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Atomfair 2,4,6-Trimethyl-N,N-diphenylaniline PTAA C21H21N

Description 2,4,6-Trimethyl-N,N-diphenylaniline (CAS No. 1333317-99-9) is a high-purity organic compound with the molecular formula C21H21N . This tertiary amine features a central aniline core substituted with two phenyl groups and three methyl groups at the 2, 4, and 6 positions, offering exceptional steric hindrance and electronic properties. Ideal for advanced research applications, this compound is meticulously synthesized and purified to meet stringent quality standards, ensuring consistency for photochemical, material science, and organic electronic studies. Available in various quantities, it is supplied with comprehensive analytical data (including1H NMR, HPLC, and GC-MS) to verify purity and structural integrity. Store under inert conditions…

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Description

Description

2,4,6-Trimethyl-N,N-diphenylaniline (CAS No. 1333317-99-9) is a high-purity organic compound with the molecular formula C21H21N. This tertiary amine features a central aniline core substituted with two phenyl groups and three methyl groups at the 2, 4, and 6 positions, offering exceptional steric hindrance and electronic properties. Ideal for advanced research applications, this compound is meticulously synthesized and purified to meet stringent quality standards, ensuring consistency for photochemical, material science, and organic electronic studies. Available in various quantities, it is supplied with comprehensive analytical data (including 1H NMR, HPLC, and GC-MS) to verify purity and structural integrity. Store under inert conditions to maintain stability.

  • CAS No: 1333317-99-9
  • Molecular Formula: C21H21N
  • Molecular Weight: 287.4
  • Exact Mass: 287.167399674
  • Monoisotopic Mass: 287.167399674
  • IUPAC Name: 2,4,6-trimethyl-N,N-diphenylaniline
  • SMILES: CC1=CC(=C(C(=C1)C)N(C2=CC=CC=C2)C3=CC=CC=C3)C
  • Synonyms: 2,4,6-Trimethyl-N,N-diphenylaniline, 603134-65-2, 1333317-99-9, N,N-diphenyl-2,4,6-triMethyl aniline, PTAA

Application

2,4,6-Trimethyl-N,N-diphenylaniline is widely utilized as a hole-transport material (HTM) in perovskite solar cells due to its excellent charge-carrier mobility and thermal stability. It also serves as a key intermediate in the synthesis of organic semiconductors and optoelectronic devices. Researchers employ this compound in photoredox catalysis and as a building block for conjugated polymers. Its sterically hindered structure makes it valuable for studying kinetic and thermodynamic control in organic reactions.

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