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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 23:19:52 UTC

Update Date

2021-09-26 22:55:18 UTC

HMDB ID

HMDB0246302

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4-(Diethylamino)benzaldehyde

Description

4-(Diethylamino)benzaldehyde, also known as p-formyl-N,N-diethylaniline or DEABZ, belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-). Based on a literature review a small amount of articles have been published on 4-(Diethylamino)benzaldehyde. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4-(diethylamino)benzaldehyde is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4-(Diethylamino)benzaldehyde is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0246302
     RDKit          3D
4-(Diethylamino)benzaldehyde
 28 28  0  0  0  0  0  0  0  0999 V2000
    2.7759   -1.3632    0.6299 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9250   -0.8564   -0.4876 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0247    0.2060   -0.0793 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913    1.4919    0.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1816    2.1781   -0.9659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3667   -0.0355   -0.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9110   -1.2919   -0.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2865   -1.5243   -0.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1744   -0.5098    0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6189   -0.7591    0.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0019   -1.9304   -0.0849 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6235    0.7283    0.3203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2592    0.9938    0.2730 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7785   -2.4731    0.5914 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8591   -1.0668    0.5406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3516   -1.1087    1.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3734   -1.6623   -0.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6209   -0.4144   -1.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9043    2.1589    0.7357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4844    1.2396    0.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2956    2.2534   -0.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8191    3.2173   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8345    1.6387   -1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3107   -2.1681   -0.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7019   -2.5268   -0.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3141    0.0355    0.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3111    1.5404    0.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9400    2.0087    0.4677 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
  3  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  9 12  1  0
 12 13  2  0
 13  6  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  2 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
 10 26  1  0
 12 27  1  0
 13 28  1  0
M  END

HMDB0246302
     RDKit          3D
4-(Diethylamino)benzaldehyde
 28 28  0  0  0  0  0  0  0  0999 V2000
    2.7759   -1.3632    0.6299 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9250   -0.8564   -0.4876 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0247    0.2060   -0.0793 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913    1.4919    0.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1816    2.1781   -0.9659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3667   -0.0355   -0.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9110   -1.2919   -0.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2865   -1.5243   -0.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1744   -0.5098    0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6189   -0.7591    0.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0019   -1.9304   -0.0849 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6235    0.7283    0.3203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2592    0.9938    0.2730 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7785   -2.4731    0.5914 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8591   -1.0668    0.5406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3516   -1.1087    1.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3734   -1.6623   -0.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6209   -0.4144   -1.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9043    2.1589    0.7357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4844    1.2396    0.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2956    2.2534   -0.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8191    3.2173   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8345    1.6387   -1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3107   -2.1681   -0.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7019   -2.5268   -0.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3141    0.0355    0.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3111    1.5404    0.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9400    2.0087    0.4677 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
  3  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  9 12  1  0
 12 13  2  0
 13  6  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  2 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
 10 26  1  0
 12 27  1  0
 13 28  1  0
M  END

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       1.334   3.850   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    6                                                  
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7   13                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12    6                                                       
MASTER        0    0    0    0    0    0    0    0   13    0   26    0
END

COMPND    HMDB0246302
HETATM    1  C1  UNL     1       2.776  -1.363   0.630  1.00  0.00           C  
HETATM    2  C2  UNL     1       1.925  -0.856  -0.488  1.00  0.00           C  
HETATM    3  N1  UNL     1       1.025   0.206  -0.079  1.00  0.00           N  
HETATM    4  C3  UNL     1       1.591   1.492   0.273  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.182   2.178  -0.966  1.00  0.00           C  
HETATM    6  C5  UNL     1      -0.367  -0.035  -0.016  1.00  0.00           C  
HETATM    7  C6  UNL     1      -0.911  -1.292  -0.244  1.00  0.00           C  
HETATM    8  C7  UNL     1      -2.287  -1.524  -0.189  1.00  0.00           C  
HETATM    9  C8  UNL     1      -3.174  -0.510   0.096  1.00  0.00           C  
HETATM   10  C9  UNL     1      -4.619  -0.759   0.152  1.00  0.00           C  
HETATM   11  O1  UNL     1      -5.002  -1.930  -0.085  1.00  0.00           O  
HETATM   12  C10 UNL     1      -2.624   0.728   0.320  1.00  0.00           C  
HETATM   13  C11 UNL     1      -1.259   0.994   0.273  1.00  0.00           C  
HETATM   14  H1  UNL     1       2.778  -2.473   0.591  1.00  0.00           H  
HETATM   15  H2  UNL     1       3.859  -1.067   0.541  1.00  0.00           H  
HETATM   16  H3  UNL     1       2.352  -1.109   1.626  1.00  0.00           H  
HETATM   17  H4  UNL     1       1.373  -1.662  -0.950  1.00  0.00           H  
HETATM   18  H5  UNL     1       2.621  -0.414  -1.263  1.00  0.00           H  
HETATM   19  H6  UNL     1       0.904   2.159   0.736  1.00  0.00           H  
HETATM   20  H7  UNL     1       2.484   1.240   0.916  1.00  0.00           H  
HETATM   21  H8  UNL     1       3.296   2.253  -0.899  1.00  0.00           H  
HETATM   22  H9  UNL     1       1.819   3.217  -1.078  1.00  0.00           H  
HETATM   23  H10 UNL     1       1.834   1.639  -1.880  1.00  0.00           H  
HETATM   24  H11 UNL     1      -0.311  -2.168  -0.463  1.00  0.00           H  
HETATM   25  H12 UNL     1      -2.702  -2.527  -0.379  1.00  0.00           H  
HETATM   26  H13 UNL     1      -5.314   0.036   0.387  1.00  0.00           H  
HETATM   27  H14 UNL     1      -3.311   1.540   0.548  1.00  0.00           H  
HETATM   28  H15 UNL     1      -0.940   2.009   0.468  1.00  0.00           H  
CONECT    1    2   14   15   16
CONECT    2    3   17   18
CONECT    3    4    6
CONECT    4    5   19   20
CONECT    5   21   22   23
CONECT    6    7    7   13
CONECT    7    8   24
CONECT    8    9    9   25
CONECT    9   10   12
CONECT   10   11   11   26
CONECT   12   13   13   27
CONECT   13   28
END

HMDB0246302
     RDKit          3D
4-(Diethylamino)benzaldehyde
 28 28  0  0  0  0  0  0  0  0999 V2000
    2.7759   -1.3632    0.6299 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9250   -0.8564   -0.4876 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0247    0.2060   -0.0793 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913    1.4919    0.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1816    2.1781   -0.9659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3667   -0.0355   -0.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9110   -1.2919   -0.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2865   -1.5243   -0.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1744   -0.5098    0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6189   -0.7591    0.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0019   -1.9304   -0.0849 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6235    0.7283    0.3203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2592    0.9938    0.2730 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7785   -2.4731    0.5914 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8591   -1.0668    0.5406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3516   -1.1087    1.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3734   -1.6623   -0.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6209   -0.4144   -1.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9043    2.1589    0.7357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4844    1.2396    0.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2956    2.2534   -0.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8191    3.2173   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8345    1.6387   -1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3107   -2.1681   -0.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7019   -2.5268   -0.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3141    0.0355    0.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3111    1.5404    0.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9400    2.0087    0.4677 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
  3  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  9 12  1  0
 12 13  2  0
 13  6  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  2 18  1  0
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
 10 26  1  0
 12 27  1  0
 13 28  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
4-(N,N-Diethylamino)benzaldehyde	ChEBI
4-Diethylaminobenzaldehyde	ChEBI
p-(Diethylamino)benzaldehyde	ChEBI
p-Formyl-N,N-diethylaniline	ChEBI
DEABZ	HMDB

Chemical Formula

C₁₁H₁₅NO

Average Molecular Weight

177.247

Monoisotopic Molecular Weight

177.115364107

IUPAC Name

4-(diethylamino)benzaldehyde

Traditional Name

4-(diethylamino)benzaldehyde

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C11H15NO/c1-3-12(4-2)11-7-5-10(9-13)6-8-11/h5-9H,3-4H2,1-2H3

InChI Key

MNFZZNNFORDXSV-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoyl derivatives

Direct Parent

Benzoyl derivatives

Alternative Parents

Substituents

Benzaldehyde
Benzoyl
Tertiary aliphatic/aromatic amine
Dialkylarylamine
Aniline or substituted anilines
Aryl-aldehyde
Tertiary amine
Organic oxide
Aldehyde
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Amine
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

tertiary amino compound (CHEBI:86194 )
aromatic amine (CHEBI:86194 )
benzaldehydes (CHEBI:86194 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

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	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	3.04	ALOGPS
logP	2.51	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Basic)	4.33	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	20.31 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	56.57 m³·mol⁻¹	ChemAxon
Polarizability	20.53 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
DeepCCS	[M+H]+	142.651	30932474
DeepCCS	[M-H]-	138.823	30932474
DeepCCS	[M-2H]-	176.37	30932474
DeepCCS	[M+Na]+	151.908	30932474
AllCCS	[M+H]+	140.2	32859911
AllCCS	[M+H-H2O]+	136.2	32859911
AllCCS	[M+NH4]+	144.0	32859911
AllCCS	[M+Na]+	145.1	32859911
AllCCS	[M-H]-	141.5	32859911
AllCCS	[M+Na-2H]-	142.5	32859911
AllCCS	[M+HCOO]-	143.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4-(Diethylamino)benzaldehyde	CCN(CC)C1=CC=C(C=O)C=C1	2182.3	Standard polar	33892256
4-(Diethylamino)benzaldehyde	CCN(CC)C1=CC=C(C=O)C=C1	1586.2	Standard non polar	33892256
4-(Diethylamino)benzaldehyde	CCN(CC)C1=CC=C(C=O)C=C1	1703.7	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 - 4-(Diethylamino)benzaldehyde GC-MS (Non-derivatized) - 70eV, Positive	splash10-002b-1900000000-93cface98806f8feeff5	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-(Diethylamino)benzaldehyde 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 - 4-(Diethylamino)benzaldehyde 10V, Positive-QTOF	splash10-004i-0900000000-47a54f606a1085b545cf	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 20V, Positive-QTOF	splash10-004i-0900000000-10b01a9c2215d1db4540	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 40V, Positive-QTOF	splash10-05cr-4900000000-eb39ba494b996bb586b2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 10V, Negative-QTOF	splash10-004i-0900000000-5232cda1d959d1ef6832	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 20V, Negative-QTOF	splash10-004i-0900000000-4e33181f7464903bccb6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 40V, Negative-QTOF	splash10-00r5-2900000000-b91490848bf9a0bdc152	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 10V, Positive-QTOF	splash10-004i-0900000000-26748d51e43e3187c79d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 20V, Positive-QTOF	splash10-004i-0900000000-259daf4cf07a32cbe250	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 40V, Positive-QTOF	splash10-006x-5900000000-82475248ad4075cfbe00	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 10V, Negative-QTOF	splash10-004i-0900000000-04fcceb4326c5f8f7d5c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 20V, Negative-QTOF	splash10-00os-0900000000-9bcc98aaf9d76ba52091	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(Diethylamino)benzaldehyde 40V, Negative-QTOF	splash10-00xr-9500000000-b8aa6b3eda3a1bdfff8b	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

60462

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

67114

PDB ID

Not Available

ChEBI ID

86194

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 4-(Diethylamino)benzaldehyde (HMDB0246302)

MOL for HMDB0246302 (4-(Diethylamino)benzaldehyde)

3D MOL for HMDB0246302 (4-(Diethylamino)benzaldehyde)

3D SDF for HMDB0246302 (4-(Diethylamino)benzaldehyde)

3D-SDF for HMDB0246302 (4-(Diethylamino)benzaldehyde)

PDB for HMDB0246302 (4-(Diethylamino)benzaldehyde)

3D PDB for HMDB0246302 (4-(Diethylamino)benzaldehyde)

SMILES for HMDB0246302 (4-(Diethylamino)benzaldehyde)

INCHI for HMDB0246302 (4-(Diethylamino)benzaldehyde)

Structure for HMDB0246302 (4-(Diethylamino)benzaldehyde)

3D Structure for HMDB0246302 (4-(Diethylamino)benzaldehyde)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra