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Details

Stereochemistry ACHIRAL
Molecular Formula C2H4O5S
Molecular Weight 140.115
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFOACETIC ACID

SMILES

OC(=O)CS(O)(=O)=O

InChI

InChIKey=AGGIJOLULBJGTQ-UHFFFAOYSA-N
InChI=1S/C2H4O5S/c3-2(4)1-8(5,6)7/h1H2,(H,3,4)(H,5,6,7)

HIDE SMILES / InChI

Molecular Formula C2H4O5S
Molecular Weight 140.115
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Sulfoacetate is degraded via a novel pathway involving sulfoacetyl-CoA and sulfoacetaldehyde in Cupriavidus necator H16.
2010-11-12
Sulfoacetate released during the assimilation of taurine-nitrogen by Neptuniibacter caesariensis: purification of sulfoacetaldehyde dehydrogenase.
2008-08
Differential inhibition of cytosolic PEPCK by substrate analogues. Kinetic and structural characterization of inhibitor recognition.
2008-02-19
The DUF81 protein TauE in Cupriavidus necator H16, a sulfite exporter in the metabolism of C2 sulfonates.
2007-09
Sulfoacetaldehyde is excreted quantitatively by Acinetobacter calcoaceticus SW1 during growth with taurine as sole source of nitrogen.
2005-04
Sulfoacetate generated by Rhodopseudomonas palustris from taurine.
2004-10
Rheological properties of sulfoacetate derivatives of cellulose.
2003-04-04
Preparation of sulfoacetate derivatives of cellulose by direct esterification.
2003-04-04
Ethanedisulfonate is degraded via sulfoacetaldehyde in Ralstonia sp. strain EDS1.
2001-07
Pyrophosphate analogues as inhibitors of herpes simplex virus type 1 DNA polymerase.
1980-03-28
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:30:33 GMT 2025
Edited
by admin
on Mon Mar 31 20:30:33 GMT 2025
Record UNII
Y4XC05H603
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-SULFOACETIC ACID
MI  
Preferred Name English
SULFOACETIC ACID
Systematic Name English
2-SULFOACETIC ACID [MI]
Common Name English
SULFOETHANOIC ACID
Systematic Name English
ACETIC ACID, 2-SULFO-
Common Name English
Code System Code Type Description
FDA UNII
Y4XC05H603
Created by admin on Mon Mar 31 20:30:33 GMT 2025 , Edited by admin on Mon Mar 31 20:30:33 GMT 2025
PRIMARY
CHEBI
50519
Created by admin on Mon Mar 31 20:30:33 GMT 2025 , Edited by admin on Mon Mar 31 20:30:33 GMT 2025
PRIMARY
EPA CompTox
DTXSID8059556
Created by admin on Mon Mar 31 20:30:33 GMT 2025 , Edited by admin on Mon Mar 31 20:30:33 GMT 2025
PRIMARY
PUBCHEM
31257
Created by admin on Mon Mar 31 20:30:33 GMT 2025 , Edited by admin on Mon Mar 31 20:30:33 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-627-2
Created by admin on Mon Mar 31 20:30:33 GMT 2025 , Edited by admin on Mon Mar 31 20:30:33 GMT 2025
PRIMARY
HSDB
2706
Created by admin on Mon Mar 31 20:30:33 GMT 2025 , Edited by admin on Mon Mar 31 20:30:33 GMT 2025
PRIMARY
CAS
123-43-3
Created by admin on Mon Mar 31 20:30:33 GMT 2025 , Edited by admin on Mon Mar 31 20:30:33 GMT 2025
PRIMARY
MERCK INDEX
m10353
Created by admin on Mon Mar 31 20:30:33 GMT 2025 , Edited by admin on Mon Mar 31 20:30:33 GMT 2025
PRIMARY Merck Index
Related Record Type Details
SOLVATE->ANHYDROUS