2,4,6-Trinitrobenzenesulfonic acid
Chemical compound
From Wikipedia, the free encyclopedia
Trinitrobenzenesulfonic acid (C6H3N3O9S) is a nitroaryl oxidizing acid and explosive, used in biochemical research.
| Names | |
|---|---|
| Preferred IUPAC name
2,4,6-Trinitrobenzene-1-sulfonic acid | |
| Other names
Picrylsulfonic acid; Trinitrobenzene sulfonate; TNBS | |
| Identifiers | |
3D model (JSmol) |
|
| 572358 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.017.925 |
| EC Number |
|
| 1051138 | |
PubChem CID |
|
| UNII | |
| UN number | 0386 |
CompTox Dashboard (EPA) |
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| Properties | |
| C6H3N3O9S | |
| Molar mass | 293.16 g·mol−1 |
| Density | 0.955 g/cm3 |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H317, H334 | |
| P261, P272, P280, P285, P302+P352, P304+P341, P321, P333+P313, P342+P311, P363, P501 | |
| NFPA 704 (fire diamond) | |
| Related compounds | |
Related compounds |
Picric acid Trinitroanisole |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Uses
Its primary usage is primarily to neutralize peptide terminal amino groups in scientific research.[1] Occasionally it is used as a detonator for certain other explosive compounds.[citation needed]
The compound is currently being investigated for its effects on the immune system.[2] It is used to induce colitis in the colon of laboratory animals in order to model inflammatory bowel disease and post-infectious irritable bowel syndrome.[3]
Safety precautions
The compound has generally not been investigated for toxicity. However, the primary hazard of working with 2,4,6-trinitrobenzenesulfonic acid is the risk of explosion. Similar to other polynitroaryl acids (e.g. picric acid, TNT), 2,4,6-trinitrobenzenesulfonic acid can explode when heated strongly and mechanically disturbed, even in the presence of common phlegmatizers such as water. It will rapidly heat to ignition if exposed to medium-strong reducing agents, including hydrides, sulfides, and nitrides.[4]


