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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:47:26 UTC

Update Date

2023-02-21 17:21:32 UTC

HMDB ID

HMDB0032044

Secondary Accession Numbers

HMDB32044

Metabolite Identification

Common Name

Hexyl 3-methylbutanoate

Description

Hexyl 3-methylbutanoate, also known as hexyl isopentanoate or hexyl isovalerate, belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. Hexyl 3-methylbutanoate is a very hydrophobic molecule, practically insoluble in water, and relatively neutral.

Structure

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

HMDB0032044
     RDKit          3D
Hexyl 3-methylbutanoate
 35 34  0  0  0  0  0  0  0  0999 V2000
    4.3218    1.1157    1.0138 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0421    0.5096    0.4659 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2962   -0.7447   -0.2990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0506   -1.3853   -0.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3507   -0.4615   -1.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0935   -1.0561   -2.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8781   -1.4235   -1.4578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4766   -0.5292   -0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1105    0.6674   -0.6722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5286   -0.9558    0.3895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9501    0.2890    1.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5162    1.3356    0.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9623   -0.0267    2.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0355    1.7120    1.9002 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0447    0.3444    1.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7878    1.7866    0.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    0.3437    1.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6497    1.2845   -0.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9763   -0.5781   -1.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8688   -1.4565    0.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2693   -2.3796   -1.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079   -1.6123    0.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1225    0.4858   -1.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9990   -0.1871   -2.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2746   -0.2872   -3.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3331   -1.9442   -2.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1569   -1.7031    1.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4099   -1.3635   -0.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0732    0.7398    1.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4452    1.7313    0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7610    0.8551   -0.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7587    2.1375    0.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4441   -0.2441    3.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5890    0.8789    2.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6439   -0.8519    1.9261 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  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
M  END

HMDB0032044
     RDKit          3D
Hexyl 3-methylbutanoate
 35 34  0  0  0  0  0  0  0  0999 V2000
    4.3218    1.1157    1.0138 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0421    0.5096    0.4659 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2962   -0.7447   -0.2990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0506   -1.3853   -0.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3507   -0.4615   -1.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0935   -1.0561   -2.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8781   -1.4235   -1.4578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4766   -0.5292   -0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1105    0.6674   -0.6722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5286   -0.9558    0.3895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9501    0.2890    1.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5162    1.3356    0.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9623   -0.0267    2.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0355    1.7120    1.9002 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0447    0.3444    1.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7878    1.7866    0.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    0.3437    1.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6497    1.2845   -0.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9763   -0.5781   -1.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8688   -1.4565    0.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2693   -2.3796   -1.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079   -1.6123    0.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1225    0.4858   -1.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9990   -0.1871   -2.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2746   -0.2872   -3.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3331   -1.9442   -2.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1569   -1.7031    1.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4099   -1.3635   -0.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0732    0.7398    1.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4452    1.7313    0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7610    0.8551   -0.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7587    2.1375    0.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4441   -0.2441    3.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5890    0.8789    2.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6439   -0.8519    1.9261 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  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
M  END

HEADER    PROTEIN                                 27-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-MAY-19         0                                  
HETATM    1  C   UNK     0      -6.724  -3.231   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.613  -3.231   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.279  -5.541   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.390  -4.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.056  -3.231   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.723  -4.001   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.389  -3.231   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.055  -4.001   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.946  -3.231   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.279  -4.001   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.612  -4.001   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.612  -5.541   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       1.278  -3.231   0.000  0.00  0.00           O+0
CONECT    1    4                                                            
CONECT    2   10                                                            
CONECT    3   10                                                            
CONECT    4    1    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7   13                                                       
CONECT    9   10   11                                                       
CONECT   10    2    3    9                                                  
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13    8   11                                                       
MASTER        0    0    0    0    0    0    0    0   13    0   24    0
END

COMPND    HMDB0032044
HETATM    1  C1  UNL     1       4.322   1.116   1.014  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.042   0.510   0.466  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.296  -0.745  -0.299  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.051  -1.385  -0.848  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.351  -0.461  -1.781  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.094  -1.056  -2.376  1.00  0.00           C  
HETATM    7  O1  UNL     1      -0.878  -1.424  -1.458  1.00  0.00           O  
HETATM    8  C7  UNL     1      -1.477  -0.529  -0.600  1.00  0.00           C  
HETATM    9  O2  UNL     1      -1.111   0.667  -0.672  1.00  0.00           O  
HETATM   10  C8  UNL     1      -2.529  -0.956   0.390  1.00  0.00           C  
HETATM   11  C9  UNL     1      -2.950   0.289   1.147  1.00  0.00           C  
HETATM   12  C10 UNL     1      -3.516   1.336   0.221  1.00  0.00           C  
HETATM   13  C11 UNL     1      -3.962  -0.027   2.217  1.00  0.00           C  
HETATM   14  H1  UNL     1       4.035   1.712   1.900  1.00  0.00           H  
HETATM   15  H2  UNL     1       5.045   0.344   1.349  1.00  0.00           H  
HETATM   16  H3  UNL     1       4.788   1.787   0.276  1.00  0.00           H  
HETATM   17  H4  UNL     1       2.329   0.344   1.273  1.00  0.00           H  
HETATM   18  H5  UNL     1       2.650   1.284  -0.250  1.00  0.00           H  
HETATM   19  H6  UNL     1       3.976  -0.578  -1.175  1.00  0.00           H  
HETATM   20  H7  UNL     1       3.869  -1.457   0.356  1.00  0.00           H  
HETATM   21  H8  UNL     1       2.269  -2.380  -1.282  1.00  0.00           H  
HETATM   22  H9  UNL     1       1.408  -1.612   0.053  1.00  0.00           H  
HETATM   23  H10 UNL     1       1.122   0.486  -1.258  1.00  0.00           H  
HETATM   24  H11 UNL     1       1.999  -0.187  -2.641  1.00  0.00           H  
HETATM   25  H12 UNL     1      -0.275  -0.287  -3.118  1.00  0.00           H  
HETATM   26  H13 UNL     1       0.333  -1.944  -2.998  1.00  0.00           H  
HETATM   27  H14 UNL     1      -2.157  -1.703   1.095  1.00  0.00           H  
HETATM   28  H15 UNL     1      -3.410  -1.363  -0.147  1.00  0.00           H  
HETATM   29  H16 UNL     1      -2.073   0.740   1.686  1.00  0.00           H  
HETATM   30  H17 UNL     1      -4.445   1.731   0.676  1.00  0.00           H  
HETATM   31  H18 UNL     1      -3.761   0.855  -0.760  1.00  0.00           H  
HETATM   32  H19 UNL     1      -2.759   2.138   0.073  1.00  0.00           H  
HETATM   33  H20 UNL     1      -3.444  -0.244   3.187  1.00  0.00           H  
HETATM   34  H21 UNL     1      -4.589   0.879   2.361  1.00  0.00           H  
HETATM   35  H22 UNL     1      -4.644  -0.852   1.926  1.00  0.00           H  
CONECT    1    2   14   15   16
CONECT    2    3   17   18
CONECT    3    4   19   20
CONECT    4    5   21   22
CONECT    5    6   23   24
CONECT    6    7   25   26
CONECT    7    8
CONECT    8    9    9   10
CONECT   10   11   27   28
CONECT   11   12   13   29
CONECT   12   30   31   32
CONECT   13   33   34   35
END

HMDB0032044
     RDKit          3D
Hexyl 3-methylbutanoate
 35 34  0  0  0  0  0  0  0  0999 V2000
    4.3218    1.1157    1.0138 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0421    0.5096    0.4659 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2962   -0.7447   -0.2990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0506   -1.3853   -0.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3507   -0.4615   -1.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0935   -1.0561   -2.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8781   -1.4235   -1.4578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4766   -0.5292   -0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1105    0.6674   -0.6722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5286   -0.9558    0.3895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9501    0.2890    1.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5162    1.3356    0.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9623   -0.0267    2.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0355    1.7120    1.9002 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0447    0.3444    1.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7878    1.7866    0.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    0.3437    1.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6497    1.2845   -0.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9763   -0.5781   -1.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8688   -1.4565    0.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2693   -2.3796   -1.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079   -1.6123    0.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1225    0.4858   -1.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9990   -0.1871   -2.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2746   -0.2872   -3.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3331   -1.9442   -2.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1569   -1.7031    1.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4099   -1.3635   -0.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0732    0.7398    1.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4452    1.7313    0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7610    0.8551   -0.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7587    2.1375    0.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4441   -0.2441    3.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5890    0.8789    2.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6439   -0.8519    1.9261 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  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Hexyl 3-methylbutanoic acid	Generator
3-Methylbutyric acid hexyl ester	HMDB
Butanoic acid, 3-methyl-, hexyl ester	HMDB
Caproyl isovalerate	HMDB
FEMA 3500	HMDB
Hexyl 3-methyl butanoate	HMDB
Hexyl 3-methyl butyrate	HMDB
Hexyl 3-methylbutyrate	HMDB
Hexyl isopentanoate	HMDB
Hexyl isovalerate	HMDB
Hexyl isovalerianate	HMDB
Hexyl isovaleriate	HMDB
Isovaleric acid, hexyl ester	HMDB
Isovaleric acid, hexyl ester (8ci)	HMDB
N-Hexyl iso-valerate	HMDB
N-Hexyl isopentanoate	HMDB

Chemical Formula

C₁₁H₂₂O₂

Average Molecular Weight

186.2912

Monoisotopic Molecular Weight

186.161979948

IUPAC Name

hexyl 3-methylbutanoate

Traditional Name

hexyl 3-methylbutanoate

CAS Registry Number

10032-13-0

SMILES

CCCCCCOC(=O)CC(C)C

InChI Identifier

InChI=1S/C11H22O2/c1-4-5-6-7-8-13-11(12)9-10(2)3/h10H,4-9H2,1-3H3

InChI Key

RSDDTPVXLMVLQE-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid esters

Alternative Parents

Substituents

Fatty acid ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Organoleptic effect

Taste

Sweet

Odor

Disposition

Biological location

Cellular substructure

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0032044)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0032044)

Source

Endogenous

Endogenous (HMDB: HMDB0032044)

Plant

Plant (HMDB: HMDB0032044)

Animal

Animal (HMDB: HMDB0032044)

Exogenous

Food

Food (HMDB: HMDB0032044)

Herb and spice

Oilseed crop

Safflower (FooDB: FOOD00042)

Exogenous (HMDB: HMDB0032044)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0032044)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0032044)

Lipid metabolism pathway (HMDB: HMDB0032044)

Cellular process

Cell signaling (HMDB: HMDB0032044)

Biochemical process

Lipid transport (HMDB: HMDB0032044)

Role

Biological role

Energy source (HMDB: HMDB0032044)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0032044)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	215.00 °C. @ 760.00 mm Hg	The Good Scents Company Information System
Water Solubility	12.56 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	4.196 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.049 g/L	ALOGPS
logP	4.17	ALOGPS
logP	3.57	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Basic)	-7	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	8	ChemAxon
Refractivity	54.26 m³·mol⁻¹	ChemAxon
Polarizability	23.29 Å³	ChemAxon
Number of Rings	0	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]+	144.945	31661259
DarkChem	[M-H]-	142.592	31661259
DeepCCS	[M+H]+	153.005	30932474
DeepCCS	[M-H]-	149.56	30932474
DeepCCS	[M-2H]-	186.977	30932474
DeepCCS	[M+Na]+	162.622	30932474
AllCCS	[M+H]+	148.4	32859911
AllCCS	[M+H-H2O]+	144.8	32859911
AllCCS	[M+NH4]+	151.8	32859911
AllCCS	[M+Na]+	152.7	32859911
AllCCS	[M-H]-	149.5	32859911
AllCCS	[M+Na-2H]-	151.2	32859911
AllCCS	[M+HCOO]-	153.2	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	7.93 minutes	32390414
Predicted by Siyang on May 30, 2022	18.7693 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.86 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	26.6 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2547.9 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	641.0 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	235.2 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	393.8 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	415.6 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	844.5 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	822.4 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	95.1 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1582.0 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	546.0 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1670.3 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	551.8 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	447.6 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	506.8 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	574.7 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	9.1 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Hexyl 3-methylbutanoate	CCCCCCOC(=O)CC(C)C	1435.0	Standard polar	33892256
Hexyl 3-methylbutanoate	CCCCCCOC(=O)CC(C)C	1224.6	Standard non polar	33892256
Hexyl 3-methylbutanoate	CCCCCCOC(=O)CC(C)C	1265.4	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental GC-MS	GC-MS Spectrum - Hexyl 3-methylbutanoate EI-B (Non-derivatized)	splash10-052o-9100000000-73d73fa328924a52408b	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Hexyl 3-methylbutanoate EI-B (Non-derivatized)	splash10-052o-9100000000-73d73fa328924a52408b	2018-05-18	HMDB team, MONA, MassBank	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Hexyl 3-methylbutanoate GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4r-9000000000-fa60e5802af8472e4f2d	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Hexyl 3-methylbutanoate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Hexyl 3-methylbutanoate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
MS	Mass Spectrum (Electron Ionization)	splash10-0pbl-9100000000-43d4d349248bf1e6dca8	2015-03-01	Not Available	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 10V, Positive-QTOF	splash10-000i-6900000000-8d7d4c714cfab8d100a8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 20V, Positive-QTOF	splash10-000i-9100000000-3d30266ad97c4f100d1d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 40V, Positive-QTOF	splash10-0a4l-9000000000-8c64e81ad6d0f829d1d5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 10V, Negative-QTOF	splash10-0019-6900000000-55ae203952b5926506d9	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 20V, Negative-QTOF	splash10-0ue9-9700000000-f953a25f7a959250619a	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 40V, Negative-QTOF	splash10-0kai-9100000000-ea3acd98c1c574f085a8	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 10V, Positive-QTOF	splash10-000l-9200000000-23949d54ec6ac8e13712	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 20V, Positive-QTOF	splash10-000l-9000000000-903fab1f1081329f770f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 40V, Positive-QTOF	splash10-052f-9000000000-7c9c180c877fa0670678	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 10V, Negative-QTOF	splash10-0udi-0900000000-48466664099e54f50de8	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 20V, Negative-QTOF	splash10-0ue9-8900000000-6396a01441e6bc4dff62	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hexyl 3-methylbutanoate 40V, Negative-QTOF	splash10-00kf-9000000000-aced5fcf3e6910982cc9	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-04	FELIX lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
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

FDB008748

KNApSAcK ID

C00030481

Chemspider ID

55377

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

61455

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1027041

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 Hexyl 3-methylbutanoate (HMDB0032044)

MOL for HMDB0032044 (Hexyl 3-methylbutanoate)

3D MOL for HMDB0032044 (Hexyl 3-methylbutanoate)

3D SDF for HMDB0032044 (Hexyl 3-methylbutanoate)

3D-SDF for HMDB0032044 (Hexyl 3-methylbutanoate)

PDB for HMDB0032044 (Hexyl 3-methylbutanoate)

3D PDB for HMDB0032044 (Hexyl 3-methylbutanoate)

SMILES for HMDB0032044 (Hexyl 3-methylbutanoate)

INCHI for HMDB0032044 (Hexyl 3-methylbutanoate)

Structure for HMDB0032044 (Hexyl 3-methylbutanoate)

3D Structure for HMDB0032044 (Hexyl 3-methylbutanoate)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

IR Spectra