| Names | |
|---|---|
| Preferred IUPAC name 2,6-Dichloro-4-nitroaniline | |
| Other names Amino-2,6-dichloro-4-nitrobenzene; Dicloran; Allisan; Batran; Bortran; Botran; Ditranil; Resisan | |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.497 |
| EC Number |
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| KEGG | |
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
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| Properties | |
| C6H4Cl2N2O2 | |
| Molar mass | 207.01 g·mol−1 |
| Appearance | yellow solid [1] |
| Density | 1.624 g/cm3 |
| Melting point | 191 °C (376 °F; 464 K) |
| Boiling point | 130 °C (266 °F; 403 K) 2 torr |
| 6.3 mg/l | |
| Hazards | |
| GHS labelling: [2] | |
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| Danger | |
| H300, H310, H330, H373, H411 | |
| P260, P262, P264, P270, P271, P273, P280, P284, P301+P316, P302+P352, P304+P340, P316, P319, P320, P321, P330, P361+P364, P391, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
2,6-Dichloro-4-nitroaniline is an organic compound with the formula O2NC6H2Cl2NH2. It is the most widely discussed isomer of dichloronitroaniline, mainly as a precursor to the azo dye disperse brown 1. It is prepared by treatment of 4-nitroaniline with a mixture of hydrochloric acid and hydrogen peroxide (a source of chlorine). [3] [4]