Diethylamine
Names | |
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IUPAC name
1-ethylaminoethane | |
Other names
Diethamine; N,N-Diethylamine; Diethylamine | |
Identifiers | |
109-89-7 | |
605268 | |
ChEBI | CHEBI:85259 |
ChEMBL | ChEMBL1189 |
ChemSpider | 7730 |
EC Number | 203-716-3 |
Jmol interactive 3D | Image |
MeSH | diethylamine |
PubChem | 8021 |
RTECS number | HZ8750000 |
UNII | B035PIS86W |
UN number | 1154 |
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Properties | |
C4H11N | |
Molar mass | 73.14 g·mol−1 |
Appearance | Colourless liquid |
Odor | fishy, ammoniacal |
Density | 0.7074 g mL−1 |
Melting point | −49.80 °C; −57.64 °F; 223.35 K |
Boiling point | 54.8 to 56.4 °C; 130.5 to 133.4 °F; 327.9 to 329.5 K |
Miscible | |
log P | 0.657 |
Vapor pressure | 24.2–97.5 kPa |
Henry's law constant (kH) |
150 μmol Pa−1 kg−1 |
Refractive index (nD) |
1.385 |
Thermochemistry | |
178.1 J K−1 mol−1 | |
Std enthalpy of formation (ΔfH |
−131 kJ mol−1 |
Std enthalpy of combustion (ΔcH |
−3.035 MJ mol−1 |
Hazards | |
Safety data sheet | hazard.com |
GHS pictograms | |
GHS signal word | DANGER |
H225, H302, H312, H314, H332 | |
P210, P280, P305+351+338, P310 | |
EU classification (DSD) |
F C |
R-phrases | R11, R20/21/22, R35 |
S-phrases | (S1/2), S3, S16, S26, S29, S36/37/39 |
NFPA 704 | |
Flash point | −23 °C (−9 °F; 250 K) |
312 °C (594 °F; 585 K) | |
Explosive limits | 1.8–10.1% |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose) |
540 mg/kg (rat, oral) 500 mg/kg (mouse, oral)[1] |
LC50 (Median concentration) |
4000 ppm (rat, 4 hr)[1] |
US health exposure limits (NIOSH): | |
PEL (Permissible) |
TWA 25 ppm (75 mg/m3)[2] |
REL (Recommended) |
TWA 10 ppm (30 mg/m3) ST 25 ppm (75 mg/m3)[2] |
IDLH (Immediate danger |
200 ppm[2] |
Related compounds | |
Related amines |
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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). | |
verify (what is ?) | |
Infobox references | |
Diethylamine is a secondary amine with the molecular structure CH3CH2NHCH2CH3 (also written as C4H11N). It is a flammable, weakly alkaline liquid. It is miscible with water and ethanol. It is a colorless liquid which often appears brown due to impurities. It is volatile and has a strong unpleasant odor.
Diethylamine is manufactured from ethanol and ammonia and is obtained together with ethylamine and triethylamine. It is used as a corrosion inhibitor and in the production of rubber, resins, dyes and pharmaceuticals.
Diethylamine is a corrosive chemical and contact with skin may cause irritation or burns.
Diethylamine can be used to produce LSD and is strictly watched by the DEA.
References
- 1 2 "Diethylamine". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
- 1 2 3 "NIOSH Pocket Guide to Chemical Hazards #0209". National Institute for Occupational Safety and Health (NIOSH).
- Merck Index, 12th Edition, 3160.
External links
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