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1. 1,3-propylenimine
2. Azacyclobutane
3. Trimethylenimine
1. 503-29-7
2. Trimethylene Imine
3. Azacyclobutane
4. Trimethylenimine
5. 1,3-propylenimine
6. Azetidine, Homopolymer
7. 37s883xdwr
8. Chebi:30968
9. 53860-05-2
10. Azetidin
11. Azetidine, L-
12. Unii-37s883xdwr
13. Acetidine
14. Trimethyleneimine
15. Azete, Tetrahydro-
16. Einecs 207-963-8
17. Azetidine, 98%
18. Mfcd00005165
19. Ai3-61395
20. Chembl2171713
21. Dtxsid8060117
22. Niosh/cm4290000
23. Bcp22506
24. Zinc14951819
25. Akos000121515
26. Gc10189
27. Sb52174
28. Ps-11989
29. Db-023025
30. Am20080889
31. Bb 0254753
32. Cm42900000
33. Ft-0649642
34. 503a297
35. A828069
36. Q425376
37. W-105973
38. 1,3-propylenimine;azacyclobutane;azetidine;trimethylene Imine
Molecular Weight | 57.09 g/mol |
---|---|
Molecular Formula | C3H7N |
XLogP3 | -0.1 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 0 |
Exact Mass | 57.057849228 g/mol |
Monoisotopic Mass | 57.057849228 g/mol |
Topological Polar Surface Area | 12 Ų |
Heavy Atom Count | 4 |
Formal Charge | 0 |
Complexity | 17.2 |
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 Azetidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azetidine, including repackagers and relabelers. The FDA regulates Azetidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azetidine 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 Azetidine supplier is an individual or a company that provides Azetidine active pharmaceutical ingredient (API) or Azetidine finished formulations upon request. The Azetidine suppliers may include Azetidine API manufacturers, exporters, distributors and traders.
Azetidine 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 Azetidine 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 Azetidine GMP manufacturer or Azetidine GMP API supplier for your needs.
A Azetidine CoA (Certificate of Analysis) is a formal document that attests to Azetidine's compliance with Azetidine specifications and serves as a tool for batch-level quality control.
Azetidine CoA mostly includes findings from lab analyses of a specific batch. For each Azetidine 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.
Azetidine may be tested according to a variety of international standards, such as European Pharmacopoeia (Azetidine EP), Azetidine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Azetidine USP).
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