Record Information
Version1.0
Creation Date2016-05-22 03:51:05 UTC
Update Date2016-11-09 01:15:30 UTC
Accession NumberCHEM016999
Identification
Common NameButanal oxime
ClassSmall Molecule
DescriptionAn aliphatic aldoxime resulting from the formal condensation of the carbonyl group of n-butanal with hydroxylamine.
Contaminant Sources
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
Butyraldehyde oximeChEBI
ButyraldoximeChEBI
N-Butyraldehyde oximeChEBI
N-ButyraldoximeChEBI
(1E)-Butanal oximeChEBI
(e)-CH3(CH2)2CH=nohChEBI
Butanal oximeChEBI
Chemical FormulaC4H9NO
Average Molecular Mass87.122 g/mol
Monoisotopic Mass87.068 g/mol
CAS Registry Number110-69-0
IUPAC NameN-butylidenehydroxylamine
Traditional Namebutyraldoxime
SMILESCCCC=NO
InChI IdentifierInChI=1S/C4H9NO/c1-2-3-4-5-6/h4,6H,2-3H2,1H3
InChI KeyKGGVGTQEGGOZRN-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as aldoximes. These are organic compounds with the general formula RC(H)=NOH (R = organyl).
KingdomOrganic compounds
Super ClassOrganic nitrogen compounds
ClassOrganonitrogen compounds
Sub ClassOximes
Direct ParentAldoximes
Alternative Parents
Substituents
  • Aldoxime
  • Organic oxygen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic 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 Solubility15.1 g/LALOGPS
logP0.87ALOGPS
logP0.77ChemAxon
logS-0.76ALOGPS
pKa (Strongest Acidic)11.34ChemAxon
pKa (Strongest Basic)3.43ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area32.59 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity24.77 m³·mol⁻¹ChemAxon
Polarizability9.85 ųChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-9000000000-e833a4561613946751e7Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-9000000000-8430bc46f0d2afbf07c2Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0006-9000000000-801cd2369deab490515cSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-000i-9000000000-863bd2f64b09c0cc3abeSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-000i-9000000000-1d34d8b2bd5b603d62b8Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0pvu-9000000000-3c5cbeecc2f90901dde7Spectrum
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 IDNot Available
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider IDNot Available
ChEBI ID59012
PubChem Compound ID8069
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available