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  2. N,N-Dimethylphenethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Dimethylphenethylamine

    N,N-Dimethylphenethylamine (N,N-DMPEA) is a substituted phenethylamine that is used as a flavoring agent. It is an alkaloid that was first isolated from the orchid Pinalia jarensis. [1] [a] Its aroma is described as "sweet, fishy". It is mainly used in cereal, cheese, dairy products, fish, fruit and meat. [3]

  3. N,α-Diethylphenethylamine - Wikipedia

    en.wikipedia.org/wiki/N,α-Diethylphenethylamine

    N,α-Diethylphenethylamine (DEPEA or NADEP), also known as 2-ethylamino-1-phenylbutane (EAPB) is a stimulant drug of the phenylisobutylamine (α-ethylphenethylamine) group. It is a close chemical analog of methamphetamine , which has been sold as a designer drug .

  4. N,N-Dimethylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Dimethylethylamine

    N,N-Dimethylethylamine (DMEA), sometimes referred to as dimethylethylamine, is an organic compound with formula (CH 3) 2 NC 2 H 5.It is an industrial chemical that is mainly used in foundries as a catalyst for epoxy resins and polyurethane as well as sand core production.

  5. N,N-Dimethyl-2-chloro-2-phenylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Dimethyl-2-chloro-2...

    N,N-Dimethyl-2-chloro-2-phenylethylamine (DMEA) is chemical compound that irreversibly inhibits the enzyme acetylcholinesterase.DMEA can cause intoxication in cats, resulting in respiratory failure to death, and progressive damage to the central nervous system in rats. [1]

  6. N,N'-Dimethylethylenediamine - Wikipedia

    en.wikipedia.org/wiki/N,N'-Dimethylethylenediamine

    N,N'-Dimethylethylenediamine (DMEDA) is the organic compound with the formula (CH 3 NH) 2 C 2 H 4. It is a colorless liquid with a fishy odor. It features two secondary amine functional groups. Regarding its name, N and N' indicate that the methyl groups are attached to different nitrogen atoms.

  7. Diphenylamine - Wikipedia

    en.wikipedia.org/wiki/Diphenylamine

    2 C 6 H 5 NH 2 → (C 6 H 5) 2 NH + NH 3. It is a weak base, with a K b of 10 −14. With strong acids, it forms salts. For example, treatment with sulfuric acid gives the bisulfate [(C 6 H 5) 2 NH 2] + [HSO 4] − as a white or yellowish powder with m.p. 123-125 °C. [8] Diphenylamine undergoes various cyclisation reactions.

  8. Red Dye 3 Just Got Banned. These Are the Foods to Avoid If ...

    www.aol.com/red-dye-3-just-got-134800003.html

    The FDA determined that the data presented in a 2022 color additive petition show that this ingredient causes cancer in male laboratory rats exposed to high levels of FD&C Red No. 3 because of a ...

  9. N,N'-Di-2-butyl-1,4-phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/N,N'-Di-2-butyl-1,4...

    N,N′-Di-2-butyl-1,4-phenylenediamine is an aromatic amine used industrially as an antioxidant to prevent degradation of turbine oils, transformer oils, hydraulic fluids, lubricants, waxes, and greases. It is particularly effective for hydrocarbon products produced by cracking or pyrolysis, which are characterized by high alkene content.