Synopsis
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JDMF
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KDMF
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VMF
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EDQM
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USP
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JP
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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1. Acid, Bichloroacetic
2. Acid, Dichloroacetic
3. Bichloroacetic Acid
4. Dichloroacetate, Potassium
5. Dichloroacetate, Sodium
6. Dichloroacetic Acid
7. Potassium Dichloroacetate
1. 2156-56-1
2. Sodium 2,2-dichloroacetate
3. Dichloroacetic Acid Sodium Salt
4. Ceresine
5. Dichloroacetate Sodium
6. Acetic Acid, Dichloro-, Sodium Salt
7. Dca Sodium
8. Cpc-211
9. Dca
10. Sodium Dichloroacetate [usan]
11. Bichloroacetic Acid
12. Cmi X-11s
13. Sodium Dichloroacetate (dca)
14. Nsc-744479
15. Ncgc00167845-01
16. 42932x67b5
17. Dsstox_cid_17207
18. Dsstox_rid_79307
19. Dsstox_gsid_37207
20. Sodium Dichloroacetate (usan)
21. Cas-2156-56-1
22. Mfcd00070489
23. Dichloroctan Sodny [czech]
24. Sodium,2,2-dichloroacetate
25. Cpc 211
26. Ccris 7697
27. Dichloroacetic Acid, Sodium Salt
28. Dichloroctan Sodny
29. Ceresine (tn)
30. Einecs 218-461-3
31. Sodium?dichloroacetate
32. Dichloroacetate Sodium Salt
33. Schembl105849
34. Chembl306823
35. Dtxsid8037207
36. Hy-y0445a
37. Hms3269p21
38. Hms3413f08
39. Hms3677f08
40. Hms3867g13
41. Unii-42932x67b5
42. Amy37987
43. Tox21_113573
44. Tox21_301394
45. Bdbm50177027
46. S8615
47. Akos015833467
48. Sodium Dichloroacetate [mart.]
49. Ccg-266211
50. Nsc 744479
51. Ncgc00255419-01
52. As-58721
53. B7174
54. Cs-0030662
55. D1048
56. D1719
57. Ft-0624702
58. D05857
59. F12025
60. 3-(1,3-benzothiazol-2-yl)propanoicacid
61. A815488
62. J-014151
63. Q27258517
| Molecular Weight | 150.92 g/mol |
|---|---|
| Molecular Formula | C2HCl2NaO2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 149.9251289 g/mol |
| Monoisotopic Mass | 149.9251289 g/mol |
| Topological Polar Surface Area | 40.1 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 64.7 |
| 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 | 2 |
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PharmaCompass offers a list of Dichloroacetic Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Dichloroacetic Acid manufacturer or Dichloroacetic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dichloroacetic Acid manufacturer or Dichloroacetic Acid supplier.
PharmaCompass also assists you with knowing the Dichloroacetic Acid API Price utilized in the formulation of products. Dichloroacetic Acid API Price is not always fixed or binding as the Dichloroacetic Acid Price is obtained through a variety of data sources. The Dichloroacetic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DCA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DCA, including repackagers and relabelers. The FDA regulates DCA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DCA 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 DCA supplier is an individual or a company that provides DCA active pharmaceutical ingredient (API) or DCA finished formulations upon request. The DCA suppliers may include DCA API manufacturers, exporters, distributors and traders.
click here to find a list of DCA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DCA DMF (Drug Master File) is a document detailing the whole manufacturing process of DCA active pharmaceutical ingredient (API) in detail. Different forms of DCA DMFs exist exist since differing nations have different regulations, such as DCA USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DCA DMF submitted to regulatory agencies in the US is known as a USDMF. DCA USDMF includes data on DCA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DCA USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DCA suppliers with USDMF on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing DCA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for DCA API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture DCA as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain DCA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a DCA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of DCA suppliers with NDC on PharmaCompass.
DCA 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 DCA 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 DCA GMP manufacturer or DCA GMP API supplier for your needs.
A DCA CoA (Certificate of Analysis) is a formal document that attests to DCA's compliance with DCA specifications and serves as a tool for batch-level quality control.
DCA CoA mostly includes findings from lab analyses of a specific batch. For each DCA 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.
DCA may be tested according to a variety of international standards, such as European Pharmacopoeia (DCA EP), DCA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DCA USP).
