Synopsis
Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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Listed Suppliers
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FDF
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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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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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EDQM
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USP
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JP
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US Patents
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US Exclusivities
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Health Canada Patents
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Data Compilation #PharmaFlow
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US Medicaid
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1. Ato 888
2. Compritol 888
3. Compritol Ato 888
4. Glyceryl Behenate
1. 18641-57-1
2. Tridocosanoin
3. Glyceryl Tribehenate
4. Docosanoin, Tri-
5. Compritol 888
6. Tribehenoyl Glycerol
7. 1,2,3-tridocosanoyl Glycerol
8. Propane-1,2,3-triyl Tridocosanoate
9. 2,3-di(docosanoyloxy)propyl Docosanoate
10. Docosanoic Acid, 1,2,3-propanetriyl Ester
11. Glycerol Tridocosanoate
12. Behenic Acid, 1,2,3-propanetriol Ester
13. 1,2,3-propenetriol Tridocosanoate
14. 8oc9u7tqz0
15. 1,2,3-tridocosanoyl-glycerol
16. 1,2,3-tridocosanoyl-sn-glycerol
17. Tg(22:0/22:0/22:0)
18. Glycerol Tribehenate
19. Einecs 242-471-7
20. Unii-8oc9u7tqz0
21. Brn 1811476
22. Dub Bg
23. Syncrowax Hr-c
24. Compritol 888 Cg
25. Compritol 888 Ato
26. Compritol 888 Cg Ato
27. Tribehenin (c22:0)
28. Tribehenin [ii]
29. Tribehenin [inci]
30. 1,2,3-tridocosanoylglycerol
31. 2-02-00-00374 (beilstein Handbook Reference)
32. Schembl2121937
33. Chembl2104418
34. Dtxsid40171900
35. Glycerol Tridocosanoate, Aldrichcpr
36. Tag 66:0
37. Lmgl03012338
38. Mfcd00056274
39. Tracylglycerol(22:0/22:0/22:0)
40. 1,2,3-propanetriyl Tridocosanoate, 9ci
41. Bs-23874
42. 1-behenoyl-2-behenoyl-3-behenoyl-glycerol
43. 2,3-bis(docosanoyloxy)propyl Docosanoate #
44. T1391
45. D04350
46. Docosanoic Acid, Triester With Glycerin
47. 1-docosanoyl-2-docosanoyl-3-docosanoyl-glycerol
48. Tag(22:0/22:0/22:0)
49. W-110483
50. Q27270813
| Molecular Weight | 1059.8 g/mol |
|---|---|
| Molecular Formula | C69H134O6 |
| XLogP3 | 31.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 68 |
| Exact Mass | 1059.01804199 g/mol |
| Monoisotopic Mass | 1059.01804199 g/mol |
| Topological Polar Surface Area | 78.9 Ų |
| Heavy Atom Count | 75 |
| Formal Charge | 0 |
| Complexity | 1070 |
| 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 |
API SUPPLIERS
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USDMF
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| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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ABOUT THIS PAGE
A Tribehenin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tribehenin, including repackagers and relabelers. The FDA regulates Tribehenin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tribehenin 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 Tribehenin supplier is an individual or a company that provides Tribehenin active pharmaceutical ingredient (API) or Tribehenin finished formulations upon request. The Tribehenin suppliers may include Tribehenin API manufacturers, exporters, distributors and traders.
click here to find a list of Tribehenin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tribehenin DMF (Drug Master File) is a document detailing the whole manufacturing process of Tribehenin active pharmaceutical ingredient (API) in detail. Different forms of Tribehenin DMFs exist exist since differing nations have different regulations, such as Tribehenin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tribehenin DMF submitted to regulatory agencies in the US is known as a USDMF. Tribehenin USDMF includes data on Tribehenin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tribehenin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tribehenin suppliers with USDMF on PharmaCompass.
Tribehenin 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 Tribehenin 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 Tribehenin GMP manufacturer or Tribehenin GMP API supplier for your needs.
A Tribehenin CoA (Certificate of Analysis) is a formal document that attests to Tribehenin's compliance with Tribehenin specifications and serves as a tool for batch-level quality control.
Tribehenin CoA mostly includes findings from lab analyses of a specific batch. For each Tribehenin 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.
Tribehenin may be tested according to a variety of international standards, such as European Pharmacopoeia (Tribehenin EP), Tribehenin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tribehenin USP).
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