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1. 573-56-8
2. O-dinitrophenol
3. Phenol, 2,6-dinitro-
4. Beta-dinitrophenol
5. 2,6-dnp
6. Dinitro-2,6-phenol
7. 2,6-dinitrofenol
8. .beta.-dinitrophenol
9. Phenol, .beta.-dinitro-
10. Chebi:39357
11. F4qm4i92kc
12. Nsc-6215
13. Phenol, Beta-dinitro-
14. 2,6-dinitrofenol [czech]
15. 2,6-dinitro-phenol
16. Ccris 3104
17. Hsdb 6306
18. Nsc 6215
19. Einecs 209-357-9
20. Unii-f4qm4i92kc
21. Brn 1913410
22. 2,6-dinitro Phenol
23. Wln: Wnr Bq Cnw
24. Epitope Id:161741
25. 2,6-dinitrophenol, 95%
26. Schembl1077970
27. Chembl3278560
28. Dtxsid5022063
29. 2,6-dinitrophenol [mi]
30. Nsc6215
31. Stl355968
32. Zinc12358884
33. Akos000274520
34. As-40741
35. Db-020252
36. Bb 0259250
37. Ft-0610716
38. 2,6-dinitrophenol 10 Microg/ml In Acetonitrile
39. Q20856130
Molecular Weight | 184.11 g/mol |
---|---|
Molecular Formula | C6H4N2O5 |
XLogP3 | 1.4 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 0 |
Exact Mass | 184.01202123 g/mol |
Monoisotopic Mass | 184.01202123 g/mol |
Topological Polar Surface Area | 112 Ų |
Heavy Atom Count | 13 |
Formal Charge | 0 |
Complexity | 198 |
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 |
/The investigators/ ... studied the pharmacokinetics of ... dinitrophenol isomers /incl 2,6-dinitrophenol/ and showed that elimination from the blood of mice, rabbits, guinea pigs, rats, and monkeys was complete within 30 hr.
National Research Council. Drinking Water & Health, Volume 4. Washington, DC: National Academy Press, 1981., p. 234
Dinitrophenol isomers are readily absorbed from the gastrointestinal tract and through the skin and lungs. The dinitrophenol isomers are not stored to any significant extent in the tissues of humans or lab animals following absorption, but are readily excreted, primarily via the urine. /Dinitrophenol/
National Research Council. Drinking Water & Health, Volume 4. Washington, DC: National Academy Press, 1981., p. 233
Absorption of dinitro compounds can take place with ease through the lungs, the gut, or the intact skin. The rate of absorption through skin is likely to be greater when the substances are applied in oily rather than aq soln. /Dinitro cmpd/
Clarke, M. L., D. G. Harvey and D. J. Humphreys. Veterinary Toxicology. 2nd ed. London: Bailliere Tindall, 1981., p. 134
... Dinitro compounds are persistent yellow dye-stuffs, staining exposed skin, hair, wool, fur, and feathers a distinct yellow or orange color which remains obvious for weeks or even months afterwards, despite the action of water and weather. Such staining provides evidence of at least external contact with the chemicals. /Dinitro cmpd/
Clarke, M. L., D. G. Harvey and D. J. Humphreys. Veterinary Toxicology. 2nd ed. London: Bailliere Tindall, 1981., p. 135
Metabolites of 2,6-Dinitrophenol: 2-amino-6-nitrophenol, 6-amino-2-nitrophenol, 2,6-diaminophenol /From table/
U.S. Dept Health & Human Services/Agency for Toxic Substances & Disease Registry; Toxicological Profile for Dinitrophenols p.168 (August 1995) Toxic Profiles 64. Available from, as of September 16, 2010: https://www.atsdr.cdc.gov/toxprofiles/index.asp
The half-lives for elimination of 2,6-dinitrophenol from the blood of mice and rats following a single large dose given intraperitoneally are 238 min and 210 min, respectively. /From table/
National Research Council. Drinking Water & Health, Volume 4. Washington, DC: National Academy Press, 1981., p. 234
... /Of/ the six isomeric dinitrophenols, those with nitro groups in the 2,4- and 3,4-positions stimulate oxygen consumption, whereas those with nitro groups in the 2,5-position do not. ...
Hayes, Wayland J., Jr. Pesticides Studied in Man. Baltimore/London: Williams and Wilkins, 1982., p. 463
All nitrophenols inhibit the microbial growth of natural aquatic systems because they uncouple the metabolic process of oxidative phosphorylation. /Nitrophenols/
Callahan, M.A., M.W. Slimak, N.W. Gabel, et al. Water-Related Environmental Fate of 129 Priority Pollutants. Volume I. EPA-440/4 79-029a. Washington, DC: U.S. Environmental Protection Agency, December 1979., p. 90-5
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