P-Anisidine
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| Names | |||
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| Preferred IUPAC name
4-Methoxyaniline | |||
| Other names
para-Anisidine; 4-Aminoanisole; p-Aminoanisole | |||
| Identifiers | |||
3D model (JSmol) |
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| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.002.959 | ||
| EC Number |
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| KEGG | |||
PubChem CID |
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| RTECS number |
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| UNII | |||
| UN number | 2431 | ||
CompTox Dashboard (EPA) |
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| Properties | |||
| C7H9NO | |||
| Molar mass | 123.155 g·mol−1 | ||
| Appearance | Light reddish brown solid | ||
| Odor | Fishy | ||
| Density | 1.071 (at 57 °C) | ||
| Melting point | 56 to 59 °C (133 to 138 °F; 329 to 332 K) | ||
| Boiling point | 243 °C (469 °F; 516 K) | ||
| Sparingly soluble | |||
| Solubility in other solvents | Soluble in ethanol, diethyl ether, acetone, benzene | ||
| Vapor pressure | 0.006 mmHg (25 °C) | ||
| −80.56·10−6 cm3/mol | |||
Refractive index (nD) |
1.5559 | ||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards |
Carcinogen | ||
| GHS labelling: | |||
| Warning | |||
| H300, H310, H330, H350, H373, H400 | |||
| P201, P202, P260, P262, P264, P270, P271, P273, P280, P281, P284, P301+P310, P302+P350, P304+P340, P308+P313, P310, P314, P320, P321, P322, P330, P361, P363, P391, P403+P233, P405, P501 | |||
| Flash point | 122 °C (252 °F; 395 K) | ||
| 515 °C (959 °F; 788 K) | |||
| Lethal dose or concentration (LD, LC): | |||
LD50 (median dose) |
145 mg/kg (rabbit, oral) 130 mg/kg (mouse, oral) 140 mg/kg (rat, oral) | ||
LDLo (lowest published) |
100 mg/kg (mouse, oral) | ||
| NIOSH (US health exposure limits): | |||
PEL (Permissible) |
TWA 0.5 mg/m3 [skin] | ||
REL (Recommended) |
TWA 0.5 mg/m3 [skin] | ||
IDLH (Immediate danger) |
50 mg/m3 | ||
| Related compounds | |||
Related compounds |
o-Anisidine m-Anisidine | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
p-Anisidine (or para-anisidine) is an organic compound with the formula CH3OC6H4NH2. A white solid, commercial samples can appear grey-brown owing to air oxidation. It is one of three isomers of anisidine, methoxy-containing anilines. It is prepared by reduction of 4-nitroanisole.