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Details Piperidine-2-carboxylic acid

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Role	Reference Substance
name	Piperidine-2-carboxylic acid
MPIMP ID	R000477
stereoisomer
isotopomer	ambient
formula	C6H11NO2
molecular mass	129.157
monoisotopic mass	129.07898
InChI	InChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)
InChIKey	HXEACLLIILLPRG-UHFFFAOYSA-N
supplier	Sigma
supplier code	P1516
lot	125H3663
purity
solubility
general
amount	1
amount unit	G
store temperature 1	RT
store temperature 2	RT
store dry	False
store under argon	False
store in dark	False
contributing author	Wrede J, Liebig F, 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 in	2000-01-01
date out
date expired
box number	40
application/atom+xml	http://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%270d7399db-65a4-49b3-aea8-8c6525d7f4d1%27)

Synonyms of Piperidine-2-carboxylic acid

property	value
CAS	4043-87-2
ChEBI ID	CHEBI:17964
ChEBI ontology	has role secondary metabolite
ChEBI ontology	is a piperidinemonocarboxylic acid
ChEBI ontology	is conjugate acid of pipecolate
ChemSpider ID	826
synonym	2-piperidinecarboxylic acid
synonym	DL-Pipecolic acid
synonym	homoproline
synonym	pipecolic acid
12 synonym(s)
Page of 2 Results per page:

Metabolites mapped to Piperidine-2-carboxylic acid

metabolite	stereoisomer	isotopomer
no hits!

Replica of Piperidine-2-carboxylic acid

reference substance	supplier	supplier code	lot
No Reference substances found!

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 6/23/2014 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	Strehmel N., Hummel J., Kopka J.

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