| Names | |
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Preferred IUPAC name
4-Chloroaniline
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Systematic IUPAC name
4-Chlorobenzenamine
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| Other names
p-Chloroaniline
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| Identifiers | |
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106-47-8 |
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| 3D model (Jmol) | Interactive image |
| ChEBI |
CHEBI:20331 |
| ChEMBL |
ChEMBL15888 |
| ChemSpider |
7524 |
| ECHA InfoCard | 100.003.093 |
| KEGG |
C14450 |
| PubChem | 7812 |
| UNII |
Z553SGH315 |
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| Properties | |
| C6H6ClN | |
| Molar mass | 127.57154 g/mol |
| Appearance | pale yellow solid |
| Density | 1.43 g·cm−3 |
| Melting point | 72.5 °C (162.5 °F; 345.6 K) |
| Boiling point | 232 °C (450 °F; 505 K) |
| 2.6 g/litre at 20 °C (Scheunert, 1981) | |
| Hazards | |
| Main hazards | Very toxic, possible carcinogen. Absorbed through skin. |
| Safety data sheet | External MSDS |
| Flash point | 113 °C (235 °F; 386 K) |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
4-Chloroaniline is an organochlorine compound with the formula ClC6H4NH2. This pale yellow solid is one of several known chloroanilines.
4-Chloroaniline is not prepared from aniline, which tends to overchlorinate. Instead, it is prepared by hydrogenation of 4-nitrochlorobenzene, which in turn is prepared by nitration of chlorobenzene.
4-Chloroaniline is an important building block used in the chemical industry for the production of pesticides, drugs, and dyestuffs. It is a precursor to the widely used antimicrobial and bacteriocide chlorhexidine and is used in the manufacture of pesticides, including pyraclostrobin, anilofos, monolinuron and chlorphthalim. Some benzodiazepine drugs use 4-chloroaniline in their manufacture.
4-Chloroaniline can be used to make dorastine (antihistamine), lorcainide (antiarrhythmic) and Ontianil.