| Name | 2-Methylbenzenesulfonamide |
| Synonyms | 2-TOLUENESULFONAMIDE TOLUENE-4-SULFONAMIDE o-Toluenesulphonamide TOLUENE-2-SULFONAMIDE O-TOLUENE SULFONAMIDE 2-Toluene Suldonamide TOLUENE-4-SULPHONAMIDE ORTHO TOLUENE SULFONAMIDE 2-Methylbenzenesulfonamide 2-methyl-benzenesulfonamid o-Methylbenzenesulfonamide 2-METHYLBENZENESULFONAMIDE 4-TOLUENESULFONIC ACID AMIDE 2-METHYLBENZENE-1-SULFONAMIDE 2-Methylbenzene-1-sulfonamide |
| CAS | 88-19-7 |
| EINECS | 201-808-8 |
| InChI | InChI=1/C7H9NO2S/c1-6-4-2-3-5-7(6)11(8,9)10/h2-5H,1H3,(H2,8,9,10) |
| InChIKey | YCMLQMDWSXFTIF-UHFFFAOYSA-N |
| Molecular Formula | C7H9NO2S |
| Molar Mass | 171.22 |
| Density | 1.2495 (rough estimate) |
| Melting Point | 156-158 °C (lit.) |
| Boling Point | 221 °C |
| Flash Point | 178°C |
| Water Solubility | Soluble in water (1.6 g/L at 25°C). |
| Solubility | DMSO (Slightly), Methanol (Very Slightly, Heated) |
| Vapor Presure | 0-0.008Pa at 25℃ |
| Appearance | Colorless crystal |
| Color | White to Off-White |
| BRN | 1102362 |
| pKa | 10.17±0.60(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.6100 (estimate) |
| MDL | MFCD00007934 |
| Physical and Chemical Properties | Properties of colorless flammable crystals, in ethanol crystallization is octahedral crystals, in water crystallization is prismatic crystals. melting point 156~158 ℃ solubility slightly soluble in water and ether, soluble in ethanol. |
| Use | The plasticizer of thermosetting resin is used as raw material in organic synthesis, preparation of nail polish, dye, fluorescent pigment and coating. |
| Risk Codes | R36 - Irritating to the eyes R40 - Limited evidence of a carcinogenic effect |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37 - Wear suitable protective clothing and gloves. |
| WGK Germany | 1 |
| RTECS | XT5075000 |
| TSCA | Yes |
| HS Code | 29350090 |
| Raw Materials | Ammonium hydroxide Toluene Toluene Chlorosulfonic acid Chlorosulfonic acid |
| Downstream Products | Sodium saccharine |
| Reference Show more | 1. [IF=5.833] Hu Wenyao et al."Flexible membrane composite based on sepiolite/chitosan/(silver nanoparticles) for enrichment and surface-enhanced Raman scattering determination of sulfamethoxazole in animal-derived food."MICROCHIMICA ACTA. 2022 May;189(5):1-12 |
colorless flammable crystals are octahedral crystals crystallized in ethanol and prismatic crystals crystallized in water. Slightly soluble in water and ether, soluble in ethanol. Melting point 156-158 °c.
chlorosulfonation of toluene with chlorosulfonic acid at low temperature gave o-Toluenesulfonyl chloride and a small amount of p-Toluenesulfonyl chloride. After separating the para-position by freezing crystallization method, the crude O-toluenesulfonamide was obtained by ammoniation with ammonia, decolorized with activated carbon, and then melted by alkali, acid, crystallized, centrifuged and dried
.
After that, the finished product was obtained.
for the preparation of plasticizers, adhesives, pesticide intermediates and saccharin. Also used in pharmaceutical, nickel plating, polishing, etc.
| LogP | 0.6-0.9 at 20-25℃ |
| NIST chemical information | information provided by: webbook.nist.gov (external link) |
| EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
| uses | used as saccharin, pharmaceutical intermediates, etc. used in the manufacture of saccharin, plasticizers, adhesives, pesticides, pharmaceutical and other products. The plasticizer of thermosetting resin is used as a raw material in organic synthesis, preparation of nail polish, dye, fluorescent pigment and coating. |
| production method | O-Toluenesulfonyl chloride is reacted with aqueous ammonia at 60 ° C. For 2H to form o-toluenesulfonamide. The reactant is cooled and filtered to obtain a crude product, which is then decolorized by activated carbon and refined by acid and alkali to obtain a finished product. |
| toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |