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线性分子式:
NH2CH2SO3H
化学文摘社编号:
分子量:
111.12
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
EC Number:
237-649-6
Beilstein/REAXYS Number:
1811756
MDL number:
产品名称
氨基甲磺酸, 97%
InChI key
OBESRABRARNZJB-UHFFFAOYSA-N
InChI
1S/CH5NO3S/c2-1-6(3,4)5/h1-2H2,(H,3,4,5)
SMILES string
NCS(O)(=O)=O
assay
97%
mp
184 °C (dec.) (lit.)
functional group
amine
sulfonic acid
Quality Level
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Application
氨基甲磺酸可用作合成以下物质的反应物:1-磺酸甲基-5-硫基四唑双钠盐,其是制备头孢尼西钠的关键中间体。通过与水杨醛反应制备的三齿 N-(2-羟基苄基)氨基甲磺酸席夫碱配体。
它还可用于单壁碳纳米管(SWCNT)或多孔金属有机框架(MOF)表面的功能化修饰,以引入磺酸官能团用于制备纳米复合材料。
它还可用于单壁碳纳米管(SWCNT)或多孔金属有机框架(MOF)表面的功能化修饰,以引入磺酸官能团用于制备纳米复合材料。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Synthesis of 1-sulfomethyltetrazole-5-thiol disodium salts
Ling Zhang, et al.
Speciality Petrochemicals (2011)
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)
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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