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Names | |
---|---|
Preferred IUPAC name
N,N-Dichloro-4-methylbenzene-1-sulfonamide | |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.006.786 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C7H7Cl2NO2S | |
Molar mass | 240.10 g·mol−1 |
Hazards | |
GHS labelling: | |
![]() ![]() | |
Danger | |
H271, H315, H319, H335 | |
P210, P220, P221, P261, P264, P271, P280, P283, P302+P352, P304+P340, P305+P351+P338, P306+P360, P312, P321, P332+P313, P337+P313, P362, P370+P378, P371+P380+P375, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Dichloramine-T or N,N-Dichloro-p-toluenesulfonamide is a chemical used as a disinfectant starting at the beginning of the 20th century. The chemical contains toluene substituted by a sulfonamide grouping, which in turn has two chlorine atoms attached to the nitrogen.
Dichloramine-T was first made by Frederick Daniel Chattaway in 1905. [1] Dichloramine-T can be made from para-toluenesulfonamide and bleaching powder, or chlorine. [2]
Dichloramine-T degrades with exposure to light or air. [3]
![]() | |
Names | |
---|---|
Preferred IUPAC name
N,N-Dichloro-4-methylbenzene-1-sulfonamide | |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.006.786 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C7H7Cl2NO2S | |
Molar mass | 240.10 g·mol−1 |
Hazards | |
GHS labelling: | |
![]() ![]() | |
Danger | |
H271, H315, H319, H335 | |
P210, P220, P221, P261, P264, P271, P280, P283, P302+P352, P304+P340, P305+P351+P338, P306+P360, P312, P321, P332+P313, P337+P313, P362, P370+P378, P371+P380+P375, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Dichloramine-T or N,N-Dichloro-p-toluenesulfonamide is a chemical used as a disinfectant starting at the beginning of the 20th century. The chemical contains toluene substituted by a sulfonamide grouping, which in turn has two chlorine atoms attached to the nitrogen.
Dichloramine-T was first made by Frederick Daniel Chattaway in 1905. [1] Dichloramine-T can be made from para-toluenesulfonamide and bleaching powder, or chlorine. [2]
Dichloramine-T degrades with exposure to light or air. [3]