127442
Aminomethanesulfonic acid
97%
동의어(들):
(Aminomethyl)sulfonic acid, 1-Aminomethanesulfonic acid, Aminomethanesulfonic acid, Aminomethanesulphonic acid, aminomethylsulfonic acid
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모든 사진(2)
About This Item
Linear Formula:
NH2CH2SO3H
CAS Number:
Molecular Weight:
111.12
Beilstein:
1811756
EC Number:
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
mp
184 °C (dec.) (lit.)
작용기
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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애플리케이션
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.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
Damla Kaner et al.
Environmental geochemistry and health, 32(4), 321-325 (2010-04-20)
A new polymeric resin with amino sulfonic acid pendant functions has been prepared for the extraction of acidic and basic dyes from water. Beaded polymer supports were prepared by suspension polymerization of vinyl benzyl chloride (0.9 mol) and ethylene glycol
H B Smith et al.
Biochemistry, 30(21), 5172-5177 (1991-05-28)
Ribulosebisphosphate carboxylase/oxygenase is reversibly activated by the reaction of CO2 with a specific lysyl residue (Lys191 of the Rhodospirillum rubrum enzyme) to form a carbamate that coordinates an essential Mg2+ cation. Surprisingly, the Lys191----Cys mutant protein, in the presence of
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)
Sonoko Ishizaki-Koizumi et al.
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
W S Lewis et al.
The Journal of biological chemistry, 266(31), 20823-20827 (1991-11-05)
The composition and structural aspects of the amino and carboxylic acid groups required for incorporation into peptides by transpeptidation and inhibition of hydrolysis in carboxypeptidase Y-catalyzed reactions were studied. Separation of these two groups by even one carbon prevents incorporation
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