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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:50:36 UTC

Update Date

2023-02-21 17:22:24 UTC

HMDB ID

HMDB0032579

Secondary Accession Numbers

HMDB32579

Metabolite Identification

Common Name

2,5-Diisopropylphenol

Description

2,5-Diisopropylphenol 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 significant number of articles have been published on 2,5-Diisopropylphenol.

Structure

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

HMDB0032579
     RDKit          3D
2,5-Diisopropylphenol
 31 31  0  0  0  0  0  0  0  0999 V2000
   -3.5859    0.9402    0.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8648    0.0258   -0.3943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4318   -1.3601   -0.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3945    0.0758   -0.1651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6298    0.7185   -1.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7492    0.7738   -0.9157 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3719    0.2091    0.1671 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8187    0.2862    0.3069 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3516    1.2439   -0.7592 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5231   -1.0304    0.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5927   -0.4317    1.0953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2120   -1.0046    2.1916 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7836   -0.4893    0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9177    1.2513    1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4958    0.4434    1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9858    1.8399    0.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1267    0.3656   -1.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8931   -2.1346   -0.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4887   -1.3148   -0.6014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4566   -1.5704    0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0704    1.1839   -1.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3240    1.2903   -1.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0668    0.7021    1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4175    1.4379   -0.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3153    0.7952   -1.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8216    2.2174   -0.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6136   -1.5241    1.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5483   -0.7926   -0.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0500   -1.6594   -0.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7454   -1.4999    2.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3966   -0.9882    1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  2  0
 13  4  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  5 21  1  0
  6 22  1  0
  8 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 10 29  1  0
 12 30  1  0
 13 31  1  0
M  END

HMDB0032579
     RDKit          3D
2,5-Diisopropylphenol
 31 31  0  0  0  0  0  0  0  0999 V2000
   -3.5859    0.9402    0.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8648    0.0258   -0.3943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4318   -1.3601   -0.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3945    0.0758   -0.1651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6298    0.7185   -1.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7492    0.7738   -0.9157 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3719    0.2091    0.1671 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8187    0.2862    0.3069 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3516    1.2439   -0.7592 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5231   -1.0304    0.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5927   -0.4317    1.0953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2120   -1.0046    2.1916 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7836   -0.4893    0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9177    1.2513    1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4958    0.4434    1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9858    1.8399    0.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1267    0.3656   -1.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8931   -2.1346   -0.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4887   -1.3148   -0.6014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4566   -1.5704    0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0704    1.1839   -1.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3240    1.2903   -1.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0668    0.7021    1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4175    1.4379   -0.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3153    0.7952   -1.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8216    2.2174   -0.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6136   -1.5241    1.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5483   -0.7926   -0.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0500   -1.6594   -0.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7454   -1.4999    2.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3966   -0.9882    1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  2  0
 13  4  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  5 21  1  0
  6 22  1  0
  8 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 10 29  1  0
 12 30  1  0
 13 31  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       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    8                                                            
CONECT    2    8                                                            
CONECT    3    9                                                            
CONECT    4    9                                                            
CONECT    5    6   10                                                       
CONECT    6    5   11                                                       
CONECT    7   10   12                                                       
CONECT    8    1    2   10                                                  
CONECT    9    3    4   11                                                  
CONECT   10    5    7    8                                                  
CONECT   11    6    9   12                                                  
CONECT   12    7   11   13                                                  
CONECT   13   12                                                            
MASTER        0    0    0    0    0    0    0    0   13    0   26    0
END

COMPND    HMDB0032579
HETATM    1  C1  UNL     1      -3.586   0.940   0.607  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.865   0.026  -0.394  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.432  -1.360  -0.218  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.394   0.076  -0.165  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.630   0.719  -1.100  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.749   0.774  -0.916  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.372   0.209   0.167  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.819   0.286   0.307  1.00  0.00           C  
HETATM    9  C9  UNL     1       3.352   1.244  -0.759  1.00  0.00           C  
HETATM   10  C10 UNL     1       3.523  -1.030   0.097  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.593  -0.432   1.095  1.00  0.00           C  
HETATM   12  O1  UNL     1       1.212  -1.005   2.192  1.00  0.00           O  
HETATM   13  C12 UNL     1      -0.784  -0.489   0.916  1.00  0.00           C  
HETATM   14  H1  UNL     1      -2.918   1.251   1.436  1.00  0.00           H  
HETATM   15  H2  UNL     1      -4.496   0.443   1.019  1.00  0.00           H  
HETATM   16  H3  UNL     1      -3.986   1.840   0.052  1.00  0.00           H  
HETATM   17  H4  UNL     1      -3.127   0.366  -1.418  1.00  0.00           H  
HETATM   18  H5  UNL     1      -2.893  -2.135  -0.779  1.00  0.00           H  
HETATM   19  H6  UNL     1      -4.489  -1.315  -0.601  1.00  0.00           H  
HETATM   20  H7  UNL     1      -3.457  -1.570   0.880  1.00  0.00           H  
HETATM   21  H8  UNL     1      -1.070   1.184  -1.978  1.00  0.00           H  
HETATM   22  H9  UNL     1       1.324   1.290  -1.679  1.00  0.00           H  
HETATM   23  H10 UNL     1       3.067   0.702   1.292  1.00  0.00           H  
HETATM   24  H11 UNL     1       4.418   1.438  -0.475  1.00  0.00           H  
HETATM   25  H12 UNL     1       3.315   0.795  -1.771  1.00  0.00           H  
HETATM   26  H13 UNL     1       2.822   2.217  -0.692  1.00  0.00           H  
HETATM   27  H14 UNL     1       3.614  -1.524   1.082  1.00  0.00           H  
HETATM   28  H15 UNL     1       4.548  -0.793  -0.249  1.00  0.00           H  
HETATM   29  H16 UNL     1       3.050  -1.659  -0.666  1.00  0.00           H  
HETATM   30  H17 UNL     1       0.745  -1.500   2.934  1.00  0.00           H  
HETATM   31  H18 UNL     1      -1.397  -0.988   1.642  1.00  0.00           H  
CONECT    1    2   14   15   16
CONECT    2    3    4   17
CONECT    3   18   19   20
CONECT    4    5    5   13
CONECT    5    6   21
CONECT    6    7    7   22
CONECT    7    8   11
CONECT    8    9   10   23
CONECT    9   24   25   26
CONECT   10   27   28   29
CONECT   11   12   13   13
CONECT   12   30
CONECT   13   31
END

HMDB0032579
     RDKit          3D
2,5-Diisopropylphenol
 31 31  0  0  0  0  0  0  0  0999 V2000
   -3.5859    0.9402    0.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8648    0.0258   -0.3943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4318   -1.3601   -0.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3945    0.0758   -0.1651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6298    0.7185   -1.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7492    0.7738   -0.9157 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3719    0.2091    0.1671 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8187    0.2862    0.3069 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3516    1.2439   -0.7592 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5231   -1.0304    0.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5927   -0.4317    1.0953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2120   -1.0046    2.1916 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7836   -0.4893    0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9177    1.2513    1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4958    0.4434    1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9858    1.8399    0.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1267    0.3656   -1.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8931   -2.1346   -0.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4887   -1.3148   -0.6014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4566   -1.5704    0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0704    1.1839   -1.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3240    1.2903   -1.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0668    0.7021    1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4175    1.4379   -0.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3153    0.7952   -1.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8216    2.2174   -0.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6136   -1.5241    1.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5483   -0.7926   -0.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0500   -1.6594   -0.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7454   -1.4999    2.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3966   -0.9882    1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  2  0
 13  4  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  5 21  1  0
  6 22  1  0
  8 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 10 29  1  0
 12 30  1  0
 13 31  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
25-Diisopropylphenol	ChEMBL, HMDB
2,5-Bis(1-methylethyl)-phenol	HMDB
2,5-Bis(1-methylethyl)phenol, 9ci	HMDB
P-DIIsopropylbenzene monoalc.	HMDB

Chemical Formula

C₁₂H₁₈O

Average Molecular Weight

178.2707

Monoisotopic Molecular Weight

178.135765198

IUPAC Name

2,5-bis(propan-2-yl)phenol

Traditional Name

2,5-diisopropylphenol

CAS Registry Number

35946-91-9

SMILES

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

InChI Identifier

InChI=1S/C12H18O/c1-8(2)10-5-6-11(9(3)4)12(13)7-10/h5-9,13H,1-4H3

InChI Key

VFNUNYPYULIJSN-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
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
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: HMDB0032579)

Source

Endogenous

Endogenous (HMDB: HMDB0032579)

Plant

Plant (HMDB: HMDB0032579)

Animal

Animal (HMDB: HMDB0032579)

Exogenous

Food

Food (HMDB: HMDB0032579)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0032579)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0032579)

Lipid metabolism pathway (HMDB: HMDB0032579)

Cellular process

Cell signaling (HMDB: HMDB0032579)

Biochemical process

Lipid transport (HMDB: HMDB0032579)

Role

Biological role

Energy source (HMDB: HMDB0032579)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0032579)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	95.5 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	35.52 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	0.19 g/L	ALOGPS
logP	3.84	ALOGPS
logP	4.16	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	10.55	ChemAxon
pKa (Strongest Basic)	-5.2	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	56.42 m³·mol⁻¹	ChemAxon
Polarizability	21.77 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]+	141.784	31661259
DarkChem	[M-H]-	139.923	31661259
DeepCCS	[M+H]+	147.967	30932474
DeepCCS	[M-H]-	145.572	30932474
DeepCCS	[M-2H]-	179.764	30932474
DeepCCS	[M+Na]+	154.355	30932474
AllCCS	[M+H]+	137.8	32859911
AllCCS	[M+H-H2O]+	133.5	32859911
AllCCS	[M+NH4]+	141.8	32859911
AllCCS	[M+Na]+	142.9	32859911
AllCCS	[M-H]-	144.2	32859911
AllCCS	[M+Na-2H]-	145.2	32859911
AllCCS	[M+HCOO]-	146.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2,5-Diisopropylphenol	CC(C)C1=CC(O)=C(C=C1)C(C)C	2152.1	Standard polar	33892256
2,5-Diisopropylphenol	CC(C)C1=CC(O)=C(C=C1)C(C)C	1367.1	Standard non polar	33892256
2,5-Diisopropylphenol	CC(C)C1=CC(O)=C(C=C1)C(C)C	1412.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2,5-Diisopropylphenol,1TMS,isomer #1	CC(C)C1=CC=C(C(C)C)C(O[Si](C)(C)C)=C1	1407.4	Semi standard non polar	33892256
2,5-Diisopropylphenol,1TBDMS,isomer #1	CC(C)C1=CC=C(C(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	1639.2	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 - 2,5-Diisopropylphenol GC-MS (Non-derivatized) - 70eV, Positive	splash10-03dr-3900000000-5980264e6ade728504fe	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2,5-Diisopropylphenol GC-MS (1 TMS) - 70eV, Positive	splash10-000i-7690000000-6580fa62c692261b7128	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2,5-Diisopropylphenol 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 - 2,5-Diisopropylphenol 10V, Positive-QTOF	splash10-004i-0900000000-5fa588b6c724d9aca640	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 20V, Positive-QTOF	splash10-004r-2900000000-767c0a5ce431c0482e05	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 40V, Positive-QTOF	splash10-02u3-8900000000-0ce07e97daf8acbce29f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 10V, Negative-QTOF	splash10-004i-0900000000-696cc2ef66414f019b5f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 20V, Negative-QTOF	splash10-004i-0900000000-1721138d9198d4397273	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 40V, Negative-QTOF	splash10-01tj-1900000000-d04ec981bcda5ca7d9bc	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 10V, Positive-QTOF	splash10-004i-0900000000-cde5c32691b816c25f52	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 20V, Positive-QTOF	splash10-004r-0900000000-63cfbaec9e2ed213f4fa	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 40V, Positive-QTOF	splash10-0006-9500000000-6ed456a13161dfe294bd	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 10V, Negative-QTOF	splash10-004i-0900000000-1c420c1b8167732abdd0	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 20V, Negative-QTOF	splash10-004i-0900000000-26d823d7cfe6619b14b6	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,5-Diisopropylphenol 40V, Negative-QTOF	splash10-02vl-6900000000-f17c7ef06324ac62f317	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]-)	2023-02-04	FELIX lab	View Spectrum
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

FDB010516

KNApSAcK ID

Not Available

Chemspider ID

84132

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

93189

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1634841

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 2,5-Diisopropylphenol (HMDB0032579)

MOL for HMDB0032579 (2,5-Diisopropylphenol)

3D MOL for HMDB0032579 (2,5-Diisopropylphenol)

3D SDF for HMDB0032579 (2,5-Diisopropylphenol)

3D-SDF for HMDB0032579 (2,5-Diisopropylphenol)

PDB for HMDB0032579 (2,5-Diisopropylphenol)

3D PDB for HMDB0032579 (2,5-Diisopropylphenol)

SMILES for HMDB0032579 (2,5-Diisopropylphenol)

INCHI for HMDB0032579 (2,5-Diisopropylphenol)

Structure for HMDB0032579 (2,5-Diisopropylphenol)

3D Structure for HMDB0032579 (2,5-Diisopropylphenol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra