MiMeDB: Showing metabocard for Butylated hydroxytoluene (MMDBc0047670)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 15:37:02 UTC

Update Date

2022-09-01 01:47:37 UTC

Metabolite ID

MMDBc0047670

Metabolite Identification

Common Name

Butylated hydroxytoluene

Description

2,6-Di-tert-butyl-4-methylphenol, also known as butylated hydroxytoluene or BHT, belongs to the class of organic compounds known as phenylpropanes. These are organic compounds containing a phenylpropane moiety. BHT is a mild, camphor, and musty tasting compound. It has been detected, but not quantified, in soft-necked garlic. This could make BHT a potential biomarker for the consumption of this food. BHT is a synthetic phenolic antioxidant (SPA). SPAs are a family of chemicals used widely in foods, polymers, and cosmetics as radical trapping agents to slow down degradation due to oxidation. Given their widespread use, human exposure is unavoidable and there is public concern regarding environmental contamination by these chemicals. BHT was detected in human urine (PMID:31265952 ).

Structure

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

HMDB0033826
     RDKit          3D
2,6-Di-tert-butyl-4-methylphenol
 40 40  0  0  0  0  0  0  0  0999 V2000
    0.0675    3.6086   -0.9678 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0536    2.1703   -0.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2171    1.5030   -0.3379 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1957    0.1628    0.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4955   -0.4852    0.2687 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7397   -1.6547   -0.6710 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6384    0.4695    0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5283   -0.9956    1.6922 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0072   -0.5285    0.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0556   -1.8591    0.4833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1766    0.1352   -0.1219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4851   -0.5653   -0.0148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7186   -1.1074    1.3738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6151   -1.6473   -1.0711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5984    0.4286   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1321    1.4767   -0.4754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9307    3.9265   -1.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2608    4.2110   -0.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8761    3.7992   -1.6989 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1456    2.0687   -0.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -1.4046   -1.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2313   -2.5722   -0.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8356   -1.8688   -0.6065 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5488    1.2708    0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6937    0.8426   -0.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5757   -0.1019    0.3231 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879   -1.1883    1.9710 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1420   -0.1827    2.3592 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9640   -1.9248    1.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7024   -2.4818    0.6012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9578   -2.1936    1.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8524   -0.9538    2.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5827   -0.6220    1.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3307   -1.3715   -1.8739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6355   -1.8140   -1.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9269   -2.6180   -0.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5016    1.2311    0.4930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5882   -0.0255   -0.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5729    0.8261   -1.3087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0392    2.0361   -0.6797 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  1  0
  5  6  1  0
  5  7  1  0
  5  8  1  0
  4  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 12 15  1  0
 11 16  2  0
 16  2  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  6 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 10 30  1  0
 13 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
M  END


  Mrv1652304282018152D          

 16 16  0  0  0  0            999 V2000
 9992.4001 9991.8056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9993.1137 9991.3931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9992.8126 9992.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9991.9877 9992.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.9729 9992.6306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9989.5420 9991.8056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.9729 9989.3307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9988.8275 9991.3931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9989.1284 9992.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9989.9534 9992.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9991.6851 9991.3931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.9713 9991.8052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.2574 9991.3930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.2573 9990.5688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.9712 9990.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9991.6851 9990.5688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  0  0  0  0
  1  4  1  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  6 10  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 11  1  0  0  0  0
  1 11  1  0  0  0  0
 12  5  1  0  0  0  0
 13  6  1  0  0  0  0
 15  7  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0047670

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3

> <INCHI_KEY>
NLZUEZXRPGMBCV-UHFFFAOYSA-N

> <FORMULA>
C15H24O

> <MOLECULAR_WEIGHT>
220.3505

> <EXACT_MASS>
220.18271539

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
27.348201983235235

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,6-di-tert-butyl-4-methylphenol

> <ALOGPS_LOGP>
5.25

> <JCHEM_LOGP>
5.273214425000001

> <ALOGPS_LOGS>
-4.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.602391152527046

> <JCHEM_PKA_STRONGEST_BASIC>
-4.559361293068014

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
70.41189999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.52e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ional

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0033826
     RDKit          3D
2,6-Di-tert-butyl-4-methylphenol
 40 40  0  0  0  0  0  0  0  0999 V2000
    0.0675    3.6086   -0.9678 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0536    2.1703   -0.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2171    1.5030   -0.3379 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1957    0.1628    0.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4955   -0.4852    0.2687 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7397   -1.6547   -0.6710 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6384    0.4695    0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5283   -0.9956    1.6922 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0072   -0.5285    0.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0556   -1.8591    0.4833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1766    0.1352   -0.1219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4851   -0.5653   -0.0148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7186   -1.1074    1.3738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6151   -1.6473   -1.0711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5984    0.4286   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1321    1.4767   -0.4754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9307    3.9265   -1.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2608    4.2110   -0.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8761    3.7992   -1.6989 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1456    2.0687   -0.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -1.4046   -1.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2313   -2.5722   -0.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8356   -1.8688   -0.6065 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5488    1.2708    0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6937    0.8426   -0.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5757   -0.1019    0.3231 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879   -1.1883    1.9710 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1420   -0.1827    2.3592 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9640   -1.9248    1.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7024   -2.4818    0.6012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9578   -2.1936    1.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8524   -0.9538    2.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5827   -0.6220    1.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3307   -1.3715   -1.8739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6355   -1.8140   -1.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9269   -2.6180   -0.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5016    1.2311    0.4930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5882   -0.0255   -0.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5729    0.8261   -1.3087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0392    2.0361   -0.6797 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  1  0
  5  6  1  0
  5  7  1  0
  5  8  1  0
  4  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 12 15  1  0
 11 16  2  0
 16  2  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  6 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 10 30  1  0
 13 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
M  END

HEADER    PROTEIN                                 28-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-20         0                                  
HETATM    1  C   UNK     0    8652.4808651.370   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8653.8128650.600   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8653.2508652.706   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8651.7108652.706   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8649.8168652.910   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0    8647.1458651.370   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8649.8168646.751   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8645.8118650.600   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8646.3738652.706   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8647.9138652.706   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8651.1468650.600   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8649.8138651.370   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8648.4818650.600   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8648.4808649.062   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8649.8138648.293   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8651.1468649.062   0.000  0.00  0.00           C+0
CONECT    1    2    3    4   11                                             
CONECT    2    1                                                            
CONECT    3    1                                                            
CONECT    4    1                                                            
CONECT    5   12                                                            
CONECT    6    8    9   10   13                                             
CONECT    7   15                                                            
CONECT    8    6                                                            
CONECT    9    6                                                            
CONECT   10    6                                                            
CONECT   11   12   16    1                                                  
CONECT   12   11   13    5                                                  
CONECT   13   12   14    6                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16    7                                                  
CONECT   16   15   11                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

COMPND    HMDB0033826
HETATM    1  C1  UNL     1       0.067   3.609  -0.968  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.054   2.170  -0.587  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.217   1.503  -0.338  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.196   0.163   0.017  1.00  0.00           C  
HETATM    5  C5  UNL     1       2.496  -0.485   0.269  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.740  -1.655  -0.671  1.00  0.00           C  
HETATM    7  C7  UNL     1       3.638   0.470   0.100  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.528  -0.996   1.692  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.007  -0.528   0.127  1.00  0.00           C  
HETATM   10  O1  UNL     1       0.056  -1.859   0.483  1.00  0.00           O  
HETATM   11  C10 UNL     1      -1.177   0.135  -0.122  1.00  0.00           C  
HETATM   12  C11 UNL     1      -2.485  -0.565  -0.015  1.00  0.00           C  
HETATM   13  C12 UNL     1      -2.719  -1.107   1.374  1.00  0.00           C  
HETATM   14  C13 UNL     1      -2.615  -1.647  -1.071  1.00  0.00           C  
HETATM   15  C14 UNL     1      -3.598   0.429  -0.279  1.00  0.00           C  
HETATM   16  C15 UNL     1      -1.132   1.477  -0.475  1.00  0.00           C  
HETATM   17  H1  UNL     1      -0.931   3.926  -1.336  1.00  0.00           H  
HETATM   18  H2  UNL     1       0.261   4.211  -0.042  1.00  0.00           H  
HETATM   19  H3  UNL     1       0.876   3.799  -1.699  1.00  0.00           H  
HETATM   20  H4  UNL     1       2.146   2.069  -0.431  1.00  0.00           H  
HETATM   21  H5  UNL     1       2.487  -1.405  -1.704  1.00  0.00           H  
HETATM   22  H6  UNL     1       2.231  -2.572  -0.301  1.00  0.00           H  
HETATM   23  H7  UNL     1       3.836  -1.869  -0.607  1.00  0.00           H  
HETATM   24  H8  UNL     1       3.549   1.271   0.852  1.00  0.00           H  
HETATM   25  H9  UNL     1       3.694   0.843  -0.944  1.00  0.00           H  
HETATM   26  H10 UNL     1       4.576  -0.102   0.323  1.00  0.00           H  
HETATM   27  H11 UNL     1       3.588  -1.188   1.971  1.00  0.00           H  
HETATM   28  H12 UNL     1       2.142  -0.183   2.359  1.00  0.00           H  
HETATM   29  H13 UNL     1       1.964  -1.925   1.831  1.00  0.00           H  
HETATM   30  H14 UNL     1      -0.702  -2.482   0.601  1.00  0.00           H  
HETATM   31  H15 UNL     1      -2.958  -2.194   1.364  1.00  0.00           H  
HETATM   32  H16 UNL     1      -1.852  -0.954   2.048  1.00  0.00           H  
HETATM   33  H17 UNL     1      -3.583  -0.622   1.893  1.00  0.00           H  
HETATM   34  H18 UNL     1      -3.331  -1.371  -1.874  1.00  0.00           H  
HETATM   35  H19 UNL     1      -1.636  -1.814  -1.602  1.00  0.00           H  
HETATM   36  H20 UNL     1      -2.927  -2.618  -0.620  1.00  0.00           H  
HETATM   37  H21 UNL     1      -3.502   1.231   0.493  1.00  0.00           H  
HETATM   38  H22 UNL     1      -4.588  -0.025  -0.123  1.00  0.00           H  
HETATM   39  H23 UNL     1      -3.573   0.826  -1.309  1.00  0.00           H  
HETATM   40  H24 UNL     1      -2.039   2.036  -0.680  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    3   16
CONECT    3    4   20
CONECT    4    5    9    9
CONECT    5    6    7    8
CONECT    6   21   22   23
CONECT    7   24   25   26
CONECT    8   27   28   29
CONECT    9   10   11
CONECT   10   30
CONECT   11   12   16   16
CONECT   12   13   14   15
CONECT   13   31   32   33
CONECT   14   34   35   36
CONECT   15   37   38   39
CONECT   16   40
END

HMDB0033826
     RDKit          3D
2,6-Di-tert-butyl-4-methylphenol
 40 40  0  0  0  0  0  0  0  0999 V2000
    0.0675    3.6086   -0.9678 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0536    2.1703   -0.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2171    1.5030   -0.3379 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1957    0.1628    0.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4955   -0.4852    0.2687 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7397   -1.6547   -0.6710 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6384    0.4695    0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5283   -0.9956    1.6922 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0072   -0.5285    0.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0556   -1.8591    0.4833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1766    0.1352   -0.1219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4851   -0.5653   -0.0148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7186   -1.1074    1.3738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6151   -1.6473   -1.0711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5984    0.4286   -0.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1321    1.4767   -0.4754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9307    3.9265   -1.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2608    4.2110   -0.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8761    3.7992   -1.6989 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1456    2.0687   -0.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -1.4046   -1.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2313   -2.5722   -0.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8356   -1.8688   -0.6065 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5488    1.2708    0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6937    0.8426   -0.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5757   -0.1019    0.3231 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879   -1.1883    1.9710 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1420   -0.1827    2.3592 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9640   -1.9248    1.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7024   -2.4818    0.6012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9578   -2.1936    1.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8524   -0.9538    2.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5827   -0.6220    1.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3307   -1.3715   -1.8739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6355   -1.8140   -1.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9269   -2.6180   -0.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5016    1.2311    0.4930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5882   -0.0255   -0.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5729    0.8261   -1.3087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0392    2.0361   -0.6797 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  1  0
  5  6  1  0
  5  7  1  0
  5  8  1  0
  4  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 12 15  1  0
 11 16  2  0
 16  2  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  6 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 10 30  1  0
 13 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
M  END

Synonyms

Value	Source
2,6-Bis(1,1-dimethylethyl)-4-methylphenol	ChEBI
2,6-Di-t-butyl-4-methylphenol	ChEBI
2,6-Di-tert-butyl-1-hydroxy-4-methylbenzene	ChEBI
2,6-Di-tert-butyl-4-cresol	ChEBI
2,6-Di-tert-butyl-p-cresol	ChEBI
BHT	ChEBI
Butylated hydroxytoluene	ChEBI
Butylhydroxytoluene	ChEBI
2,6 Di t butyl 4 methylphenol	MeSH
2,6 Di tert butyl 4 methylphenol	MeSH
2,6 Di tert butyl p cresol	MeSH
4 Methyl 2,6 ditertbutylphenol	MeSH
4-Methyl-2,6-ditertbutylphenol	MeSH
Di tert butyl methylphenol	MeSH
Dibunol	MeSH
Hydroxytoluene, butylated	MeSH
Ionol	MeSH
Ionol (BHT)	MeSH
Di-tert-butyl-methylphenol	MeSH
2,6-Bis(1,1-dimethylethyl)-4-methylphenol, 9ci	HMDB
2,6-Di-tert-butyl-P-cresol, 8ci	HMDB
Butyl hydroxy toluene	HMDB
e321	HMDB
FEMA 2184	HMDB
Popol	HMDB
2,6-Bis(tert-butyl)-4-methylphenol	HMDB
2,6-Di(tert-butyl)hydroxytoluene	HMDB
2,6-Di-tert-butyl-4-hydroxytoluene	HMDB
2,6-Di-tert-butyl-4-methyl phenol	HMDB
2,6-Di-tert-butyl-4-methyl-1-hydroxybenzene	HMDB
2,6-Di-tert-butyl-4-methylhydroxybenzene	HMDB
2,6-Di-tert-butyl-4-methylphenol	HMDB
2,6-Di-tert-butyl-p-cresole	HMDB
2,6-Di-tert-butyl-p-methylphenol	HMDB
2,6-Di-tert-butylcresol	HMDB
2,6-Di-tert-butylmethylphenol	HMDB
2,6-Ditertbutyl paracresol	HMDB
2,6-tert-Butyl-4-methylphenol	HMDB
3,5-Bis(1,1-dimethylethyl)-4-hydroxytoluene	HMDB
3,5-Di-tert-butyl-4-hydroxytoluene	HMDB
3,5-Di-tert-butyl-p-hydroxytoluene	HMDB
4-Hydroxy-3,5-di-tert-butyltoluene	HMDB
4-Methyl-2,6-bis(1,1-dimethylethyl)phenol	HMDB
4-Methyl-2,6-di-tert-butylphenol	HMDB
4-Methyl-2,6-ditertbutyl phenol	HMDB
Di-tert-Butyl-4-methylphenol	HMDB
Di-tert-butyl-p-cresol	HMDB
Di-tert-butylcresol	HMDB
Dibutyl paracresol	HMDB
Dibutylated hydroxytoluene	HMDB
Dibutylcresol	HMDB
Dibutylhydroxytoluene	HMDB
o-Di-tert-butyl-p-methylphenol	HMDB

Molecular Formula

C₁₅H₂₄O

Average Mass

220.3505

Monoisotopic Mass

220.18271539

IUPAC Name

2,6-di-tert-butyl-4-methylphenol

Traditional Name

ional

CAS Registry Number

Not Available

SMILES

CC1=CC(=C(O)C(=C1)C(C)(C)C)C(C)(C)C

InChI Identifier

InChI=1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3

InChI Key

NLZUEZXRPGMBCV-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpropanes. These are organic compounds containing a phenylpropane moiety.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Phenylpropanes

Direct Parent

Phenylpropanes

Alternative Parents

Substituents

Phenylpropane
P-cresol
Toluene
Phenol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

phenols (CHEBI:34247 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.015 g/L	ALOGPS
logP	5.25	ALOGPS
logP	5.27	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	11.6	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	70.41 m³·mol⁻¹	ChemAxon
Polarizability	27.35 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Blood
Saliva
Urine

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Unknown

Exposure Sources

Food Exposures

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Age	Sex	Health Condition	Data Source	Reference
Human	Detected and Quantified	0.000174	Adult (>18 years old)	Both	Normal	HMDB	31265952
Human Saliva	Detected but not Quantified		Adult (>18 years old)	Male	Normal	HMDB	1268322
Human	Detected but not Quantified					HMDB

External Links

HMDB ID

HMDB0033826

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Butylated_hydroxytoluene

METLIN ID

Not Available

PubChem Compound

31404

PDB ID

Not Available

ChEBI ID

34247

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Liu R, Mabury SA: Unexpectedly high concentrations of 2,4-di-tert-butylphenol in human urine. Environ Pollut. 2019 Sep;252(Pt B):1423-1428. doi: 10.1016/j.envpol.2019.06.077. Epub 2019 Jun 21. [PubMed:31265952 ]
Yannai, Shmuel (2004). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. Boca Raton: Chapman & Hall/CRC..

Showing metabocard for Butylated hydroxytoluene (MMDBc0047670)

MOL for #<Metabolite:0x0000560be235eb40>

3D MOL for #<Metabolite:0x0000560be235eb40>

3D SDF for #<Metabolite:0x0000560be235eb40>

3D-SDF for #<Metabolite:0x0000560be235eb40>

PDB for #<Metabolite:0x0000560be235eb40>

3D PDB for #<Metabolite:0x0000560be235eb40>

SMILES for #<Metabolite:0x0000560be235eb40>

INCHI for #<Metabolite:0x0000560be235eb40>

Structure for #<Metabolite:0x0000560be235eb40>

3D Structure for #<Metabolite:0x0000560be235eb40>