<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-03 00:44:03 UTC</creation_date>
  <update_date>2026-08-25 15:28:48 UTC</update_date>
  <accession/>
  <common_name>1-Hydroxy-2,2,6,6-tetramethylpiperidine</common_name>
  <class>SmallMolecule</class>
  <description>1-Hydroxy-2,2,6,6-tetramethylpiperidine is an organic compound with the formula C9H19N1O1 and an average molecular weight of 157.26 g/mol. 1-Hydroxy-2,2,6,6-tetramethylpiperidine belongs to the piperidines, a class of organoheterocyclic compounds within the organic compounds.

This compound is found in or released from 28 recorded sources. Within electrical and electronic equipment, it is associated with amplifiers, antennas, adjustable resistors, auxiliary devices, and colour television systems, among 11 other items. It is also linked to the building and construction sector, specifically appearing in floors, ceilings, roofs, and stairs and ramps. In the context of food, food processing and cookware, the compound is found in the processing of meats and fish, as well as the preparation of wort, wine or sparkling wine, and vinegar. Additionally, it is identified in household items such as badges and household cleaning and consumer products, including pipe accessories and other smoking requisites.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>(2,2,6,6-Tetramethylpiperidin-1-yl)oxidanyl</synonym>
    <synonym>1,1,5,5-tetramethylpentamethylene nitroxide</synonym>
    <synonym>1-$l^{1}-oxidanyl-2,2,6,6-tetramethylpiperidine</synonym>
    <synonym>1-hydroxy-2,2,6,6-tetramethyl-piperidine</synonym>
    <synonym>1-hydroxy-2,2,6,6-tetramethylpiperidine</synonym>
    <synonym>1-Oxy-2,2,6,6-tetramethylpiperidine</synonym>
    <synonym>1-Oxy-2,2,6,6-tetramethylpiperidine, free radical</synonym>
    <synonym>1H-imidazole, 2-ethyl-5-methyl-</synonym>
    <synonym>2,2,6,6-???????????????-1-????????????</synonym>
    <synonym>2,2,6,6-Tetramethyl-1-piperadinyloxy, free radical</synonym>
    <synonym>2,2,6,6-Tetramethyl-1-piperidinol</synonym>
    <synonym>2,2,6,6-tetramethyl-1-piperidinyloxy</synonym>
    <synonym>2,2,6,6-Tetramethyl-1-piperidinyloxy (TEMPO)</synonym>
    <synonym>2,2,6,6-Tetramethyl-1-piperidinyloxy (TEMPO.)</synonym>
    <synonym>2,2,6,6-tetramethyl-1-piperidinyloxy,free radical</synonym>
    <synonym>2,2,6,6-Tetramethyl-piperidin-1-ol</synonym>
    <synonym>2,2,6,6-tetramethyl-piperidine-N-oxyl</synonym>
    <synonym>2,2,6,6-tetramethylpiperidin-1-ol</synonym>
    <synonym>2,2,6,6-Tetramethylpiperidine-1-N-Oxyl (en)Tempo (en)</synonym>
    <synonym>2,2,6,6-Tetramethylpiperidine-1-oxyl</synonym>
    <synonym>2,2,6,6-Tetramethylpiperidine-N-oxyl, TEMPO, free radical</synonym>
    <synonym>2,2,6,6-Tetramethylpiperidinooxy</synonym>
    <synonym>2,2,6,6-tetramethylpiperidinooxy radical</synonym>
    <synonym>2,2,6,6-Tetramethylpiperidinoxy free radical</synonym>
    <synonym>2,2,6,6-tetramethylpiperidinyl-1-oxide</synonym>
    <synonym>2,2,6,6-tetramethylpiperidinyloxy,free radical</synonym>
    <synonym>2,2,6,6-Tetramethylpiperidoxyl</synonym>
    <synonym>4-Oxypiperidol</synonym>
    <synonym>free radical</synonym>
    <synonym>MFCD00873840</synonym>
    <synonym>ol</synonym>
    <synonym>Piperidine, 1-hydroxy-2,2,6,6-tetramethyl-</synonym>
    <synonym>PIPERIDINOL, 2,2,6,6-TETRAMETHYL-</synonym>
    <synonym>polylactide</synonym>
    <synonym>TEMPO (1 2,2,6,6-tetrametylpiperidÃƒÆ’Ã‚Â­n-1-oxyl)</synonym>
    <synonym>Tempol</synonym>
    <synonym>TN8991900</synonym>
    <synonym>UNII:VQN7359ICQ</synonym>
    <synonym>[2564-83-2]</synonym>
  </synonyms>
  <chemical_formula>C9H19N1O1</chemical_formula>
  <average_molecular_weight>157.257</average_molecular_weight>
  <monisotopic_moleculate_weight>157.146664</monisotopic_moleculate_weight>
  <iupac_name>2,2,6,6-tetramethylpiperidin-1-ol</iupac_name>
  <traditional_iupac>2,2,6,6-tetramethylpiperidoxyl</traditional_iupac>
  <cas_registry_number>7031-93-8</cas_registry_number>
  <smiles>CC1(C)CCCC(C)(C)N1O</smiles>
  <inchi>InChI=1S/C9H19NO/c1-8(2)6-5-7-9(3,4)10(8)11/h11H,5-7H2,1-4H3</inchi>
  <inchikey>VUZNLSBZRVZGIK-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Organoheterocyclic compounds</super_class>
    <class>Piperidines</class>
    <sub_class/>
    <direct_parent>Piperidines</direct_parent>
    <alternate_parents>
      <alternative_parent>Azacyclic compounds</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>N-organohydroxylamines</alternative_parent>
      <alternative_parent>Organic oxygen compounds</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>Aliphatic heteromonocyclic compound</substituent>
      <substituent>Azacycle</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>N-organohydroxylamine</substituent>
      <substituent>Organic nitrogen compound</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organonitrogen compound</substituent>
      <substituent>Organopnictogen compound</substituent>
      <substituent>Piperidine</substituent>
    </substituents>
    <molecular_framework>Aliphatic heteromonocyclic compounds</molecular_framework>
    <descriptors/>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways/>
  <state/>
  <appearance/>
  <experimental_properties>
    <property>
      <kind>logp</kind>
      <value>1.4</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>2.30</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-0.97</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>1.67e+01 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>1.67</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>14.74</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>3.85</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>2,2,6,6-tetramethylpiperidin-1-ol</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>157.257</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>157.146664</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CC1(C)CCCC(C)(C)N1O</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C9H19N1O1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C9H19NO/c1-8(2)6-5-7-9(3,4)10(8)11/h11H,5-7H2,1-4H3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>VUZNLSBZRVZGIK-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>23.47</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>46.71</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>18.7</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>2</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>
  </predicted_properties>
  <route_of_exposure/>
  <mechanism_of_toxicity/>
  <metabolism/>
  <toxicity/>
  <lethaldose/>
  <carcinogenicity/>
  <use_source/>
  <min_risk_level/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f726a177260&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>549976</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>2006285</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
  <actor_id/>
  <pdb_id/>
  <wikipidia/>
  <general_references/>
  <targets>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
    <target>
      <target_id/>
      <mechanism_of_action/>
      <constants/>
      <references/>
    </target>
  </targets>
</compound>
