<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">5001</id>
  <title>T3D4946</title>
  <common-name>1-Methyl-2-pyrrolidone</common-name>
  <description>1-Methyl-2-pyrrolidone, or N-Methyl-2-pyrrolidone (NMP), is a chemical compound with 5-membered lactam structure. It is a colorless to slightly yellow liquid miscible with water. It is used in petrochemical processing, and as a solvent for surface treatment of textiles, resins and metal coated plastics or as a paint stripper. In the pharmaceutical industry, N-methyl-2-pyrrolidone is used in the formulation for drugs by both oral and transdermal delivery routes. NMP has been identified as a reproductive toxicant, first by California in 2001[3] and then by the European Commission in 2003. In the face of increasing regulation, some manufacturers are considering alternative solvents for some applications, especially where worker exposure is difficult to control, such as in paint stripping, graffiti removal, and agriculture. (Wikipedia)</description>
  <cas>872-50-4</cas>
  <pubchem-id>13387</pubchem-id>
  <chemical-formula>C5H9NO</chemical-formula>
  <weight>99.13</weight>
  <appearance>Colorless to slightly yellow liquid.</appearance>
  <melting-point>-24°C</melting-point>
  <boiling-point></boiling-point>
  <density nil="true"/>
  <solubility></solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure></route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity></mechanism-of-toxicity>
  <metabolism>1-Methyl-2-pyrrolidone is rapidly biotransformed by hydroxylation to 5-hydroxy- N -methyl-2-pyrrolidone, which is further oxidized to N -methylsuccinimide; this intermediate is further hydroxylated to 2-hydroxy- N - methylsuccinimide. These metabolites are all colourless. The excreted amounts of NMP metabolites in the urine after inhalation or oral intake represented about 100% and 65% of the administered doses, respectively.</metabolism>
  <toxicity></toxicity>
  <lethaldose></lethaldose>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>1-Methyl-2-pyrrolidone is used in petrochemical processing, and as a solvent for surface treatment of textiles, resins and metal coated plastics or as a paint stripper. In the pharmaceutical industry, N-methyl-2-pyrrolidone is used in the formulation for drugs by both oral and transdermal delivery routes.</use-source>
  <min-risk-level></min-risk-level>
  <health-effects></health-effects>
  <symptoms>Rapid, irregular respiration, shortnessof breath, decreased pain reflex, and slight bloody nasalsecretion.</symptoms>
  <treatment></treatment>
  <created-at type="dateTime">2014-09-17T20:01:58Z</created-at>
  <updated-at type="dateTime">2026-04-17T19:29:27Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia></wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id>13387</kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id></chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id></ctd-id>
  <stitch-id></stitch-id>
  <drugbank-id>DB12521</drugbank-id>
  <pdb-id></pdb-id>
  <actor-id></actor-id>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CN1CCCC1=O</moldb-smiles>
  <moldb-formula>C5H9NO</moldb-formula>
  <moldb-inchi>InChI=1S/C5H9NO/c1-6-4-2-3-5(6)7/h2-4H2,1H3</moldb-inchi>
  <moldb-inchikey>SECXISVLQFMRJM-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">99.1311</moldb-average-mass>
  <moldb-mono-mass type="decimal">99.068413915</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Liquid</state>
  <logp></logp>
  <hmdb-id></hmdb-id>
  <chembl-id>CHEMBL12543</chembl-id>
  <chemspider-id>12814</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference></synthesis-reference>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003902</chemdb-id>
  <dsstox-id>DTXSID6020856</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>1-methylpyrrolidin-2-one</iupac>
</compound>
