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2,4-Dinitrophenol (2,4-DNP or simply DNP) is an organic compound with the formula HOC 6 H 3 (NO 2) 2. It has been used in explosives manufacturing and as a pesticide and herbicide. In humans, DNP causes dose-dependent mitochondrial uncoupling , causing the rapid loss of ATP as heat and leading to uncontrolled hyperthermia —up to 44 °C (111 ...
2,4-dinitrophenol picric acid 2,4-Dinitrophenol (m.p. 83 °C) is a moderately strong acid (pK a = 4.89). 2,4,6-Trinitrophenol is better known as picric acid , which has a well-developed chemistry.
Dinitrophenols are chemical compounds which are nitro derivatives of phenol.. There are six isomers of dinitrophenol: Chemical structure of 2,4-Dinitrophenol. 2,3-Dinitrophenol; 2,4-Dinitrophenol
2,4-Dinitrophenylhydrazine (2,4-DNPH or DNPH) is the organic compound C 6 H 3 (NO 2) 2 NHNH 2. DNPH is a red to orange solid. It is a substituted hydrazine.
2,4-DNP can mean: 2,4-Dinitrophenol , a small organic molecule formerly marketed as a pharmaceutical "diet aid" 2,4-Dinitrophenylhydrazine , Brady's reagent, used in organic chemical analysis
A solution of 4-nitrophenol appears colorless below pH 5.4 and yellow above pH 7.5. [3] This color-changing property makes this compound useful as a pH indicator. The yellow color of the 4-nitrophenolate form (or 4-nitrophenoxide) is due to a maximum of absorbance at 405 nm (ε = 18.3 to 18.4 mM −1 cm −1 in strong alkali). [4]
2,3-Dinitrophenol This page was last edited on 7 September 2024, at 12:23 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
2,4-Dinitrotoluene (DNT) or dinitro is an organic compound with the formula C 7 H 6 N 2 O 4. This pale yellow crystalline solid is well known as a precursor to trinitrotoluene (TNT) but is mainly produced as a precursor to toluene diisocyanate .