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Pentyl alcohol

C5H120 PENTYL-ALCOHOL -305.155 5.0637E-01 4.5232E-05 -149.75 270 C6H12 METHYLCYCLO- -110.437 4.7401 E-01 4.9123E-05 35,77... [Pg.379]

Ethyl ( , 7-1,3-pen tadiene-l-carbamate, 59,8 3-Ethyl-3-pentanol, 58, 25, 26, 27, 31 3-Ethyl-3-pentyl alcohol, 58, 78 3-Ethyl-3-pentyl fluoride, 58, 78... [Pg.117]

Pentanone, see Methyl n-propyl ketone 3- Pentanone, see Diethyl ketone Pentene, see Amylene n-Pentyl acetate, see n-Amyl acetate sec-Pentyl acetate, see sec-Amyl acetate Pentyl alcohol, see n-Amyl alcohol Pentyl amine, see n-Amylamine iso-Pentyl nitrite, see Amyl nitrite Peracetic acid (40% acetic acid 1.23 41... [Pg.129]

The most widely used complexing agents are alcohols (butanol, n-propyl alcohol and n-pentyl alcohol1). Schoch33 now recommends the use of Pen-tasol, a commercial mixture of pentyl alcohols, for the first precipitation, and 1-butanol for recrystallizations. For com (maize) starch, this avoids contamination of the amylopectin with an intermediate fraction which is sufficiently linear to be precipitated with Pentasol and yet has a degree of branching which prevents complex formation with butanol. [Pg.344]

DIMETHYL-l-PROPANOL tert-PENTYL-ALCOHOL 2-METHYL-1-BUTANOL... [Pg.37]

Pillai and Pines (84) found that neopentyl alcohol, mixed with 10% by weight of piperidine and passed over alumina prepared from aluminum isopropoxide, yielded 2-methyl-l-butene and 2-methyl-2-butene, in a maximum ratio of 3, and small amounts of 1,1-dimethylcyclo-propane. However, lert-pentyl alcohol yielded these two olefins in a maximum ratio of only 1.4, and none of the cyclopropane was produced (Table VI). Because of these facts a carbonium ion mechanism which is applicable to ferf-pentyl alcohol is not adequate to explain the rearrangement taking place during the dehydration of neopentyl alcohol,... [Pg.80]

Dehydration of Neopentyl Alcohol and terl-Pentyl Alcohols" over Alumina ... [Pg.80]

As a consequence of the wide choice of hydride reagents the classical methods such as reduction with sodium in ethanol almost fell into oblivion [579, 520]. Nevertheless some old reductions were resuscitated. Sodium di-thionite was found to be an effective reducing agent [262], and the reduction by alcohols [309] was modified to cut down on the temperature [755] or the time required [527], or to furnish chiral alcohols ( in good yields and excellent optical purity ) by using optically active pentyl alcohol and its aluminum salt [522]. Formation of chiral alcohols by reduction of pro-chiral ketones is... [Pg.107]

Hydrogenation of benzo[/]quinoline over Raney nickel at 150 °C and 70 atm gives l,2,3,4,7,8,9,10-octahydrobenzo[/]quinoline (52) as the main product, together with some m-l,2,3,4,4a,5,6,10b-octahydro isomer (53 Scheme 38). Use of sodium in pentyl alcohol gives the trans isomer of (53) together with (52) (64JOC1419). [Pg.328]

Pentanedial Solution 2,4-Pentanedione 1-Pentanethiol 1-Pentanol Pentek 1-Pentene Pentyl Acetates Pentyl Alcohol Sec-Pentyl Carbinol 1-Pentyl Chloride Pentyl Methyl Ketone Pentylsilicon Trichloride Peracetic Acid Percarbamide Perchloric Acid Perchloric Acid Solution... [Pg.74]

Ethylenedioxybutyl)-3-trichloro-acetamido 1 cyclohexene, 58, 9, 11 Ethylene, 1,1-diphenyl-, 56, 32 Ethylene glycol, 56, 44 Ethylene glycol, phenyl-, 55, 116 Ethylene, tetramethyl-, 56, 35 Ethyl-or-fluoro-l-naphthaleneacetate, 57, 73 Ethyl 2-fluoropropanoate, 57, 73 3-Ethylhexane, 58, 3, 4 3-ETHYL-1-HEXYNE, 58,1, 2, 3, 4 Ethyl levuhnates, 5-substituted, 58, 81 Fthyl nitrite, 58, 113, 115 Ethyl V-nitroso-A-fp-tolylsulfonylmethyl)-carbamate, 57, 96 3-Ethyl-3-pentanol, 58, 25, 26, 31 3-Ethyl-3-pentyl alcohol, 58, 78 3-Ethyl-3-pentyl fluoride, 58, 78 Ethyl A -(p-tolylsulfonylmethyl)carbamate, 57, 95... [Pg.184]

Toxicology and Carcinogenesis Studies of Pentyl Alcohol, National Toxicology Program, U.S. Department of Health and Human Services, Washington, D.C., May 1989. [Pg.63]

Silica A 2096 tm-pentyl-alcohol/ hexane B hexane g xanthophylls 50... [Pg.829]

Ethyl alcohol, CH3CH2OH, is miscible with water at 20°C, but pentyl alcohol, CH3CH2CH2CH2CH2OH, is soluble in water only to the extent of 2.7 g/100 mL. Explain. [Pg.465]

Pentyl alcohol (Problem 11.42) is miscible with octane, CgHi8, but methyl alcohol, CH3OH, is insoluble in octane. Explain. [Pg.465]

Cognate preparation. 2-ChIoro-2-methylbutane. Use 22 g (27 ml, 0.25 mol) of 2-methylbutan-2-ol (t-pentyl alcohol) and 65 ml of concentrated hydrochloric acid. Distil the chloride twice from a Claisen flask with fractionating side-arm or through a short column. Collect the 2-chloro-2-methylbutane at 83-85 °C the yield is 18 g (68%). Record the p.m.r. spectrum (CC14, TMS) and assign the signals which appear at 51.01 (t, 3H), 1.51 (s, 6H) and 1.73 (q, 2H) note the overlap of the latter two signals. [Pg.556]


See other pages where Pentyl alcohol is mentioned: [Pg.739]    [Pg.218]    [Pg.212]    [Pg.182]    [Pg.122]    [Pg.223]    [Pg.682]    [Pg.407]    [Pg.293]    [Pg.293]    [Pg.293]    [Pg.328]    [Pg.11]    [Pg.64]    [Pg.92]    [Pg.119]    [Pg.157]    [Pg.183]    [Pg.80]    [Pg.111]    [Pg.154]    [Pg.96]    [Pg.297]    [Pg.297]    [Pg.165]    [Pg.273]    [Pg.140]    [Pg.739]    [Pg.794]    [Pg.1304]    [Pg.1304]    [Pg.551]   
See also in sourсe #XX -- [ Pg.140 ]

See also in sourсe #XX -- [ Pg.506 ]




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