Isobutyl alcohol isobutanol

Isobutyl alcohol, isobutanol, 2-methyl-propanol, isopropyl carbinol, Me2CHCH20H. B.p. 108°C. Occurs in fusel-oil. Oxidized by potassium permanganate to 2-methyl-propanoic acid dehydrated by strong sulphuric acid to 2-methylpropene. [Pg.71]

ISOBUTYL ALCOHOL Isobutanol, Isopropylcarbinol, 2-Methyl- 1-propanol Flammable Liquid, III 1 3 0... [Pg.103]

Isobutyl Alcohol Isobutanol Isopropylcarbinol 2-Methyl-1-Propanol Fermentation Butyl Alcohol ... [Pg.249]

Isobutyl alcohol (Isobutanol) tert-Butyl alcohol (r rr-Butanol)... [Pg.284]

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]

Since alcohols and aldehydes are both formed in the Oxo reaction, acetals are formed (158). A recent paper by Macho (87) studied their further reactions under Oxo conditions, hydrolysis, hydrogenolysis, and thermal decomposition. Decomposition to saturated and unsaturated ethers increased with temperature from 12% at 120° to 41% at 170° C. Thus isobutyl ether, isobutenyl isobutyl ether, isobutanol, and isobutyraldehyde were identified by gas-phase chromatography among the reaction products of the decomposition of isobutyraldehyde diisobutyl acetal. [Pg.138]

Chemical Name isobutanol, isobutyl alcohol, 2-methyl-1-propanol... [Pg.255]

B.ll) (B.11) 1-Propanol,2-methyl, 2-methylpropan-l-ol, isobutanol, isobutyl alcohol, isopropyl carbinol 178-83-1] FEMA 2179... [Pg.99]

Bellstein Handbook Reference) AI3-01777 Alcool isobutyllque BRN 1730878 CCRIS 2300 EINECS 201-148-0 FEMA Number 2179 Fermentation butyl alcohol HSDB 49 Iso-butyl alcohol Isobutanol Isobutyl alcohol Isobutylalkohol Isopropyloarbinol NSC 5708 RCRA waste number U140 UN1212. Used as a solvent and chemical feedstock. Clear liquid mp = -107,8° bp B 108" d ° = 0.8018 soluble In H = 720 (5 g/100 ml), more soluble in organic solvents LDsO (rat orl) = 2,46 g/kg. BASF Corp. Eastman Cham. Co. Hoechst Celanese Neste UK Shell UK Shell Usines de Melle. [Pg.343]

Commonly used water-immiscible solvents in industrial-scale processes include alcohols (isobutanol, -butanol), ketones (particularly methyl isobutyl ketone), acetates (butyl, ethyl, isopropyl), hydrocarbons (toluene, hexanes), and methylene chloride. These solvents are inexpensive, readily available, and exhibit physical properties of low viscosity and density significantly different from water. Common water-miscible solvents are the alcohols (particularly methanol). For laboratory-scale processes, the selection is greater since selection is not constrained by economics. Craig and Sogn (16) have prepared an extensive compilation of such solvents. [Pg.61]

Isobutanethiol. See 2-Methyl-1-propanethiol Isobutanoic acid. See Isobutyric acid isobutanol HP, Isobutanol. See Isobutyl alcohol Isobutanolamine Isobutanol-2 amine. See Aminomethyl propanol Isobutene. See Isobutylene Isobutene homopolymer Isobutene polymer. See Polyisobutene Isobutene trimer. See Triisobutylene Isobutenol. See Methallyl alcohol Isobutenyl chloride. See 3-Chloro-2-methylpropene... [Pg.2197]

Ucar Ethanol. See Alcohol Ucar Ethyl Acetate. See Ethyl acetate Ucar 2-Ethylhexanol. See 2-Ethylhexanol Ucar Filmer IBT. See 2,2,4-Trimethyl-1,3-pentanediol isobutyrate Ucar Isobutanol. See Isobutyl alcohol Ucar Isobutyl Acetate. See Isobutyl acetate Ucar Isophorone. See Isophorone Ucar Isopropanol. See Isopropyl alcohol Ucar Isopropyl Acetate. See Isopropyl acetate Ucar Latex 100. See Styrene/acrylates copolymer... [Pg.4622]

Choline bicarbonate DuCoa Choline Bicarbonate 78-78-4 Isopentane 78-79-5 Isoprene 78-81-9 Isobutylamine 78-82-0 Isobutyronitrile 78-83-1 Isobutanol HP Isobutyl alcohol Ucar Isobutanol 78-84-2... [Pg.6061]

Tetrahydrolinalool 201-134-4 Linalool Linalool 95 Linalool 925 201-137-0 Choline bicarbonate DuCoa Choline Bicarbonate 201-142-8 Isopentane 201-143-1 Isoprene 201-145-4 Isobutylamine 201-147-5 Isobutyronitrile 201-148-0 Isobutanol HP Isobutyl alcohol Ucar Isobutanol 201-149-6... [Pg.6706]

CH3.CH(CH3) CH3 2-methyl propane (isobutane) Primary CH3-CH(CH3) CH20H 2-methylpropan-l-ol (isobutyl alcohol or isobutanol)... [Pg.39]

Alcohols that contain more than two carbons are known as higher alcohols, or fusel oils. Isobutanol, n-propanol, isoamyl alcohol, and active amyl alcohol are produced in various proportions by various yeasts including Candida, Hansenula, Pichia, and Saccharomyces (Rankine, 1967 Edwards et al., 1990 Holloway and Subden, 1991 Webster et al., 1993 Lambrechts and Pretorius, 2000) and, potentially, play an important role in the sensory character of wine (Rankine, 1967). Sensory descriptors that are commonly used to describe higher alcohols include fusel (butanol), alcoholic (isobutyl alcohol), marzipan (active amyl alcohol and isoamyl alcohols), and floral or rose (phenethyl alcohol) (Lambrechts and Pretorius, 2000). [Pg.26]

ISOBUTYL ALCOHOL (CHj,CHCH,OH Isobutanol, IBa, 2-Methyl-l propanol, Isopropylcarblnol Strong oxidizers S2 1.2 (212T) 10,9 (2irn... [Pg.223]

Methylpropan-l-ol, known as isobutyl alcohol or isobutanol (resulting from valine via 2-oxoisovalerate) and 3-methyl-... [Pg.523]

Iron Vrtnol Isobutanol Isobutyl Alcohol Iso-Octane Isopropanpi... [Pg.830]

Formation of alcohol names must be carried out systematically. Propan-2-ol is correct isopropanol is incorrect because there is no parent isopropane from which this name can be derived isopropyl alcohol is a correct alternative, because there is a radical isopropyl CHMe2— (sodium isopropoxide is similarly correct). Moreover, though there is isobutane, isobutanol is ambiguous whereas isobutyl alcohol is specific (from the radical CHMc2 CH2—). [Pg.80]

Isobutanolamine Isobutanol-2 amine. See Aminomethyi propanol Isobutene homopolymer Isobutene polymer. See Polyisobutene Isobutyl adipate. See Diisobutyl adipate Isobutyl alcohol... [Pg.2164]

The proper choice of catalysts for the vapor phase hydration of olefins under pressure to form alcohols is a very important factor. Apparently, catalysts active in promoting the hydration reaction are likewise active toward promotion of the undesirable polymerization reactions since this latter reaction often proceeds at a more rapid rate than that of alcohol formation as evidenced by the high yields of polymers and low yields of alcohols. The use of catalysts to lower the temperature for the reaction is necessitated by the fact that as the temperature is increased to obtain more favorable rates, the equilibrium conversion to alcohol becomes lower, and the tendency to polymerize is increased. Also, the catalyst must not promote dehydrogenation of the alcohol to form hydrogen and aldehyde since at the temperature of operation the equilibrium is very favorable for this reaction as has been pointed out in a previous chapter. Thus, the reaction, isobutanol = isobutyl aldehyde -f hydrogen has an equilibrium constant corresponding to about 72 per cent decomposition at 450° C even with 100 atmospheres of hydrogen pressure. [Pg.223]

Heteropolyacids contain 10, 11, or 12 molybdenum atoms per phosphorus atom. Indirect methods for the determination of phosphate are given in Figure 97. The most suitable organic solvents for extracting heteropolyacids are oxygen-containing solvents such as alcohols (n-butanol, isobutanol, hexanol, heptanol), ketones (MIBK), and esters (isobutyl acetate, butyl acetate). [Pg.139]

A - 1,1-diethoxyrethane (acetal) B - Acetaldehyde C - Acetone D - Benzene E - Cyclohexane F - Methanol G -Butan-2-one (methyl ethyl ketone) H - 4-methylpentan-2-one (methyl isobutyl ketone) I - Propanol J -Propan-2-ol K - Butanol L - Butan-2-ol M - 2-methylpropanol (isobutanol) N - Furan-2-carbaldehyde (furfural) O - 2-methylpropan-2-ol (1,1-dimethyl alcohol) P - 2-methylbutan-2-ol Q - Pentan-2-ol R - Pentanol S - Hexanol T - Heptan-2-ol U - Hexan-2-ol V - Hexan-3-ol... [Pg.994]

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