p-Aminotoluene

• Formula: C₇H₉N
• Molecular weight: 107.1531
• IUPAC Standard InChI: InChI=1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3 Copy

  
• IUPAC Standard InChIKey: RZXMPPFPUUCRFN-UHFFFAOYSA-N Copy
• CAS Registry Number: 106-49-0
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Other names: p-Toluidine; p-Methylaniline; p-Methylbenzenamine; p-Tolylamine; C.I. Azoic coupling component 107; 1-Amino-4-methylbenzene; 4-Aminotoluene; 4-Methylaniline; 4-Methylbenzenamine; 4-Toluidine; Benzenamine, 4-methyl-; 4-Amino-1-methylbenzene; 4-Tolylamine; p-Toluidin; Aniline, p-methyl-; 4-Aminotoluen; Rcra waste number U353; C.I. 37107; Naphtol AS-KG; Naphtol AS-KGLL; NSC 15350
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
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Normal melting point

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

Go To: Top, Normal melting point, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Meva'a and Lichanot, 1990
Meva'a, L.M.; Lichanot, A., Thermodynamic properties in condensed phase of ortho, meta and para fluorotoluene, cresol and toluidine, Thermochim. Acta, 1990, 158, 335. [all data]

Kemula, Buchowski, et al., 1968
Kemula, W.; Buchowski, H.; Pawlowski, W., Effect of the position of substituents in an aromatic ring on R(f) and partition coefficients: II. aromatic amines, Rocz. Chem., 1968, 42, 1951. [all data]

Assal, 1966
Assal, F.A., Binary Systems of Phenol, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1966, 14, 599. [all data]

Rastogi, Nigam, et al., 1963
Rastogi, R.P.; Nigam, R.K.; Sharma, R.N.; Girdhar, H.L., Entropy of Fusion of Molecular Complexes, J. Chem. Phys., 1963, 39, 11, 3042, https://doi.org/10.1063/1.1734140 . [all data]

Anonymous, 1954
Anonymous, R., , Am. Pet. Inst. Res. Proj. 45, Tech. Rep. 13, Ohio State Univ., 1954. [all data]

Berliner and Berliner, 1954
Berliner, E.; Berliner, F., Relative Rates of Iodination of p-Alkylanilines, J. Am. Chem. Soc., 1954, 76, 6179-85. [all data]

Barcelo, Le Fevre, et al., 1951
Barcelo, J.R.; Le Fevre, R.J.W.; Smythe, B.M., Variations of dipole moment with state for n-propyl and n-butylamines with notes on the apparent moments of in solutions of certain other amines., Trans. Faraday Soc., 1951, 47, 357. [all data]

Campbell and Campbell, 1940
Campbell, A.N.; Campbell, A.J.R., The heats of solution, heats of formation, specific heats and equilibrium diagrams of certain molecular compounds. J. Am. Chem. Soc., 1940, 62, 291-297. [all data]

Timmermans and Hennaut-Roland, 1937
Timmermans, J.; Hennaut-Roland, M., Works from International Bureau at Physical-Chemical Standards. VIII. Physical constants of 20 organic compounds, J. Chim. Phys. Phys.-Chim. Biol., 1937, 34, 693. [all data]

Glass and Madgin, 1934
Glass, H.M.; Madgin, W.M., Equilibrium constants in terms of activities (cryoscopic): IV the dissociation of p-toluidine o-tolyloxide in benzene and in p- dichlorobenzene, J. Chem. Soc., 1934, 1934, 1292-96. [all data]

Bernoulli and Veillon, 1932
Bernoulli, A.L.; Veillon, E.A., Analysis of the Constitution of Aromatic Two-component System by Means of the Gradients of Viscosity and Density., Helv. Chim. Acta, 1932, 15, 810. [all data]

Buehler, Wood, et al., 1932
Buehler, C.A.; Wood, J.H.; Hull, D.C.; Erwin, E.C., A Study of Molecular Organic Compounds. IV. The Molecular Organic Compounds of Phenol, their Parachors and Refractivities, J. Am. Chem. Soc., 1932, 54, 2398. [all data]

Gans and Harkins, 1930
Gans, D.M.; Harkins, W.D., The Surface Tension of Aqueous Solutions of Para-Toluidine, J. Am. Chem. Soc., 1930, 52, 2289. [all data]

Pushin and Sladovic, 1928
Pushin, N.A.; Sladovic, L., Equilibrium in the binary systems cresols-amines, J. Chem. Soc., 1928, 1928, 2474. [all data]

Berliner and May, 1927
Berliner, J.F.T.; May, O.E., Studies in vapor pressure. III. The Toluidines, J. Am. Chem. Soc., 1927, 49, 1007. [all data]

O'Connor, 1924
O'Connor, E.A., Some Binary Systems Composed of Acetic Acid and the Homologues of Anil, J. Chem. Soc., 1924, 125, 1422. [all data]

Cauwood and Turner, 1915
Cauwood, J.D.; Turner, W.E.S., XXXI. The Dielectric Constants of Some Organic Solvents at their Melting or Boiling Points, J. Chem. Soc., Trans., 1915, 107, 276. [all data]

Beck, 1907
Beck, K., The Relative Viscosity., Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1907, 58, 425. [all data]

Beck and Ebbinghaus, 1906
Beck, K.; Ebbinghaus, K., On Transition Temperatures and A Method of Meauring Them, Ber. Dtsch. Chem. Ges., 1906, 39, 3870. [all data]

Buechner, 1906
Buechner, E.H., Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1906, 54, 665. [all data]

Philip and Smith, 1905
Philip, J.C.; Smith, S.H., Researches on the freezing points of binary mixtures of organic substances: the behavior of the dihydric phenols towards p-toluidine,alpha-naphthylamine, and picric acid, J. Chem. Soc., 1905, 87, 1735. [all data]

Demerliac, 1898
Demerliac, M.R., J. Phys. Radium, 1898, 7, 591. [all data]

Perkin, 1896
Perkin, W.H., LXIX. On Magnetic Rotatory Power, especially of Aromatic Compounds, J. Chem. Soc., 1896, 69, 1025-1257. [all data]

Bruhl, 1895
Bruhl, J.W., Spectrochemistry of Nitrogen-Containing Compounds. I., Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1895, 16, 193. [all data]

Eykman, 1889
Eykman, J.F., Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1889, 4, 497. [all data]

Neubeck, 1887
Neubeck, F., Molecular Volumes of Aromatic Compounds, Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1887, 1, 649. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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