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Names | |||
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Preferred IUPAC name
Ethanamine | |||
Other names
Ethylamine
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Identifiers | |||
3D model (JSmol)
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3DMet | |||
505933 | |||
ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.000.759 | ||
EC Number |
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897 | |||
KEGG | |||
MeSH | ethylamine | ||
PubChem CID
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RTECS number |
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UNII | |||
UN number | 1036 | ||
CompTox Dashboard (EPA)
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Properties | |||
C2H7N | |||
Molar mass | 45.085 g·mol−1 | ||
Appearance | Colourless gas | ||
Odor | fishy, ammoniacal | ||
Density | 688 kg m−3 (at 15 °C) | ||
Melting point | −85 to −79 °C; −121 to −110 °F; 188 to 194 K | ||
Boiling point | 16 to 20 °C; 61 to 68 °F; 289 to 293 K | ||
Miscible | |||
log P | 0.037 | ||
Vapor pressure | 116.5 kPa (at 20 °C) | ||
Henry's law
constant (kH) |
350 μmol Pa−1 kg−1 | ||
Acidity (pKa) | 10.8 (for the Conjugate acid) | ||
Basicity (pKb) | 3.2 | ||
Thermochemistry | |||
Std enthalpy of
formation (ΔfH⦵298) |
−57.7 kJ mol−1 | ||
Hazards | |||
GHS labelling: | |||
Danger | |||
H220, H319, H335 | |||
P210, P261, P305+P351+P338, P410+P403 | |||
NFPA 704 (fire diamond) | |||
Flash point | −37 °C (−35 °F; 236 K) | ||
383 °C (721 °F; 656 K) | |||
Explosive limits | 3.5–14% | ||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
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LC50 (median concentration)
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1230 ppm (mammal)[3] | ||
LCLo (lowest published)
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3000 ppm (rat, 4 hr) 4000 ppm (rat, 4 hr)[3] | ||
NIOSH (US health exposure limits): | |||
PEL (Permissible)
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TWA 10 ppm (18 mg/m3)[2] | ||
REL (Recommended)
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TWA 10 ppm (18 mg/m3)[2] | ||
IDLH (Immediate danger)
|
600 ppm[2] | ||
Related compounds | |||
Related alkanamines
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Related compounds
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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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Ethylamine, also known as ethanamine, is an organic compound with the formula CH3CH2NH2. This colourless gas has a strong ammonia-like odor. It condenses just below room temperature to a liquid miscible with virtually all solvents. It is a nucleophilic base, as is typical for amines. Ethylamine is widely used in chemical industry and organic synthesis.[4] It is a DEA list I chemical by 21 CFR § 1310.02.
Ullmann
was invoked but never defined (see the help page).