CAS 25346-09-2

3-aminopropane-1-sulfinic acid

Description:

3-Aminopropane-1-sulfinic acid, with the CAS number 25346-09-2, is an organosulfur compound characterized by the presence of both an amino group and a sulfinic acid functional group. It is a colorless to pale yellow solid that is soluble in water, reflecting its polar nature due to the sulfinic acid moiety. The compound features a three-carbon chain (propane) with an amino group (-NH2) attached to the first carbon and a sulfinic acid group (-SO2H) on the terminal carbon. This structure imparts unique chemical properties, making it a useful intermediate in organic synthesis and a potential reagent in various chemical reactions. The sulfinic acid group is known for its ability to act as a reducing agent, while the amino group can participate in nucleophilic reactions. Additionally, 3-aminopropane-1-sulfinic acid may exhibit biological activity, which has led to interest in its applications in pharmaceuticals and biochemistry. Overall, its dual functional groups make it a versatile compound in both synthetic and biological contexts.

Formula: C₃H₉NO₂S

InChI: InChI=1/C3H9NO2S/c4-2-1-3-7(5)6/h1-4H2,(H,5,6)

SMILES: C(CN)CS(=O)O

Synonyms:

• 1-Propanesulfinic Acid, 3-Amino-

3-Aminopropane-1-sulfinic acid

CAS: 25346-09-2

3-Aminopropane-1-sulfinic acid is a reactive molecule that is found in the body and has been shown to be reactive with pancreatic tissue. It has been shown to activate the enzyme hplc analysis, which hydrolyzes 3-aminopropane-1-sulfinic acid into its metabolites. The sulfonic acids have been found to have an inflammatory effect on the pancreas. This drug has been shown to be effective in treating a number of inflammatory diseases, such as rheumatoid arthritis and ulcerative colitis. 3-Aminopropane-1-sulfinic acid may also act as a regulatory or allosteric modulator by binding to an allosteric site on the enzyme β-cell and inhibiting insulin release.

Formula: C₃H₉NO₂S

Purity: Min. 95%

Molecular weight: 123.18 g/mol

Ref: 3D-ABA34609