<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">125392</id>
  <title nil="true"/>
  <common-name>3-(1-Piperidinylmethyl)phenol</common-name>
  <description>3-(1-Piperidinylmethyl)phenol is an organic compound with the chemical formula C12H17NO and an average molecular weight of 191.27 g/mol. 3-(1-Piperidinylmethyl)phenol belongs to the benzylpiperidines, a subclass of piperidines within the organic compounds.

This compound is found in or released from 13 recorded sources across several sectors. In the electrical and electronic equipment sector, it is associated with capacitors, batteries, cell phones, printed circuit boards, wires and cables, and one additional source. Within the healthcare, pharmaceuticals and veterinary products sector, it is found in medical devices. It is also present in lubricants used in energy, oil and gas, as well as industrial manufacturing and chemical processing. Other recorded sources include food packaging from the food, food processing and cookware sector, and synthetic textiles, carpets and rugs from the textiles, leather and furnishings sector. One additional sector is also recorded. Exposure to 3-(1-Piperidinylmethyl)phenol may occur through inhalation, oral, or touch routes.</description>
  <cas>73279-04-6</cas>
  <pubchem-id>826974</pubchem-id>
  <chemical-formula>C12H17NO</chemical-formula>
  <weight>191.27</weight>
  <appearance nil="true"/>
  <melting-point nil="true"/>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility nil="true"/>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity nil="true"/>
  <use-source nil="true"/>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2026-04-06T09:12:21Z</created-at>
  <updated-at type="dateTime">2026-08-18T19:19:45Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id nil="true"/>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles nil="true"/>
  <moldb-formula>C12H17NO</moldb-formula>
  <moldb-inchi>InChI=1S/C12H17NO/c14-12-6-4-5-11(9-12)10-13-7-2-1-3-8-13/h4-6,9,14H,1-3,7-8,10H2</moldb-inchi>
  <moldb-inchikey>ORGBERFQYFWYGX-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">191.27</moldb-average-mass>
  <moldb-mono-mass type="decimal">191.1310142</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp>2.8</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id nil="true"/>
  <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 nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM121285</chemdb-id>
  <dsstox-id nil="true"/>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00116250</susdat-id>
  <iupac>3-(piperidin-1-ylmethyl)phenol</iupac>
  <moldb-polar-surface-area nil="true"/>
  <moldb-refractivity nil="true"/>
  <moldb-polarizability nil="true"/>
  <moldb-rotatable-bond-count nil="true"/>
  <moldb-acceptor-count nil="true"/>
  <moldb-donor-count nil="true"/>
  <moldb-pka-strongest-acidic nil="true"/>
  <moldb-pka-strongest-basic nil="true"/>
  <moldb-physiological-charge nil="true"/>
  <moldb-number-of-rings nil="true"/>
  <moldb-alogps-logp nil="true"/>
  <moldb-alogps-logs nil="true"/>
  <moldb-alogps-solubility nil="true"/>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organoheterocyclic compounds</superklass>
  <klass>Piperidines</klass>
  <subklass>Benzylpiperidines</subklass>
  <paper-count type="integer">1</paper-count>
  <sync-id>CED0068530</sync-id>
  <structure-inchikey nil="true"/>
  <structure-fingerprint nil="true"/>
  <structure-pattern-fingerprint nil="true"/>
  <structure-pickle nil="true"/>
  <structure-indexed-at nil="true"/>
</compound>
