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  1. en.wikipedia.org › wiki › AcetoneAcetone - Wikipedia

    Acetone, or propanone, is an organic compound with the formula (CH 3) 2 CO. It is the simplest and smallest ketone. It is a colourless, highly volatile and flammable liquid with a characteristic pungent odour. Acetone is miscible with water and serves as an important organic solvent in its own right, in

    • C₃H₆O
    • 58.080 g·mol−1
    • −94.7 °C (−138.5 °F; 178.5 K)
    • Miscible
  2. 144.5. 181.0. 214.5. —. Table data obtained from CRC Handbook of Chemistry and Physics 44th ed. Vapor pressure of acetone based on formula, P m m H g = 10 7.02447 − 1161.0 224 + T {\displaystyle \scriptstyle P_ {mmHg}=10^ {7.02447- {\frac {1161.0} {224+T}}}} from Lange's Handbook of Chemistry, 10th ed. vapor pressure of acetone (log scale ...

    • 20.7 ε 0 at 25°C
    • 26.2 dyn/cm at 0°23.7 dyn/cm at 20°C
    • 1.3561
  3. Acetone, or propanone, is an organic compound with the chemical formula (CH3)2CO. This clear, mobile, easy-to-burn liquid is the simplest example of the ketones. Acetone can be mixed with water. It is an important solvent, often to clean things in the laboratory. Common uses of acetone in the home are as the active ingredient in nail polish remover and as paint thinner.

    • 635.7K
    • 1466
    • 200-662-2
    • AL3150000
  4. Acetone were an American alternative rock band formed in 1992 in Los Angeles, California, United States, from the three core members of the group Spinout, formed in 1987. The group consisted of Mark Lightcap on guitar, Richie Lee on bass and Steve Hadley on drums. It disbanded after Lee committed suicide on July 23, 2001, aged 34. The group's influences included The Beach Boys, Gram Parsons and the Velvet Underground. Establishing themselves as an alternative rock group, they had also incorporat

    • Overview
    • History
    • Chemistry
    • Industrial uses
    • Use in improvised explosive devices

    Acetone peroxide is an organic peroxide and a primary explosive. It is produced by the reaction of acetone and hydrogen peroxide to yield a mixture of linear monomer and cyclic dimer, trimer, and tetramer forms. The dimer is known as diacetone diperoxide. The trimer is known as triacetone triperoxide or tri-cyclic acetone peroxide. Acetone peroxide takes the form of a white crystalline powder with a distinctive bleach-like odor or a fruit-like smell when pure, and can explode powerfully if subje

    Acetone peroxide was discovered in 1895 by the German chemist Richard Wolffenstein. Wolffenstein combined acetone and hydrogen peroxide, and then he allowed the mixture to stand for a week at room temperature, during which time a small quantity of crystals precipitated, which had a melting point of 97 °C. In 1899 Adolf von Baeyer and Victor Villiger described the first synthesis of the dimer and described use of acids for the synthesis of both peroxides. Baeyer and Villiger prepared the ...

    The chemical name acetone peroxide is most commonly used to refer to the cyclic trimer, the product of a reaction between two precursors, hydrogen peroxide and acetone, in an acid-catalyzed nucleophilic addition, although various further monomeric and dimeric forms are possible. Synthesis of tri-cyclic acetone peroxide. Specifically, two dimers, one cyclic (C6H12O4) and one open chain (C6H14O4), as well as an open chain monomer, can also be formed; under a particular set of conditions of reagent

    Ketone peroxides, including acetone peroxide and methyl ethyl ketone peroxide, find application as initiators for polymerization reactions, e.g., silicone or polyester resins, in the making of fiberglass-reinforced composites. For these uses, the peroxides are typically in the form of a dilute solution in an organic solvent; methyl ethyl ketone peroxide is more common for this purpose, as it is stable in storage. Acetone peroxide is used as a flour bleaching agent to bleach and "mature" flour. A

    TATP has been used in bomb and suicide attacks and in improvised explosive devices, including the London bombings on 7 July 2005, where four suicide bombers killed 52 people and injured more than 700. It was one of the explosives used by the "shoe bomber" Richard Reid in his 2001 failed shoe bomb attempt and was used by the suicide bombers in the November 2015 Paris attacks, 2016 Brussels bombings, Manchester Arena bombing, June 2017 Brussels attack, Parsons Green bombing, the Surabaya bombings,

    • 17088-37-8
    • 131.5 to 133 °C (dimer), 91 °C (trimer)
    • C₆H₁₂O₄ (dimer), C₉H₁₈O₆ (trimer), C₁₂H₂₄O₈ (tetramer)
    • Insoluble
  5. Acetone imine. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Acetone imine, or 2-propanimine is an organic compound and an imine with the chemical formula (CH 3) 2 CNH. It is a volatile and flammable liquid at room temperature. It is the simplest ketimine.

    • colorless liquid
    • 0.8 g cm−3 (25 °C)
    • C₃H₇N
    • 57.096 g·mol−1
  6. Acetone azine can be prepared from acetone and hydrazine: 2 (CH 3) 2 CO + N 2 H 4 → 2 H 2 O + [ (CH 3) 2 C=N] 2. It can also be produced from acetone (2 eq.), ammonia (2 eq.) and hydrogen peroxide (1 eq.). The first step is the formation of acetone imine, Me 2 C=NH; this is then oxidized by hydrogen peroxide through a complex mechanism to ...

    • 133 °C (271 °F; 406 K)
    • −125 °C (−193 °F; 148 K)
    • C₆H₁₂N₂
    • 112.17 g mol−1
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