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Showing metabocard for 4-Aminobenzohydrazide (HMDB0246354)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-10 23:22:52 UTC
Update Date2021-09-26 22:55:23 UTC
HMDB IDHMDB0246354
Secondary Accession NumbersNone
Metabolite Identification
Common Name4-Aminobenzohydrazide
Description4-Aminobenzohydrazide, also known as aminostimil, belongs to the class of organic compounds known as aminobenzoic acids and derivatives. These are benzoic acids (or derivative thereof) containing an amine group attached to the benzene moiety. Based on a literature review a significant number of articles have been published on 4-Aminobenzohydrazide. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4-aminobenzohydrazide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4-Aminobenzohydrazide 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
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MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0246354 (4-Aminobenzohydrazide)


  Mrv1652309112101232D          

 11 11  0  0  0  0            999 V2000
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -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
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 11  1  0  0  0  0
M  END
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3D MOL for HMDB0246354 (4-Aminobenzohydrazide)

HMDB0246354
     RDKit          3D
4-Aminobenzohydrazide
 20 20  0  0  0  0  0  0  0  0999 V2000
   -3.9904   -0.9639    0.7369 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6118   -0.6901    0.8169 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8419   -0.3769   -0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4245   -0.3462   -1.4360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4305   -0.0978   -0.2296 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2710   -0.1112    0.9436 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6389    0.1622    1.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3331    0.4611   -0.1409 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7237    0.7416   -0.0912 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6399    0.4778   -1.3260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2921    0.2058   -1.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3856   -0.5717   -0.1440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4633   -0.6151    1.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1616   -0.7224    1.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2370   -0.3423    1.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1233    0.1331    1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3837    0.5174   -0.8775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779    1.1944    0.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1796    0.7144   -2.2535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2166    0.2300   -2.3310 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11  5  1  0
  1 12  1  0
  1 13  1  0
  2 14  1  0
  6 15  1  0
  7 16  1  0
  9 17  1  0
  9 18  1  0
 10 19  1  0
 11 20  1  0
M  END
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3D SDF for HMDB0246354 (4-Aminobenzohydrazide)


  Mrv1652309112101232D          

 11 11  0  0  0  0            999 V2000
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -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
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 11  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0246354

> <DATABASE_NAME>
hmdb

> <SMILES>
NNC(=O)C1=CC=C(N)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C7H9N3O/c8-6-3-1-5(2-4-6)7(11)10-9/h1-4H,8-9H2,(H,10,11)

> <INCHI_KEY>
WPBZMCGPFHZRHJ-UHFFFAOYSA-N

> <FORMULA>
C7H9N3O

> <MOLECULAR_WEIGHT>
151.169

> <EXACT_MASS>
151.074561922

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
20

> <JCHEM_AVERAGE_POLARIZABILITY>
15.407986886482902

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-aminobenzohydrazide

> <ALOGPS_LOGP>
-0.51

> <JCHEM_LOGP>
-0.3015155366666667

> <ALOGPS_LOGS>
-1.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.212029739610788

> <JCHEM_PKA_STRONGEST_BASIC>
3.413058017422083

> <JCHEM_POLAR_SURFACE_AREA>
81.14

> <JCHEM_REFRACTIVITY>
44.32090000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.01e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-aminobenzoylhydrazine

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0246354 (4-Aminobenzohydrazide)

HMDB0246354
     RDKit          3D
4-Aminobenzohydrazide
 20 20  0  0  0  0  0  0  0  0999 V2000
   -3.9904   -0.9639    0.7369 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6118   -0.6901    0.8169 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8419   -0.3769   -0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4245   -0.3462   -1.4360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4305   -0.0978   -0.2296 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2710   -0.1112    0.9436 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6389    0.1622    1.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3331    0.4611   -0.1409 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7237    0.7416   -0.0912 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6399    0.4778   -1.3260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2921    0.2058   -1.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3856   -0.5717   -0.1440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4633   -0.6151    1.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1616   -0.7224    1.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2370   -0.3423    1.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1233    0.1331    1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3837    0.5174   -0.8775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779    1.1944    0.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1796    0.7144   -2.2535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2166    0.2300   -2.3310 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11  5  1  0
  1 12  1  0
  1 13  1  0
  2 14  1  0
  6 15  1  0
  7 16  1  0
  9 17  1  0
  9 18  1  0
 10 19  1  0
 11 20  1  0
M  END
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PDB for HMDB0246354 (4-Aminobenzohydrazide)

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   1.540   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       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0      -0.000   4.620   0.000  0.00  0.00           N+0
HETATM   10  N   UNK     0      -0.000   6.160   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0       1.334  -2.310   0.000  0.00  0.00           N+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9                                                            
CONECT   11    3                                                            
MASTER        0    0    0    0    0    0    0    0   11    0   22    0
END
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3D PDB for HMDB0246354 (4-Aminobenzohydrazide)

COMPND    HMDB0246354
HETATM    1  N1  UNL     1      -3.990  -0.964   0.737  1.00  0.00           N  
HETATM    2  N2  UNL     1      -2.612  -0.690   0.817  1.00  0.00           N  
HETATM    3  C1  UNL     1      -1.842  -0.377  -0.321  1.00  0.00           C  
HETATM    4  O1  UNL     1      -2.424  -0.346  -1.436  1.00  0.00           O  
HETATM    5  C2  UNL     1      -0.430  -0.098  -0.230  1.00  0.00           C  
HETATM    6  C3  UNL     1       0.271  -0.111   0.944  1.00  0.00           C  
HETATM    7  C4  UNL     1       1.639   0.162   1.011  1.00  0.00           C  
HETATM    8  C5  UNL     1       2.333   0.461  -0.141  1.00  0.00           C  
HETATM    9  N3  UNL     1       3.724   0.742  -0.091  1.00  0.00           N  
HETATM   10  C6  UNL     1       1.640   0.478  -1.326  1.00  0.00           C  
HETATM   11  C7  UNL     1       0.292   0.206  -1.374  1.00  0.00           C  
HETATM   12  H1  UNL     1      -4.386  -0.572  -0.144  1.00  0.00           H  
HETATM   13  H2  UNL     1      -4.463  -0.615   1.595  1.00  0.00           H  
HETATM   14  H3  UNL     1      -2.162  -0.722   1.742  1.00  0.00           H  
HETATM   15  H4  UNL     1      -0.237  -0.342   1.878  1.00  0.00           H  
HETATM   16  H5  UNL     1       2.123   0.133   1.968  1.00  0.00           H  
HETATM   17  H6  UNL     1       4.384   0.517  -0.877  1.00  0.00           H  
HETATM   18  H7  UNL     1       4.178   1.194   0.743  1.00  0.00           H  
HETATM   19  H8  UNL     1       2.180   0.714  -2.254  1.00  0.00           H  
HETATM   20  H9  UNL     1      -0.217   0.230  -2.331  1.00  0.00           H  
CONECT    1    2   12   13
CONECT    2    3   14
CONECT    3    4    4    5
CONECT    5    6    6   11
CONECT    6    7   15
CONECT    7    8    8   16
CONECT    8    9   10
CONECT    9   17   18
CONECT   10   11   11   19
CONECT   11   20
END
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SMILES for HMDB0246354 (4-Aminobenzohydrazide)

NNC(=O)C1=CC=C(N)C=C1
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INCHI for HMDB0246354 (4-Aminobenzohydrazide)

InChI=1S/C7H9N3O/c8-6-3-1-5(2-4-6)7(11)10-9/h1-4H,8-9H2,(H,10,11)
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
4-AminobenzhydrazideHMDB
4-Aminobenzoic acid-hydrazideHMDB
AminostimilHMDB
p-Aminobenzoic acid hydrazideHMDB
Para-aminobenzhydrazideHMDB
Chemical FormulaC7H9N3O
Average Molecular Weight151.169
Monoisotopic Molecular Weight151.074561922
IUPAC Name4-aminobenzohydrazide
Traditional Name4-aminobenzoylhydrazine
CAS Registry NumberNot Available
SMILES
NNC(=O)C1=CC=C(N)C=C1
InChI Identifier
InChI=1S/C7H9N3O/c8-6-3-1-5(2-4-6)7(11)10-9/h1-4H,8-9H2,(H,10,11)
InChI KeyWPBZMCGPFHZRHJ-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as aminobenzoic acids and derivatives. These are benzoic acids (or derivative thereof) containing an amine group attached to the benzene moiety.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassBenzoic acids and derivatives
Direct ParentAminobenzoic acids and derivatives
Alternative Parents
Substituents
  • Aminobenzoic acid or derivatives
  • Benzoyl
  • Aniline or substituted anilines
  • Amino acid or derivatives
  • Carboxylic acid hydrazide
  • Carboxylic acid derivative
  • Amine
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
logP-0.51ALOGPS
logP-0.3ChemAxon
logS-1.2ALOGPS
pKa (Strongest Acidic)15.21ChemAxon
pKa (Strongest Basic)3.41ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area81.14 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity44.32 m³·mol⁻¹ChemAxon
Polarizability15.41 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+134.95830932474
DeepCCS[M-H]-131.39530932474
DeepCCS[M-2H]-168.7730932474
DeepCCS[M+Na]+144.30830932474
AllCCS[M+H]+134.032859911
AllCCS[M+H-H2O]+129.532859911
AllCCS[M+NH4]+138.132859911
AllCCS[M+Na]+139.332859911
AllCCS[M-H]-130.932859911
AllCCS[M+Na-2H]-132.332859911
AllCCS[M+HCOO]-133.932859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Predicted by Siyang on May 30, 20229.7606 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20224.57 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid837.5 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid307.2 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid71.1 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid175.6 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid49.7 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid253.9 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid314.9 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)132.5 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid674.3 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid110.6 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid780.1 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid217.0 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid220.1 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate465.2 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA322.7 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water189.0 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
4-AminobenzohydrazideNNC(=O)C1=CC=C(N)C=C13009.5Standard polar33892256
4-AminobenzohydrazideNNC(=O)C1=CC=C(N)C=C11730.8Standard non polar33892256
4-AminobenzohydrazideNNC(=O)C1=CC=C(N)C=C11911.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
4-Aminobenzohydrazide,1TMS,isomer #1C[Si](C)(C)NNC(=O)C1=CC=C(N)C=C12055.6Semi standard non polar33892256
4-Aminobenzohydrazide,1TMS,isomer #1C[Si](C)(C)NNC(=O)C1=CC=C(N)C=C12049.6Standard non polar33892256
4-Aminobenzohydrazide,1TMS,isomer #1C[Si](C)(C)NNC(=O)C1=CC=C(N)C=C12815.5Standard polar33892256
4-Aminobenzohydrazide,1TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)NN)C=C12112.7Semi standard non polar33892256
4-Aminobenzohydrazide,1TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)NN)C=C12168.2Standard non polar33892256
4-Aminobenzohydrazide,1TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)NN)C=C12867.5Standard polar33892256
4-Aminobenzohydrazide,1TMS,isomer #3C[Si](C)(C)N(N)C(=O)C1=CC=C(N)C=C11924.2Semi standard non polar33892256
4-Aminobenzohydrazide,1TMS,isomer #3C[Si](C)(C)N(N)C(=O)C1=CC=C(N)C=C11965.7Standard non polar33892256
4-Aminobenzohydrazide,1TMS,isomer #3C[Si](C)(C)N(N)C(=O)C1=CC=C(N)C=C13113.6Standard polar33892256
4-Aminobenzohydrazide,2TMS,isomer #1C[Si](C)(C)NNC(=O)C1=CC=C(N[Si](C)(C)C)C=C12259.6Semi standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #1C[Si](C)(C)NNC(=O)C1=CC=C(N[Si](C)(C)C)C=C12233.4Standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #1C[Si](C)(C)NNC(=O)C1=CC=C(N[Si](C)(C)C)C=C12411.8Standard polar33892256
4-Aminobenzohydrazide,2TMS,isomer #2C[Si](C)(C)N(NC(=O)C1=CC=C(N)C=C1)[Si](C)(C)C2174.3Semi standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #2C[Si](C)(C)N(NC(=O)C1=CC=C(N)C=C1)[Si](C)(C)C2087.3Standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #2C[Si](C)(C)N(NC(=O)C1=CC=C(N)C=C1)[Si](C)(C)C2677.4Standard polar33892256
4-Aminobenzohydrazide,2TMS,isomer #3C[Si](C)(C)NN(C(=O)C1=CC=C(N)C=C1)[Si](C)(C)C2005.2Semi standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #3C[Si](C)(C)NN(C(=O)C1=CC=C(N)C=C1)[Si](C)(C)C2016.1Standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #3C[Si](C)(C)NN(C(=O)C1=CC=C(N)C=C1)[Si](C)(C)C2551.7Standard polar33892256
4-Aminobenzohydrazide,2TMS,isomer #4C[Si](C)(C)N(C1=CC=C(C(=O)NN)C=C1)[Si](C)(C)C2177.0Semi standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #4C[Si](C)(C)N(C1=CC=C(C(=O)NN)C=C1)[Si](C)(C)C2193.5Standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #4C[Si](C)(C)N(C1=CC=C(C(=O)NN)C=C1)[Si](C)(C)C2646.3Standard polar33892256
4-Aminobenzohydrazide,2TMS,isomer #5C[Si](C)(C)NC1=CC=C(C(=O)N(N)[Si](C)(C)C)C=C12071.0Semi standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #5C[Si](C)(C)NC1=CC=C(C(=O)N(N)[Si](C)(C)C)C=C12173.4Standard non polar33892256
4-Aminobenzohydrazide,2TMS,isomer #5C[Si](C)(C)NC1=CC=C(C(=O)N(N)[Si](C)(C)C)C=C12715.9Standard polar33892256
4-Aminobenzohydrazide,3TMS,isomer #1C[Si](C)(C)NC1=CC=C(C(=O)NN([Si](C)(C)C)[Si](C)(C)C)C=C12334.2Semi standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #1C[Si](C)(C)NC1=CC=C(C(=O)NN([Si](C)(C)C)[Si](C)(C)C)C=C12279.2Standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #1C[Si](C)(C)NC1=CC=C(C(=O)NN([Si](C)(C)C)[Si](C)(C)C)C=C12301.8Standard polar33892256
4-Aminobenzohydrazide,3TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)N(N[Si](C)(C)C)[Si](C)(C)C)C=C12108.5Semi standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)N(N[Si](C)(C)C)[Si](C)(C)C)C=C12158.0Standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)N(N[Si](C)(C)C)[Si](C)(C)C)C=C12189.0Standard polar33892256
4-Aminobenzohydrazide,3TMS,isomer #3C[Si](C)(C)NNC(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C12233.8Semi standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #3C[Si](C)(C)NNC(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C12176.4Standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #3C[Si](C)(C)NNC(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C12257.6Standard polar33892256
4-Aminobenzohydrazide,3TMS,isomer #4C[Si](C)(C)N(C(=O)C1=CC=C(N)C=C1)N([Si](C)(C)C)[Si](C)(C)C2042.7Semi standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #4C[Si](C)(C)N(C(=O)C1=CC=C(N)C=C1)N([Si](C)(C)C)[Si](C)(C)C2112.9Standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #4C[Si](C)(C)N(C(=O)C1=CC=C(N)C=C1)N([Si](C)(C)C)[Si](C)(C)C2471.8Standard polar33892256
4-Aminobenzohydrazide,3TMS,isomer #5C[Si](C)(C)N(N)C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C12043.6Semi standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #5C[Si](C)(C)N(N)C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C12200.0Standard non polar33892256
4-Aminobenzohydrazide,3TMS,isomer #5C[Si](C)(C)N(N)C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C12604.4Standard polar33892256
4-Aminobenzohydrazide,4TMS,isomer #1C[Si](C)(C)N(NC(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C2297.2Semi standard non polar33892256
4-Aminobenzohydrazide,4TMS,isomer #1C[Si](C)(C)N(NC(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C2283.4Standard non polar33892256
4-Aminobenzohydrazide,4TMS,isomer #1C[Si](C)(C)N(NC(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C2207.5Standard polar33892256
4-Aminobenzohydrazide,4TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C=C12159.1Semi standard non polar33892256
4-Aminobenzohydrazide,4TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C=C12211.4Standard non polar33892256
4-Aminobenzohydrazide,4TMS,isomer #2C[Si](C)(C)NC1=CC=C(C(=O)N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C=C12162.6Standard polar33892256
4-Aminobenzohydrazide,4TMS,isomer #3C[Si](C)(C)NN(C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C2074.3Semi standard non polar33892256
4-Aminobenzohydrazide,4TMS,isomer #3C[Si](C)(C)NN(C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C2162.8Standard non polar33892256
4-Aminobenzohydrazide,4TMS,isomer #3C[Si](C)(C)NN(C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C2105.8Standard polar33892256
4-Aminobenzohydrazide,5TMS,isomer #1C[Si](C)(C)N(C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C2219.2Semi standard non polar33892256
4-Aminobenzohydrazide,5TMS,isomer #1C[Si](C)(C)N(C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C2290.2Standard non polar33892256
4-Aminobenzohydrazide,5TMS,isomer #1C[Si](C)(C)N(C(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C2036.4Standard polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N)C=C12301.5Semi standard non polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N)C=C12220.8Standard non polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N)C=C12852.8Standard polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)NN)C=C12374.0Semi standard non polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)NN)C=C12372.7Standard non polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)NN)C=C12886.0Standard polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)N(N)C(=O)C1=CC=C(N)C=C12127.7Semi standard non polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)N(N)C(=O)C1=CC=C(N)C=C12154.7Standard non polar33892256
4-Aminobenzohydrazide,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)N(N)C(=O)C1=CC=C(N)C=C13154.3Standard polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N[Si](C)(C)C(C)(C)C)C=C12788.8Semi standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N[Si](C)(C)C(C)(C)C)C=C12603.7Standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N[Si](C)(C)C(C)(C)C)C=C12532.0Standard polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(NC(=O)C1=CC=C(N)C=C1)[Si](C)(C)C(C)(C)C2632.8Semi standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(NC(=O)C1=CC=C(N)C=C1)[Si](C)(C)C(C)(C)C2459.2Standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(NC(=O)C1=CC=C(N)C=C1)[Si](C)(C)C(C)(C)C2682.9Standard polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)NN(C(=O)C1=CC=C(N)C=C1)[Si](C)(C)C(C)(C)C2461.4Semi standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)NN(C(=O)C1=CC=C(N)C=C1)[Si](C)(C)C(C)(C)C2433.8Standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)NN(C(=O)C1=CC=C(N)C=C1)[Si](C)(C)C(C)(C)C2623.3Standard polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C1=CC=C(C(=O)NN)C=C1)[Si](C)(C)C(C)(C)C2668.0Semi standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C1=CC=C(C(=O)NN)C=C1)[Si](C)(C)C(C)(C)C2569.3Standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C1=CC=C(C(=O)NN)C=C1)[Si](C)(C)C(C)(C)C2623.9Standard polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N)[Si](C)(C)C(C)(C)C)C=C12600.2Semi standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N)[Si](C)(C)C(C)(C)C)C=C12576.7Standard non polar33892256
4-Aminobenzohydrazide,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N)[Si](C)(C)C(C)(C)C)C=C12794.7Standard polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C13034.0Semi standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12809.0Standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12580.0Standard polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12874.2Semi standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12723.0Standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12527.4Standard polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12985.7Semi standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12781.8Standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)NNC(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12530.4Standard polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2716.5Semi standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2687.9Standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2624.4Standard polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)N(N)C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12790.1Semi standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)N(N)C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12775.0Standard non polar33892256
4-Aminobenzohydrazide,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)N(N)C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12801.1Standard polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(NC(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C3185.1Semi standard non polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(NC(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C3007.6Standard non polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(NC(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C2574.9Standard polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C13115.3Semi standard non polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12960.8Standard non polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(C(=O)N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12575.2Standard polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)NN(C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C3029.8Semi standard non polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)NN(C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C2941.4Standard non polar33892256
4-Aminobenzohydrazide,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)NN(C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C2532.2Standard polar33892256
4-Aminobenzohydrazide,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3288.4Semi standard non polar33892256
4-Aminobenzohydrazide,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3186.2Standard non polar33892256
4-Aminobenzohydrazide,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2538.4Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 4-Aminobenzohydrazide GC-MS (Non-derivatized) - 70eV, Positivesplash10-00di-0900000000-889bc6fc64536c97be0b2021-09-24Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 4-Aminobenzohydrazide GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminobenzohydrazide 10V, Positive-QTOFsplash10-0fk9-0900000000-bba71451ecf96c1aa9a32021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminobenzohydrazide 20V, Positive-QTOFsplash10-00di-1900000000-3c7e055767e5c79c83722021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminobenzohydrazide 40V, Positive-QTOFsplash10-014l-9100000000-d815a80c0bbcb84cfb9b2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminobenzohydrazide 10V, Negative-QTOFsplash10-0udi-3900000000-a8182455261ea4463ae42021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminobenzohydrazide 20V, Negative-QTOFsplash10-0006-9400000000-8f5606ac38c45aba589c2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminobenzohydrazide 40V, Negative-QTOFsplash10-0002-4900000000-9a999eea0c89a734ddaa2021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID20160
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound21450
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. 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 ]