<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2010-04-08 22:08:18 UTC</creation_date>
  <update_date>2018-05-28 23:20:25 UTC</update_date>
  <accession>FDB008895</accession>
  <name>Acrylamide-acrylic acid resin</name>
  <description>It is used as a food additive .</description>
  <synonyms>
    <synonym>2-Propenamide-2-propenoic acid polymer</synonym>
    <synonym>2-Propenamide, polymer with 2-propenoic acid</synonym>
    <synonym>2-Propenoic acid, polymer with 2-propenamide</synonym>
    <synonym>Acrylamide - acrylic acid resin</synonym>
    <synonym>Acrylamide acrylic acid polymer</synonym>
    <synonym>Acrylamide-acrylate copolymer</synonym>
    <synonym>Acrylamide-acrylate polymer</synonym>
    <synonym>Acrylamide-acrylic acid copolymer</synonym>
    <synonym>Acrylamide-acrylic acid polymer</synonym>
    <synonym>Acrylamide-acrylic resin</synonym>
    <synonym>Acrylic acid-acrylamide copolymer</synonym>
    <synonym>Acrylic acid-acrylamide polymer</synonym>
    <synonym>Acrylic acid, polymer with acrylamide</synonym>
    <synonym>Acrylic acid, polymer with acrylamide (8CI)</synonym>
    <synonym>Acrysol 51</synonym>
    <synonym>Cyanamer P 26</synonym>
    <synonym>Cyanamer P26</synonym>
    <synonym>Hydrolyzed polyacrylamide</synonym>
    <synonym>Nalco 623</synonym>
    <synonym>Poly(acrylamide-co-acrylic acid)</synonym>
    <synonym>Poly(acrylic acid-acrylamide)</synonym>
    <synonym>Polyacrylamide, hydrolyzed</synonym>
    <synonym>Polyacrylamide, partially hydrolyzed</synonym>
    <synonym>Polyhall</synonym>
    <synonym>Sansapol am</synonym>
  </synonyms>
  <chemical_formula>C6H9NO3</chemical_formula>
  <average_molecular_weight>143.1406</average_molecular_weight>
  <monisotopic_moleculate_weight>143.058243159</monisotopic_moleculate_weight>
  <iupac_name>prop-2-enamide; prop-2-enoic acid</iupac_name>
  <traditional_iupac>acrylamide; acrylic acid</traditional_iupac>
  <cas_registry_number>9003-06-9</cas_registry_number>
  <smiles>NC(=O)C=C.OC(=O)C=C</smiles>
  <inchi>InChI=1S/C3H5NO.C3H4O2/c2*1-2-3(4)5/h2H,1H2,(H2,4,5);2H,1H2,(H,4,5)</inchi>
  <inchikey>RNIHAPSVIGPAFF-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <description> belongs to the class of organic compounds known as acrylic acids. These are organic compounds containing acrylic acid CH2=CHCO2H.</description>
    <direct_parent>Acrylic acids</direct_parent>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organic acids and derivatives</super_class>
    <class>Carboxylic acids and derivatives</class>
    <sub_class>Acrylic acids and derivatives</sub_class>
    <molecular_framework/>
    <alternative_parents>
      <alternative_parent>Carbonyl compounds</alternative_parent>
      <alternative_parent>Carboximidic acids</alternative_parent>
      <alternative_parent>Carboxylic acids</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Monocarboxylic acids and derivatives</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
      <alternative_parent>Organonitrogen compounds</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
    </alternative_parents>
    <substituents>
      <substituent>Acrylic acid</substituent>
      <substituent>Aliphatic acyclic compound</substituent>
      <substituent>Carbonyl group</substituent>
      <substituent>Carboximidic acid</substituent>
      <substituent>Carboximidic acid derivative</substituent>
      <substituent>Carboxylic acid</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Monocarboxylic acid or derivatives</substituent>
      <substituent>Organic nitrogen compound</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organonitrogen compound</substituent>
      <substituent>Organooxygen compound</substituent>
      <substituent>Organopnictogen compound</substituent>
    </substituents>
    <external_descriptors>
    </external_descriptors>
  </taxonomy>
  <state/>
  <predicted_properties>
  </predicted_properties>
  <experimental_properties>
  </experimental_properties>
  <property>
    <kind>logp</kind>
    <value>-0.27</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>pka_strongest_acidic</kind>
    <value>16.7</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>pka_strongest_basic</kind>
    <value>0.83</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>iupac</kind>
    <value>prop-2-enamide; prop-2-enoic acid</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>average_mass</kind>
    <value>143.1406</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>mono_mass</kind>
    <value>143.058243159</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>smiles</kind>
    <value>NC(=O)C=C.OC(=O)C=C</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>formula</kind>
    <value>C6H9NO3</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>inchi</kind>
    <value>InChI=1S/C3H5NO.C3H4O2/c2*1-2-3(4)5/h2H,1H2,(H2,4,5);2H,1H2,(H,4,5)</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>inchikey</kind>
    <value>RNIHAPSVIGPAFF-UHFFFAOYSA-N</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>polar_surface_area</kind>
    <value>43.09</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>refractivity</kind>
    <value>19.11</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>polarizability</kind>
    <value>6.88</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>rotatable_bond_count</kind>
    <value>2</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>acceptor_count</kind>
    <value>1</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>donor_count</kind>
    <value>1</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>physiological_charge</kind>
    <value>0</value>
    <source>ChemAxon</source>
  </property>
  <property>
    <kind>formal_charge</kind>
    <value>0</value>
    <source>ChemAxon</source>
  </property>
  <pathways>
  </pathways>
  <spectra>
    <spectrum>
      <type>Specdb::CMs</type>
      <spectrum_id>42778</spectrum_id>
    </spectrum>
    <spectrum>
      <type>Specdb::MsMs</type>
      <spectrum_id>86646</spectrum_id>
    </spectrum>
    <spectrum>
      <type>Specdb::MsMs</type>
      <spectrum_id>86647</spectrum_id>
    </spectrum>
    <spectrum>
      <type>Specdb::MsMs</type>
      <spectrum_id>86648</spectrum_id>
    </spectrum>
    <spectrum>
      <type>Specdb::MsMs</type>
      <spectrum_id>148995</spectrum_id>
    </spectrum>
    <spectrum>
      <type>Specdb::MsMs</type>
      <spectrum_id>148996</spectrum_id>
    </spectrum>
    <spectrum>
      <type>Specdb::MsMs</type>
      <spectrum_id>148997</spectrum_id>
    </spectrum>
  </spectra>
  <hmdb_id>HMDB32161</hmdb_id>
  <pubchem_compound_id/>
  <chemspider_id/>
  <kegg_id/>
  <chebi_id>415036</chebi_id>
  <biocyc_id/>
  <het_id/>
  <wikipidia/>
  <vmh_id/>
  <fbonto_id/>
  <foodb_id/>
  <general_references>
    <reference>#&lt;Reference:0x000055ce324ed990&gt;</reference>
  </general_references>
  <foods>
  </foods>
  <flavors>
  </flavors>
  <enzymes>
  </enzymes>
  <health_effects>
  </health_effects>
</compound>
