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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:32:50 UTC

Update Date

2023-02-21 17:19:16 UTC

HMDB ID

HMDB0029820

Secondary Accession Numbers

HMDB29820

Metabolite Identification

Common Name

2,6-Diisopropyl-3-methylphenol

Description

2,6-Diisopropyl-3-methylphenol belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. Based on a literature review a small amount of articles have been published on 2,6-Diisopropyl-3-methylphenol.

Structure

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

HMDB0029820
     RDKit          3D
2,6-Diisopropyl-3-methylphenol
 34 34  0  0  0  0  0  0  0  0999 V2000
   -2.2046    2.4000   -0.3806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9655    1.5792   -0.2289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2228    2.1465    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3696    1.3769    0.2753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3907    0.0311    0.0886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5976   -0.7901    0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2980   -1.1415    1.3125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6502    0.2234   -0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1264   -0.5833   -0.2839 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3076   -1.9202   -0.4402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9950    0.1647   -0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3473   -0.3265   -0.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1618   -0.2430    0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3760   -1.8563   -0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7287    2.5146    0.6121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9059    3.4498   -0.6338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8609    2.0773   -1.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2324    3.1981    0.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3091    1.8860    0.5589 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5291   -1.5966   -0.7183 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5846   -2.2326    1.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6145   -1.0463    2.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2412   -0.6285    1.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3718   -0.4033   -1.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    0.8621   -1.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1609    0.7476    0.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1445   -2.6826   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8199    0.1689   -1.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9771    0.4710    0.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4753    0.0613    1.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6042   -1.1987    0.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -2.1684   -0.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0408   -2.1958   -1.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0107   -2.3447    0.0328 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
  6  8  1  0
  5  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 11  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  0
  7 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END

  Mrv0541 02241218302D          

 14 14  0  0  0  0            999 V2000
   -0.7136    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7136   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7123   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7123    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.4111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4273    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4274    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1423    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4274    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1423    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4273    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4273   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  1  9  1  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
  4 14  1  0  0  0  0
  5  6  2  0  0  0  0
  5  8  1  0  0  0  0
  6  7  1  0  0  0  0
  8 12  1  0  0  0  0
  8 13  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029820

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C1=CC=C(C)C(C(C)C)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C13H20O/c1-8(2)11-7-6-10(5)12(9(3)4)13(11)14/h6-9,14H,1-5H3

> <INCHI_KEY>
KEGGEHPMMDYTGB-UHFFFAOYSA-N

> <FORMULA>
C13H20O

> <MOLECULAR_WEIGHT>
192.2973

> <EXACT_MASS>
192.151415262

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
23.56951147452191

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-methyl-2,6-bis(propan-2-yl)phenol

> <ALOGPS_LOGP>
4.15

> <JCHEM_LOGP>
4.673120185

> <ALOGPS_LOGS>
-3.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.068582886321014

> <JCHEM_PKA_STRONGEST_BASIC>
-4.984132735171248

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
61.46169999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.50e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,6-diisopropyl-3-methylphenol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0029820
     RDKit          3D
2,6-Diisopropyl-3-methylphenol
 34 34  0  0  0  0  0  0  0  0999 V2000
   -2.2046    2.4000   -0.3806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9655    1.5792   -0.2289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2228    2.1465    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3696    1.3769    0.2753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3907    0.0311    0.0886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5976   -0.7901    0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2980   -1.1415    1.3125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6502    0.2234   -0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1264   -0.5833   -0.2839 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3076   -1.9202   -0.4402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9950    0.1647   -0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3473   -0.3265   -0.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1618   -0.2430    0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3760   -1.8563   -0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7287    2.5146    0.6121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9059    3.4498   -0.6338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8609    2.0773   -1.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2324    3.1981    0.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3091    1.8860    0.5589 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5291   -1.5966   -0.7183 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5846   -2.2326    1.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6145   -1.0463    2.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2412   -0.6285    1.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3718   -0.4033   -1.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    0.8621   -1.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1609    0.7476    0.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1445   -2.6826   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8199    0.1689   -1.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9771    0.4710    0.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4753    0.0613    1.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6042   -1.1987    0.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -2.1684   -0.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0408   -2.1958   -1.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0107   -2.3447    0.0328 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
  6  8  1  0
  5  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 11  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  0
  7 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -1.332   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.332  -1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.330  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.330   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.767   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.000   2.307   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.664   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.664   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.999   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.664   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.999   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.664   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.664  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2    6    9                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6    8                                                  
CONECT    6    1    5    7                                                  
CONECT    7    6                                                            
CONECT    8    5   12   13                                                  
CONECT    9    1   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8                                                            
CONECT   13    8                                                            
CONECT   14    4                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   28    0
END

COMPND    HMDB0029820
HETATM    1  C1  UNL     1      -2.205   2.400  -0.381  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.966   1.579  -0.229  1.00  0.00           C  
HETATM    3  C3  UNL     1       0.223   2.147   0.117  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.370   1.377   0.275  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.391   0.031   0.089  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.598  -0.790   0.009  1.00  0.00           C  
HETATM    7  C7  UNL     1       3.298  -1.141   1.313  1.00  0.00           C  
HETATM    8  C8  UNL     1       3.650   0.223  -0.637  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.126  -0.583  -0.284  1.00  0.00           C  
HETATM   10  O1  UNL     1       0.308  -1.920  -0.440  1.00  0.00           O  
HETATM   11  C10 UNL     1      -0.995   0.165  -0.424  1.00  0.00           C  
HETATM   12  C11 UNL     1      -2.347  -0.326  -0.706  1.00  0.00           C  
HETATM   13  C12 UNL     1      -3.162  -0.243   0.635  1.00  0.00           C  
HETATM   14  C13 UNL     1      -2.376  -1.856  -0.930  1.00  0.00           C  
HETATM   15  H1  UNL     1      -2.729   2.515   0.612  1.00  0.00           H  
HETATM   16  H2  UNL     1      -1.906   3.450  -0.634  1.00  0.00           H  
HETATM   17  H3  UNL     1      -2.861   2.077  -1.199  1.00  0.00           H  
HETATM   18  H4  UNL     1       0.232   3.198   0.263  1.00  0.00           H  
HETATM   19  H5  UNL     1       2.309   1.886   0.559  1.00  0.00           H  
HETATM   20  H6  UNL     1       2.529  -1.597  -0.718  1.00  0.00           H  
HETATM   21  H7  UNL     1       3.585  -2.233   1.180  1.00  0.00           H  
HETATM   22  H8  UNL     1       2.614  -1.046   2.182  1.00  0.00           H  
HETATM   23  H9  UNL     1       4.241  -0.628   1.456  1.00  0.00           H  
HETATM   24  H10 UNL     1       4.372  -0.403  -1.152  1.00  0.00           H  
HETATM   25  H11 UNL     1       3.111   0.862  -1.330  1.00  0.00           H  
HETATM   26  H12 UNL     1       4.161   0.748   0.218  1.00  0.00           H  
HETATM   27  H13 UNL     1      -0.145  -2.683  -0.819  1.00  0.00           H  
HETATM   28  H14 UNL     1      -2.820   0.169  -1.524  1.00  0.00           H  
HETATM   29  H15 UNL     1      -3.977   0.471   0.471  1.00  0.00           H  
HETATM   30  H16 UNL     1      -2.475   0.061   1.428  1.00  0.00           H  
HETATM   31  H17 UNL     1      -3.604  -1.199   0.888  1.00  0.00           H  
HETATM   32  H18 UNL     1      -3.499  -2.168  -0.873  1.00  0.00           H  
HETATM   33  H19 UNL     1      -2.041  -2.196  -1.866  1.00  0.00           H  
HETATM   34  H20 UNL     1      -2.011  -2.345   0.033  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3    3   11
CONECT    3    4   18
CONECT    4    5    5   19
CONECT    5    6    9
CONECT    6    7    8   20
CONECT    7   21   22   23
CONECT    8   24   25   26
CONECT    9   10   11   11
CONECT   10   27
CONECT   11   12
CONECT   12   13   14   28
CONECT   13   29   30   31
CONECT   14   32   33   34
END

HMDB0029820
     RDKit          3D
2,6-Diisopropyl-3-methylphenol
 34 34  0  0  0  0  0  0  0  0999 V2000
   -2.2046    2.4000   -0.3806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9655    1.5792   -0.2289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2228    2.1465    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3696    1.3769    0.2753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3907    0.0311    0.0886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5976   -0.7901    0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2980   -1.1415    1.3125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6502    0.2234   -0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1264   -0.5833   -0.2839 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3076   -1.9202   -0.4402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9950    0.1647   -0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3473   -0.3265   -0.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1618   -0.2430    0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3760   -1.8563   -0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7287    2.5146    0.6121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9059    3.4498   -0.6338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8609    2.0773   -1.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2324    3.1981    0.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3091    1.8860    0.5589 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5291   -1.5966   -0.7183 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5846   -2.2326    1.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6145   -1.0463    2.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2412   -0.6285    1.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3718   -0.4033   -1.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    0.8621   -1.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1609    0.7476    0.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1445   -2.6826   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8199    0.1689   -1.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9771    0.4710    0.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4753    0.0613    1.4279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6042   -1.1987    0.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -2.1684   -0.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0408   -2.1958   -1.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0107   -2.3447    0.0328 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
  6  8  1  0
  5  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 11  2  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  0
  7 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2,6-Diisopropyl-3-methyl-phenol	HMDB
2,6-Diisopropyl-m-cresol	HMDB
2,6-Diisopropyl-m-cresol, 8ci	HMDB
3-Methyl-2,6-bis(1-methylethyl)phenol, 9ci	HMDB

Chemical Formula

C₁₃H₂₀O

Average Molecular Weight

192.2973

Monoisotopic Molecular Weight

192.151415262

IUPAC Name

3-methyl-2,6-bis(propan-2-yl)phenol

Traditional Name

2,6-diisopropyl-3-methylphenol

CAS Registry Number

28434-93-7

SMILES

CC(C)C1=CC=C(C)C(C(C)C)=C1O

InChI Identifier

InChI=1S/C13H20O/c1-8(2)11-7-6-10(5)12(9(3)4)13(11)14/h6-9,14H,1-5H3

InChI Key

KEGGEHPMMDYTGB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Aromatic monoterpenoids

Alternative Parents

Substituents

Monocyclic monoterpenoid
Aromatic monoterpenoid
P-cymene
Phenylpropane
Cumene
M-cresol
1-hydroxy-4-unsubstituted benzenoid
Toluene
Phenol
Benzenoid
Monocyclic benzene moiety
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0029820)

Source

Endogenous

Endogenous (HMDB: HMDB0029820)

Plant

Plant (HMDB: HMDB0029820)

Animal

Animal (HMDB: HMDB0029820)

Exogenous

Food

Food (HMDB: HMDB0029820)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Exogenous (HMDB: HMDB0029820)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0029820)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0029820)

Lipid metabolism pathway (HMDB: HMDB0029820)

Cellular process

Cell signaling (HMDB: HMDB0029820)

Biochemical process

Lipid transport (HMDB: HMDB0029820)

Role

Biological role

Energy source (HMDB: HMDB0029820)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0029820)

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	54.92 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.15 g/L	ALOGPS
logP	4.15	ALOGPS
logP	4.67	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	11.07	ChemAxon
pKa (Strongest Basic)	-5	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	61.46 m³·mol⁻¹	ChemAxon
Polarizability	23.57 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]+	143.235	31661259
DarkChem	[M-H]-	142.487	31661259
DeepCCS	[M+H]+	151.002	30932474
DeepCCS	[M-H]-	148.644	30932474
DeepCCS	[M-2H]-	183.311	30932474
DeepCCS	[M+Na]+	158.891	30932474
AllCCS	[M+H]+	141.4	32859911
AllCCS	[M+H-H2O]+	137.3	32859911
AllCCS	[M+NH4]+	145.2	32859911
AllCCS	[M+Na]+	146.3	32859911
AllCCS	[M-H]-	148.5	32859911
AllCCS	[M+Na-2H]-	149.4	32859911
AllCCS	[M+HCOO]-	150.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2,6-Diisopropyl-3-methylphenol	CC(C)C1=CC=C(C)C(C(C)C)=C1O	1978.7	Standard polar	33892256
2,6-Diisopropyl-3-methylphenol	CC(C)C1=CC=C(C)C(C(C)C)=C1O	1465.9	Standard non polar	33892256
2,6-Diisopropyl-3-methylphenol	CC(C)C1=CC=C(C)C(C(C)C)=C1O	1436.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2,6-Diisopropyl-3-methylphenol,1TMS,isomer #1	CC1=CC=C(C(C)C)C(O[Si](C)(C)C)=C1C(C)C	1520.0	Semi standard non polar	33892256
2,6-Diisopropyl-3-methylphenol,1TBDMS,isomer #1	CC1=CC=C(C(C)C)C(O[Si](C)(C)C(C)(C)C)=C1C(C)C	1737.2	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2,6-Diisopropyl-3-methylphenol GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-2900000000-1d986533863d4d0d5ce9	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2,6-Diisopropyl-3-methylphenol GC-MS (1 TMS) - 70eV, Positive	splash10-0002-5290000000-f6d5c580e5667cfe6d9a	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2,6-Diisopropyl-3-methylphenol 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 - 2,6-Diisopropyl-3-methylphenol 10V, Positive-QTOF	splash10-0006-0900000000-059de6804df3c558eac2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 20V, Positive-QTOF	splash10-0006-1900000000-df0ee16b7165583fcc12	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 40V, Positive-QTOF	splash10-0pdi-6900000000-c965429c89ebe98ef743	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 10V, Negative-QTOF	splash10-0006-0900000000-1dc705c7898023571189	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 20V, Negative-QTOF	splash10-0006-0900000000-d634cc4532718c80a6c9	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 40V, Negative-QTOF	splash10-054n-1900000000-557f356b1e538a5a7804	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 10V, Negative-QTOF	splash10-0006-0900000000-14436e4d9ff8d032db54	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 20V, Negative-QTOF	splash10-0006-0900000000-e0b1f94019a714de6169	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 40V, Negative-QTOF	splash10-0a7i-2900000000-291711f0003c7f6c0452	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 10V, Positive-QTOF	splash10-0006-1900000000-ba399d89d881ed25fc67	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 20V, Positive-QTOF	splash10-01ox-0900000000-d1623b0110c4486c4e60	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,6-Diisopropyl-3-methylphenol 40V, Positive-QTOF	splash10-000x-9300000000-8ccd77b3121ef647b1e1	2021-09-24	Wishart Lab	View Spectrum

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)	2023-02-03	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)	2023-02-03	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-03	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

FDB001031

KNApSAcK ID

Not Available

Chemspider ID

107095

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

119956

PDB ID

Not Available

ChEBI ID

138017

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1516901

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 2,6-Diisopropyl-3-methylphenol (HMDB0029820)

MOL for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

3D MOL for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

3D SDF for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

3D-SDF for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

PDB for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

3D PDB for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

SMILES for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

INCHI for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

Structure for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

3D Structure for HMDB0029820 (2,6-Diisopropyl-3-methylphenol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra