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1. Thiazoles
1. 288-47-1
2. 1,3-thiazole
3. Fema No. 3615
4. 320rcw8pef
5. Chebi:43732
6. Thiazol
7. Thiazoles
8. Tz
9. Ccris 3205
10. Einecs 206-021-3
11. Unii-320rcw8pef
12. Brn 0103852
13. A Thiazole
14. Racemic Thiazole
15. Thiazole-
16. Thiazole, 99%
17. 5h-1,3-thiazole
18. 1,3-thiazole #
19. Thiazole, >=99%
20. Thiazole [fhfi]
21. Thiazole [mi]
22. 4-27-00-00960 (beilstein Handbook Reference)
23. Chembl15605
24. Dtxsid2059776
25. Fema 3615
26. Amy5749
27. Bcp27450
28. Zinc1484626
29. Bbl027512
30. Mfcd00005315
31. Stl372725
32. Akos005146301
33. Cs-w001237
34. Lom
35. Cb7853436
36. Db-000360
37. Ft-0631899
38. T0185
39. En300-22312
40. 288t471
41. A819630
42. Q413426
43. Q-100366
| Molecular Weight | 85.13 g/mol |
|---|---|
| Molecular Formula | C3H3NS |
| XLogP3 | 0.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 84.99862027 g/mol |
| Monoisotopic Mass | 84.99862027 g/mol |
| Topological Polar Surface Area | 41.1 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 30.1 |
| 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 |
API SUPPLIERS
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USDMF
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Average Price (USD/KGS) |
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ABOUT THIS PAGE
A Thiazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thiazole, including repackagers and relabelers. The FDA regulates Thiazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thiazole 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 Thiazole supplier is an individual or a company that provides Thiazole active pharmaceutical ingredient (API) or Thiazole finished formulations upon request. The Thiazole suppliers may include Thiazole API manufacturers, exporters, distributors and traders.
click here to find a list of Thiazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Thiazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Thiazole active pharmaceutical ingredient (API) in detail. Different forms of Thiazole DMFs exist exist since differing nations have different regulations, such as Thiazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Thiazole DMF submitted to regulatory agencies in the US is known as a USDMF. Thiazole USDMF includes data on Thiazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Thiazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Thiazole suppliers with USDMF on PharmaCompass.
Thiazole 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 Thiazole 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 Thiazole GMP manufacturer or Thiazole GMP API supplier for your needs.
A Thiazole CoA (Certificate of Analysis) is a formal document that attests to Thiazole's compliance with Thiazole specifications and serves as a tool for batch-level quality control.
Thiazole CoA mostly includes findings from lab analyses of a specific batch. For each Thiazole 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.
Thiazole may be tested according to a variety of international standards, such as European Pharmacopoeia (Thiazole EP), Thiazole JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Thiazole USP).
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