Record Information
Version1.0
Creation Date2016-05-22 04:46:13 UTC
Update Date2016-11-09 01:15:42 UTC
Accession NumberCHEM017945
Identification
Common NameProcaine hydrochloride
ClassSmall Molecule
Description
Contaminant Sources
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
NovocainKegg
GeriocaineMeSH
AnujectMeSH
Lophakomp-procain NMeSH
GerokitMeSH
Hydrochloride, procaineMeSH
Procain steigerwaldMeSH
ProcaineMeSH
Hewedolor-procainMeSH
NovocaineMeSH
Pröcaine chlorhydrate lavoisierMeSH
Procain-logesMeSH
Procain jenapharmMeSH
Procain curasanMeSH
Röwo procainMeSH
Procain braunMeSH
Procaina serraMeSH
Procain rödlerMeSH
Chaix et du marais brand OF procaine hydrochlorideMeSH
Loges brand OF procaine hydrochlorideMeSH
Curasan brand OF procaine hydrochlorideMeSH
Lomapharm brand OF procaine hydrochlorideMeSH
Pharmakon brand OF procaine hydrochlorideMeSH
Abbott brand OF procaine hydrochlorideMeSH
Aventis brand OF procaine hydrochlorideMeSH
Braun brand OF procaine hydrochlorideMeSH
Hevert brand OF procaine hydrochlorideMeSH
Jenapharm brand OF procaine hydrochlorideMeSH
Serra pamies brand OF procaine hydrochlorideMeSH
Steigerwald brand OF procaine hydrochlorideMeSH
2-(Diethylamino)ethyl 4-aminobenzoic acid hydrochlorideGenerator
Chemical FormulaC13H21ClN2O2
Average Molecular Mass272.771 g/mol
Monoisotopic Mass272.129 g/mol
CAS Registry Number51-05-8
IUPAC Name2-(diethylamino)ethyl 4-aminobenzoate hydrochloride
Traditional Nameprocaine hydrochloride
SMILESCl.CCN(CC)CCOC(=O)C1=CC=C(N)C=C1
InChI IdentifierInChI=1S/C13H20N2O2.ClH/c1-3-15(4-2)9-10-17-13(16)11-5-7-12(14)8-6-11;/h5-8H,3-4,9-10,14H2,1-2H3;1H
InChI KeyHCBIBCJNVBAKAB-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassBenzoic acids and derivatives
Direct ParentBenzoic acid esters
Alternative Parents
Substituents
  • Aminobenzoic acid or derivatives
  • Benzoate ester
  • Benzoyl
  • Aniline or substituted anilines
  • Carboxylic acid ester
  • Amino acid or derivatives
  • Tertiary amine
  • Tertiary aliphatic amine
  • Carboxylic acid derivative
  • Monocarboxylic acid or derivatives
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organopnictogen compound
  • Amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Primary amine
  • Hydrochloride
  • 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 Solubility6.81 g/LALOGPS
logP2.1ALOGPS
logP1.88ChemAxon
logS-1.5ALOGPS
pKa (Strongest Basic)8.96ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area55.56 ŲChemAxon
Rotatable Bond Count7ChemAxon
Refractivity70.3 m³·mol⁻¹ChemAxon
Polarizability27.33 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
LC-MS/MSLC-MS/MS Spectrum - LC-ESI-qTof , Positivesplash10-0f76-0190000000-ce053a8c64308bc3ebbbSpectrum
LC-MS/MSLC-MS/MS Spectrum - LC-ESI-qTof , Positivesplash10-00di-4900000000-65f3e23c6772211b3048Spectrum
LC-MS/MSLC-MS/MS Spectrum - , positivesplash10-01w0-1950000000-1f4de90a31c5658a10d3Spectrum
LC-MS/MSLC-MS/MS Spectrum - , positivesplash10-00di-4900000000-65f3e23c6772211b3048Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00di-0090000000-e33f0b449ea0e065c241Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00di-0090000000-e33f0b449ea0e065c241Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00di-0090000000-e33f0b449ea0e065c241Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00di-0090000000-afa912b41755f6c33c27Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-00di-0090000000-afa912b41755f6c33c27Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00di-0090000000-afa912b41755f6c33c27Spectrum
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 IDDBSALT000551
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 IDNot Available
PubChem Compound ID5795
Kegg Compound IDC07894
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available