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Details 2-[[Amino(imino)methyl]amino]ethane-1-sulfonic acid

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Role	Reference Substance
name	2-[[Amino(imino)methyl]amino]ethane-1-sulfonic acid
MPIMP ID	R000337
stereoisomer
isotopomer	ambient
formula	C3H9N3O3S
molecular mass	167.188
monoisotopic mass	167.03646
InChI	InChI=1S/C3H9N3O3S/c4-3(5)6-1-2-10(7,8)9/h1-2H2,(H4,4,5,6)(H,7,8,9)
InChIKey	JKLRIMRKZBSSED-UHFFFAOYSA-N
supplier	Acros
supplier code	BTB09138DA
lot
purity	97
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	Boelling 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 order	2005-02-28
date in	2005-03-31
date out
date expired
box number	35
application/atom+xml	http://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%27ace62a59-f697-49cc-8547-3252a0f25801%27)

Synonyms of 2-[[Amino(imino)methyl]amino]ethane-1-sulfonic acid

property	value
CAS	543-18-0
ChEBI ID	CHEBI:17228
ChEBI ontology	has functional parent taurine
ChEBI ontology	is a guanidines
ChEBI ontology	is tautomer of taurocyamine zwitterion
ChemSpider ID	61635
MetaCyc	TAUROCYAMINE
synonym	2-(carbamimidamido)ethanesulfonic acid
synonym	2-[[Amino(imino)methyl]amino]ethane-1-sulfonic acid
synonym	2-{[amino(imino)methyl]amino}ethanesulfonic acid
13 synonym(s)
Page of 2 Results per page:

Metabolites mapped to 2-[[Amino(imino)methyl]amino]ethane-1-sulfonic acid

metabolite	stereoisomer	isotopomer
no hits!

Replica of 2-[[Amino(imino)methyl]amino]ethane-1-sulfonic 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 8/7/2013 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
modified by users	Kopka J., Hummel J.

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