N,N,N',N'-Tetra(p-aminophenyl)-p-phenylenediamine - ≥98% , CAS No.3283-07-6

CAS: 3283-07-6 Cat. No.: N303455 Molecular Weight: 472.58

GRADE & PURITY ≥98%

Synonyms

N,N,N',N'-Tetrakis(4-aminophenyl)-1,4-benzenediamine | N,N,N,N-Tetrakis(4-aminophenyl)-1,4-benzenediamine | LVPYYSKDNVAARK-UHFFFAOYSA-N | N1-(4-aminophenyl)-N1-{4-[bis(4-aminophenyl)amino]phenyl}benzene-1,4-diamine | DTXSID2062951 | N,N,N',N'-tetrakis(p-a

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Shipped In

Normal

Specifications

Synonyms

N, N, N', N'-Tetrakis(4-aminophenyl)-1, 4-benzenediamine | N, N, N, N-Tetrakis(4-aminophenyl)-1, 4-benzenediamine | LVPYYSKDNVAARK-UHFFFAOYSA-N | N1-(4-aminophenyl)-N1-{4-[bis(4-aminophenyl)amino]phenyl}benzene-1, 4-diamine | DTXSID2062951 | N, N, N', N'-tetrakis(p-a

Specifications & Purity

≥98%

Storage

Protected from light, Room temperature, Argon charged, Desiccated

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488185328
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185328
• Canonical Smiles: C1=CC(=CC=C1N)N(C2=CC=C(C=C2)N)C3=CC=C(C=C3)N(C4=CC=C(C=C4)N)C5=CC=C(C=C5)N
• IUPAC Name: 4-N-[4-(4-amino-N-(4-aminophenyl)anilino)phenyl]-4-N-(4-aminophenyl)benzene-1,4-diamine
• InChIKey: LVPYYSKDNVAARK-UHFFFAOYSA-N
• INCHI: 1S/C30H28N6/c31-21-1-9-25(10-2-21)35(26-11-3-22(32)4-12-26)29-17-19-30(20-18-29)36(27-13-5-23(33)6-14-27)28-15-7-24(34)8-16-28/h1-20H,31-34H2
• Isomeric SMILES: C1=CC(=CC=C1N)N(C2=CC=C(C=C2)N)C3=CC=C(C=C3)N(C4=CC=C(C=C4)N)C5=CC=C(C=C5)N
• Molecular Weight: 472.58
• Reaxy-Rn: 3076080
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3076080&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Tertiary amines
          • Level6 Triarylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Tertiary amines
• Direct Parent: Triarylamines
• Alternative Parents: Aniline and substituted anilines Primary amines Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Tertiary aromatic amine - Aniline or substituted anilines - Benzenoid - Monocyclic benzene moiety - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as triarylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three aryl groups bonded to the amino nitrogen.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Light sensitive
• Flash Point(°C): 409.3℃
• Boil Point(°C): 765.6℃ at 760 mmHg
• Melt Point(°C): >300℃
• Molecular Weight: 472.600 g/mol
• XLogP3: 5.700
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 6
• Exact Mass: 472.238 Da
• Monoisotopic Mass: 472.238 Da
• Topological Polar Surface Area: 111.000 Ų
• Heavy Atom Count: 36
• Formal Charge: 0
• Complexity: 534.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

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2. Lei Huang, Rong Guo, Qingqing Qiu, Huan Li, Putrakumar Balla, Jinming Zeng, Tongxiang Liang, Xiaopeng Qi, Ping Liu.  (2024)  Triarylamine-based polyimide COFs for achieving high performance ambipolar multi-color electrochromic energy-storage films.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.155018]

3. Shunli Wang, Yinsheng Li, Limei Tian.  (2025)  Woven cross-linked elastomer strategy for extremely tear-resistant, recyclable elastomer/carbon fiber composites.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.163541]

4. Shunli Wang, Yinsheng Li, Limei Tian.  (2025)  High-toughness polyurethane elastomers for recyclable carbon fiber-reinforced composites with excellent tear resistance.  COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING,      [PMID:] [10.1016/j.compositesa.2025.109140]

5. Wenping Shi, Xiao Yang, Haitao Li, Chunxia Zhao, Jing Zhou, Yuli Xiong, Wen Chen.  (2025)  Enhancement of long-cycle electrochromic stability of covalent organic framework films via linkage conversion.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:41455346] [10.1016/j.jcis.2025.139776]