Information about Ethylamine
| Ethylamine | |
|---|---|
| IUPAC name | Ethanamine |
| Other names | Ethylamine, Monoethylamine, Aminoethane, 1-Aminoethane |
| Identifiers | |
| CAS number | |
| PubChem | |
| EINECS number | |
| RTECS number | KH2100000 |
| SMILES | CCN |
| InChI | InChI=1/C2H7N/c1-2-3/h2-3H2,1H3 |
| Properties | |
| Molecular formula | C2H7N |
| Molar mass | 45.08 g/mol |
| Appearance | Light yellow liquid |
| Density | 0.689 g/cm3 |
| Melting point | -81 °C |
| Boiling point | 16.6 °C |
| Solubility in water | Miscible |
| Vapor pressure | 121 kPa (20 °C) |
| Hazards | |
| Main hazards | Harmful, corrosive, highly flammable |
| NFPA 704 |
|
| R-phrases | R12, R20, R22, R34, R36, R37, R38 |
| S-phrases | S16, S26, S29 |
| Flash point | -17 °C |
| Autoignition temperature | 385 °C |
| Explosive limits | 3.5-14 %V |
| Except where noted otherwise, data are given for materials in their standard state (at 25 C, 100 kPa) | |
Ethylamine is a chemical compound with the formula CH3CH2NH2. It has a strong ammonia-like odor. It is miscible with virtually all solvents and is considered to be a weak base, as is typical for amines. Ethylamine is widely used in chemical industry and organic synthesis.
Ethylamine, like some other amines, has the unusual property of dissolving lithium metal to give the ion [Li(amine)4]+ and the solvated electron. Evaporation of these solutions, gives back lithium metal. Such solutions are used for the reduction of unsaturated organic compounds, such as naphthalenes[1] and alkynes.
Synthesis and reactions
Ethylamine can be prepared in a laboratory by reaction of ethylene with ammonia in the presence of a catalyst.- H2C=CH2 + NH3 → CH3CH2NH2
It can also be synthesized from acetaldehyde and ammonium chloride.
- 2 CH3CHO + NH4Cl → CH3CH2NH3Cl + CH3CO2H
- CH3CH2NH3Cl + NaOH → CH3CH2NH2 + NaCl + H2O
Reaction of ethylamine with sulfuryl chloride followed by oxidaton of the sulfonamide give diethyldiazene, EtN=NEt.[2]
It is a basic compound.
References
1. ^ Kaiser, E. M.; Benkeser R. A. "Δ9,10-Octalin" Organic Syntheses, Collected Volume 6, p.852 (1988). [1]
2. ^ Ohme, R.; Preuschhof, H.; Heyne, H.-U. "Azoethane" Organic Syntheses, Collected Volume 6, p.78 (1988). [2]
2. ^ Ohme, R.; Preuschhof, H.; Heyne, H.-U. "Azoethane" Organic Syntheses, Collected Volume 6, p.78 (1988). [2]
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boiling point of a liquid is the temperature at which the vapor pressure of the liquid equals the environmental pressure surrounding the liquid.[1][2][3][4]
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Solubility is a physical property referring to the ability for a given substance, the solute, to dissolve in a solvent.[1] It is measured in terms of the maximum amount of solute dissolved in a solvent at equilibrium. The resulting solution is called a saturated solution.
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Water is a common chemical substance that is essential to all known forms of life.[1] In typical usage, water refers only to its liquid form or state, but the substance also has a solid state, ice, and a gaseous state, water vapor.
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standard state of a material is its state at 1 bar (100 kilopascals exactly). This pressure was changed from 1 atm (101.325 kilopascals) by IUPAC in 1990.[1] The standard state of a material can be defined at any given temperature, most commonly 25 degrees Celsius,
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Ammonia is a compound with the formula NH3. It is normally encountered as a gas with a characteristic pungent odor. Ammonia contributes significantly to the nutritional needs of the planet as a precursor to foodstuffs and fertilizers.
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Amines are organic compounds and a type of functional group that contain nitrogen as the key atom. Structurally amines resemble ammonia, wherein one or more hydrogen atoms are replaced by organic substituents such as alkyl and aryl groups.
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Lithium (IPA: /ˈlɪθiəm/) is a chemical element with the symbol Li and atomic number 3. It is a soft alkali metal with a silver-white color.
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The Birch reduction is the organic reduction of aromatic rings with sodium in liquid ammonia to form 1,4-cyclohexadienes. The reaction was reported by the Australian chemist Arthur John Birch (1915–1995) in 1944.
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