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N-Butyl methyl ether

Methyl-n-butyl ether CsHi O 628284 88.150 1.7785E-105 -1.7157E-I-02... [Pg.216]

The formal isomerization enthalpies of methyl n-butyl ether to methyl terf-butyl ether and of di-n-butyl ether to n-butyl ferf-butyl ether are about —24kJmoU (Iq) and —26.5 kJmol (g), respectively. From these, and the experimental enthalpy of formation of di-ferf-butyl peroxide, the enthalpies of formation of di-n-butyl peroxide are ca —333 kJmol (Iq) and —288 kJmol (g), wildly divergent from the reported values. [Pg.151]

Methyl n-amyl carbinol. 247, 254 Methyl n-amyl ketone, 482 Methylaniline (mono), pure, from commercial methylaniline, 562, 570 P-Methylanthraquinone, 728, 740 Methyl benzoate, 780, 781 p-Methyl benzyl alcohol, 811,812 Methyl benzyl ketone, 727, 735 Methyl y-bromocrotonate, 926, 927 2-Methyl-2-butene, 239 Methyl n-butyl carbinol, 247,255 Methyl n-butyl ether, 314 Methyl n-butyl ketone, 475, 481 4-Methylcarbostyril, 855 p-Methylcinnamic acid, 719 4-Methylcoumarin, 853, 854 Methyl crotonate, 926, 927 Methylethylacetic acid, 354, 358 Methylethylethynyl carbinol, 468 Methyl ethyl ketone, 335, 336 purification of, 172 Methyl n-hexyl ether, 314 Methyl n-hexyl ketone, 335, 336 Methyl n-hexyl ketoxime, 348 Methyl hydrogen adipate, 938 Methyl hydrogen sebacate, 938,939 4-Methyl-7-hydroxycoumarin, 834 Methyl iodide, 287 Methyl isopropyl carbinol, 247,255 Methyl 4-keto-octanoate, 936... [Pg.1179]

Methyl-n-butyl ether CsHijO 628284 88.150 1.7785E+05 -1.7157E+02... [Pg.213]

METHYLBUTYI- ETHANOATE see IHO850 METHYL BUTYL ETHER see BRU780 METHYL n-BUTYL ETHER see BRU780 METHYL tert-BUTYL ETHER see MHV859 METHYL tert-BUTYL ETHER (DOT) see MHV859 3-METHYLBUTYL FORMATE see IHSOOO 3-METHYLBUTYL 2-HYDROXYBENZOATE see IMEOOO... [Pg.1769]

Again cleavage reactions can be followed by NMR spectroscopy as in the case of methyl n-butyl ether... [Pg.56]

The reaction of NO3 with methyl n-butyl ether has not been studied. On the basis of structure-activity relationships developed later in this chapter (section III-H), a rate coefficient of fe 2.5 x 10" cm molecule" s" is estimated at 298 K. [Pg.304]

Table lll-B-IO. Rate coefficients k = Ax e cm molecule s ) for reaction of OH with methyl n-butyl ether [CH30(CH2)3CH3]... [Pg.305]

III-B-4.3. Summary of the Atmospheric Fate of Methyl n-Butyl Ether, and... [Pg.306]

The atmospheric destruction of methyl n-butyl ether will occur primarily via reaction with OH, with NO3 and Cl-atoms potentially playing a role. The lifetime against OH attack is estimated to be about 8 h, for a daytime [OH] 2.5 x 10 molecule cm . ... [Pg.306]

The OH-initiated oxidation of methyl n-butyl ether has been studied in detail by Aschmann and Atkinson (1999a). Observed products, with molar yields in parentheses, were as follows methyl formate (51 11%), propanal (43 6%), butanal (4.5 1%), methyl butyrate ( 1.6%), and CH3C(0)CH2CH20CH3 and/or CH3CH2C(0)CH20CH3 (19 4%). Products with molecular weights of 118, 149, and 165, corresponding to five-carbon hydroxycarbonyls, nitrates, and hydroxynitrates, were also identified. [Pg.306]


See other pages where N-Butyl methyl ether is mentioned: [Pg.314]    [Pg.822]    [Pg.618]    [Pg.95]    [Pg.139]    [Pg.181]    [Pg.201]    [Pg.223]    [Pg.314]    [Pg.1091]    [Pg.314]    [Pg.618]    [Pg.65]    [Pg.92]    [Pg.136]    [Pg.178]    [Pg.198]    [Pg.220]    [Pg.238]    [Pg.569]    [Pg.80]    [Pg.314]    [Pg.289]    [Pg.278]    [Pg.314]    [Pg.99]    [Pg.143]    [Pg.185]    [Pg.205]    [Pg.220]    [Pg.227]    [Pg.409]    [Pg.18]    [Pg.304]   
See also in sourсe #XX -- [ Pg.314 ]

See also in sourсe #XX -- [ Pg.314 ]

See also in sourсe #XX -- [ Pg.314 ]

See also in sourсe #XX -- [ Pg.314 ]




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