Record Information
Version1.0
Creation Date2016-05-22 03:59:31 UTC
Update Date2016-11-09 01:15:32 UTC
Accession NumberCHEM017178
Identification
Common NameN-Phenylhydroxylamine
ClassSmall Molecule
DescriptionAn N-substituted amine that is a derivative of aniline in which one of the amino hydrogen atoms is replaced with a hydroxy substituent.
Contaminant Sources
  • STOFF IDENT Compounds
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
(Hydroxyamino)benzeneChEBI
HydroxylaminobenzeneChEBI
N-HydroxyanilineChEBI
N-HydroxybenzenamineChEBI
N-HydroxylanilineChEBI
PhenylhydroxylamineChEBI
Phenylhydroxylamine hydrochlorideMeSH
Chemical FormulaC6H7NO
Average Molecular Mass109.126 g/mol
Monoisotopic Mass109.053 g/mol
CAS Registry Number100-65-2
IUPAC NameN-phenylhydroxylamine
Traditional Namephenylhydroxylamine
SMILESONC1=CC=CC=C1
InChI IdentifierInChI=1S/C6H7NO/c8-7-6-4-2-1-3-5-6/h1-5,7-8H
InChI KeyCKRZKMFTZCFYGB-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as n-phenylhydroxylamines. These are hydroxylamines that are N-substituted with a phenyl group.
KingdomOrganic compounds
Super ClassBenzenoids
ClassN-phenylhydroxylamines
Sub ClassNot Available
Direct ParentN-phenylhydroxylamines
Alternative Parents
Substituents
  • N-phenylhydroxylamine
  • 1-hydroxylamino, 4-unsubstituted benzenoid
  • 1-hydroxylamino, 2-unsubstituted benzenoid
  • Arylhydroxamate
  • Monocyclic benzene moiety
  • N-organohydroxylamine
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • 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 Solubility41.1 g/LALOGPS
logP1.06ALOGPS
logP1.48ChemAxon
logS-0.42ALOGPS
pKa (Strongest Acidic)15.03ChemAxon
pKa (Strongest Basic)5.22ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area32.26 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity33.05 m³·mol⁻¹ChemAxon
Polarizability11.28 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-0a4i-9500000000-15e3a2408b196f0da05bSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-03di-0900000000-51b69367ae8ff36838e6Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-03di-2900000000-57822fb69be9854441e4Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0296-9100000000-b00292874f87427e5c4bSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a4i-5900000000-be5cbec6896f82c96176Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0a4i-3900000000-dd4848a9d018d69002c1Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-052f-9100000000-e1ac31071b46f20c29a2Spectrum
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 IDNot Available
HMDB IDHMDB0186195
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkPhenylhydroxylamine
Chemspider IDNot Available
ChEBI ID28902
PubChem Compound ID7518
Kegg Compound IDC02720
YMDB IDNot Available
ECMDB IDECMDB20159
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
1. https://www.ncbi.nlm.nih.gov/pubmed/?term=11304127
2. https://www.ncbi.nlm.nih.gov/pubmed/?term=23766821