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Alba-Simionesco, C.; Fan, J.; Angell, C. A. (1999). "Thermodynamic aspects of the glass transition phenomenon. II. Molecular liquids with variable interactions".
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Pratesi, G.; Bartolini, P.; Senatra, D.; Ricci, M.; Righini, R.; Barocchi, F.; Torre, R. (2003). "Experimental studies of the
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is substituted onto the benzene ring. The difference between these three isomers is the position where the methyl group (–CH
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isomer is produced on the largest scale. Its primary application is as a precursor to the pesticides
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amines. Due to the amino group bonded to the aromatic ring, the toluidines are
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The chemical properties of the toluidines are quite similar to those of
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419:. This difference is related to the fact that the
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478:. They are a component of accelerators for
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645:CDC – NIOSH Pocket to Chemical Hazards
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399:salts, as usual for organic amines.
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521:Bowers, Joseph S. "Toluidines".
431:-Toluidine can be obtained from
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592:The Journal of Chemical Physics
563:-toluidine glass transition".
489:-toluidine is a metabolite of
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497:. This is then treated with
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577:10.1103/PhysRevE.67.021505
395:water due to formation of
363:Disclaimer and references
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533:10.1002/14356007.a27_159
407:-toluidines are viscous
293:Magnetic susceptibility
527:. Weinheim: Wiley-VCH.
446:-Toluidine reacts with
427:are more symmetrical.
415:-toluidine is a flaky
391:but dissolve well in
42:. These isomers are
458:Uses and occurrence
85:chemical structures
493:, which may cause
116:Toluidine isomers
565:Physical Review E
495:methemoglobinemia
485:In some patients
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302:72.1 × 10 cm/mol
299:74.6 × 10 cm/mol
296:76.0 × 10 cm/mol
40:organic compounds
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239:Glass not formed
200:Chemical formula
194:4-methylaniline
191:3-methylaniline
188:2-methylaniline
121:Methyl position
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104:functional group
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30:There are three
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178:-methylaniline
172:-methylaniline
166:-methylaniline
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440:-nitrotoluene
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331:Cc1ccc(N)cc1
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328:Cc1cccc(N)c1
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381:weakly basic
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160:Other names
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135:Common name
93:methyl group
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38:, which are
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468:metolachlor
423:-toluidine
325:Cc1ccccc1N
269:203–204 °C
266:199–200 °C
155:-toluidine
149:-toluidine
18:P-Toluidine
653:Categories
643:-Toluidine
636:-Toluidine
629:-Toluidine
505:References
491:prilocaine
472:acetochlor
308:CAS number
288:1.05 g/cm
285:0.98 g/cm
282:1.00 g/cm
142:-toluidine
63:-toluidine
56:-toluidine
48:-toluidine
433:reduction
425:molecules
36:toluidine
664:Toluenes
659:Anilines
450:to form
397:ammonium
387:in pure
377:aromatic
482:glues.
409:liquids
385:soluble
373:aniline
278:Density
272:200 °C
253:−30 °C
250:−23 °C
89:aniline
32:isomers
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411:, but
403:- and
393:acidic
321:SMILES
256:43 °C
235:187 K
232:189 K
124:ortho
74:; and
58:, and
571:(2).
561:ortho
464:ortho
417:solid
401:ortho
389:water
130:para
127:meta
101:amino
68:ortho
621:MSDS
537:ISBN
476:dyes
470:and
462:The
413:para
405:meta
106:(–NH
81:aryl
76:para
72:meta
600:doi
596:110
573:doi
529:doi
435:of
34:of
655::
638:,
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567:.
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212:N
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641:p
634:m
627:o
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444:p
438:p
429:p
421:p
210:9
208:H
206:7
204:C
176:p
170:m
164:o
153:p
147:m
140:o
108:2
97:3
61:p
54:m
46:o
20:)
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