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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:58:20 UTC

Update Date

2022-03-07 02:55:28 UTC

HMDB ID

HMDB0037713

Secondary Accession Numbers

HMDB37713

Metabolite Identification

Common Name

Octyl phenylacetate

Description

Octyl phenylacetate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. Based on a literature review a small amount of articles have been published on Octyl phenylacetate.

Structure

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

HMDB0037713
     RDKit          3D
Octyl phenylacetate
 42 42  0  0  0  0  0  0  0  0999 V2000
    6.2299    0.2808    0.4389 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3809    1.4283    0.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1077    1.5428    0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3227    0.2310    0.2151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0861    0.3844   -0.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2004   -0.8320   -0.5872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.1797    0.7794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1597   -2.4180    0.6527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2626   -2.2263   -0.1785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2550   -1.2950    0.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1889   -0.5457    1.0178 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3579   -1.2398   -0.9818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3586   -0.1981   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4514   -0.4828    0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3988    0.4729    0.4535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2789    1.7593   -0.0132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1928    2.0770   -0.8075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2492    1.1006   -1.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8210   -0.6614    0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2435    0.4248    0.8898 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3715    0.2983   -0.6558 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9559    2.3702    0.7180 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1608    1.3169    1.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3784    1.6957   -0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4760    2.3395    0.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9620   -0.5922   -0.1641 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1342    0.1025    1.2805 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4775    1.2573   -0.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4066    0.5525   -1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3197   -0.7296   -1.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7688   -1.7110   -0.9739 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1456   -0.3521    1.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5586   -1.4887    1.4626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4309   -2.8162    1.6553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -3.1999    0.1794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8938   -2.2277   -0.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9798   -1.1042   -2.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5364   -1.4974    0.4961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2572    0.2261    1.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0063    2.5410    0.2174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0607    3.0756   -1.1949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3954    1.3201   -1.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 13  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 12 36  1  0
 12 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
M  END


  Mrv0541 05061309582D          

 18 18  0  0  0  0            999 V2000
    3.5724    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  6  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  2  0  0  0  0
 13 10  1  0  0  0  0
 15 11  2  0  0  0  0
 15 12  1  0  0  0  0
 15 14  1  0  0  0  0
 16 14  1  0  0  0  0
 17 16  2  0  0  0  0
 18 13  1  0  0  0  0
 18 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037713

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCOC(=O)CC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H24O2/c1-2-3-4-5-6-10-13-18-16(17)14-15-11-8-7-9-12-15/h7-9,11-12H,2-6,10,13-14H2,1H3

> <INCHI_KEY>
VGYPAVUJUMQTGE-UHFFFAOYSA-N

> <FORMULA>
C16H24O2

> <MOLECULAR_WEIGHT>
248.3606

> <EXACT_MASS>
248.177630012

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
30.55584478998032

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
octyl 2-phenylacetate

> <ALOGPS_LOGP>
5.50

> <JCHEM_LOGP>
4.8590618359999995

> <ALOGPS_LOGS>
-5.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.086204852056523

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
74.4123

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.66e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
octyl 2-phenylacetate

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0037713
     RDKit          3D
Octyl phenylacetate
 42 42  0  0  0  0  0  0  0  0999 V2000
    6.2299    0.2808    0.4389 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3809    1.4283    0.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1077    1.5428    0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3227    0.2310    0.2151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0861    0.3844   -0.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2004   -0.8320   -0.5872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.1797    0.7794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1597   -2.4180    0.6527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2626   -2.2263   -0.1785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2550   -1.2950    0.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1889   -0.5457    1.0178 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3579   -1.2398   -0.9818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3586   -0.1981   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4514   -0.4828    0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3988    0.4729    0.4535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2789    1.7593   -0.0132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1928    2.0770   -0.8075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2492    1.1006   -1.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8210   -0.6614    0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2435    0.4248    0.8898 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3715    0.2983   -0.6558 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9559    2.3702    0.7180 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1608    1.3169    1.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3784    1.6957   -0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4760    2.3395    0.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9620   -0.5922   -0.1641 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1342    0.1025    1.2805 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4775    1.2573   -0.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4066    0.5525   -1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3197   -0.7296   -1.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7688   -1.7110   -0.9739 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1456   -0.3521    1.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5586   -1.4887    1.4626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4309   -2.8162    1.6553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -3.1999    0.1794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8938   -2.2277   -0.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9798   -1.1042   -2.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5364   -1.4974    0.4961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2572    0.2261    1.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0063    2.5410    0.2174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0607    3.0756   -1.1949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3954    1.3201   -1.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 13  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 12 36  1  0
 12 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       6.668  11.550   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002  10.780   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336  11.550   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669  10.780   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.003  11.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.337  10.780   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      24.006   9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      24.006  10.780   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.673   8.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.671  11.550   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.673  11.550   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      21.339   9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.004  10.780   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.005  11.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.339  10.780   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      18.672  10.780   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      18.672   9.240   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      17.338  11.550   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5   10                                                       
CONECT    7    8    9                                                       
CONECT    8    7   11                                                       
CONECT    9    7   12                                                       
CONECT   10    6   13                                                       
CONECT   11    8   15                                                       
CONECT   12    9   15                                                       
CONECT   13   10   18                                                       
CONECT   14   15   16                                                       
CONECT   15   11   12   14                                                  
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   13   16                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

COMPND    HMDB0037713
HETATM    1  C1  UNL     1       6.230   0.281   0.439  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.381   1.428   0.914  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.108   1.543   0.075  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.323   0.231   0.215  1.00  0.00           C  
HETATM    5  C5  UNL     1       2.086   0.384  -0.620  1.00  0.00           C  
HETATM    6  C6  UNL     1       1.200  -0.832  -0.587  1.00  0.00           C  
HETATM    7  C7  UNL     1       0.715  -1.180   0.779  1.00  0.00           C  
HETATM    8  C8  UNL     1      -0.160  -2.418   0.653  1.00  0.00           C  
HETATM    9  O1  UNL     1      -1.263  -2.226  -0.179  1.00  0.00           O  
HETATM   10  C9  UNL     1      -2.255  -1.295   0.020  1.00  0.00           C  
HETATM   11  O2  UNL     1      -2.189  -0.546   1.018  1.00  0.00           O  
HETATM   12  C10 UNL     1      -3.358  -1.240  -0.982  1.00  0.00           C  
HETATM   13  C11 UNL     1      -4.359  -0.198  -0.654  1.00  0.00           C  
HETATM   14  C12 UNL     1      -5.451  -0.483   0.134  1.00  0.00           C  
HETATM   15  C13 UNL     1      -6.399   0.473   0.453  1.00  0.00           C  
HETATM   16  C14 UNL     1      -6.279   1.759  -0.013  1.00  0.00           C  
HETATM   17  C15 UNL     1      -5.193   2.077  -0.807  1.00  0.00           C  
HETATM   18  C16 UNL     1      -4.249   1.101  -1.118  1.00  0.00           C  
HETATM   19  H1  UNL     1       5.821  -0.661   0.826  1.00  0.00           H  
HETATM   20  H2  UNL     1       7.243   0.425   0.890  1.00  0.00           H  
HETATM   21  H3  UNL     1       6.372   0.298  -0.656  1.00  0.00           H  
HETATM   22  H4  UNL     1       5.956   2.370   0.718  1.00  0.00           H  
HETATM   23  H5  UNL     1       5.161   1.317   1.978  1.00  0.00           H  
HETATM   24  H6  UNL     1       4.378   1.696  -0.972  1.00  0.00           H  
HETATM   25  H7  UNL     1       3.476   2.339   0.500  1.00  0.00           H  
HETATM   26  H8  UNL     1       3.962  -0.592  -0.164  1.00  0.00           H  
HETATM   27  H9  UNL     1       3.134   0.102   1.280  1.00  0.00           H  
HETATM   28  H10 UNL     1       1.477   1.257  -0.314  1.00  0.00           H  
HETATM   29  H11 UNL     1       2.407   0.553  -1.668  1.00  0.00           H  
HETATM   30  H12 UNL     1       0.320  -0.730  -1.250  1.00  0.00           H  
HETATM   31  H13 UNL     1       1.769  -1.711  -0.974  1.00  0.00           H  
HETATM   32  H14 UNL     1       0.146  -0.352   1.259  1.00  0.00           H  
HETATM   33  H15 UNL     1       1.559  -1.489   1.463  1.00  0.00           H  
HETATM   34  H16 UNL     1      -0.431  -2.816   1.655  1.00  0.00           H  
HETATM   35  H17 UNL     1       0.492  -3.200   0.179  1.00  0.00           H  
HETATM   36  H18 UNL     1      -3.894  -2.228  -0.937  1.00  0.00           H  
HETATM   37  H19 UNL     1      -2.980  -1.104  -2.008  1.00  0.00           H  
HETATM   38  H20 UNL     1      -5.536  -1.497   0.496  1.00  0.00           H  
HETATM   39  H21 UNL     1      -7.257   0.226   1.080  1.00  0.00           H  
HETATM   40  H22 UNL     1      -7.006   2.541   0.217  1.00  0.00           H  
HETATM   41  H23 UNL     1      -5.061   3.076  -1.195  1.00  0.00           H  
HETATM   42  H24 UNL     1      -3.395   1.320  -1.733  1.00  0.00           H  
CONECT    1    2   19   20   21
CONECT    2    3   22   23
CONECT    3    4   24   25
CONECT    4    5   26   27
CONECT    5    6   28   29
CONECT    6    7   30   31
CONECT    7    8   32   33
CONECT    8    9   34   35
CONECT    9   10
CONECT   10   11   11   12
CONECT   12   13   36   37
CONECT   13   14   14   18
CONECT   14   15   38
CONECT   15   16   16   39
CONECT   16   17   40
CONECT   17   18   18   41
CONECT   18   42
END

HMDB0037713
     RDKit          3D
Octyl phenylacetate
 42 42  0  0  0  0  0  0  0  0999 V2000
    6.2299    0.2808    0.4389 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3809    1.4283    0.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1077    1.5428    0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3227    0.2310    0.2151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0861    0.3844   -0.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2004   -0.8320   -0.5872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.1797    0.7794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1597   -2.4180    0.6527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2626   -2.2263   -0.1785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2550   -1.2950    0.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1889   -0.5457    1.0178 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3579   -1.2398   -0.9818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3586   -0.1981   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4514   -0.4828    0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3988    0.4729    0.4535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2789    1.7593   -0.0132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1928    2.0770   -0.8075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2492    1.1006   -1.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8210   -0.6614    0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2435    0.4248    0.8898 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3715    0.2983   -0.6558 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9559    2.3702    0.7180 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1608    1.3169    1.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3784    1.6957   -0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4760    2.3395    0.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9620   -0.5922   -0.1641 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1342    0.1025    1.2805 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4775    1.2573   -0.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4066    0.5525   -1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3197   -0.7296   -1.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7688   -1.7110   -0.9739 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1456   -0.3521    1.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5586   -1.4887    1.4626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4309   -2.8162    1.6553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -3.1999    0.1794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8938   -2.2277   -0.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9798   -1.1042   -2.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5364   -1.4974    0.4961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2572    0.2261    1.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0063    2.5410    0.2174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0607    3.0756   -1.1949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3954    1.3201   -1.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 13  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 12 36  1  0
 12 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Octyl phenylacetic acid	Generator
Acetic acid, phenyl-, octyl ester	HMDB
Benzeneacetic acid, octyl ester	HMDB
FEMA 2812	HMDB
Octyl alpha-toluate	HMDB
Octyl benzeneacetate	HMDB

Chemical Formula

C₁₆H₂₄O₂

Average Molecular Weight

248.3606

Monoisotopic Molecular Weight

248.177630012

IUPAC Name

octyl 2-phenylacetate

Traditional Name

octyl 2-phenylacetate

CAS Registry Number

122-45-2

SMILES

CCCCCCCCOC(=O)CC1=CC=CC=C1

InChI Identifier

InChI=1S/C16H24O2/c1-2-3-4-5-6-10-13-18-16(17)14-15-11-8-7-9-12-15/h7-9,11-12H,2-6,10,13-14H2,1H3

InChI Key

VGYPAVUJUMQTGE-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohol esters

Direct Parent

Fatty alcohol esters

Alternative Parents

Substituents

Fatty alcohol ester
Benzenoid
Monocyclic benzene moiety
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Urine (HMDB: HMDB0037713)

Cytoplasm (HMDB: HMDB0037713)
Cell membrane (HMDB: HMDB0037713)

Cellular substructure

Membrane (HMDB: HMDB0037713)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037713)

Source

Endogenous

Endogenous (HMDB: HMDB0037713)

Animal

Animal (HMDB: HMDB0037713)

Exogenous

Food

Food (HMDB: HMDB0037713)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0037713)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0037713)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0037713)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0037713)

Nutrient

Nutrient (HMDB: HMDB0037713)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0037713)

Food and nutrition

Food additive

Flavoring agent

Flavoring agent (HMDB: HMDB0037713)

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
Water Solubility	0.00077 g/L	ALOGPS
logP	5.5	ALOGPS
logP	4.86	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	74.41 m³·mol⁻¹	ChemAxon
Polarizability	30.56 Å³	ChemAxon
Number of Rings	1	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
DarkChem	[M+H]+	161.159	31661259
DarkChem	[M-H]-	160.943	31661259
DeepCCS	[M+H]+	164.55	30932474
DeepCCS	[M-H]-	161.428	30932474
DeepCCS	[M-2H]-	197.395	30932474
DeepCCS	[M+Na]+	173.224	30932474
AllCCS	[M+H]+	161.5	32859911
AllCCS	[M+H-H2O]+	158.1	32859911
AllCCS	[M+NH4]+	164.6	32859911
AllCCS	[M+Na]+	165.5	32859911
AllCCS	[M-H]-	165.7	32859911
AllCCS	[M+Na-2H]-	166.5	32859911
AllCCS	[M+HCOO]-	167.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Octyl phenylacetate	CCCCCCCCOC(=O)CC1=CC=CC=C1	2379.9	Standard polar	33892256
Octyl phenylacetate	CCCCCCCCOC(=O)CC1=CC=CC=C1	1778.3	Standard non polar	33892256
Octyl phenylacetate	CCCCCCCCOC(=O)CC1=CC=CC=C1	1868.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental GC-MS	GC-MS Spectrum - Octyl phenylacetate EI-B (Non-derivatized)	splash10-0006-9100000000-c9aa0ac707d694f5661f	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Octyl phenylacetate EI-B (Non-derivatized)	splash10-0006-9100000000-c9aa0ac707d694f5661f	2018-05-18	HMDB team, MONA, MassBank	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Octyl phenylacetate GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-9200000000-d4a497a0a077e4c870f2	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Octyl phenylacetate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Octyl phenylacetate 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 - Octyl phenylacetate 10V, Positive-QTOF	splash10-0002-2790000000-6785ff681aa684dd7af9	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 20V, Positive-QTOF	splash10-03xr-4910000000-f6e9940254355a5f7ecf	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 40V, Positive-QTOF	splash10-0006-9200000000-402237fd57553506198f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 10V, Negative-QTOF	splash10-00kb-0970000000-7eb9667ada76cb6f2c57	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 20V, Negative-QTOF	splash10-014r-1910000000-2289a15d8a875601dda2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 40V, Negative-QTOF	splash10-014i-5900000000-d9be7b0235501e7854a9	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 10V, Positive-QTOF	splash10-0002-1390000000-ced7676c43ed5987d4f8	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 20V, Positive-QTOF	splash10-0006-9200000000-e75cfe6f4216edcc1956	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 40V, Positive-QTOF	splash10-0006-9300000000-6562825e1fe79cfff5b2	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 10V, Negative-QTOF	splash10-0002-2290000000-38fd8f2b1d514c138a74	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 20V, Negative-QTOF	splash10-0007-9550000000-9c40d079b6c31df9cead	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Octyl phenylacetate 40V, Negative-QTOF	splash10-0006-9200000000-edfc143ebe6c503f5a9b	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

FDB016841

KNApSAcK ID

Not Available

Chemspider ID

55009

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

61050

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Octyl phenylacetate (HMDB0037713)

MOL for HMDB0037713 (Octyl phenylacetate)

3D MOL for HMDB0037713 (Octyl phenylacetate)

3D SDF for HMDB0037713 (Octyl phenylacetate)

3D-SDF for HMDB0037713 (Octyl phenylacetate)

PDB for HMDB0037713 (Octyl phenylacetate)

3D PDB for HMDB0037713 (Octyl phenylacetate)

SMILES for HMDB0037713 (Octyl phenylacetate)

INCHI for HMDB0037713 (Octyl phenylacetate)

Structure for HMDB0037713 (Octyl phenylacetate)

3D Structure for HMDB0037713 (Octyl phenylacetate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra