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An over-the-counter shampoo is a good place to start - we use an oatmeal-based Luvsome anti-itch dog shampoo and it's been a lifesaver. These DIY allergy pops are like a treat, and can be ...
1,3-Dimethylbutylamine (1,3-DMBA, dimethylbutylamine, DMBA, 4-amino-2-methylpentane, or AMP), is a stimulant drug structurally related to methylhexanamine where a butyl group replaces the pentyl group. The compound is an aliphatic amine.
3-Methylpentane is a branched alkane with the molecular formula C 6 H 14. It is a structural isomer of hexane composed of a methyl group bonded to the third carbon atom in a pentane chain. It is of similar structure to the isomeric 2-methylpentane , which has the methyl group located on the second carbon of the pentane chain.
2-Methylpentane, trivially known as isohexane, is a branched-chain alkane with the molecular formula C 6 H 14. It is a structural isomer of hexane composed of a methyl group bonded to the second carbon atom in a pentane chain.
2-Methylpentamethylenediamine is an organic compound part of the amine family with the formula H 2 NCH 2 CH 2 CH 2 CH(CH 3)CCH 2 NCH 2. A colorless liquid, this diamine is obtained by the hydrogenation of 2-methylglutaronitrile. [1] It is better known by the trade name "Dytek A". [2]
Shampoo lather in hair Bottles of shampoo and lotions manufactured in the early 20th century by the C.L. Hamilton Co. of Washington, D.C., United States. Shampoo (/ ʃ æ m ˈ p uː /) is a hair care product, typically in the form of a viscous liquid, that is formulated to be used for cleaning (scalp) hair.
N-Methyl-1,3-benzodioxolylpentanamine (MBDP; Methyl-K, UWA-091), also known as 3,4-methylenedioxy-α-propyl-N-methylphenethylamine, is a psychoactive drug of the phenethylamine chemical class. It is the N-methyl analogue of 1,3-benzodioxolylpentanamine (BDP; K). Methyl-K was first synthesized by Alexander Shulgin ("Sasha" Shulgin).
2-Methyl-3-pentanol (IUPAC name: 2-methylpentan-3-ol) is an organic chemical compound. It is a secondary alcohol [2] that is used as a fuel. [3] References
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