Hemimellitene (1,2,3-TMB), in addition to pseudocumene (1,2,4-TMB) and mesitylene
(1,3,5-TMB), is one of TMB isomers.
Addition of nonpolar cosolvents, such as toluene, p-xylene, and mesitylene
, resulted in materials with enhanced gelation rates and enlarged pores.
Abdul-Latif, "Viscosities, densities, and speeds of sound of binary mixtures of benzene, toluene, o-xylene, m-xylene, p-xylene, and mesitylene
with anisole at (288.15, 293.15, 298.15, and 303.15) K," Journal of Chemical and Engineering Data, vol.
Viscosities, densities and speeds of sound of binary mixtures of benzene, toluene, o-xylene, m-xylene, p-xylene and mesitylene
with anisole at 288.15.
Viscosities, densities, speeds of sound and refractive indices of binary mixtures of o-xylene, m-xylene, p-xylene, ethylbenzene and mesitylene
with 1-decanol at 298.15 and 308.15 K, Journal of Molecular Liquids, 159, 132-141
Indeed, some processes to produce MXDA were disclosed using m-xylene, pseudocumene, mesitylene
, ethylbenzene, methylpyridine, benzonitrile, m-tolunitrile, isopropanol, MXDA and cyanopyridine (Kurek, 1984; Nakamura et al., 2002; Otsuka et al., 2003; Takamizawa et al., 2001).
The aldol condensation of acetone affords a variety of dimers such as diacetone alcohol and mesityl oxide and trimers including phorone, isophorone, semiphorone, triacetone alcohol, 2,2,6,6-tetramethyltetrahydropyran-4-one, and mesitylene
. The components of mixtures of these substances and derivatives of them have been identified and quantified in gas chromatograms using a mass-selective detector (GC-MS).
They are very soluble in a variety of common organic solvents including toluene, xylene, mesitylene
and methylene chloride.
Synthesis of spherical SBA-15 with large pore size : Pluronic P123 and a certain amount of KCl were dissolved in [H.sub.2]O and hydrochloric acid (36-38%) at room temperature until the solution became transparent, then mesitylene
The next heavier aromatic, xylene or C8, comes in three differently shaped isomers and so does the next heavier one, mesitylene
Ni [([[eta].sup.4]-[C.sub.8][H.sub.12]).sub.2] (STREM, 98%) and 1-hexadecylamine (ACROS, 90%) were used as received; mesitylene
(ACROS, 97%) was dried, degassed, and stored on molecular sieve in the glove box.
(Acetone is a waste product from butanol production.) The Swift process converts acetone into mesitylene
or tri-methylbenzene, the primary constituent of its fuel, so it depends on cheap acetone to make the conversion economic.