Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (5) Show 5 proteins XML

Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2009-01-30 15:39:15 UTC

Update Date

2022-03-07 02:51:12 UTC

HMDB ID

HMDB0011638

Secondary Accession Numbers

HMDB11638

Metabolite Identification

Common Name

Tetradecanol

Description

1-Tetradecanol, or commonly myristyl alcohol, is a straight-chain saturated fatty alcohol, with the molecular formula C14H30O. It is a white crystalline solid that is practically insoluble in water, soluble in diethyl ether, and slightly soluble in ethanol. 1-Tetradecanol may be prepared by the reduction of myristic acid or some fatty acid esters with reagents such as lithium aluminium hydride or sodium. As with other fatty alcohols, 1-tetradecanol is used as an ingredient in cosmetics such as cold creams for its emollient properties. It is also used as an intermediate in the chemical synthesis of other products such sulfated alcohol (Wikipedia ).

Structure

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

HMDB0011638
     RDKit          3D
Tetradecanol
 45 44  0  0  0  0  0  0  0  0999 V2000
   -6.0043   -1.6514    1.6914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0355   -0.7253    0.9559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1711   -1.5231    0.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2401   -0.6344   -0.7231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3363    0.1075    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4035    0.9899   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5408    0.2078   -1.4929 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4304    1.0757   -2.2741 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3704    1.8599   -1.4251 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1905    0.8733   -0.5939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655    1.5962    0.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9433    0.5890    1.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -0.3558    0.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5001   -1.3642    1.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6414   -2.1163    1.8257 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8031   -1.0062    2.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3767   -2.3963    0.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4291   -2.0890    2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3584   -0.2392    1.7192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6013    0.0276    0.3878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7573   -2.1028   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5670   -2.2692    0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8329    0.1504   -1.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6939   -1.1797   -1.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9142    0.7567    0.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7082   -0.6092    0.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8138    1.5916    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0817    1.7085   -1.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0103   -0.5851   -0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1430   -0.3258   -2.2780 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0552    0.3535   -2.8725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1024    1.6855   -3.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8914    2.5835   -0.7574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0287    2.4339   -2.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6703    0.2113   -1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5197    0.2824    0.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8239    2.2790   -0.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    2.2553    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1724   -0.0112    1.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5567    1.0861    1.8514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0256   -0.9673   -0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3820    0.2088   -0.4434 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1557   -0.7910    1.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0509   -2.0327    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0169   -3.0084    2.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
M  END


  Mrv1652304272018522D          

 15 14  0  0  0  0            999 V2000
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4290    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1435    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8580    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2869    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0014    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7159    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4304    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1449    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8593    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5739    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2883    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0028    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0011638

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCCCCCCCO

> <INCHI_IDENTIFIER>
InChI=1S/C14H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h15H,2-14H2,1H3

> <INCHI_KEY>
HLZKNKRTKFSKGZ-UHFFFAOYSA-N

> <FORMULA>
C14H30O

> <MOLECULAR_WEIGHT>
214.3874

> <EXACT_MASS>
214.229665582

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
30.11209765779862

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
tetradecan-1-ol

> <ALOGPS_LOGP>
6.21

> <JCHEM_LOGP>
5.251008596

> <ALOGPS_LOGS>
-5.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.84394282199214

> <JCHEM_PKA_STRONGEST_BASIC>
-1.9922594096606376

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
68.14489999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.44e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
myristyl alcohol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0011638
     RDKit          3D
Tetradecanol
 45 44  0  0  0  0  0  0  0  0999 V2000
   -6.0043   -1.6514    1.6914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0355   -0.7253    0.9559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1711   -1.5231    0.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2401   -0.6344   -0.7231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3363    0.1075    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4035    0.9899   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5408    0.2078   -1.4929 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4304    1.0757   -2.2741 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3704    1.8599   -1.4251 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1905    0.8733   -0.5939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655    1.5962    0.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9433    0.5890    1.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -0.3558    0.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5001   -1.3642    1.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6414   -2.1163    1.8257 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8031   -1.0062    2.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3767   -2.3963    0.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4291   -2.0890    2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3584   -0.2392    1.7192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6013    0.0276    0.3878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7573   -2.1028   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5670   -2.2692    0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8329    0.1504   -1.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6939   -1.1797   -1.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9142    0.7567    0.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7082   -0.6092    0.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8138    1.5916    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0817    1.7085   -1.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0103   -0.5851   -0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1430   -0.3258   -2.2780 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0552    0.3535   -2.8725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1024    1.6855   -3.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8914    2.5835   -0.7574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0287    2.4339   -2.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6703    0.2113   -1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5197    0.2824    0.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8239    2.2790   -0.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    2.2553    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1724   -0.0112    1.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5567    1.0861    1.8514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0256   -0.9673   -0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3820    0.2088   -0.4434 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1557   -0.7910    1.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0509   -2.0327    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0169   -3.0084    2.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
M  END

HEADER    PROTEIN                                 27-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-APR-20         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.669   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.670   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.671   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.005   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.338   0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      18.672   0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   28    0
END

COMPND    HMDB0011638
HETATM    1  C1  UNL     1      -6.004  -1.651   1.691  1.00  0.00           C  
HETATM    2  C2  UNL     1      -5.035  -0.725   0.956  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.171  -1.523   0.031  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.240  -0.634  -0.723  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.336   0.107   0.209  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.404   0.990  -0.577  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.541   0.208  -1.493  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.430   1.076  -2.274  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.370   1.860  -1.425  1.00  0.00           C  
HETATM   10  C10 UNL     1       2.190   0.873  -0.594  1.00  0.00           C  
HETATM   11  C11 UNL     1       3.165   1.596   0.286  1.00  0.00           C  
HETATM   12  C12 UNL     1       3.943   0.589   1.088  1.00  0.00           C  
HETATM   13  C13 UNL     1       4.711  -0.356   0.217  1.00  0.00           C  
HETATM   14  C14 UNL     1       5.500  -1.364   1.034  1.00  0.00           C  
HETATM   15  O1  UNL     1       4.641  -2.116   1.826  1.00  0.00           O  
HETATM   16  H1  UNL     1      -6.803  -1.006   2.107  1.00  0.00           H  
HETATM   17  H2  UNL     1      -6.377  -2.396   0.987  1.00  0.00           H  
HETATM   18  H3  UNL     1      -5.429  -2.089   2.530  1.00  0.00           H  
HETATM   19  H4  UNL     1      -4.358  -0.239   1.719  1.00  0.00           H  
HETATM   20  H5  UNL     1      -5.601   0.028   0.388  1.00  0.00           H  
HETATM   21  H6  UNL     1      -4.757  -2.103  -0.715  1.00  0.00           H  
HETATM   22  H7  UNL     1      -3.567  -2.269   0.593  1.00  0.00           H  
HETATM   23  H8  UNL     1      -3.833   0.150  -1.273  1.00  0.00           H  
HETATM   24  H9  UNL     1      -2.694  -1.180  -1.523  1.00  0.00           H  
HETATM   25  H10 UNL     1      -2.914   0.757   0.918  1.00  0.00           H  
HETATM   26  H11 UNL     1      -1.708  -0.609   0.790  1.00  0.00           H  
HETATM   27  H12 UNL     1      -0.814   1.592   0.152  1.00  0.00           H  
HETATM   28  H13 UNL     1      -2.082   1.709  -1.127  1.00  0.00           H  
HETATM   29  H14 UNL     1      -0.010  -0.585  -0.942  1.00  0.00           H  
HETATM   30  H15 UNL     1      -1.143  -0.326  -2.278  1.00  0.00           H  
HETATM   31  H16 UNL     1       1.055   0.354  -2.873  1.00  0.00           H  
HETATM   32  H17 UNL     1      -0.102   1.686  -3.028  1.00  0.00           H  
HETATM   33  H18 UNL     1       0.891   2.584  -0.757  1.00  0.00           H  
HETATM   34  H19 UNL     1       2.029   2.434  -2.107  1.00  0.00           H  
HETATM   35  H20 UNL     1       2.670   0.211  -1.318  1.00  0.00           H  
HETATM   36  H21 UNL     1       1.520   0.282   0.060  1.00  0.00           H  
HETATM   37  H22 UNL     1       3.824   2.279  -0.291  1.00  0.00           H  
HETATM   38  H23 UNL     1       2.623   2.255   1.007  1.00  0.00           H  
HETATM   39  H24 UNL     1       3.172  -0.011   1.653  1.00  0.00           H  
HETATM   40  H25 UNL     1       4.557   1.086   1.851  1.00  0.00           H  
HETATM   41  H26 UNL     1       4.026  -0.967  -0.409  1.00  0.00           H  
HETATM   42  H27 UNL     1       5.382   0.209  -0.443  1.00  0.00           H  
HETATM   43  H28 UNL     1       6.156  -0.791   1.713  1.00  0.00           H  
HETATM   44  H29 UNL     1       6.051  -2.033   0.345  1.00  0.00           H  
HETATM   45  H30 UNL     1       5.017  -3.008   2.019  1.00  0.00           H  
CONECT    1    2   16   17   18
CONECT    2    3   19   20
CONECT    3    4   21   22
CONECT    4    5   23   24
CONECT    5    6   25   26
CONECT    6    7   27   28
CONECT    7    8   29   30
CONECT    8    9   31   32
CONECT    9   10   33   34
CONECT   10   11   35   36
CONECT   11   12   37   38
CONECT   12   13   39   40
CONECT   13   14   41   42
CONECT   14   15   43   44
CONECT   15   45
END

HMDB0011638
     RDKit          3D
Tetradecanol
 45 44  0  0  0  0  0  0  0  0999 V2000
   -6.0043   -1.6514    1.6914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0355   -0.7253    0.9559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1711   -1.5231    0.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2401   -0.6344   -0.7231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3363    0.1075    0.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4035    0.9899   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5408    0.2078   -1.4929 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4304    1.0757   -2.2741 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3704    1.8599   -1.4251 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1905    0.8733   -0.5939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655    1.5962    0.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9433    0.5890    1.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -0.3558    0.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5001   -1.3642    1.0338 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6414   -2.1163    1.8257 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8031   -1.0062    2.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3767   -2.3963    0.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4291   -2.0890    2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3584   -0.2392    1.7192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6013    0.0276    0.3878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7573   -2.1028   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5670   -2.2692    0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8329    0.1504   -1.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6939   -1.1797   -1.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9142    0.7567    0.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7082   -0.6092    0.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8138    1.5916    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0817    1.7085   -1.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0103   -0.5851   -0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1430   -0.3258   -2.2780 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0552    0.3535   -2.8725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1024    1.6855   -3.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8914    2.5835   -0.7574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0287    2.4339   -2.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6703    0.2113   -1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5197    0.2824    0.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8239    2.2790   -0.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    2.2553    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1724   -0.0112    1.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5567    1.0861    1.8514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0256   -0.9673   -0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3820    0.2088   -0.4434 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1557   -0.7910    1.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0509   -2.0327    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0169   -3.0084    2.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-Hydroxytetradecane	ChEBI
1-Tetradecanol	ChEBI
1-Tetradecyl alcohol	ChEBI
Myristic alcohol	ChEBI
Myristyl alcohol	ChEBI
N-Tetradecanol	ChEBI
N-Tetradecanol-1	ChEBI
N-Tetradecyl alcohol	ChEBI
Tetradecyl alcohol	ChEBI
Adol 18	HMDB
Alfol 14	HMDB
Conol 1495	HMDB
Kalcohl 40	HMDB
Kalcohl 4098	HMDB
Kalcol 4098	HMDB
Lanette 14	HMDB
Lanette K	HMDB
Lanette wax KS	HMDB
Lorol C 14	HMDB
Loxanol V	HMDB
N-Tetradecan-1-ol	HMDB
Nacol 14-95	HMDB
Tetradecanol (7ci)	HMDB
Tetradecan-1-ol	HMDB
Myristyl alcohol, aluminum salt	HMDB
Tetradecanol	ChEBI

Chemical Formula

C₁₄H₃₀O

Average Molecular Weight

214.3874

Monoisotopic Molecular Weight

214.229665582

IUPAC Name

tetradecan-1-ol

Traditional Name

myristyl alcohol

CAS Registry Number

112-72-1

SMILES

CCCCCCCCCCCCCCO

InChI Identifier

InChI=1S/C14H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h15H,2-14H2,1H3

InChI Key

HLZKNKRTKFSKGZ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Long-chain fatty alcohols

Alternative Parents

Substituents

Long chain fatty alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

long-chain primary fatty alcohol (CHEBI:77417 )
fatty alcohol 14:0 (CHEBI:77417 )
Fatty alcohols (LMFA05000041 )
a long-chain alcohol (CPD-7875 )
a primary alcohol (CPD-7875 )
a fatty alcohol (CPD-7875 )

Ontology

Cytoplasm (HMDB: HMDB0011638)
Cell membrane (HMDB: HMDB0011638)

Biofluid or Excreta

Feces (HMDB: HMDB0011638)
Urine (HMDB: HMDB0011638)

Excreta

Biofluid or Excreta

Feces (PMID: 24029555)

Cellular substructure

Extracellular (HMDB: HMDB0011638)
Membrane (HMDB: HMDB0011638)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0011638)

Source

Endogenous

Endogenous (HMDB: HMDB0011638)

Plant

Plant (HMDB: HMDB0011638)

Animal

Animal (HMDB: HMDB0011638)

Exogenous

Food

Food (HMDB: HMDB0011638)

Animal origin

Poultry

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Vegetable

Root vegetable

Kohlrabi (FooDB: FOOD00033)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0011638)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0011638)

Cellular process

Cell signaling (HMDB: HMDB0011638)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0011638)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0011638)

Nutrient

Nutrient (HMDB: HMDB0011638)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0011638)

Emulsifier (HMDB: HMDB0011638)

Pharmaceutical industry

Biomarker

Celiac disease (MarkerDB: MDB00029970)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	39.5 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	6.03	BURKHARD,LP ET AL. (1985B)

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00044 g/L	ALOGPS
logP	6.21	ALOGPS
logP	5.25	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	16.84	ChemAxon
pKa (Strongest Basic)	-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	12	ChemAxon
Refractivity	68.14 m³·mol⁻¹	ChemAxon
Polarizability	30.11 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	155.634	31661259
DarkChem	[M-H]-	155.775	31661259
DeepCCS	[M+H]+	158.063	30932474
DeepCCS	[M-H]-	154.101	30932474
DeepCCS	[M-2H]-	191.677	30932474
DeepCCS	[M+Na]+	167.34	30932474
AllCCS	[M+H]+	159.4	32859911
AllCCS	[M+H-H2O]+	155.9	32859911
AllCCS	[M+NH4]+	162.6	32859911
AllCCS	[M+Na]+	163.5	32859911
AllCCS	[M-H]-	160.8	32859911
AllCCS	[M+Na-2H]-	162.1	32859911
AllCCS	[M+HCOO]-	163.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tetradecanol	CCCCCCCCCCCCCCO	2220.7	Standard polar	33892256
Tetradecanol	CCCCCCCCCCCCCCO	1673.9	Standard non polar	33892256
Tetradecanol	CCCCCCCCCCCCCCO	1680.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Tetradecanol,1TMS,isomer #1	CCCCCCCCCCCCCCO[Si](C)(C)C	1764.6	Semi standard non polar	33892256
Tetradecanol,1TBDMS,isomer #1	CCCCCCCCCCCCCCO[Si](C)(C)C(C)(C)C	1986.4	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental GC-MS	GC-MS Spectrum - Tetradecanol GC-MS (1 TMS)	splash10-00di-7590000000-977855648ce1bb3be347	2014-06-16	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Tetradecanol EI-B (Non-derivatized)	splash10-0a4l-9000000000-32d5eef1c4d74b3ec3ba	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Tetradecanol EI-B (Non-derivatized)	splash10-052f-9000000000-acacbf10a3263c94194f	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Tetradecanol EI-B (Non-derivatized)	splash10-0a5c-9100000000-2616129ec4a43b6c0102	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Tetradecanol GC-MS (Non-derivatized)	splash10-00di-7590000000-977855648ce1bb3be347	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetradecanol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0563-9600000000-eec06d9397af9c3a7e99	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetradecanol GC-MS (1 TMS) - 70eV, Positive	splash10-00di-9620000000-4b25e0c0e809382e8217	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetradecanol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetradecanol 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
Experimental LC-MS/MS	LC-MS/MS Spectrum - Tetradecanol NA , positive-QTOF	splash10-006x-4900000000-9984d821b36fbb9446e6	2020-07-21	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 10V, Positive-QTOF	splash10-00kb-0960000000-3c72c9bef17048b10a31	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 20V, Positive-QTOF	splash10-0002-4910000000-9c450227835d31d57a2a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 40V, Positive-QTOF	splash10-052f-9300000000-e8c01d4094b22e4ad7a0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 10V, Negative-QTOF	splash10-03di-0390000000-24c96d483d78255edac3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 20V, Negative-QTOF	splash10-03di-1980000000-7c6d57144abbe039abdd	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 40V, Negative-QTOF	splash10-000w-8900000000-c66ca1bb8fdb18f90e99	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 10V, Positive-QTOF	splash10-014i-9340000000-c451e7bae87af519149a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 20V, Positive-QTOF	splash10-0ab9-9000000000-2e144a890203dcbb17fb	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 40V, Positive-QTOF	splash10-052f-9000000000-cbaa89cc20f0bcb181ab	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 10V, Negative-QTOF	splash10-03di-0090000000-66f23677a88c1ed92476	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 20V, Negative-QTOF	splash10-03di-0090000000-d479398c0f5329e2e292	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetradecanol 40V, Negative-QTOF	splash10-08fu-9640000000-3871dae38884d89b8f4d	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Feces

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected and Quantified	6452.494-293269.723 nmol/g wet feces	Children (1-13 years old)	Not Specified	Normal	21970810	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	24029555	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected and Quantified	0-1246326.354 nmol/g wet feces	Children (1-13 years old)	Not Specified	Treated celiac disease	21970810	details

Associated Disorders and Diseases

Disease References

Celiac disease
Di Cagno R, De Angelis M, De Pasquale I, Ndagijimana M, Vernocchi P, Ricciuti P, Gagliardi F, Laghi L, Crecchio C, Guerzoni ME, Gobbetti M, Francavilla R: Duodenal and faecal microbiota of celiac children: molecular, phenotype and metabolome characterization. BMC Microbiol. 2011 Oct 4;11:219. doi: 10.1186/1471-2180-11-219. [PubMed:21970810 ]

Associated OMIM IDs

212750 (Celiac disease)

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB002891

KNApSAcK ID

C00032309

Chemspider ID

7917

KEGG Compound ID

Not Available

BioCyc ID

CPD-7875

BiGG ID

Not Available

Wikipedia Link

1-Tetradecanol

METLIN ID

Not Available

PubChem Compound

8209

PDB ID

Not Available

ChEBI ID

77417

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

MDB00029970

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Download (PDF)

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 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Enzymes

Enzyme Details

1. Alkyldihydroxyacetonephosphate synthase, peroxisomal

General function:: Involved in catalytic activity
Specific function:: 1-acyl-glycerone 3-phosphate + a long-chain alcohol = an alkyl-glycerone 3-phosphate + a long-chain acid anion
Gene Name:: AGPS
Uniprot ID:: O00116
Molecular weight:: 72911.2

Enzyme Details

2. Fatty acyl-CoA reductase 1

General function:: Involved in catalytic activity
Specific function:: Catalyzes the reduction of saturated fatty acyl-CoA with chain length C16 or C18 to fatty alcohols.
Gene Name:: FAR1
Uniprot ID:: Q8WVX9
Molecular weight:: 59356.25

Enzyme Details

3. Fatty acyl-CoA reductase 2

General function:: Involved in catalytic activity
Specific function:: Catalyzes the reduction of fatty acyl-CoA to fatty alcohols. The preferred substrates are C16, C18, C18:1 and C18:2 but low activity can be observed with C10-C14 substrates.
Gene Name:: FAR2
Uniprot ID:: Q96K12
Molecular weight:: 59437.92

Enzyme Details

4. Acyl-CoA wax alcohol acyltransferase 1

General function:: Involved in transferase activity, transferring acyl groups other than amino-acyl groups
Specific function:: Acyltransferase that predominantly esterify long chain (wax) alcohols with acyl-CoA-derived fatty acids to produce wax esters. Wax esters are enriched in sebum, suggesting that it plays a central role in lipid metabolism in skin. Has a preference for arachidyl alcohol as well as decyl alcohol, demonstrating its relatively poor activity using saturated long chain alcohols (C16, C18, and C20).
Gene Name:: AWAT1
Uniprot ID:: Q58HT5
Molecular weight:: 37758.815

Enzyme Details

5. Acyl-CoA wax alcohol acyltransferase 2

General function:: Involved in transferase activity, transferring acyl groups other than amino-acyl groups
Specific function:: Acyltransferase that predominantly esterify long chain (wax) alcohols with acyl-CoA-derived fatty acids to produce wax esters. Wax esters are enriched in sebum, suggesting that it plays a central role in lipid metabolism in skin. Has no activity using decyl alcohol and significantly prefers the C16 and C18 alcohols. May also have 2-acylglycerol O-acyltransferase (MGAT) and acyl-CoA:retinol acyltransferase (ARAT) activities, to catalyze the synthesis of diacylglycerols and retinyl esters; however this activity is unclear in vivo.
Gene Name:: AWAT2
Uniprot ID:: Q6E213
Molecular weight:: 38093.25

Showing metabocard for Tetradecanol (HMDB0011638)

MOL for HMDB0011638 (Tetradecanol)

3D MOL for HMDB0011638 (Tetradecanol)

3D SDF for HMDB0011638 (Tetradecanol)

3D-SDF for HMDB0011638 (Tetradecanol)

PDB for HMDB0011638 (Tetradecanol)

3D PDB for HMDB0011638 (Tetradecanol)

SMILES for HMDB0011638 (Tetradecanol)

INCHI for HMDB0011638 (Tetradecanol)

Structure for HMDB0011638 (Tetradecanol)

3D Structure for HMDB0011638 (Tetradecanol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes