|
| | Sulfamide Chemical Properties |
| Melting point | 90-92 °C(lit.) | | density | 1.611 g/mL at 25 °C(lit.) | | storage temp. | Inert atmosphere,Room Temperature | | solubility | water: soluble50mg/mL, clear, colorless to faintly yellow | | form | Crystalline Powder, Free From Visible Impurities | | pka | 10.87±0.60(Predicted) | | color | White to practically white , free from visible impurities | | PH | 5.67 at 21.7℃ and 10g/L | | Water Solubility | soluble | | Sensitive | Moisture Sensitive | | Merck | 14,8922 | | InChIKey | NVBFHJWHLNUMCV-UHFFFAOYSA-N | | CAS DataBase Reference | 7803-58-9(CAS DataBase Reference) | | NIST Chemistry Reference | Sulfamide(7803-58-9) | | EPA Substance Registry System | Sulfamide (7803-58-9) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | F | 9 | | TSCA | Yes | | HazardClass | IRRITANT | | HS Code | 28530090 |
| | Sulfamide Usage And Synthesis |
| Description | Sulfamide is a white solid substance that is normally produced by reacting sulfuryl chloride with ammonia. Sulfamide is stable under normal conditions and soluble in acetone and DMSO. Sulfamide may also refer to the functional group in organic chemistry, and it consists of at least one group attached to a nitrogen atom of sulfamide.
It is a carbonic anhydrase inhibitor and is widely used as a pharmaceutical intermediate.
Sulfamide is sensitive to moisture, thus should be kept away from water and humidity. It should also be stored away from oxidizing agents. Sulfamide should be kept in a tightly closed container and placed in a cool, dry, and well-ventilated condition.
| | Chemical Properties | White Solid | | Uses | Similar to urea in many of its reactions, but is more acidic, and can act as a dibasic acid. | | Uses | A carbonic anhydrase inhibitor; used for treatment of cancer. | | Uses | Sulfamide and its derivatives can also be used to prepare fused thiadiazine systems, Reaction with 2-aminoacetophenones affords IH-2,1,3-benzothia- diazine 2,2-dioxides 77 (65JOC3960). The corresponding 3,4-dihydro deriv- atives are readily available from 2-aminobenzylamines with either sulfuryl chloride (70M1443) or sulfamide (66USP3278532; 71MI055). These kinds of compounds can also be obtained from N-aryl-N'-alkylsulfamides and s-trioxane in a reaction involving cyclization by intramolecular sulfamido- methylation (79JOC2032) (Scheme 30). | | Definition | ChEBI: The simplest of the sulfamic acids consisting of a single sulfur atom covalently bound by single bonds to two amino groups and by double bonds to two oxygen atoms. | | Purification Methods | Crystallise sulfamide from absolute EtOH. It decomposes at 250o. [Schenk in Handbook of Preparative Inorganic Chemistry (Ed. Brauer) Academic Press Vol I pp 482-483 1963.] |
| | Sulfamide Preparation Products And Raw materials |
|
