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Details Piperidine-2-carboxylic acid

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Role Reference Substance
namePiperidine-2-carboxylic acid
MPIMP IDR001471
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
supplier code80615
lot1094978
purity99
solubility 
generalirritant
amount500
amount unitMG
store temperature 1RT
store temperature 2RT
store dryFalse
store under argonFalse
store in darkFalse
contributing authorBoelling C, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
date of order2004-11-23
date in2004-12-08
date out 
date expired 
box number9
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%2743578815-a35f-4fb5-952e-b2c2bf5931ed%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

reference substancesuppliersupplier codelot
Piperidine-2-carboxylic acidSigma-Aldrich P2519MKBK3901V
1 reference substance(s)
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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