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1. Tetrapropoxysilane
2. 682-01-9
3. Tetra-n-propoxysilane
4. Tetrapropyl Silicate
5. Propyl Orthosilicate
6. Silicic Acid (h4sio4), Tetrapropyl Ester
7. Dynasil P
8. Tetra-n-propyl Silicate
9. Tetra-n-propyl Orthosilicate
10. 4pe821g3gh
11. Unii-4pe821g3gh
12. Propyl Silicate
13. Tetrapropyloxysilane
14. Einecs 211-659-0
15. Silicon Orthopropoxide
16. Silicon Tetrapropoxide
17. N-propyl Orthosilicate
18. Silane, Tetrapropoxy-
19. Tetrapropylorthosilicate
20. Tetra-n-propoxy-silane
21. Silicon Tetra-n-propoxide
22. Ec 211-659-0
23. Si(och2ch2ch3)4
24. Dsstox_cid_22382
25. Dsstox_rid_80010
26. Dsstox_gsid_42382
27. Schembl23873
28. Si(o-n-c3h7)4
29. Tetra-n-propyl Ortho Silicate
30. Propyl Silicate ((pro)4si)
31. Tetrapropyl Orthosilicate, 95%
32. Chembl3181871
33. Dtxsid9042382
34. Zqzcobsuofhdee-uhfffaoysa-
35. Propyl Orthosilicate [ii]
36. Tox21_301445
37. Ct2090
38. Mfcd00009364
39. Akos016013013
40. Zinc169745019
41. S16425
42. Ncgc00255743-01
43. Cas-682-01-9
44. Ls-14170
45. Db-055120
46. Cs-0187692
47. Ft-0632791
48. T1174
49. Tetra-n-propoxysilane(tetra Propylorthosilicate)
50. Tetrapropyl Orthosilicate, >=98%, Deposition Grade
51. Q27260328
| Molecular Weight | 264.43 g/mol |
|---|---|
| Molecular Formula | C12H28O4Si |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 12 |
| Exact Mass | 264.17568590 g/mol |
| Monoisotopic Mass | 264.17568590 g/mol |
| Topological Polar Surface Area | 36.9 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 129 |
| 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 Tetrapropyl Orthosilicate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetrapropyl Orthosilicate, including repackagers and relabelers. The FDA regulates Tetrapropyl Orthosilicate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetrapropyl Orthosilicate 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 Tetrapropyl Orthosilicate supplier is an individual or a company that provides Tetrapropyl Orthosilicate active pharmaceutical ingredient (API) or Tetrapropyl Orthosilicate finished formulations upon request. The Tetrapropyl Orthosilicate suppliers may include Tetrapropyl Orthosilicate API manufacturers, exporters, distributors and traders.
Tetrapropyl Orthosilicate 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 Tetrapropyl Orthosilicate 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 Tetrapropyl Orthosilicate GMP manufacturer or Tetrapropyl Orthosilicate GMP API supplier for your needs.
A Tetrapropyl Orthosilicate CoA (Certificate of Analysis) is a formal document that attests to Tetrapropyl Orthosilicate's compliance with Tetrapropyl Orthosilicate specifications and serves as a tool for batch-level quality control.
Tetrapropyl Orthosilicate CoA mostly includes findings from lab analyses of a specific batch. For each Tetrapropyl Orthosilicate 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.
Tetrapropyl Orthosilicate may be tested according to a variety of international standards, such as European Pharmacopoeia (Tetrapropyl Orthosilicate EP), Tetrapropyl Orthosilicate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tetrapropyl Orthosilicate USP).
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