| Names | |
|---|---|
| Preferred IUPAC name
2,3-Dichloronaphthalene-1,4-dione | |
| Identifiers | |
| |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.003.828 |
| EC Number |
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PubChem CID
|
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| UNII | |
| UN number | 2902 2761 |
CompTox Dashboard (EPA)
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| |
| |
| Properties | |
| C10H4Cl2O2 | |
| Molar mass | 227.04 g·mol−1 |
| Appearance | Yellow crystals1 |
| Melting point | 193 °C (379 °F; 466 K)1 |
| 0.1 ppm1 | |
| Hazards | |
| GHS labelling:[1] | |
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| |
| Warning | |
| H302, H315, H317, H319, H410 | |
| P261, P264, P264+P265, P270, P272, P273, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P333+P317, P337+P317, P362+P364, P391, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Dichlone (trade names Phygon and Quintar) is a fungicide and algicide of the quinone class. It is a general use fungicide applied to fruits, vegetables, field crops, ornamentals, and residential and commercial outdoor areas.1 It is also used to control blue algae.2
Dichlone is not persistent in soil and has moderate mammalian toxicity.2
Dichlone can be manufactured by the chlorination and oxidation of naphthalene.3

Synthesis of dichlone from naphthalene source ↗
References
References
- "Dichlone (Phygon, Quintar) Chemical Profile". Pesticide Management Education Program, Cornell Cooperative Extension.
- "Dichlone". Pesticide Properties DataBase, University of Hertfordshire.
- Thomas A. Unger (1996). Pesticide Synthesis Handbook. William Andrew. p. 966. ISBN 0-8155-1853-6.


