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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 20:10:30 UTC

Update Date

2021-09-26 22:50:31 UTC

HMDB ID

HMDB0243487

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N,N-Diphenyl-p-phenylenediamine

Description

N,N-Diphenyl-p-phenylenediamine 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. Based on a literature review a significant number of articles have been published on N,N-Diphenyl-p-phenylenediamine. This compound has been identified in human blood as reported by (PMID: 31557052 ). N,n-diphenyl-p-phenylenediamine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N,N-Diphenyl-p-phenylenediamine is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0243487
     RDKit          3D
N,N-Diphenyl-p-phenylenediamine
 36 38  0  0  0  0  0  0  0  0999 V2000
   -4.8133   -2.0458    0.2238 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4797   -1.5716    0.1492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2456   -0.3720   -0.5063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9707    0.1009   -0.5886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539   -0.5751   -0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4339    0.0389   -0.2228 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4111    1.4539    0.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2579    1.8715    1.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3593    3.2074    1.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2122    4.1347    0.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8581    3.7047   -0.4883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9717    2.3413   -0.8292 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6064   -0.6957   -0.4347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4251   -0.4765   -1.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6458   -1.1149   -1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0864   -1.9928   -0.6841 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3004   -2.2368    0.4145 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0847   -1.5968    0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1415   -1.7325    0.5892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4344   -2.2507    0.6952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2328   -2.6061   -0.5281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3580   -1.8089    1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0536    0.2009   -0.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8044    1.0378   -1.1030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7147    1.1572    1.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8703    3.5539    2.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1280    5.2055    0.8893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3118    4.4260   -1.1589 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4932    2.0899   -1.7393 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1151    0.1760   -2.3499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2501   -0.8992   -2.5337 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0563   -2.5033   -0.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6523   -2.9394    1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5446   -1.7867    1.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3877   -2.3277    1.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6093   -3.1682    1.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
  6 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  5 19  1  0
 19 20  2  0
 20  2  1  0
 12  7  1  0
 18 13  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  4 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  1  0
M  END


  Mrv1652309102122102D          

 20 22  0  0  0  0            999 V2000
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 17 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0243487

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=CC=C(C=C1)N(C1=CC=CC=C1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H16N2/c19-15-11-13-18(14-12-15)20(16-7-3-1-4-8-16)17-9-5-2-6-10-17/h1-14H,19H2

> <INCHI_KEY>
UXKQNCDDHDBAPD-UHFFFAOYSA-N

> <FORMULA>
C18H16N2

> <MOLECULAR_WEIGHT>
260.34

> <EXACT_MASS>
260.131348523

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
29.523606628429157

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N1,N1-diphenylbenzene-1,4-diamine

> <ALOGPS_LOGP>
4.71

> <JCHEM_LOGP>
4.465880151666667

> <ALOGPS_LOGS>
-4.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
4.776137051009219

> <JCHEM_POLAR_SURFACE_AREA>
29.259999999999998

> <JCHEM_REFRACTIVITY>
83.91890000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.32e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N1,N1-diphenylbenzene-1,4-diamine

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0243487
     RDKit          3D
N,N-Diphenyl-p-phenylenediamine
 36 38  0  0  0  0  0  0  0  0999 V2000
   -4.8133   -2.0458    0.2238 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4797   -1.5716    0.1492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2456   -0.3720   -0.5063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9707    0.1009   -0.5886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539   -0.5751   -0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4339    0.0389   -0.2228 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4111    1.4539    0.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2579    1.8715    1.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3593    3.2074    1.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2122    4.1347    0.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8581    3.7047   -0.4883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9717    2.3413   -0.8292 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6064   -0.6957   -0.4347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4251   -0.4765   -1.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6458   -1.1149   -1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0864   -1.9928   -0.6841 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3004   -2.2368    0.4145 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0847   -1.5968    0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1415   -1.7325    0.5892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4344   -2.2507    0.6952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2328   -2.6061   -0.5281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3580   -1.8089    1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0536    0.2009   -0.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8044    1.0378   -1.1030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7147    1.1572    1.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8703    3.5539    2.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1280    5.2055    0.8893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3118    4.4260   -1.1589 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4932    2.0899   -1.7393 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1151    0.1760   -2.3499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2501   -0.8992   -2.5337 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0563   -2.5033   -0.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6523   -2.9394    1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5446   -1.7867    1.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3877   -2.3277    1.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6093   -3.1682    1.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
  6 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  5 19  1  0
 19 20  2  0
 20  2  1  0
 12  7  1  0
 18 13  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  4 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  1  0
M  END

HEADER    PROTEIN                                 10-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-21         0                                  
HETATM    1  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       4.001  -0.770   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       9.336   2.310   0.000  0.00  0.00           N+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8   14                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14    7   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   17                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

COMPND    HMDB0243487
HETATM    1  N1  UNL     1      -4.813  -2.046   0.224  1.00  0.00           N  
HETATM    2  C1  UNL     1      -3.480  -1.572   0.149  1.00  0.00           C  
HETATM    3  C2  UNL     1      -3.246  -0.372  -0.506  1.00  0.00           C  
HETATM    4  C3  UNL     1      -1.971   0.101  -0.589  1.00  0.00           C  
HETATM    5  C4  UNL     1      -0.854  -0.575  -0.033  1.00  0.00           C  
HETATM    6  N2  UNL     1       0.434   0.039  -0.223  1.00  0.00           N  
HETATM    7  C5  UNL     1       0.411   1.454   0.001  1.00  0.00           C  
HETATM    8  C6  UNL     1      -0.258   1.871   1.155  1.00  0.00           C  
HETATM    9  C7  UNL     1      -0.359   3.207   1.472  1.00  0.00           C  
HETATM   10  C8  UNL     1       0.212   4.135   0.630  1.00  0.00           C  
HETATM   11  C9  UNL     1       0.858   3.705  -0.488  1.00  0.00           C  
HETATM   12  C10 UNL     1       0.972   2.341  -0.829  1.00  0.00           C  
HETATM   13  C11 UNL     1       1.606  -0.696  -0.435  1.00  0.00           C  
HETATM   14  C12 UNL     1       2.425  -0.476  -1.526  1.00  0.00           C  
HETATM   15  C13 UNL     1       3.646  -1.115  -1.647  1.00  0.00           C  
HETATM   16  C14 UNL     1       4.086  -1.993  -0.684  1.00  0.00           C  
HETATM   17  C15 UNL     1       3.300  -2.237   0.414  1.00  0.00           C  
HETATM   18  C16 UNL     1       2.085  -1.597   0.533  1.00  0.00           C  
HETATM   19  C17 UNL     1      -1.142  -1.733   0.589  1.00  0.00           C  
HETATM   20  C18 UNL     1      -2.434  -2.251   0.695  1.00  0.00           C  
HETATM   21  H1  UNL     1      -5.233  -2.606  -0.528  1.00  0.00           H  
HETATM   22  H2  UNL     1      -5.358  -1.809   1.066  1.00  0.00           H  
HETATM   23  H3  UNL     1      -4.054   0.201  -0.956  1.00  0.00           H  
HETATM   24  H4  UNL     1      -1.804   1.038  -1.103  1.00  0.00           H  
HETATM   25  H5  UNL     1      -0.715   1.157   1.831  1.00  0.00           H  
HETATM   26  H6  UNL     1      -0.870   3.554   2.357  1.00  0.00           H  
HETATM   27  H7  UNL     1       0.128   5.206   0.889  1.00  0.00           H  
HETATM   28  H8  UNL     1       1.312   4.426  -1.159  1.00  0.00           H  
HETATM   29  H9  UNL     1       1.493   2.090  -1.739  1.00  0.00           H  
HETATM   30  H10 UNL     1       2.115   0.176  -2.350  1.00  0.00           H  
HETATM   31  H11 UNL     1       4.250  -0.899  -2.534  1.00  0.00           H  
HETATM   32  H12 UNL     1       5.056  -2.503  -0.777  1.00  0.00           H  
HETATM   33  H13 UNL     1       3.652  -2.939   1.184  1.00  0.00           H  
HETATM   34  H14 UNL     1       1.545  -1.787   1.432  1.00  0.00           H  
HETATM   35  H15 UNL     1      -0.388  -2.328   1.026  1.00  0.00           H  
HETATM   36  H16 UNL     1      -2.609  -3.168   1.197  1.00  0.00           H  
CONECT    1    2   21   22
CONECT    2    3    3   20
CONECT    3    4   23
CONECT    4    5    5   24
CONECT    5    6   19
CONECT    6    7   13
CONECT    7    8    8   12
CONECT    8    9   25
CONECT    9   10   10   26
CONECT   10   11   27
CONECT   11   12   12   28
CONECT   12   29
CONECT   13   14   14   18
CONECT   14   15   30
CONECT   15   16   16   31
CONECT   16   17   32
CONECT   17   18   18   33
CONECT   18   34
CONECT   19   20   20   35
CONECT   20   36
END

HMDB0243487
     RDKit          3D
N,N-Diphenyl-p-phenylenediamine
 36 38  0  0  0  0  0  0  0  0999 V2000
   -4.8133   -2.0458    0.2238 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4797   -1.5716    0.1492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2456   -0.3720   -0.5063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9707    0.1009   -0.5886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539   -0.5751   -0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4339    0.0389   -0.2228 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4111    1.4539    0.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2579    1.8715    1.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3593    3.2074    1.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2122    4.1347    0.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8581    3.7047   -0.4883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9717    2.3413   -0.8292 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6064   -0.6957   -0.4347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4251   -0.4765   -1.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6458   -1.1149   -1.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0864   -1.9928   -0.6841 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3004   -2.2368    0.4145 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0847   -1.5968    0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1415   -1.7325    0.5892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4344   -2.2507    0.6952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2328   -2.6061   -0.5281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3580   -1.8089    1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0536    0.2009   -0.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8044    1.0378   -1.1030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7147    1.1572    1.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8703    3.5539    2.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1280    5.2055    0.8893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3118    4.4260   -1.1589 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4932    2.0899   -1.7393 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1151    0.1760   -2.3499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2501   -0.8992   -2.5337 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0563   -2.5033   -0.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6523   -2.9394    1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5446   -1.7867    1.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3877   -2.3277    1.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6093   -3.1682    1.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
  6 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  5 19  1  0
 19 20  2  0
 20  2  1  0
 12  7  1  0
 18 13  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  4 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₈H₁₆N₂

Average Molecular Weight

260.34

Monoisotopic Molecular Weight

260.131348523

IUPAC Name

N1,N1-diphenylbenzene-1,4-diamine

Traditional Name

N1,N1-diphenylbenzene-1,4-diamine

CAS Registry Number

Not Available

SMILES

NC1=CC=C(C=C1)N(C1=CC=CC=C1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C18H16N2/c19-15-11-13-18(14-12-15)20(16-7-3-1-4-8-16)17-9-5-2-6-10-17/h1-14H,19H2

InChI Key

UXKQNCDDHDBAPD-UHFFFAOYSA-N

Chemical Taxonomy

Description

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.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Amines

Direct Parent

Triarylamines

Alternative Parents

Substituents

Tertiary aromatic amine
Aniline or substituted anilines
Benzenoid
Monocyclic benzene moiety
Organopnictogen compound
Hydrocarbon derivative
Primary amine
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	4.71	ALOGPS
logP	4.47	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Basic)	4.78	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.26 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	83.92 m³·mol⁻¹	ChemAxon
Polarizability	29.52 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	163.4	30932474
DeepCCS	[M-H]-	161.042	30932474
DeepCCS	[M-2H]-	193.928	30932474
DeepCCS	[M+Na]+	169.493	30932474
AllCCS	[M+H]+	161.6	32859911
AllCCS	[M+H-H2O]+	157.9	32859911
AllCCS	[M+NH4]+	165.0	32859911
AllCCS	[M+Na]+	166.0	32859911
AllCCS	[M-H]-	164.3	32859911
AllCCS	[M+Na-2H]-	163.2	32859911
AllCCS	[M+HCOO]-	162.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N,N-Diphenyl-p-phenylenediamine	NC1=CC=C(C=C1)N(C1=CC=CC=C1)C1=CC=CC=C1	3714.4	Standard polar	33892256
N,N-Diphenyl-p-phenylenediamine	NC1=CC=C(C=C1)N(C1=CC=CC=C1)C1=CC=CC=C1	2568.9	Standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine	NC1=CC=C(C=C1)N(C1=CC=CC=C1)C1=CC=CC=C1	2408.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N,N-Diphenyl-p-phenylenediamine,1TMS,isomer #1	C[Si](C)(C)NC1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1	2595.2	Semi standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine,1TMS,isomer #1	C[Si](C)(C)NC1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1	2529.0	Standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine,1TMS,isomer #1	C[Si](C)(C)NC1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1	3170.5	Standard polar	33892256
N,N-Diphenyl-p-phenylenediamine,2TMS,isomer #1	C[Si](C)(C)N(C1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1)[Si](C)(C)C	2512.6	Semi standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine,2TMS,isomer #1	C[Si](C)(C)N(C1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1)[Si](C)(C)C	2415.5	Standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine,2TMS,isomer #1	C[Si](C)(C)N(C1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1)[Si](C)(C)C	3029.6	Standard polar	33892256
N,N-Diphenyl-p-phenylenediamine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1	2794.0	Semi standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1	2690.6	Standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1	3271.2	Standard polar	33892256
N,N-Diphenyl-p-phenylenediamine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1)[Si](C)(C)C(C)(C)C	2907.7	Semi standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1)[Si](C)(C)C(C)(C)C	2841.8	Standard non polar	33892256
N,N-Diphenyl-p-phenylenediamine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C1=CC=C(N(C2=CC=CC=C2)C2=CC=CC=C2)C=C1)[Si](C)(C)C(C)(C)C	3132.1	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N,N-Diphenyl-p-phenylenediamine GC-MS (Non-derivatized) - 70eV, Positive	splash10-01q9-4390000000-96153d34c287f3f32b0b	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N,N-Diphenyl-p-phenylenediamine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N,N-Diphenyl-p-phenylenediamine 10V, Positive-QTOF	splash10-03di-0090000000-2f16209866e7f29988de	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N,N-Diphenyl-p-phenylenediamine 20V, Positive-QTOF	splash10-03di-0090000000-2f16209866e7f29988de	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N,N-Diphenyl-p-phenylenediamine 40V, Positive-QTOF	splash10-0059-9760000000-3a982ea727dc3359640a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N,N-Diphenyl-p-phenylenediamine 10V, Negative-QTOF	splash10-0a4i-0090000000-cd7631b883f8a7ce97fa	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N,N-Diphenyl-p-phenylenediamine 20V, Negative-QTOF	splash10-0a4i-0090000000-cd7631b883f8a7ce97fa	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N,N-Diphenyl-p-phenylenediamine 40V, Negative-QTOF	splash10-0a4i-0290000000-13acc2cef019f8900189	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

67906

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

75371

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for N,N-Diphenyl-p-phenylenediamine (HMDB0243487)

MOL for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

3D MOL for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

3D SDF for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

3D-SDF for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

PDB for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

3D PDB for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

SMILES for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

INCHI for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

Structure for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

3D Structure for HMDB0243487 (N,N-Diphenyl-p-phenylenediamine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra