Short description:


  • Reference FOB pretium:
    US $ 1,389
    / Ton
  • Portus:SINARUM
  • Terms:L / c, T / T, Western Unionis
  • CAS:78-93-3
  • Product Detail

    Product Tags

    Product Name:Methyl ethyl ketone

    Molecular format:C4h8o

    CAS non:78-93-3

    Product Molecular structuram:

    Methyl ethyl ketone

    Specification:

    Item

    Unitas

    Valor

    Pudicitia

    %

    99.8min

    Colo

    APHA

    8max

    Acidum valorem (ut acetate acidum)

    %

    0.002MAX

    humor

    %

    0.03max

    Species

    -

    SCRUTUM

     

    Eget proprietatibus:

    Methyl ethyl ketone est susceptibilis ad variis motus propter suam carbonyl coetus et activae hydrogenii adjacent ad carbonyl coetus. Condensatio occurs cum hydrochloric acidum aut sodium hydroxide ad producendum 3,4-Dimethyl, III-hexen-II-unum aut III-methyl-III-hepten-V-unum. Cum expositae solis diu, ethane, acetic acidum et condensationem products produci. Generate Draceyl cum oxidized cum nitric acidum. Cum oxidized cum fortis oxidizing agentia ut Chromic acidum, acetic acidum generatur. Butanone est relative firmum ad calorem, et scelerisque CISTRUM ad altius temperaturis producit enone seu methyl enone. Cum Condensed cum Aliphatic aut aromaticum aldehydes, altum M. Weight Ketones, Cyclic Composita, Ketone Condensia et Resinam producuntur. Exempli gratia, condensatio cum formaldehyde in conspectu Domini sodium hydroxide primo producit II-methyl-I-butanol-III-unum, sequitur siccitatibus ad methacrylatone.
    Resinificatio occurs super nuditate solis aut UV lux. Condensacio cum phenol cedit 2,2-bis (IV-hydroxyphen) butane. Reacts cum aliphatic esters in praesentia a basic catalyst ad producendum β-diketones. Acylation cum acidic anhydride in conspectu de acidic catalyst ad formam β-diketones. Reacts cum hydrogenii cyanide ad formare cyanohydrin. Reacts cum ammonia ad formare ketopiperidine derivationes. Et α-hydrogenium atom de Butanone est libenter substituatur cum hogalos ad formare variis halogenated KETTONES, ut III-Chloro-II-butanone per commercium cum CHLORUM. 2,4-dinitrophendrazine cum 2,4-dinitrophendhylydrazine producit flavo-2,4-dinitrophendhylydrazone.

    Butanone

     

    Application:

    Methyl ethyl ketone (II-butanone, ethyl ketone, methyl acetone) est organicum solvendo relative humilis toxicity, quae in multis applications. Hoc est in industriae et commercial products ut solvendo ad adhesives, depingit et purgatio agentibus et quasi de-crescis solvendo. A naturalis pars quaedam cibis, methyl ethyl ketone potest dimisit in environment per Volcanoes et silva Fires.it adhibetur in themanufacture de Smokeless pulveris et colore syntheticum, ut solvente, et insurma coating. Est etiam usus est ut a flavoringsubstance in cibo.

    MEK adhibetur ut solvendo pro variis coating systems, exempli gratia, Vinyl, adhesives, nitrocellulose et acrylic coatings. Est usus in Poena Remitters, lacquers, Varnishes, imbre pingit, sealers, glues, magnetica tapes, printing inks, Rosins, Purgato solutions, et polymerization. Non est in aliis dolor products, exempli gratia, familia et amat in cements et lignum, saturitatem products. MEK adhibetur in dewaxing lubricating olea, quod degreasing of metallorum, in productionem in synthetica Leathers, transparent charta et aluminium ffoyle, et sicut chemical medium et aluminium ffoyle, et quasi eget medium et catalyst. Est extractionem solvendo in processus of windeststuffs et cibum ingredientia. Mek potest etiam esse ad sterilitatem chirurgicam et dentalis apparatu.
    In addition ad suum fabricantium, environmental fontes de Mek includit exhauriunt a jet et internum combustione machinas, et industriae actionibus ut gasification de carbo. Non est in substantial amounts in Tabaci fumus. Mek est produci biologicam et iam identified as a uber of microbial metabolism. Hoc etiam in plantis, animal pheromones et animal textuum, et MEK est verisimile a minor uber of normalis mammalian metabolismus. Est firmum sub Ordinarius condiciones sed potest formare peroxides in longum differentur repono; Hi ut explosivae.


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