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  2. 2,4-Dinitrophenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine

    Melting point: 198 to 202 °C (388 to 396 °F; 471 to 475 K) dec. ... 2,4-Dinitrophenylhydrazine ... orange or red precipitate of the dinitrophenylhydrazone.

  3. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    R 2 C=N−NR' 2 + H 2 O → R 2 C=O + H 2 N−NR' 2. Alkyl hydrazones are 10 2 - to 10 3-fold more sensitive to hydrolysis than analogous oximes. [10] When derived from hydrazine itself, hydrazones condense with a second equivalent of a carbonyl to give azines: [11] R 2 C=N−NH 2 + R 2 C=O → R 2 C=N−N=CR 2 + H 2 O. Hydrazones are ...

  4. Derivative (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Derivative_(chemistry)

    For example, melting point (MP) analysis can assist in identification of many organic compounds. A crystalline derivative may be prepared, such as a semicarbazone or 2,4-dinitrophenylhydrazone (derived from aldehydes or ketones ), as a simple way of verifying the identity of the original compound, assuming that a table of derivative MP values ...

  5. 2,4-Dinitrophenol - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenol

    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 ...

  6. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon groups. [1]

  7. Derivatization - Wikipedia

    en.wikipedia.org/wiki/Derivatization

    These products may be purified by recrystallization, and their melting points taken. An example is the formation of 2,4-dinitrophenylhydrazones from ketones and 2,4-dinitrophenylhydrazine . By consulting an appropriate reference table such as in Vogel's, the identity of the starting material may be deduced.

  8. 2,4-Dinitrotoluene - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrotoluene

    C 7 H 6 N 2 O 4: Molar mass: 182.134 g/mol Appearance Pale yellow to orange crystalline solid Density: 1.52 g/cm 3 [1] Melting point: 70 °C (158 °F; 343 K) [1] Boiling point: Decomposes at 250–300 °C [1] Vapor pressure: 1.47X10-4 mm Hg @ 22 C [2] Hazards Occupational safety and health (OHS/OSH):

  9. 2,4-Dichlorophenoxyacetic acid - Wikipedia

    en.wikipedia.org/wiki/2,4-Dichlorophenoxyacetic_acid

    2,4-Dichlorophenoxyacetic acid is an organic compound with the chemical formula Cl 2 C 6 H 3 OCH 2 CO 2 H.It is usually referred to by its ISO common name 2,4-D. [4] It is a systemic herbicide that kills most broadleaf weeds by causing uncontrolled growth, but most grasses such as cereals, lawn turf, and grassland are relatively unaffected.