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Details Piperidine-2-carboxylic acid

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Role Reference Substance
namePiperidine-2-carboxylic acid
MPIMP IDR003176
stereoisomer(S)-
isotopomerambient
formulaC6H11NO2
molecular mass129.157
monoisotopic mass129.07898
InChIInChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m0/s1
InChIKeyHXEACLLIILLPRG-YFKPBYRVSA-N
supplierSigma-Aldrich 
supplier codeP2519
lotMKBK3901V
purity99
solubility 
general 
amount100
amount unitMG
store temperature 1RT
store temperature 2 
store dry 
store under argon 
store in dark 
contributing authorFehrle I, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
date of order 
date in2014-03-12
date out 
date expired 
box number91
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%2700537702-3080-40da-aab1-bdc183b7f764%27)

Synonyms of Piperidine-2-carboxylic acid

propertyvalue
Beilstein81093
BRENDA59615
CAS3105-95-1
ChEBI IDChEBI:30913
ChEBI ontologyis a pipecolic acid
ChEBI ontologyis conjugate base of L-pipecolate
ChEBI ontologyis enantiomer of D-pipecolic acid
ChEBI ontologyis tautomer of L-pipecolic acid zwitterion
ChemSpider ID388365
MetaCycL-PIPECOLATE
22 synonym(s)
    of 3    

Metabolites mapped to Piperidine-2-carboxylic acid

Replica of Piperidine-2-carboxylic acid

compound timestamp information
deposited at 8/29/2006 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
last changed at 6/19/2014 by Kopka J., Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
modified by users Hummel J., Fehrle I., Kopka J.
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