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HCID 88539Erstellt: 26. Oktober 2026

N-Phenyl-N-(p-tolyl)-p-toluidin

DMTPA · BIS(4-METHYLPHENYL)PHENYLAMINE · 4-Methyl-N-phenyl-N-(p-tolyl)aniline · 4,4'-Dimethyltriphen · N,N-DI-P-TOLYLANILINE · PHENYL(DI-P-TOLYL)AMINE · n-phenyl di-p-tolylamine · 4,4DimehtylTriphenylamine

https://huagongshe.com/de/chemical/88539

Molekülstruktur von N-Phenyl-N-(p-tolyl)-p-toluidin

Identifikatoren & physikalische Daten

CAS No.20440-95-3
SummenformelC20H19N
Durchschnittliche Molmasse273,4 g/mol
Monoisotopische Masse273,15174961 g/mol
SMILESCc1ccc(N(c2ccccc2)c2ccc(C)cc2)cc1
InChIKeyYWKKLBATUCJUHI-UHFFFAOYSA-N
PubChem CID88539
EC No.243-822-7
DTXSIDDTXSID5066611
Lokaler NameN-Phenyl-N-(p-tolyl)-p-toluidin

Chemische & physikalische Eigenschaften

XLogP6,5
Polarare Oberfläche (TPSA)3,2
H-Brücken-Donoren0
H-Brücken-Akzeptoren1
Frei drehbare Bindungen3
Schwere Atome21
Formalladung0
Komplexität269
Schmelzpunkt112°C
Siedepunkt289.3 °C
Dichte1.079±0.06 g/cm3(Predicted)
LagerbedingungenSealed in dry,Room Temperature
Aggregatzustandpowder to crystal
pKa (Säurekonstante)-2.19±0.50(Predicted)
FarbeWhite to Orange to Green
InChIInChI=1S/C20H19N/c1-16-8-12-19(13-9-16)21(18-6-4-3-5-7-18)20-14-10-17(2)11-15-20/h3-15H,1-2H3
InChIKeyYWKKLBATUCJUHI-UHFFFAOYSA-N
SMILESC1(N(C2=CC=C(C)C=C2)C2=CC=CC=C2)=CC=C(C)C=C1
CAS Datenbank20440-95-3(CAS DataBase Reference)
EPA chemische InformationenBenzenamine, 4-methyl-N-(4-methylphenyl)-N-phenyl- (20440-95-3)

Sicherheit & Vorschriften

GHS-EinstufungWarningH302 (97.5%): Harmful if swallowed [Warning Acute toxicity, oral]P264, P270, P273, P301+P317, P330, P391, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 40 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesAcute Tox. 4 (97.5%)
TSCA-Inventar-StatusTSCA listed
Zollcode29214990

Anwendungen & Verwendung

Verwenden

4,4'-Dimethyltriphenylamine (DMTPA) can be used as a starting material for the synthesis of 4-[bis(4-methylphenyl)amino]benzaldehyde (BMABA). BMABA is a molecule exhibiting mechanophluorescence, and it has applications in fields such as sensors, data storage and smart switches [5]. The reaction process and mechanism are as follows:This synthesis method is carried out via the Vilsmeier-Haack reaction. DMTPA (1.37 g, 5.01 mmol) was dissolved in DMF (2.3 mL, 29.8 mmol), and trichlorooxaphosphorane (0.46 mL, 5.02 mmol) was slowly added under an ice-water bath. Upon completion of the addition, the reaction temperature was adjusted to 100 °C and the mixture was heated for 3 h. After cooling to room temperature, the product was dissolved in dichloromethane, then neutralised with a sodium bicarbonate solution, extracted, dried over anhydrous Na₂SO₄, and the solid product was collected by vacuum distillation. Chromatographic separation was performed on a silica gel column using a mobile phase of dichloromethane and methanol (Vdichloromethane:Vmethanol = 100:1), yielding pale yellow BMABA (1.14 g, 75.6% yield).