual or a company that provides Eupatorin active pharmaceutical ingredient (API) or Eupatorin finished formulations upon request. The Eupatorin suppliers may include Eupatorin API manufacturers, exporters, distributors and traders.
Eupatorin 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 Eupatorin 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 Eupatorin GMP manufacturer or Eupatorin GMP API supplier for your needs.
A Eupatorin CoA (Certificate of Analysis) is a formal document that attests to Eupatorin's compliance with Eupatorin specifications and serves as a tool for batch-level quality control.
Eupatorin CoA mostly includes findings from lab analyses of a specific batch. For each Eupatorin 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.
Eupatorin may be tested according to a variety of international standards, such as European Pharmacopoeia (Eupatorin EP), Eupatorin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eupatorin USP).
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