Record Information
Version1.0
Creation Date2016-05-19 01:48:45 UTC
Update Date2016-11-09 01:09:22 UTC
Accession NumberCHEM004524
Identification
Common NameDinitrobenzene (mixed isomers)
ClassSmall Molecule
DescriptionA dinitrobenzene that is benzene disubstituted at positions 1 and 3 with nitro groups.
Contaminant Sources
  • Clean Air Act Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
1,3-DinitrobenzolChEBI
2,4-DinitrobenzeneChEBI
DINITROPHENYLENEChEBI
m-DinitrobenzeneChEBI
m-DNBChEBI
Meta-dinitrobenzeneChEBI
3-DinitrobenzeneHMDB
Chemical FormulaC6H4N2O4
Average Molecular Mass168.107 g/mol
Monoisotopic Mass168.017 g/mol
CAS Registry Number25154-54-5
IUPAC Name1,3-dinitrobenzene
Traditional Name2,4-dinitrobenzene
SMILES[O-][N+](=O)C1=CC(=CC=C1)[N+]([O-])=O
InChI IdentifierInChI=1S/C6H4N2O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H
InChI KeyWDCYWAQPCXBPJA-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as nitrobenzenes. Nitrobenzenes are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassNitrobenzenes
Direct ParentNitrobenzenes
Alternative Parents
Substituents
  • Nitrobenzene
  • Nitroaromatic compound
  • Organic nitro compound
  • C-nitro compound
  • Organic 1,3-dipolar compound
  • Propargyl-type 1,3-dipolar organic compound
  • Allyl-type 1,3-dipolar organic compound
  • Organic oxoazanium
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organonitrogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility0.15 g/LALOGPS
logP1.7ALOGPS
logP1.85ChemAxon
logS-3.1ALOGPS
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area91.64 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity40.71 m³·mol⁻¹ChemAxon
Polarizability13.59 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
GC-MSGC-MS Spectrum - EI-B (Non-derivatized)splash10-0fb9-9100000000-ce6bfeb5ef2ced4681a2Spectrum
GC-MSGC-MS Spectrum - EI-B (Non-derivatized)splash10-00pi-9200000000-c1a87d65c320c33184e3Spectrum
GC-MSGC-MS Spectrum - EI-B (Non-derivatized)splash10-00pi-9200000000-97cd4c3ebec0ccbd0bcaSpectrum
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-014j-9700000000-f21228ba810672e35569Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableSpectrum
LC-MS/MSLC-MS/MS Spectrum - APCI-ITFT , negativesplash10-000i-0900000000-38869faeae4bd7e73217Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014i-0900000000-8e6e1e3044163af9bb88Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-03xu-0900000000-fc0ea1a311a8f1fbd289Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03xu-1900000000-8fe9c8f85ceb745b0962Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014i-0900000000-b1ee7d966d12380fc8d4Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014i-0900000000-66896cdfc20c56dcfd5dSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-014i-1900000000-648609457021263ea5adSpectrum
MSMass Spectrum (Electron Ionization)splash10-00pi-9200000000-1fab7ad275aef5be69adSpectrum
1D NMR1H NMR SpectrumNot AvailableSpectrum
1D NMR13C NMR SpectrumNot AvailableSpectrum
Toxicity Profile
Route of ExposureNot Available
Mechanism of ToxicityNot Available
MetabolismNot Available
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)Not Available
Uses/SourcesNot Available
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
DrugBank IDDB02680
HMDB IDHMDB0244170
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc ID13-DINITROBENZENE
METLIN IDNot Available
PDB IDNot Available
Wikipedia Link1,3-Dinitrobenzene
Chemspider ID7172
ChEBI ID51397
PubChem Compound ID7452
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
1. https://www.ncbi.nlm.nih.gov/pubmed/?term=12119003
2. https://www.ncbi.nlm.nih.gov/pubmed/?term=7744316
3. https://www.ncbi.nlm.nih.gov/pubmed/?term=9291486
4. 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.