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1. 3992-42-5
2. Deoxycytidine Hydrochloride
3. Cytidine, 2'-deoxy-, Monohydrochloride
4. 2'-deoxycytidine Hcl
5. 2'-deoxycytidine (hydrochloride)
6. 2'-deoxycytidine Monohydrochloride
7. 25203-63-8
8. X8fx60e66d
9. Cytidine, 2'-deoxy-, Hydrochloride (1:)
10. 4-amino-1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one;hydrochloride
11. 4-amino-1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one Hydrochloride
12. Smr000718803
13. Dc.hcl
14. Unii-x8fx60e66d
15. 2-deoxycytidine Hydrochloride
16. Nsc-83251
17. Cytosine Deoxyriboside Hydrochloride
18. Einecs 223-639-9
19. Einecs 246-732-6
20. Mfcd00012840
21. Nsc 83251
22. Cytidine, 2'-deoxy-, Hydrochloride (1:1)
23. 2'-deoxycytidinehydrochloride
24. 2'-deoycytidine Hydrochloride
25. Mls001306453
26. Mls001332443
27. Mls001332444
28. Schembl552284
29. 2\'-deoxycytidine Hydrochloride
30. Chembl1356971
31. Dtxsid2074956
32. Akos015843820
33. Akos015961323
34. 4-amino-1-((2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1h)-one Hydrochloride
35. As-63599
36. Hy-17564
37. D0048
38. 992d425
39. A824806
40. J-700039
41. Q27293693
42. 2'-deoxycytidine Hydrochloride, Analytical Standard, >=99%
43. 1-(2-deoxy-.beta.-d-ribofuranosyl)cytosine Hydrochloride
44. 2'-deoxycytidine Hydrochloride, Suitable For Cell Culture, Bioreagent
45. 1-(2-deoxy-beta-d-ribofuranosyl)cytosine Hydrochloride, Cytosine Deoxyriboside Hydrochloride
| Molecular Weight | 263.68 g/mol |
|---|---|
| Molecular Formula | C9H14ClN3O4 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 263.0672836 g/mol |
| Monoisotopic Mass | 263.0672836 g/mol |
| Topological Polar Surface Area | 108 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 355 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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A Deoxycytidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deoxycytidine Hydrochloride, including repackagers and relabelers. The FDA regulates Deoxycytidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deoxycytidine Hydrochloride 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 Deoxycytidine Hydrochloride supplier is an individual or a company that provides Deoxycytidine Hydrochloride active pharmaceutical ingredient (API) or Deoxycytidine Hydrochloride finished formulations upon request. The Deoxycytidine Hydrochloride suppliers may include Deoxycytidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Deoxycytidine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Deoxycytidine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Deoxycytidine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Deoxycytidine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Deoxycytidine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Deoxycytidine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Deoxycytidine Hydrochloride USDMF includes data on Deoxycytidine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Deoxycytidine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Deoxycytidine Hydrochloride suppliers with USDMF on PharmaCompass.
Deoxycytidine Hydrochloride 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 Deoxycytidine Hydrochloride 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 Deoxycytidine Hydrochloride GMP manufacturer or Deoxycytidine Hydrochloride GMP API supplier for your needs.
A Deoxycytidine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Deoxycytidine Hydrochloride's compliance with Deoxycytidine Hydrochloride specifications and serves as a tool for batch-level quality control.
Deoxycytidine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Deoxycytidine Hydrochloride 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.
Deoxycytidine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Deoxycytidine Hydrochloride EP), Deoxycytidine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Deoxycytidine Hydrochloride USP).
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