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See-Butyl alcohol

Methyl ethyl ketone. Use the apparatus of Fig. Ill, 61, 1 but with a 500 ml. round-bottomed flask. Place 40 g. (50 ml.) of see. butyl alcohol, 100 ml. of water and a few fragments of porous porcelain in the flask. Dissolve 100 g. of sodium dichromate dihydrate in 125 ml. of water in a beaker and add very slowly and with constant sturing 80 ml. of concentrated sulphuric acid allow to cool, and transfer the resulting solution to the dropping funnel. Heat the flask on a wire gauze or in an air bath until the alcohol mixture commences to boil. Remove the flame and run in the dichromate solution slowly and at such a rate that the temperature... [Pg.336]

Propylene oxide [75-56-9] (methyloxirane, 1,2-epoxypropane) is a significant organic chemical used primarily as a reaction intermediate for production of polyether polyols, propylene glycol, alkanolamines (qv), glycol ethers, and many other useful products (see Glycols). Propylene oxide was first prepared in 1861 by Oser and first polymerized by Levene and Walti in 1927 (1). Propylene oxide is manufactured by two basic processes the traditional chlorohydrin process (see Chlorohydrins) and the hydroperoxide process, where either / fZ-butanol (see Butyl alcohols) or styrene (qv) is a co-product. Research continues in an effort to develop a direct oxidation process to be used commercially. [Pg.133]

A typical feed to a commercial process is a refinery stream or a steam cracker B—B stream (a stream from which butadiene has been removed by extraction and isobutylene by chemical reaction). The B—B stream is a mixture of 1-butene, 2-butene, butane, and isobutane. This feed is extracted with 75—85% sulfuric acid at 35—50°C to yield butyl hydrogen sulfate. This ester is diluted with water and stripped with steam to yield the alcohol. Both 1-butene and 2-butene give j -butyl alcohol. The sulfuric acid is generally concentrated and recycled (109) (see Butyl alcohols). [Pg.372]

The 0X0 process is not limited to simple olefins. The terrninal-to-branched ratio of products can be controlled by ligand addition (130). Butanol is produced from propylene and CO using a similar process (see Butyl alcohols). The catalyst in this case is Fe(CO) (131). [Pg.69]

However, the 0x0 reaction starting frompropylene and proceeding via the hydrogenation of butyraldehyde, has become the more widely employed commercial route for preparing / -butanol (see BuTYL ALCOHOLS Oxo PROCESS). [Pg.416]

Butanoic acid, 3-amino-, N-coco alkyl derivs. See Cocaminobutyric acid Butanoic acid, 3-oxo-, 2-[(1-oxo-2-propenyl) oxy] ethyl ester. See 2-(Acetoacetoxy) ethyl acrylate Butanol 1-Butanol Butan-1-ol. See Butyl alcohol... [Pg.1004]

Butyl alcohol. See 2-Butanol n-Bulyl alcohol. See Butyl alcohol s-Butyl alcohol. See 2-Butanol... [Pg.1008]

Butyl hydroxide. See Butyl alcohol t-Butyl hydroxide. See l-Bulyl alcohol... [Pg.1011]

Butyric acid lactone. See Butyrolactone Butyric alcohol. See Butyl alcohol Butyric aldehyde. See n-Butyraldehyde Butyrolactam y-Butyrolactam. See 2-Pyrrolidone... [Pg.1015]

Methylolpropane. See Butyl alcohol Methylolurea resin. See Urea-formaldehyde resin... [Pg.1203]

Butanoic acid propyl ester. See Propyl butyrate Butanoic acid, 1,7,7-trimethylbicyclo -2.2.1] hept-2-yl ester, endo. See Bomyl butyrate Butanoic anhydride. See Butyric anhydride Butanol 1-Butanol Butan-1-ol. See Butyl alcohol 2-Butanol... [Pg.585]

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]

Butyl hydroxide. See Butyl alcohol t-Butyl hydroxide. See t-Butyl alcohol Butyl hydroxyacetate n-Butyl hydroxyacetate. See Butyl glycolate Butyl hydroxyanisole 2(3)-t-Butyl-4-hydroxyanisole. See BHA... [Pg.624]

Eastman n-Butanol. See Butyl alcohol Eastman n-Butyl Acetate, Urethane Grade. [Pg.1595]

Methylolpentane. See 2-Ethyl-1-butanol Methylolpropane. See Butyl alcohol 2-Methyloltetrahydro-1,4-pyran. See... [Pg.2666]

Nacol 4-99. See Butyl alcohol Nacol 6-98. See Hexyl alcohol Nacol 8-98, Nacol 8-99. See Caprylic alcohol Nacol 10-97, Nacol 10-99. See Decyl alcohol Nacol 12-96, Nacol 12-99. See Lauryl alcohol Nacol 14-95, Nacol 14-98. See Myristyl alcohol... [Pg.2763]

Propyl caproate. See Propyl hexanoate Propyl caprylate. See Propyl octanoate Propyl carbinol. See Butyl alcohol N-Propylcarbinyl chloride. See Butyl chloride Propyl Cellosolve Propyi Ceiiosoive . See Ethylene glycol propyl ether Propyl chlorocarbonate n-Propyl chlorocarbonate Propyl chloroformate. See n-Propyl chloroformate n-Propyl chloroformate CAS 109-61-5 EINECS/ELINCS 203-687-7 UN 2740 (DOT)... [Pg.3735]

Propyl mercaptan. See Isopropyl mercaptan n-Propyl mercaptan. See Propyl mercaptan n-Propyl methanoate. See Propyl formate Propylmethanol. See Butyl alcohol... [Pg.3761]

Ucar Butanol. See Butyl alcohol Ucar Butyl Acetate. See n-Butyl acetate Ucar n-Butyl Propionate. See n-Butyl propionate... [Pg.4622]


See other pages where See-Butyl alcohol is mentioned: [Pg.382]    [Pg.79]    [Pg.131]    [Pg.407]    [Pg.79]    [Pg.50]    [Pg.79]    [Pg.1004]    [Pg.1146]    [Pg.1321]    [Pg.1325]    [Pg.142]    [Pg.360]    [Pg.2108]    [Pg.2185]    [Pg.196]    [Pg.362]    [Pg.962]    [Pg.243]    [Pg.74]    [Pg.910]    [Pg.935]   
See also in sourсe #XX -- [ Pg.5 , Pg.76 ]




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Butyl alcohol alcohols

Butyl alcohol—

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