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L-Pipecolic acid (PC000820)

Record Information
Version1.0
Creation date2015-10-09 22:32:55 UTC
Update date2017-01-19 02:36:37 UTC
FoodComEx IDPC000820
FoodDB RecordFDB000546
Chemical Information
NameL-Pipecolic acid
DescriptionPresent in beans and other legumes, and in lesser quantities in other plants including barley, hops, malt and mushrooms. L-Pipecolic acid is found in many foods, some of which are macadamia nut (m. tetraphylla), linden, tinda, and cumin.
CAS Number3105-95-1
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
SynonymSource
(-)-Pipecolatebiospider
(-)-Pipecolic acidbiospider
(2S)-Piperidine-2-carboxylic acidbiospider
(S)-(-)-2-Piperidinecarboxylatebiospider
(S)-(-)-2-Piperidinecarboxylic acidbiospider
(s)-(-)-pipecolatebiospider
(s)-(-)-pipecolic acidbiospider
(S)-2-Piperidinecarboxylatebiospider
(S)-2-Piperidinecarboxylic acidbiospider
(s)-pipecolatebiospider
(s)-pipecolic acidbiospider
(s)-pipecolinatebiospider
(s)-pipecolinic acidbiospider
(S)-Piperidine-2-carboxylatebiospider
(S)-Piperidine-2-carboxylic acidbiospider
2-Piperidinecarboxylic acid, 9CI; L-formdb_source
L-(-)-pipecolatebiospider
L-(-)-pipecolic acidbiospider
L-homoprolinebiospider
L-pipecolatebiospider
L-pipecolic acidbiospider
L-pipecolinatebiospider
L-pipecolinic acidbiospider
L-Piperidine-2-carboxylatebiospider
L-Piperidine-2-carboxylic acidbiospider
Pipecolic acid, (s)-(-)-biospider
Pipecolic acid, l-biospider
Pipecolic acid, l-(-)-biospider
Chemical FormulaC6H11NO2
IUPAC name(2S)-piperidine-2-carboxylic acid
InChI IdentifierInChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m0/s1
InChI KeyHXEACLLIILLPRG-YFKPBYRVSA-N
Isomeric SMILESOC(=O)[C@@H]1CCCCN1
Average Molecular Weight129.157
Monoisotopic Molecular Weight129.078978601
Chemical Taxonomy
Description Belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentL-alpha-amino acids
Alternative Parents
Substituents
  • L-alpha-amino acid
  • Piperidinecarboxylic acid
  • Piperidine
  • Amino acid
  • Carboxylic acid
  • Secondary aliphatic amine
  • Monocarboxylic acid or derivatives
  • Secondary amine
  • Organoheterocyclic compound
  • Azacycle
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organooxygen compound
  • Organonitrogen compound
  • Amine
  • Carbonyl group
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External Descriptors
Physico-Chemical Properties - Experimental
PropertyValueReference
Experimental logPNot Available
Experimental Water SolubilityNot Available
Melting PointMp 259-260°DFC
Foods of Origin
FoodContent Range AverageReference
FoodReference
Production Data
Production Methodcommercial
Production Method ReferenceNot Available
Production Method Reference FileNot Available
Quantity AvailableProduction upon request, up to 1 g
Delivery TimeNot Available
Storage Formsolid
Storage Conditions-80°C
StabilityNot Available
PurityNot Available
Spectra
Spectral Data Upon RequestNot Available
Provider Information
Contact NameContact InstitutionContact Email
Rosa Vazquez Fresnovazquezf@ualberta.ca
Commercial Vendors
AKSci E692
AKSci J92544
Toronto Research Chemicals P479750