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1. Citric Acid Tributyl Ester
2. Tributyl Citric Acid
1. 77-94-1
2. Tributyl 2-hydroxypropane-1,2,3-tricarboxylate
3. Butyl Citrate
4. Tri-n-butyl Citrate
5. Citroflex 4
6. Citric Acid, Tributyl Ester
7. N-butyl Citrate
8. 1,2,3-propanetricarboxylic Acid, 2-hydroxy-, Tributyl Ester
9. Morflex Tbc
10. Citroflex C 4
11. Nsc 8491
12. Nsc-8491
13. 2-hydroxy-1,2,3-propanetricarboxylic Acid, Tributyl Ester
14. 827d5b1b6s
15. 1,2,3-propanetricarboxylic Acid, 2-hydroxy-, 1,2,3-tributyl Ester
16. Butyl Citrate (van)
17. Mfcd00027217
18. Tributyl 2-hydroxypropane-1,2,3-tricarboxylate (tributyl Citrate)
19. Citric Acid Tributyl Ester
20. Einecs 201-071-2
21. Brn 1806072
22. Unii-827d5b1b6s
23. Ai3-00394
24. Tributyl 2-hydroxy-1,2,3-propanetricarboxylate
25. Citric Acid Tributyl
26. Tributyl Citrate [nf]
27. Ec 201-071-2
28. Tributyl2-hydroxypropane-1,2,3-tricarboxylate
29. Butyl Citrate [mi]
30. Schembl24668
31. Citric Acid Tri-n-butyl Ester
32. Tributyl Citrate, >=97.0%
33. Tributyl Citrate [inci]
34. Chembl2107619
35. Dtxsid5051442
36. Nsc8491
37. Tributyl Citrate [mart.]
38. Chebi:176825
39. Tributyl Citrate [usp-rs]
40. Zinc3875494
41. Akos015839595
42. Tributyl Citrate [ep Impurity]
43. Ds-4667
44. Db-056272
45. C0366
46. Ft-0631337
47. A839297
48. Tributyl 2-hydroxy-1,2,3-propanetricarboxylate #
49. Q1954892
50. W-104292
51. Tributyl Acetylcitrate Impurity A [ep Impurity]
52. 2-hydroxy-1,3-propanetricarboxylic Acid, Tributyl Ester
53. 1,3-propanetricarboxylic Acid, 2-hydroxy-, Tributyl Ester
54. 2-hydroxy-1,2,3-propanetricarboxylic Acidtributyl Ester
55. Tributyl Citrate, United States Pharmacopeia (usp) Reference Standard
56. Tributyl Citrate, Pharmaceutical Secondary Standard; Certified Reference Material
Molecular Weight | 360.4 g/mol |
---|---|
Molecular Formula | C18H32O7 |
XLogP3 | 2.7 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 7 |
Rotatable Bond Count | 17 |
Exact Mass | 360.21480336 g/mol |
Monoisotopic Mass | 360.21480336 g/mol |
Topological Polar Surface Area | 99.1 Ų |
Heavy Atom Count | 25 |
Formal Charge | 0 |
Complexity | 382 |
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 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Tributyl Citrate API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tributyl Citrate API, including repackagers and relabelers. The FDA regulates Tributyl Citrate API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tributyl Citrate API 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 Tributyl Citrate API manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tributyl Citrate API supplier is an individual or a company that provides Tributyl Citrate API active pharmaceutical ingredient (API) or Tributyl Citrate API finished formulations upon request. The Tributyl Citrate API suppliers may include Tributyl Citrate API API manufacturers, exporters, distributors and traders.
click here to find a list of Tributyl Citrate API suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tributyl Citrate API DMF (Drug Master File) is a document detailing the whole manufacturing process of Tributyl Citrate API active pharmaceutical ingredient (API) in detail. Different forms of Tributyl Citrate API DMFs exist exist since differing nations have different regulations, such as Tributyl Citrate API USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tributyl Citrate API DMF submitted to regulatory agencies in the US is known as a USDMF. Tributyl Citrate API USDMF includes data on Tributyl Citrate API's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tributyl Citrate API USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tributyl Citrate API suppliers with USDMF on PharmaCompass.
Tributyl Citrate API 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 Tributyl Citrate API 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 Tributyl Citrate API GMP manufacturer or Tributyl Citrate API GMP API supplier for your needs.
A Tributyl Citrate API CoA (Certificate of Analysis) is a formal document that attests to Tributyl Citrate API's compliance with Tributyl Citrate API specifications and serves as a tool for batch-level quality control.
Tributyl Citrate API CoA mostly includes findings from lab analyses of a specific batch. For each Tributyl Citrate API 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.
Tributyl Citrate API may be tested according to a variety of international standards, such as European Pharmacopoeia (Tributyl Citrate API EP), Tributyl Citrate API JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tributyl Citrate API USP).
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