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1. Imizol
1. 55750-06-6
2. Imizol
3. Imidocarb (dipropionate)
4. Imidocarb Propionate
5. Zsm1m03shc
6. Ncgc00166399-01
7. N,n'-bis(3-(4,5-dihydro-1h-imidazol-2-yl)phenyl)urea Dipropionate
8. Dsstox_cid_26604
9. Dsstox_rid_81759
10. Dsstox_gsid_46604
11. 1,3-bis[3-(4,5-dihydro-1h-imidazol-2-yl)phenyl]urea;propanoic Acid
12. 1,3-bis(3-(4,5-dihydro-1h-imidazol-2-yl)phenyl)urea Dipropionate
13. N,n'-bis[3-(4,5-dihydro-1h-imidazol-2-yl)phenyl]urea, Dipropanoate
14. Propanoic Acid, Compd. With N,n'-bis(3-(4,5-dihydro-1h-imidazol-2-yl)phenyl)urea (2:1)
15. Einecs 259-791-8
16. Cas-55750-06-6
17. Imidocarb 100 Microg/ml In Methanol
18. Unii-zsm1m03shc
19. Propanoic Acid, Compd. With N,n'-bis[3-(4,5-dihydro-1h-imidazol-2-yl)phenyl]urea (2:1)
20. 2-yl)phenyl)urea Dipropionate
21. Schembl2885201
22. Chembl1362780
23. Dtxsid4046604
24. Ex-a981
25. Bcp12142
26. Tox21_112415
27. 1,3-bis[3-(4,5-dihydro-1h-imidazol-2-yl)phenyl]urea,propanoic Acid
28. Mfcd00013161
29. S5214
30. Akos015888295
31. Imidocarb Dipropionate [mart.]
32. Tox21_112415_1
33. Ccg-269667
34. Ncgc00174046-02
35. Ac-20135
36. As-17387
37. 1,3-bis(3-(4,5-dihydro-1h-imidazol-
38. Imidocarb Dipropionate [green Book]
39. Db-050101
40. Hy-107496
41. Cs-0028632
42. Ft-0630686
43. I0957
44. F17388
45. A830788
46. Q-201233
47. Q27295871
48. N,n'-bis(3-(4,5-dihydro-1h-imidazol-2-yl)-phenyl)
49. 3,3'-di-2-imidazolin-2-ylcarbanilide Dipropionate
50. Imidocarb Dipropionate, Vetranal(tm), Analytical Standard
51. Imidocarb Dipropionate, Antibiotic For Culture Media Use Only
52. 1,3-bis[3-(4,5-dihydro-1h-imidazol-2-yl)phenyl]urea; Propanoic Acid
53. Propanoic Acid, Compd. With Urea, N,n'-bis[3-(4,5-dihydro-1h-imidazol-2-yl)phenyl]- (2:1)
| Molecular Weight | 496.6 g/mol |
|---|---|
| Molecular Formula | C25H32N6O5 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 6 |
| Exact Mass | 496.24341814 g/mol |
| Monoisotopic Mass | 496.24341814 g/mol |
| Topological Polar Surface Area | 165 Ų |
| Heavy Atom Count | 36 |
| Formal Charge | 0 |
| Complexity | 567 |
| 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 | 3 |
Antiprotozoal Agents
Substances that are destructive to protozoans. (See all compounds classified as Antiprotozoal Agents.)
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ABOUT THIS PAGE
A Imidocarb Dipropionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imidocarb Dipropionate, including repackagers and relabelers. The FDA regulates Imidocarb Dipropionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imidocarb Dipropionate 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 Imidocarb Dipropionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Imidocarb Dipropionate supplier is an individual or a company that provides Imidocarb Dipropionate active pharmaceutical ingredient (API) or Imidocarb Dipropionate finished formulations upon request. The Imidocarb Dipropionate suppliers may include Imidocarb Dipropionate API manufacturers, exporters, distributors and traders.
click here to find a list of Imidocarb Dipropionate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Imidocarb Dipropionate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Imidocarb Dipropionate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Imidocarb Dipropionate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Imidocarb Dipropionate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Imidocarb Dipropionate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Imidocarb Dipropionate suppliers with NDC on PharmaCompass.
Imidocarb Dipropionate 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 Imidocarb Dipropionate 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 Imidocarb Dipropionate GMP manufacturer or Imidocarb Dipropionate GMP API supplier for your needs.
A Imidocarb Dipropionate CoA (Certificate of Analysis) is a formal document that attests to Imidocarb Dipropionate's compliance with Imidocarb Dipropionate specifications and serves as a tool for batch-level quality control.
Imidocarb Dipropionate CoA mostly includes findings from lab analyses of a specific batch. For each Imidocarb Dipropionate 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.
Imidocarb Dipropionate may be tested according to a variety of international standards, such as European Pharmacopoeia (Imidocarb Dipropionate EP), Imidocarb Dipropionate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Imidocarb Dipropionate USP).
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