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It is the N-ethyl analog of 1,3-benzodioxolylpentanamine (BDP; K). Ethyl-K was first synthesized by Alexander Shulgin. In his book PiHKAL ("Phenethylamines i Have Known And Loved"), the minimum dosage is listed as 40 mg and the duration is unknown. [1] [2] Very little is known about the pharmacology, pharmacokinetics, effects, and toxicity of ...
1-Aminopentane is an organic compound with the formula CH 3 (CH 2) 4 NH 2. It is used as a solvent , as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers , and pharmaceutical products, [ 1 ] and as a flavoring agent .
Ethyl-[2-[2-(ethyl-dimethyl-ammonio)ethyl-methyl-amino]ethyl]-dimethyl-ammonium. CAS Number: ... C 13 H 33 N 3: Molar mass: 231.428 g·mol −1: 3D model ...
N-Ethylpentylone (β-keto-ethylbenzodioxolylpentanamine, βk-ethyl-K, βk-EBDP, ephylone) is a substituted cathinone and stimulant drug which was developed in the 1960s. [2] [3] It has been reported as a novel designer drug in several countries including the United Kingdom, [4] South Africa, [5] New Zealand, [6] the United States, [7] and ...
3-Methyl-2-pentanone (methyl sec-butyl ketone) is an aliphatic ketone and isomer of 2-hexanone. [2] References This page was last edited on 17 November 2024, at 23: ...
Ethylnaphthylaminopropane (ENAP; developmental code name PAL-1045) is a monoamine releasing agent (MRA) of the amphetamine and naphthylaminopropane families that is related to naphthylaminopropane (NAP; PAL-287) and methamnetamine (MNAP; PAL-1046).
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Like other simple aliphatic amines, ethylamine is a weak base: the pK a of [CH 3 CH 2 NH 3] + has been determined to be 10.8 [8] [9] Ethylamine undergoes the reactions anticipated for a primary alkyl amine, such as acylation and protonation. Reaction with sulfuryl chloride followed by oxidation of the sulfonamide give diethyldiazene, EtN=NEt. [10]