127442
Aminomethanesulfonic acid
97%
Synonym(s):
(Aminomethyl)sulfonic acid, 1-Aminomethanesulfonic acid, Aminomethanesulfonic acid, Aminomethanesulphonic acid, aminomethylsulfonic acid
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All Photos(2)
About This Item
Linear Formula:
NH2CH2SO3H
CAS Number:
Molecular Weight:
111.12
Beilstein:
1811756
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
mp
184 °C (dec.) (lit.)
functional group
amine
sulfonic acid
SMILES string
NCS(O)(=O)=O
InChI
1S/CH5NO3S/c2-1-6(3,4)5/h1-2H2,(H,3,4,5)
InChI key
OBESRABRARNZJB-UHFFFAOYSA-N
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Application
Aminomethanesulfonic acid can be used as a reactant to synthesize: 1-Sulfomethyltetrazole-5-thiol disodium salts, which are useful key intermediates for the preparation of cefonicid sodium. Tridentate N-(2-hydroxybenzyl)aminomethane sulfonic acid Schiff-base ligand by reacting with salicylaldehyde.
It can also be used to functionalize the surface of single-walled carbon nanotubes (SWCNT) or porous metal-organic frameworks (MOF) to introduce the sulfonic acid functional groups for the preparation of nanocomposites.
It can also be used to functionalize the surface of single-walled carbon nanotubes (SWCNT) or porous metal-organic frameworks (MOF) to introduce the sulfonic acid functional groups for the preparation of nanocomposites.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of 1-sulfomethyltetrazole-5-thiol disodium salts
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Speciality Petrochemicals (2011)
Nigel G Ternan et al.
FEMS microbiology letters, 207(1), 49-53 (2002-03-12)
Chromohalobacter marismortui VH1 was screened for its ability to utilise organosulfonate compounds at a range of NaCl concentrations. Only aminomethane sulfonate, of seven sulfonates tested, was utilised. Length of lag phase during growth on aminomethane sulfonate, as either nitrogen and/or
J B Lombardini
European journal of pharmacology, 110(3), 385-387 (1985-04-16)
It is well known that taurine stimulates ATP-dependent calcium ion uptake at low calcium ion concentrations. However, aminomethanesulfonic acid, the lower homologue of taurine, inhibits calcium ion uptake under the same experimental conditions. The higher homologue of taurine, 3-aminopropanesulfonic acid
Copper (II) complexes of Schiff-base and reduced Schiff-base ligands: Influence of weakly coordinating sulfonate groups on the structure and oxidation of 3, 5-DTBC
Sreenivasulu B, et al.
European Journal of Inorganic Chemistry, 2005(22), 4635-4645 (2005)
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Biochemical and biophysical research communications, 322(2), 514-519 (2004-08-25)
The activation of Kupffer cells represents a central mechanism of liver injury involving the production of TNF-alpha. It is known that glycine prevents LPS-induced production of TNF-alpha in isolated Kupffer cells. In this study, the possibility that glycine analogues might
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