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  2. Phenylacetone - Wikipedia

    en.wikipedia.org/wiki/Phenylacetone

    Phenylacetone, also known as phenyl-2-propanone, is an organic compound with the chemical formula C 6 H 5 CH 2 COCH 3. It is a colorless oil that is soluble in organic solvents. It is a mono-substituted benzene derivative, consisting of an acetone attached to a phenyl group. As such, its systematic IUPAC name is 1-phenyl-2-propanone.

  3. 3,4-Methylenedioxyphenylpropan-2-one - Wikipedia

    en.wikipedia.org/wiki/3,4-Methylenedioxyphenyl...

    3,4-Methylenedioxyphenylpropan-2-one [1] or piperonyl methyl ketone (MDP2P or PMK) is a chemical compound consisting of a phenylacetone moiety substituted with a methylenedioxy functional group. It is commonly synthesized from either safrole (which, for comparison, is 3-[3,4-(methylenedioxy)phenyl]-2-propene) or its isomer isosafrole via ...

  4. How to make non-Newtonian liquid at home - AOL

    www.aol.com/.../21/diy-non-newtonian-liquid/24626004

    How to make non-Newtonian liquid: 2.5 cups of corn starch. 1 cup of water. 1 tablespoons of paint. After all ingredients are in a medium-sized mixing bowl, mix until well incorporated.

  5. Propiophenone - Wikipedia

    en.wikipedia.org/wiki/Propiophenone

    Propiophenone can be prepared by Friedel–Crafts reaction of propanoyl chloride and benzene.It is also prepared commercially by ketonization of benzoic acid and propionic acid over calcium acetate and alumina at 450–550 °C: [1]

  6. Cumene process - Wikipedia

    en.wikipedia.org/wiki/Cumene_process

    The cumene process (cumene-phenol process, Hock process) is an industrial process for synthesizing phenol and acetone from benzene and propylene. The term stems from cumene (isopropyl benzene), the intermediate material during the process. It was invented by R. Ūdris and P. Sergeyev in 1942 (USSR), [1] and independently by Heinrich Hock in ...

  7. 2,4-Dinitrophenylhydrazine - Wikipedia

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

    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. The solid is relatively sensitive to shock and friction. For this reason DNPH is usually handled as a wet powder. DNPH is a precursor to the drug Sivifene.

  8. Vinyl sulfone dyes - Wikipedia

    en.wikipedia.org/wiki/Vinyl_sulfone_dyes

    Vinyl sulfone dyes are reactive dyes comprising a vinyl sulfone group as reactive group (a fiber-bonding site of the reactive dye, "reactive hook"). Due to the relatively high reactivity of the vinyl sulfone group with water (residual moisture, air humidity), it is present in many commercial products in a protected form.

  9. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Pigment Yellow 97, a popular yellow colorant, is a hydrazone. [6]Hydrazones are the basis for various analyses of ketones and aldehydes. For example, dinitrophenylhydrazine coated onto a silica sorbent is the basis of an adsorption cartridge.