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Toluene (/ ˈ t ɒ l. j u iː n /), also known as toluol (/ ˈ t ɒ l. j u. ɒ l , - ɔː l , - oʊ l / ), is a substituted aromatic hydrocarbon [ 15 ] with the chemical formula C 6 H 5 CH 3 , often abbreviated as PhCH 3 , where Ph stands for the phenyl group.
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Many different solvents are suitable, including sulfolane (C 4 H 8 O 2 S), furfural (C 5 H 4 O 2), tetraethylene glycol (C 8 H 18 O 5), dimethylsulfoxide (C 2 H 6 OS), and N-methyl-2-pyrrolidone (C 5 H 9 NO). Below is a schematic flow diagram of one method, involving extractive distillation, for extraction of the BTX aromatics from a catalytic ...
Ethyltoluene describes organic compounds with the formula CH 3 C 6 H 4 CH 2 CH 3. Three isomers exist: 1,2- 1,3-, and 1,4-. All are colorless liquids, immiscible in water, with similar boiling points. They are classified are aromatic hydrocarbons. The ring bears two substituents: a methyl group and an ethyl group. [1]
Also called resource cost advantage. The ability of a party (whether an individual, firm, or country) to produce a greater quantity of a good, product, or service than competitors using the same amount of resources. absorption The total demand for all final marketed goods and services by all economic agents resident in an economy, regardless of the origin of the goods and services themselves ...
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Chemicals produced from toluene. toluene – methylbenzene; can be a solvent or precursor for other chemicals benzene; toluene diisocyanate (TDI) – used as co-monomers with polyether polyols to form polyurethanes or with di- or polyamines to form polyureas polyurethanes; benzoic acid – carboxybenzene caprolactam; Chemicals produced from xylenes