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  2. Isopropylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Isopropylbenzylamine

    [citation needed] [dubious – discuss] The toxicity of N-isopropylbenzylamine has been studied as of 2022 and it has been found to produces toxicity via increasing nitric oxide in vitro. In this study, in vitro toxicity of N-isopropylbenzylamine and its toxicity-related targets were investigated in SN4741, SH-SY5Y or PC12 cell lines that model ...

  3. Methylenedioxybenzylamphetamine - Wikipedia

    en.wikipedia.org/wiki/Methylenedioxybenzyl...

    Methylenedioxybenzylamphetamine, abbreviated MDBZ, and systematically named 3,4-methylenedioxy-N-benzylamphetamine, is a psychedelic drug.It is the N-benzyl ...

  4. Propylamine - Wikipedia

    en.wikipedia.org/wiki/Propylamine

    Propylamine, also known as n-propylamine, is an amine with the chemical formula CH 3 (CH 2) 2 NH 2. [1] It is a colorless volatile liquid. [2] Propylamine is a weak base. Its K b (base dissociation constant) is 4.7 × 10 −4.

  5. Isopropylamine - Wikipedia

    en.wikipedia.org/wiki/Isopropylamine

    Isopropylamine can be obtained by reaction of isopropyl alcohol with ammonia in presence of a catalyst: [3] (CH 3) 2 CHOH + NH 3 → (CH 3) 2 CHNH 2 + H 2 O. Isopropylamine is a building block for the preparation of many herbicides and pesticides including atrazine, bentazon, glyphosate, imazapyr, ametryne, desmetryn, prometryn, pramitol, dipropetryn, propazine, fenamiphos, and iprodione. [3]

  6. Naphthylpropylaminopentane - Wikipedia

    en.wikipedia.org/wiki/Naphthylpropylaminopentane

    1-(2-Naphthyl)-2-propylaminopentane (NPAP), also known as 2-naphthyl-α,N-dipropylphenethylamine, is a monoaminergic activity enhancer (MAE) of the α-propylphenethylamine and naphthylaminopropane families related to phenylpropylaminopentane (PPAP). [1] It is the analogue of PPAP in which the phenyl ring has been replaced with a naphthalene ...

  7. Tribenzylamine - Wikipedia

    en.wikipedia.org/wiki/Tribenzylamine

    Tribenzylamine is an organic compound with the formula N(CH 2 C 6 H 5) 3. It is a symmetrical tertiary amine. It is of some historic interest as one of the first compounds produced by the Leuckart reaction. [1] The compound is a common target in the development of new synthetic methods, e.g. from benzyl alcohol. [2] [3]

  8. Substituted methylenedioxyphenethylamine - Wikipedia

    en.wikipedia.org/wiki/Substituted_methylenedioxy...

    Structure Chemical Name Abbreviations Other Names CAS number Ref 3,4-Methylenedioxyphenethylamine: MDPEA: Homopiperonylamine: 1484-85-1: 3,4-Methylenedioxy-N-methylphenethylamine

  9. Propyleneimine - Wikipedia

    en.wikipedia.org/wiki/Propyleneimine

    Propyleneimine (or propylene imine) is the organic compound with the formula CH 3 CH(NH)CH 2. It is a secondary amine and the smallest chiral aziridine (ring containing C 2 N). It is a flammable colorless liquid. Its derivatives, copolymers and oligomers, are of commercial interest. [4]