| Names | |
|---|---|
| IUPAC name Aminomethanesulfonic acid | |
| Other names Aminomethylenesulfonic acid | |
| Identifiers | |
3D model (JSmol) | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.034.212 |
| EC Number |
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PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
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| Properties | |
| CH5NO3S | |
| Molar mass | 111.12 g·mol−1 |
| Melting point | 190–194 °C (374–381 °F; 463–467 K) [1] |
| Hazards | |
| GHS labelling: | |
| | |
| Danger | |
| H314 | |
| P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Aminomethylsulfonic acid (also called aminomethylenesulfonic acid and aminomethanesulfonic acid) is an organic chemical compound, with amino (-NH2) and sulfonic acid (-SO3H) groups on the carbon atom. Its chemical formula is N H 2 CH2 S O 3H, and it has a molar mass of 111.12 g/mol.
Aminomethanesulfonic acid is a corrosive solid. It could be thought of as the sulfonic acid analogue of glycine, just like aminomethylphosphonic acid is the phosphonic analogue of glycine. [2] Its density is ~1.7 g/cm3. [3]
Aminomethane sulfonic acid can be made by the reaction between hexamethylenetetramine (hexamine) with sulfur dioxide (SO2) in an aqueous environment. [4]
Aminomethanesulfonic acid can cause skin and eye burns, it is an dermatotoxin.