Propyleneimine
Appearance
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Names | |||
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IUPAC name
2-Methylaziridine
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Other names
1,2-Propylenimine
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Identifiers | |||
3D model (JSmol)
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ChemSpider | |||
ECHA InfoCard | 100.000.799 | ||
EC Number |
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PubChem CID
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RTECS number |
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UN number | 1921 (inhibited) | ||
CompTox Dashboard (EPA)
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Properties | |||
C3H7N | |||
Molar mass | 57.096 g·mol−1 | ||
Appearance | Colorless, oily liquid[1] | ||
Odor | ammonia-like[1] | ||
Density | 0.9 g/mL[2] | ||
Melting point | −63 °C (−81 °F; 210 K)[2] | ||
Boiling point | 67 °C (153 °F; 340 K)[2] | ||
Miscible[2] | |||
Vapor pressure | 112 mmHg (20°C)[1] | ||
Hazards | |||
Flash point | −4 °C (25 °F; 269 K)[2] | ||
Lethal dose or concentration (LD, LC): | |||
LCLo (lowest published)
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500 ppm (rat, 4 hr)[3] | ||
NIOSH (US health exposure limits): | |||
PEL (Permissible)
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TWA 2 ppm (5 mg/m3) [skin][1] | ||
REL (Recommended)
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Ca TWA 2 ppm (5 mg/m3) [skin][1] | ||
IDLH (Immediate danger)
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Ca [100 ppm][1] | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Propyleneimine is the organic compound with the formula CH3CH(NH)CH2. It is a secondary amine]] and the smallest chiral aziridine (ring containing C2N). It is a colorless liquid.
The compound is mainly of academic interest, e.g. for the synthesis of dendrimers, a process that exploits the tendency of aziridines to undergo ring-opening reactions.[4] [2]
References
- ^ a b c d e f NIOSH Pocket Guide to Chemical Hazards. "#0537". National Institute for Occupational Safety and Health (NIOSH).
- ^ a b c d e f g h Propyleneimine International Chemical Safety Card at actrav.itcilo.org
- ^ "Propylene imine". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
- ^ "Dendrimers: Relationship between structure and biocompatibility in vitro, and preliminary studies on the biodistribution of 125I-labeled polyamidoamine dendrimers in vivo". Journal of Controlled Release. 65: 133–148. 2000. doi:10.1016/S0168-3659(99)00246-1.
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