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Methyl iodide isobutyl ketone

Methyl ethyl ketone peroxide Methyl formate Methyl iodide Methyl isoamyl acetate Methyl isobutyl carbinol Methyl isobutyl ketone (hexone)... [Pg.368]

To 1,320 parts of methyl isobutyl ketone is added 570 parts of 3-diethylamino-1 -cyclohexyl-1 -phenylpropanol-1 (2 mols) and the mixture is stirred until solution is complete. Then 500 parts (3.2 mols or 60% excess) of ethyl iodide are added. After filtration, the filtrate is diluted with an additional 300 parts of methyl isobutyl ketone and the solution is then heated at the reflux temperature (108°C to 110°C) for 9 hours. After cooling to 0°C, the precipitated solid material is removed by filtration, washed with isopropyl acetate and dried. Approximately 111 parts of product is obtained or a yield of 88.6% based on as-is starting material or 92.5% based on real starting material. [Pg.1537]

Similarly to quantitative determination of high surfactant concentrations, many alternative methods have been proposed for the quantitative determination of low surfactant concentrations. Tsuji et al. [270] developed a potentio-metric method for the microdetermination of anionic surfactants that was applied to the analysis of 5-100 ppm of sodium dodecyl sulfate and 1-10 ppm of sodium dodecyl ether (2.9 EO) sulfate. This method is based on the inhibitory effect of anionic surfactants on the enzyme system cholinesterase-butyryl-thiocholine iodide. A constant current is applied across two platinum plate electrodes immersed in a solution containing butyrylthiocholine and surfactant. Since cholinesterase produces enzymatic hydrolysis of the substrate, the decrease in the initial velocity of the hydrolysis caused by the surfactant corresponds to its concentration. Amounts up to 60 pg of alcohol sulfate can be spectrometrically determined with acridine orange by extraction of the ion pair with a mixture 3 1 (v/v) of benzene/methyl isobutyl ketone [271]. [Pg.282]

Indenopyrene, see Indeno[l,2,3-crf pyrene l//-Indole, see Indole Indolene, see Indoline Inexit, see Lindane Inhibisol, see 1,1,1-Trichloroethane Insecticide 497, see Dieldrin Insecticide 4049, see Malathion Insectophene, see a-Endosulfan, p-Endosulfan Intox 8, see Chlordane Inverton 245, see 2,4,5-T lodomethane, see Methyl iodide IP, see Indeno[l,2,3-crf pyrene IP3, see Isoamyl alcohol Ipaner, see 2,4-D IPE, see Isopropyl ether IPH, see Phenol Ipersan, see Trifluralin Iphanon, see Camphor Isceon 11, see Trichlorofluoromethane Isceon 122, see Dichlorodifluoromethane Iscobrome, see Methyl bromide Iscobrome D, see Ethylene dibromide Isoacetophorone, see Isophorone a-Isoamylene, see 3-Methyl-l-butene Isoamyl ethanoate, see Isoamyl acetate Isoamylhydride, see 2-Methylbutane Isoamylol, see Isoamyl alcohol Isobac, see 2,4-Dichlorophenol Isobenzofuran-l,3-dione, see Phthalic anhydride 1,3-Isobenzofurandione, see Phthalic anhydride IsoBuAc, see Isobutyl acetate IsoBuBz, see Isobutylbenzene Isobutane, see 2-Methylpropane Isobutanol, see Isobutyl alcohol Isobutene, see 2-Methylpropene Isobutenyl methyl ketone, see Mesityl oxide Isobutyl carbinol, see Isoamyl alcohol Isobutylene, see 2-Methylpropene Isobutylethylene, see 4-Methyl-l-pentene Isobutyl ketone, see Diisobutyl ketone Isobutyl methyl ketone, see 4-Methyl-2-pentanone Isobutyltrimethylmethane, see 2,2,4-Trimethylpentane Isocumene, see Propylbenzene Isocyanatomethane, see Methyl isocyanate Isocyanic acid, methyl ester, see Methyl isocyanate Isocyanic acid, methylphenylene ester, see 2,4-Toluene-diisocyanate... [Pg.1492]

Mercury compounds Methanol Methoxychlor Methyl bromide Methyl chloride Methyl ethyl ketone Methyl hydrazine Methyl iodide Methyl isobutyl ketone Methyl isocyanate Methyl methacrylate Methyl f-butyl ether... [Pg.68]

Use Chemicals (methyl isobutyl ketone methyl isobutyl carbinol methyl methacrylate bisphenol-A) paint, varnish, and lacquer solvent cellulose acetate, especially as spinning solvent to clean and dry parts of precision equipment solvent for potassium iodide and permanganate delusterant for cellulose acetate fibers specification testing of vulcanized rubber products. [Pg.9]

Methylindole, 22, 94 Methyl iodide, 28, 6 Methyl isobutyl ketone, 28, 45 Methyl isothiocyanate, 21, 81, 83 Methyl isothiourea, reaction of sulfate... [Pg.58]

Alkylation (R" = alkyl or substituted alkyl) is most satisfactorily accomplished with active halogen compounds such as allyl, benzyl, and propargyl halides, but a-halo ketones, esters, and nitriles can also be used.467,474 Treating l-(l-cyclohexenyl)pyrrolidine with allyl bromide in the presence of /V-ethyl-dicyclohexylamine as base leads to introduction of two allyl groups, i.e., formation of 2,6-diallylcyclohexanone.475 Arylation can be effected by, for example, l-chloro-2,4-dinitrobenzene (R" = 2,4-dinitrophenyl).476 A-Isobutyl-fl-butylamine477 and pyrrolidine478 have been recommended as amine components for C-alkylation by simple alkyl halides such as ethyl and methyl iodides. The following two examples are illustrative ... [Pg.928]

Methyl iodide (iodomethane) [74-88-4] Methyl isobutyl ketone (hexane) [108-10-1] Methyl isocyanate [624-83-9]... [Pg.913]

Methyl iodide Methyl isobutyl ketone Methyl isocyanate Methyl morpholine oxide Methyinaphthalene... [Pg.5496]

If the water sample contains Ge, Te, Co, Ni, Cu, Cr, V, fluoride, bromide or iodide in concentrations of 1 mg/1 or more, boron may be separated from these interfering substances by extraction with 2-ethyl-1,3-hexane-diol in methyl isobutyl ketone and subsequent reextraction with 0.5 m sodium hydroxide solution (see Section 3.5.1,4). [Pg.422]

Unless otherwise noted, acetone was the solvent. b Yield of deoxyiodo-sugar derivative. 0 Yield of sodium sulfonate. Yield by determination of sodium iodide consumed. Free iodine liberated. / Acetonylacetone. Corrected for solubility of sodium sulfonate in acetone. A Acetic anhydride. Isobutyl methyl ketone. [Pg.184]

A mixture of cyanuric iodide and 2-chloro-4,6-diiodo-l,3,5-triazine is formed by reaction of cyanuric chloride with hydrogen iodide at low temperature.139 Sodium iodide and cyanuric chloride also react in isobutyl methyl ketone to give cyanuric iodide in 83% yield.60... [Pg.754]


See other pages where Methyl iodide isobutyl ketone is mentioned: [Pg.165]    [Pg.273]    [Pg.67]    [Pg.154]    [Pg.636]    [Pg.212]    [Pg.901]    [Pg.1414]    [Pg.1774]    [Pg.7]    [Pg.594]    [Pg.560]    [Pg.273]    [Pg.273]    [Pg.353]    [Pg.127]    [Pg.469]    [Pg.1531]    [Pg.29]   
See also in sourсe #XX -- [ Pg.50 , Pg.123 ]




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Isobutyl

Isobutyl iodide

Isobutyl ketone

Methyl iodide

Methyl isobutyl ketone

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