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Details

Stereochemistry ACHIRAL
Molecular Formula CH4NO3S.Na
Molecular Weight 133.102
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM AMINOMETHANESULFONATE

SMILES

[Na+].NCS([O-])(=O)=O

InChI

InChIKey=UZHDDUOPWFLWPC-UHFFFAOYSA-M
InChI=1S/CH5NO3S.Na/c2-1-6(3,4)5;/h1-2H2,(H,3,4,5);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula CH4NO3S
Molecular Weight 110.112
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Removal of dyes from water using crosslinked aminomethane sulfonic acid based resin.
2010-08
Comparison of zwitterionic N-alkylaminomethanesulfonic acids to related compounds in the Good buffer series.
2010-04-01
The effects of taurine, hypotaurine, and taurine homologs on erythrocyte morphology, membrane fluidity and cytoskeletal spectrin alterations due to diabetes, alcoholism and diabetes-alcoholism in the rat.
2009
The effects of taurine, taurine homologs and hypotaurine on cell and membrane antioxidative system alterations caused by type 2 diabetes in rat erythrocytes.
2009
(Acetato-κO)bis-(2,2'-bipyridyl-κN,N')copper(II)-ethyl sulfate-methyl sulfate (1/0.5/0.5).
2008-11-20
Diaqua-bis(4-bromo-2-formyl-phenolato-κO,O')cobalt(II).
2008-09-06
cis-Aqua-bis(2,4-dichloro-6-formyl-phenolato-κO,O')(N,N-dimethyl-formamide-κO)nickel(II).
2008-07-26
Bis(2,4-dibromo-6-formyl-phenolato-κO,O')copper(II).
2007-12-06
The glycine analogue, aminomethanesulfonic acid, inhibits LPS-induced production of TNF-alpha in isolated rat Kupffer cells and exerts hepatoprotective effects in mice.
2004-09-17
Utilisation of aminomethane sulfonate by Chromohalobacter marismortui VH1.
2002-01-22
Sweetness and enzymatic activity of lysozyme.
2001-10
Inhibition of HIV replication by derivatives of naphthalenedisulfonic acids.
1990-08
Aromatic sulfonic acids as viral inhibitors. Structure-activity study using rhino, adeno 3, herpes simplex, and influenza viruses.
1971-07
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:20:09 GMT 2025
Edited
by admin
on Wed Apr 02 09:20:09 GMT 2025
Record UNII
JQ5RQ6235B
Record Status Validated (UNII)
Record Version
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Name Type Language
SODIUM AMINOMETHANESULFONATE
Systematic Name English
METHANESULFONIC ACID, 1-AMINO-, SODIUM SALT (1:1)
Preferred Name English
SODIUM AMINOMETHANESULPHONATE
Systematic Name English
METHANESULFONIC ACID, AMINO-, SODIUM SALT
Systematic Name English
METHANESULFONIC ACID, AMINO-, MONOSODIUM SALT
Systematic Name English
Code System Code Type Description
FDA UNII
JQ5RQ6235B
Created by admin on Wed Apr 02 09:20:09 GMT 2025 , Edited by admin on Wed Apr 02 09:20:09 GMT 2025
PRIMARY
CAS
6939-85-1
Created by admin on Wed Apr 02 09:20:09 GMT 2025 , Edited by admin on Wed Apr 02 09:20:09 GMT 2025
PRIMARY
PUBCHEM
23667279
Created by admin on Wed Apr 02 09:20:09 GMT 2025 , Edited by admin on Wed Apr 02 09:20:09 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE