Methacrylonitrile
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| Names | |||
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| Preferred IUPAC name
2-Methylprop-2-enenitrile | |||
| Other names
Methylacrylonitrile
2-Cyanopropene 2-Cyano-1-propene Isopropenecyanide Isopropenylcyanid Isopropene cyanide | |||
| Identifiers | |||
3D model (JSmol)
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| Abbreviations | MeAN | ||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.004.380 | ||
| EC Number |
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PubChem CID
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| RTECS number |
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| UNII | |||
| UN number | 3079 | ||
CompTox Dashboard (EPA)
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| Properties | |||
| C4H5N | |||
| Molar mass | 67.091 g·mol−1 | ||
| Appearance | Clear colorless to very slightly yellow liquid | ||
| Odor | Bitter almonds | ||
| Density | 0.8 g/mL | ||
| Melting point | −35.8 °C (−32.4 °F; 237.3 K) | ||
| Boiling point | 90 to 92 °C (194 to 198 °F; 363 to 365 K) | ||
| 2.57 g/100 mL (20 °C) | |||
| Vapor pressure | 71 mmHg (25 °C) | ||
| Hazards | |||
| GHS labelling: | |||
| Danger | |||
| H225, H301, H311, H317, H331 | |||
| P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P272, P280, P301+P310, P302+P352, P303+P361+P353, P304+P340, P311, P312, P321, P322, P330, P333+P313, P361, P363, P370+P378, P403+P233, P403+P235, P405, P501 | |||
| Flash point | 13 °C (55 °F; 286 K) | ||
| Explosive limits | 2%-6.8% | ||
| NIOSH (US health exposure limits): | |||
PEL (Permissible)
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none | ||
REL (Recommended)
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TWA 1 ppm (3 mg/m3) [skin] | ||
IDLH (Immediate danger)
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N.D. | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Methacrylonitrile (or 2-Methylprop-2-enenitrile), MeAN in short, is a chemical compound that is an unsaturated aliphatic nitrile, widely used in the preparation of homopolymers, copolymers, elastomers, and plastics and as a chemical intermediate in the preparation of acids, amides, amines, esters, and other nitriles. MeAN is also used as a replacement for acrylonitrile in the manufacture of an acrylonitrile/butadiene/styrene-like polymer. It is a clear and colorless (to slightly yellow) liquid, that has a bitter almond smell.
It is toxic by ingestion, inhalation, and skin absorption.