Record Information
Version1.0
Creation Date2016-05-19 01:52:43 UTC
Update Date2016-11-09 01:09:23 UTC
Accession NumberCHEM004617
Identification
Common NameACRYLAMIDE-ACRYLIC ACID RESIN
ClassSmall Molecule
DescriptionIt is used as a food additive .
Contaminant Sources
  • EAFUS Chemicals
  • FooDB Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
Acrylamide-acrylate resinGenerator
2-Propenamide, polymer with 2-propenoic acidHMDB
2-Propenamide-2-propenoic acid polymerHMDB
2-Propenoic acid, polymer with 2-propenamideHMDB
Acrylamide - acrylic acid resinHMDB
Acrylamide acrylic acid polymerHMDB
Acrylamide-acrylate copolymerHMDB
Acrylamide-acrylate polymerHMDB
Acrylamide-acrylic acid copolymerHMDB
Acrylamide-acrylic acid polymerHMDB
Acrylamide-acrylic resinHMDB
Acrylic acid, polymer with acrylamideHMDB
Acrylic acid, polymer with acrylamide (8ci)HMDB
Acrylic acid-acrylamide copolymerHMDB
Acrylic acid-acrylamide polymerHMDB
Acrysol 51HMDB
Cyanamer P 26HMDB
Cyanamer P26HMDB
Hydrolyzed polyacrylamideHMDB
nalco 623HMDB
Poly(acrylamide-CO-acrylic acid)HMDB, MeSH
Poly(acrylic acid-acrylamide)HMDB
Polyacrylamide, hydrolyzedHMDB
Polyacrylamide, partially hydrolyzedHMDB
PolyhallHMDB
Sansapol amHMDB
Poly(aam-CO-aa)MeSH
Poly(am-CO-aa)MeSH
PAM-aacMeSH
Prop-2-enimidate
prop-2-enoate
Chemical FormulaC6H9NO3
Average Molecular Mass143.141 g/mol
Monoisotopic Mass143.058 g/mol
CAS Registry Number9003-06-9
IUPAC Nameprop-2-enamide; prop-2-enoic acid
Traditional Nameacrylamide; acrylic acid
SMILESNC(=O)C=C.OC(=O)C=C
InChI IdentifierInChI=1S/C3H5NO.C3H4O2/c2*1-2-3(4)5/h2H,1H2,(H2,4,5);2H,1H2,(H,4,5)
InChI KeyRNIHAPSVIGPAFF-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as acrylic acids. These are organic compounds containing acrylic acid CH2=CHCO2H.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAcrylic acids and derivatives
Direct ParentAcrylic acids
Alternative Parents
Substituents
  • Acrylic acid
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboximidic acid derivative
  • Carboximidic acid
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organonitrogen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkNot Available
External DescriptorsNot Available
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
logP-0.27ChemAxon
pKa (Strongest Acidic)16.7ChemAxon
pKa (Strongest Basic)0.83ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area43.09 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity19.11 m³·mol⁻¹ChemAxon
Polarizability6.88 ųChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS ( TMS) - 70eV, Positivesplash10-05di-9100000000-9bb15bc91b0dbc41366eSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-0900000000-1d8fc77a39e34130d1b4Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-0900000000-1d8fc77a39e34130d1b4Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0006-0900000000-1d8fc77a39e34130d1b4Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0006-0900000000-7a9fc1380b65c2883817Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0006-0900000000-7a9fc1380b65c2883817Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0006-0900000000-7a9fc1380b65c2883817Spectrum
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 IDHMDB0032161
FooDB IDFDB008895
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 ID62693
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available