<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4263</id>
  <title>T3D4209</title>
  <common-name>Acetamide</common-name>
  <description>Acetamide is found in red beetroot. Acetamide (or acetic acid amide or ethanamide), CH3CONH2, the amide of acetic acid, is a white crystalline solid in pure form. It is produced by dehydrating ammonium acetate. Acetamide has been shown to exhibit anti-microbial, anti-inflammatory, anti-arthritic and antibiotic functions. Acetamide belongs to the family of Primary Carboxylic Acid Amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2. (A3310, A3311, A3311, A3312).</description>
  <cas>60-35-5</cas>
  <pubchem-id>178</pubchem-id>
  <chemical-formula>C2H5NO</chemical-formula>
  <weight>59.07</weight>
  <appearance>White powder.</appearance>
  <melting-point>82 - 83°C</melting-point>
  <boiling-point>223°C (433.4°F)</boiling-point>
  <density nil="true"/>
  <solubility>2250 mg/mL at 25°C</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></metabolism>
  <toxicity></toxicity>
  <lethaldose></lethaldose>
  <carcinogenicity>2B, possibly carcinogenic to humans. (L135)</carcinogenicity>
  <use-source>This is an endogenously produced metabolite found in the human body. It is used in metabolic reactions, catabolic reactions or waste generation.</use-source>
  <min-risk-level></min-risk-level>
  <health-effects></health-effects>
  <symptoms></symptoms>
  <treatment></treatment>
  <created-at type="dateTime">2014-08-29T05:53:06Z</created-at>
  <updated-at type="dateTime">2026-04-17T17:54:53Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Acetamide</wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id>C06244</kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id>27856</chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id></ctd-id>
  <stitch-id></stitch-id>
  <drugbank-id>DB02736</drugbank-id>
  <pdb-id>ACM</pdb-id>
  <actor-id></actor-id>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CC(N)=O</moldb-smiles>
  <moldb-formula>C2H5NO</moldb-formula>
  <moldb-inchi>InChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)</moldb-inchi>
  <moldb-inchikey>DLFVBJFMPXGRIB-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">59.0672</moldb-average-mass>
  <moldb-mono-mass type="decimal">59.037113787</moldb-mono-mass>
  <origin>Endogenous</origin>
  <state>Solid</state>
  <logp>-1.26</logp>
  <hmdb-id>HMDB31645</hmdb-id>
  <chembl-id>CHEMBL16081</chembl-id>
  <chemspider-id>173</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>&lt;p&gt;Youichi Shiokawa, Kazuo Okumura, Kazuhiko Take, Kazunori Tsubaki, &amp;#8220;Novel substituted-acetamide compound and a process for the preparation thereof.&amp;#8221; U.S. Patent US5066680, issued February, 1963.&lt;/p&gt;</synthesis-reference>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003169</chemdb-id>
  <dsstox-id>DTXSID7020005</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00006888</susdat-id>
  <iupac>acetamide</iupac>
</compound>
