「toluene」の共起表現一覧(1語右で並び替え)
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The o- and p-isotoluenes isomerise to | toluene, a reaction driven by aromatic stabilisation. |
This enzyme participates in | toluene and xylene degradation. |
id insoluble in water and soluble in acetone, | toluene, and benzene. |
substrate, benzylsuccinate, and two products, | toluene and fumarate. |
paringly soluble in solvents such as benzene, | toluene, and dichloromethane. |
in benzoate degradation via hydroxylation and | toluene and xylene degradation. |
tum dots are typically soluble in chloroform, | toluene, and (to a lesser extent) hexane. |
equality of the chemical potentials of liquid | toluene and toluene vapour, and the corresponding equ |
ays: gamma-hexachlorocyclohexane degradation, | toluene and xylene degradation, and naphthalene and a |
8 ml of | toluene and 1 gram of butanedioic anhydride are added |
ays: gamma-hexachlorocyclohexane degradation, | toluene and xylene degradation, naphthalene and anthr |
n metabolism, and the degradation pathway for | toluene and xylene. |
ar I, the gas industry's by-products, phenol, | toluene and ammonia and sulphurous compounds were val |
k bluish-black powder, soluble in benzene and | toluene and insoluble in water, with melting point 10 |
itration: The sample is normally dissolved in | toluene and propanol with a little water and titrated |
erved the hydrogenolysis of benzyl alcohol to | toluene, and as early as 1906, Padoa and Ponti had ob |
ways: benzoate degradation via hydroxylation, | toluene and xylene degradation, 1,4-dichlorobenzene d |
romatics, which means that it has less of the | toluene and other solvents which produce the intoxica |
of highly volatile components like benzene or | toluene, and almost no sulfur, oxygen, and nitrogen i |
1,3-dioxolane and | toluene are possible substitutes as solvents. |
ly liquid phase chlorination and oxidation of | toluene are the main routes. |
y aromatic compounds such as benzoic acid and | toluene are taken internally, they are converted to h |
It can be prepared by the bromination of | toluene at room temperature in air, using manganese(I |
produced by the free radical chlorination of | toluene, being preceded in the process by benzyl chlo |
of 2,4,6-trichlorophenol in a solution of dry | toluene by reaction with oxalyl chloride in the prese |
Toluene can be used to break open red blood cells in | |
ncludes several proteins that are involved in | toluene catabolism and degradation of aromatic hydroc |
nd a catalyst to form a mixture of isomers of | toluene diamine (TDA) |
Most DNT is used in the production of | toluene diisocyanate which is used to produce flexibl |
toluene diisocyanate (TDI) - used as co-monomers with | |
EC 1.14.12.11 | toluene dioxygenase |
In enzymology, a | toluene dioxygenase (EC 1.14.12.11) is an enzyme that |
Immiscible liquids, such as water and | toluene, easily form azeotropes. Commonly, these azeo |
toluene, ethyl acetate, acetone, ethanol, acetonitril | |
These include BTEX compounds (benzene, | toluene, ethylbenzene, and xylene found in gasoline, |
e nitrogen, whereas nonpolar solvents such as | toluene favour C-3 attack. |
Toluene, found in glue, paint, thinner, etc. See also | |
The nitration of | toluene gives sequentially mononitrotoluene, DNT, and |
with non-polar organic solvents (chloroform, | toluene, hexane etc) and form a two-phase system. |
Toluene hydrodealkylation to benzene | |
ves reacting an aromatic hydrocarbon, such as | toluene, in the presence of hydrogen gas to form a si |
Industrial uses of | toluene include dealkylation to benzene, and the disp |
trations of hippuric acid may also indicate a | toluene intoxication, however, scientists have called |
Polyvinyltoluene (PVT, polyvinyl | toluene) is a synthetic polymer. |
Toluene is separated from the mixture by steam distil | |
First, | toluene is nitrated with a mixture of sulfuric and ni |
Toluene is an organic compound which is mostly harmle | |
nes in organic chemistry are the non-aromatic | toluene isomers with an exocyclic double bond. |
of asphaltenes at very low concentrations (in | toluene) led to aggregate weights being misinterprete |
It may be synthesized from | toluene; more interesting is its production when acet |
The 4 substrates of this enzyme are | toluene, NADH, H+, and O2, whereas its two products a |
anol, acetone, and ether, but not in benzene, | toluene, or chloroform. |
is prepared by heating the Petasis reagent in | toluene or THF to 60 °C. |
The liquid used can be pure ethanol or | toluene or kerosene or Isoamyl acetate, depending on |
n sulfide is formed, then recrystallized from | toluene or xylene. |
trol contains 25% aromatics, such as benzene, | toluene, ortho-xylene and para-xylene. |
ured several other tankers, spilling styrene, | toluene, propane, caustic soda, and chlorine onto the |
Toluene reacts as a normal aromatic hydrocarbon towar | |
librated using a strong, known scatterer like | toluene since the Rayleigh Ratio of toluene and a few |
Aromatics: Benzene | Toluene Solvent Xylene Orthoxylene Paraxylene Solgad |
Fetal | Toluene Syndrome has been defined and resembles Fetal |
The isomerisation of p-isotoluene to | toluene takes place at 100 °C in benzene with bimolec |
on of a boronic acid (1) such as one based on | toluene to a boroxine (2). |
was commissioned for production of benzene & | toluene using feedstock available from CRU. |
mporary shut down after traces of benzene and | toluene were detected in groundwater monitoring bores |
The primary VOC at Love Canal is | toluene, which is found along with dioxins and other |
Nitration: Reaction of | toluene with nitric acid and a catalyst to form dinit |
es and heavier aromatics are used in place of | toluene, with similar efficiency. |
s for analyte (the solution) and T is for the | toluene with the Rayleigh Ratio of toluene, RT being |
-chlorotoluene (benzyl chloride), consists of | toluene with chlorine substitution on the methyl grou |
ls that occur in TPH include hexane, benzene, | toluene, xylenes, naphthalene, and fluorene, other co |
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