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1. Uridine-5'-triphosphoric Acid Trisodium Salt
2. 19817-92-6
3. Uridine 5'-triphosphate Trisodium Salt
4. Uridine Triphosphate Trisodium
5. Gm3e161i3c
6. Uridine 5'-(disodium Dihydrogen Triphosphate)
7. Uridine 5'-(tetrahydrogen Triphosphate), Sodium Salt (1:3)
8. Uridine 5'-triphosphate Trisodium Salt Hydrate
9. Utp Na3
10. Utp Trisodium Salt
11. Mfcd00044310
12. Utp, Trisodium Salt
13. Uridine 5'-triphosphate Sodium Salt
14. Uridine-5'-triphosphate Trisodium Salt
15. Unii-gm3e161i3c
16. Einecs 243-347-5
17. Utipina
18. Utp-na
19. Trisodium Utp
20. Nsc-20260
21. Utipina [who-dd]
22. 5'-utp 3na
23. Spectrum1503346
24. Hms500n11
25. Uridine-5'-triphosphate Trisodium
26. Act02629
27. Ccg-38717
28. Hg1376
29. Nsc 20260
30. Akos015895705
31. Ac-8222
32. Uridine-5'-triphosphoricacidtrisodiumsalt
33. As-80622
34. U0022
35. Uridine Triphosphate Trisodium [who-dd]
36. Q27279174
37. Uridine 5'-triphosphate Trisodium Salt Hydrate, Type Iv, 90-95%
38. Uridine 5'-triphosphate Trisodium Salt Hydrate, From Yeast, Type Iii, >=96%
39. Sodium ((2r,3s,4r,5r)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl Hydrogentriphosphate
40. Trisodium;[[[(2r,3s,4r,5r)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] Hydrogen Phosphate
41. Uridine 5'-triphosphate Trisodium Salt Solution, Hplc Purified, Aqueous Solution For Rna Polymerase Transcription
Molecular Weight | 550.09 g/mol |
---|---|
Molecular Formula | C9H12N2Na3O15P3 |
Hydrogen Bond Donor Count | 4 |
Hydrogen Bond Acceptor Count | 15 |
Rotatable Bond Count | 8 |
Exact Mass | 549.91436152 g/mol |
Monoisotopic Mass | 549.91436152 g/mol |
Topological Polar Surface Area | 267 Ų |
Heavy Atom Count | 32 |
Formal Charge | 0 |
Complexity | 820 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 4 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 4 |
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ABOUT THIS PAGE
A Uridine Triphosphate Trisodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uridine Triphosphate Trisodium, including repackagers and relabelers. The FDA regulates Uridine Triphosphate Trisodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uridine Triphosphate Trisodium 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 Uridine Triphosphate Trisodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Uridine Triphosphate Trisodium supplier is an individual or a company that provides Uridine Triphosphate Trisodium active pharmaceutical ingredient (API) or Uridine Triphosphate Trisodium finished formulations upon request. The Uridine Triphosphate Trisodium suppliers may include Uridine Triphosphate Trisodium API manufacturers, exporters, distributors and traders.
click here to find a list of Uridine Triphosphate Trisodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Uridine Triphosphate Trisodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Uridine Triphosphate Trisodium active pharmaceutical ingredient (API) in detail. Different forms of Uridine Triphosphate Trisodium DMFs exist exist since differing nations have different regulations, such as Uridine Triphosphate Trisodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Uridine Triphosphate Trisodium DMF submitted to regulatory agencies in the US is known as a USDMF. Uridine Triphosphate Trisodium USDMF includes data on Uridine Triphosphate Trisodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Uridine Triphosphate Trisodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Uridine Triphosphate Trisodium suppliers with USDMF on PharmaCompass.
Uridine Triphosphate Trisodium 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 Uridine Triphosphate Trisodium 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 Uridine Triphosphate Trisodium GMP manufacturer or Uridine Triphosphate Trisodium GMP API supplier for your needs.
A Uridine Triphosphate Trisodium CoA (Certificate of Analysis) is a formal document that attests to Uridine Triphosphate Trisodium's compliance with Uridine Triphosphate Trisodium specifications and serves as a tool for batch-level quality control.
Uridine Triphosphate Trisodium CoA mostly includes findings from lab analyses of a specific batch. For each Uridine Triphosphate Trisodium 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.
Uridine Triphosphate Trisodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Uridine Triphosphate Trisodium EP), Uridine Triphosphate Trisodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Uridine Triphosphate Trisodium USP).
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