Anodyne

Piperidine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Phosphate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
[]
Conformer structure via JSmol
Physical properties
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85.15 g/mol [1]
Density0.8622 at 68 °F (EPA, 1998) - Less dense than water; will float g/cm3 [1]
AppearanceCLEAR, COLORLESS LIQUID [1]
OdorAMINE-LIKE ODOR [1]
TasteBURNING PEPPERY TASTE [1]
Melting point16 to 19 °F (EPA, 1998) [1]
Boiling point223 ° [1]
Decomposition... When heated to decomposition, it emits highly toxic fumes of oxides of /nitrogen oxides/. ... . [1]
SolubilityMiscible (NTP, 1992) [1]
0.8 [1]
Structural Identifiers
[]
C5H11[1]
piperidine [1]
C1CCNCC1 [1]
InChI=1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2 [1]
InChIKeyNQRYJNQNLNOLGT-UHFFFAOYSA-N [1]

Piperidine

Piperidine (also known as Hexahydropyridine, Cyclopentimine, Azacyclohexane, Piperidin, Cypentil, Hexazane, Pentamethyleneimine, Pentamethylenimine, Perhydropyridine or Pyridine, hexahydro-) is a substance of the piperidine class.

Chemistry

Salts []

Piperidine is typically found in the form of its hydrochloride and phosphate salts.

 []

Piperidine is a achiral mixture

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 8082, Piperidine. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/8082

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Piperidine. UNII: 67I85E138Y. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/67I85E138Y