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Names | |||
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Preferred IUPAC name
1,4-Dichlorobenzene
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Other names
para-Dichlorobenzene
p-Dichlorobenzene p-DCB PDB Paramoth Para crystals Paracide Dichlorocide |
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Identifiers | |||
106-46-7 | |||
3D model (Jmol) | Interactive image | ||
ChEBI | CHEBI:28618 | ||
ChEMBL | ChEMBL190982 | ||
ChemSpider | 13866817 | ||
ECHA InfoCard | 100.003.092 | ||
KEGG | C07092 | ||
RTECS number | CZ4550000 | ||
UNII | D149TYB5MK | ||
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Properties | |||
C6H4Cl2 | |||
Molar mass | 147.00 g·mol−1 | ||
Appearance | Colorless/white crystals | ||
Odor | mothball-like | ||
Density | 1.25 g/cm3, solid | ||
Melting point | 53.5 °C (128.3 °F; 326.6 K) | ||
Boiling point | 174 °C (345 °F; 447 K) | ||
10.5 mg/100 mL (20 °C) | |||
Vapor pressure | 1.3 mmHg (20°C) | ||
-82.93·10−6 cm3/mol | |||
Hazards | |||
Main hazards | Suspected carcinogen | ||
EU classification (DSD)
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Xn N Carc. Cat. 3 |
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R-phrases | R36 R40 R50/53 | ||
S-phrases | (S2) S36/37 S46 S60 S61 | ||
NFPA 704 | |||
Flash point | 66 °C (151 °F; 339 K) | ||
Explosive limits | 2.5%-? | ||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
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500 mg/kg (oral, rat) 2950 mg/kg (oral, mouse) 2512 mg/kg (oral, rat) 2830 mg/kg (oral, rabbit) |
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LDLo (lowest published)
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857 mg/kg (human, oral) 4000 mg/kg (rat, oral) 2800 mg/kg (guinea pig, oral) |
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US health exposure limits (NIOSH): | |||
PEL (Permissible)
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TWA 75 ppm (450 mg/m3) | ||
REL (Recommended)
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Ca | ||
IDLH (Immediate danger)
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Ca [150 ppm] | ||
Related compounds | |||
Related compounds
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1,2-Dichlorobenzene 1,3-Dichlorobenzene |
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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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what is ?) | (|||
Infobox references | |||
1,4-Dichlorobenzene (p-DCB or para-dichlorobenzene, sometimes abbreviated as PDB or para) is an organic compound with the formula C6H4Cl2. This colorless solid has a strong odor. The molecule consists of a benzene ring with two chlorine atoms (replacing hydrogen atoms) on opposing sites of the ring. It is used as a pesticide and a deodorant, most familiarly in mothballs in which it is a replacement for the more traditional naphthalene because of naphthalene's greater flammability (though both chemicals have the same NFPA 704 rating). It is also used as a precursor in the production of the polymer poly(p-phenylene sulfide).
p-DCB is produced by chlorination of benzene using ferric chloride as a catalyst:
The chief impurity is the 1,2 isomer. The compound can be purified by fractional crystallisation, taking advantage of its relatively high melting point of 53.5 °C; the isomeric dichlorobenzenes and chlorobenzene melt well below room temperature.
p-DCB is used to control moths, molds, and mildew. It also finds use as a disinfectant in waste containers and restrooms and is the characteristic smell associated with urinal cakes. Its usefulness for these applications arises from p-DCB's low solubility in water and its relatively high volatility: it sublimes readily near room temperature.