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N-Butanol butyl alcohol

Butanol, see sec-Butyl alcohol n-Butanol, see 1-Butanol n-Butan-l-ol, see 1-Butanol s-Butanol, see sec-Butyl alcohol sec-Butanol, see sec-Butyl alcohol f-Butanol, see ferf-Butyl alcohol ferf-Butanol, see ferf-Butyl alcohol Butan-l-ol, see 1-Butanol Butan-2-ol, see sec-Butyl alcohol... [Pg.1466]

Butyl alcohol, n-butanol Butyl alcohol, n-butanol Calcium chloride, saturated Diesel... [Pg.1195]

Butyl Alcohol n-butanol 23 365 8 Satisfactory 1 year good appearance 0.34 Barex 210 BP Chemicals Specimen 6 oz bottles, capped, per method PT-60, 50% Relative Humidity... [Pg.156]

Butyl Alcohol n-butanol 100 23 28 7 Very slight clouding/discoloration expected life months to years Tyril Dow Chemical Specimen In accordance with ASTM D543-84... [Pg.2941]

Butyl Alcohol n-butanol 20 0-365 8 Resistant for months Polystyrol 456M Monsanto Specimen Uncolored, unstressed... [Pg.3156]

Butyl Alcohol n-butanol 23 2 8 No change in exterior lupiace AV60 Mitsubishi Gas Chemical... [Pg.610]

CH3CH2CH2CH20H 1-Butanol Butyl alcohol, n-butanol 118 Perfumery, extraction of essential oils. Water soluble. [Pg.86]

Substitutive name Functional class names 1 Butanol n Butyl alcohol or butyl alcohol 2 Butanol sec Butyl alcohol or 1 methylpropyl alcohol... [Pg.1205]

Methanol, ethanol, isopropylalcohol, n-propylalcohol, ferf-butyl alcohol, 2-butanol, 2-methyl-l-propanol, 1-butanol, 2-pentanol. 2-methyl-l-butanol, 1-pentanol... [Pg.36]

Synonyms AI3-00405 BRN 0969148 1-BuOH Butan-l-ol /3-Butan-l-ol /3-Butanol Butyl alcohol 1-Butyl alcohol n-Butyl alcohol Butyl hydroxide Butyric alcohol n-Butyric alcohol CCRIS 4321 CCS 203 EINECS 200-752-6 EINECS 238-128-6 FEMA No. 2178 Hemostyp 1-Hydroxybutane Methylolpropane NA 1120 NBA NSC 62782 Propyl carbinol Propylmeth-anol RCRA waste number U031 UN 1120. [Pg.206]

Still in the forties, butyl benzyl phthalate (BBP) was introduced by Monsanto Co. This ester is based on the monohydric alcohol n-butanol, but the benzyl group is derived from benzyl chloride rather then benzyl alcohol. This route was selected to make possible manufacture of pure coester which showed a better balance of properties than if made from the two alcohols. BBP was destined to make its mark in PVC, particularly in the flooring industry. [Pg.187]

Many anhydrous metal halides will form alcoholates if the presence of water is avoided during the preparations. The reactions of alcohols with vanadium trichloride were originally thought,1 to produce hexaalcoholates, but subsequent work cast some doubt on this.23 In a recent publication4 it was established that the species formed in solution by treating vanadium trichloride with methanol, ethanol, n- and z-propyl alcohol (1- and 2-propanol), n-, i-, and s-butyl alcohol (1-butanol, 2-mothyl-l-propanol, and 2-butanol), and cyclohexanol are of the type [V(R0H)4C12]C1 in each ease. In some cases the species precipitated from the above solutions have the same structural type,... [Pg.177]

The author selected the system containing salt which is not dissolved with other components but only with a particular component of a solvent mixture as a system with which the phenomenon of preferential solvate can be understood easily. Calcium chloride is dissolved with alcohol but it is not dissolved well with ester. Thus, calcium chloride forms a preferential solvate with alcohol and does not with ester. For the component system which consists of calcium chloride, alcohol, and ester, the author selected the following three systems for which vapor-liquid equibrium relations have been measured methanol-ethyl acetate-calcium chloride (I) methyl acetate-methanol-calcium chloride (3) and n-butyl acetate-n-butanol-calcium chloride (3). [Pg.36]

B) n-Butyl Bromide (M.). Enter in your notebook the calculated amounts of alcohol, hydrobromic acid, and sulfuric acid required for the preparation of n-butyl bromide, starting with 0.5 mole of n-butyl alcohol (1-butanol). If the sodium bromide method is to be used, calculate the amoxmts as shown in the introduction, and use 50 ml of water to dissolve the sodium bromide. Have the instructor approve the calculations. [Pg.136]

N-Butyl Alcohol Butanol Butyl Alcohol 1-Butanol 1 -Hydroxybutane Propylcarbinol... [Pg.232]

Propyl alcohol n-Butyl alcohol n-Heptyl alcohol 2-Propanol 2-Butanol 2-Pentanol ieri-Butyl alcohol. [Pg.431]

The mother liquor was extracted with n-Butyl alcohol,the butanol fraction (80g) was rechromatographed on silica gel using CHCb-MeOH-HaO as eluent. Two isospirostanol saponins (gracillin and zingibermiin A) and two fiirostanol saponins (protogracillin and protozingiberrin A) were also obtained. [Pg.231]

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]

Butan-2-ol. See 2-Butanol n-Butanol. See Butyl alcohol s-Butanol. See,2-Butanol t-Butanol. See t-Butyl alcohol 2-Butanol acetate. See s-Butyl acetate Butanol-2-amine 1-Butanol-2-amino-. See2-Aminobutanol... [Pg.586]

Bomyl butyrate Bornyl formate Bomyl isovalerate Bornyl valerate p-Bourbonene 2-Butanol Butan-3-one-2-yl butyrate Butter acids Butter esters n-Butyl acetate Butyl acetoacetate Butyl alcohol n-Butylamine Butyl anthranilate Butyl butyrate Butyl butyryl lactate a-Butylcinnamaldehyde Butyl cinnamate Butyl 2-decenoate Butyl ethyl malonate... [Pg.5282]

In this experiment, you will compare the relative nucleophilidties of chloride ions and bromide ions toward each of the following alcohols 1-butanol (n-butyl alcohol), 2-butanol (scc-butyl alcohol), and 2-methyl-2-propanol (f-butyl alcohol). The two nucleophiles will be present at the same time in each reaction, in equimolar concentrations, and they will be competing for substrate. A protic solvent is used in these reactions. [Pg.191]

Try this test with 1-butanol (n-butyl alcohol), 2-butanol (scc-butyl alcohol), and 2-methyl-2-propanol (f-butyl alcohol). [Pg.494]

There are four isomers of butanol n-butanol, isobutanol, 2-butanol, and tert butyl alcohol. The butanol produced in fementation is n-butanol. Water and n-butanol form a heterogeneous azeotrope at atmospheric pressure and 364.6 K with a composition of 76.33 mol% water. [Pg.201]

Chemical Designations — Synonyms Butanol Butyl Alcohol 1-Butanol 1-Hydroxybutane n-Propylcarbinol Chemical Formula CH3(CH2)2CH20H. Observable Characteristics — Physical State (as normally shipped) Liquid Color Colorless Odor Alcohol-like pungent strong characteristic mildly alcoholic, non residual. Physical and Chemical Properties — Physical State at 15 C and 1 atm. Liquid Molecular Weight 74.12 Boiling Point at 1 atm. 243.9,... [Pg.42]

See other pages where N-Butanol butyl alcohol is mentioned: [Pg.228]    [Pg.469]    [Pg.1869]    [Pg.2077]    [Pg.2381]    [Pg.2471]    [Pg.3066]    [Pg.228]    [Pg.469]    [Pg.1869]    [Pg.2077]    [Pg.2381]    [Pg.2471]    [Pg.3066]    [Pg.97]    [Pg.372]    [Pg.7]    [Pg.258]    [Pg.245]    [Pg.245]    [Pg.107]    [Pg.20]    [Pg.237]    [Pg.124]    [Pg.421]    [Pg.124]    [Pg.139]    [Pg.202]    [Pg.195]    [Pg.231]    [Pg.450]   
See also in sourсe #XX -- [ Pg.141 ]



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