- InChI
- InChI=1S/C8H20N.BrH/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;1H/q+1;/p-1
- InChI Key
- HWCKGOZZJDHMNC-UHFFFAOYSA-M
- Formula
- C8H20BrN
- SMILES
- CC[N+](CC)(CC)CC.[Br-]
- Molecular Weight1
- 210.16
- CAS
- 71-91-0
- Other Names
-
- Ammonium, tetraethyl-, bromide
- Beparon
- Bromethyl
- Bromure de tetraethylammonium
- Etambro
- Etamon
- Ethanaminium, N,N,N-triethyl-, bromide
- Ethylon
- Etylon
- Sympatektoman
- TEA
- TEA bromide
- TEAB
- TMD 10
- Teamon
- Tetranium
- Tetrylammonium Bromide
- USAF do-32
- Cp,solid : Solid phase heat capacity (J/mol×K).
- ΔfusH : Enthalpy of fusion at a given temperature (kJ/mol).
- ΔfusS : Entropy of fusion at a given temperature (J/mol×K).
- Tfus : Normal melting (fusion) point (K).
- 1: Molecular weight from the IUPAC atomic weights tables.
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Physical Properties
| Property | Value | Unit | Source |
|---|---|---|---|
| Tfus | [447.00; 447.00] | K |
|
| Tfus | 447.00 ± 2.00 | K | NIST |
| Tfus | 447.00 ± 2.00 | K | NIST |
Cheméo can also estimate Normal Boiling Point Temperature, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.
Temperature Dependent Properties
| Property | Value | Unit | Temperature (K) | Source |
|---|---|---|---|---|
| Cp,solid | 246.90 | J/mol×K | 298.00 | NIST |
| ΔfusH | [20.30; 20.30] | kJ/mol | [447.00; 447.00] |
|
| ΔfusH | 20.30 | kJ/mol | 447.00 | NIST |
| ΔfusH | 20.30 | kJ/mol | 447.00 | NIST |
| ΔfusS | [45.00; 45.00] | J/mol×K | [447.00; 447.00] |
|
| ΔfusS | 45.00 | J/mol×K | 447.00 | NIST |
| ΔfusS | 45.00 | J/mol×K | 447.00 | NIST |
Similar Compounds
Find more compounds similar to Tetraethylammonium bromide.
Mixtures
- Tetraethylammonium bromide + Water
- Tetraethylammonium bromide + Glycine + Water
- D-Alanine + Tetraethylammonium bromide + Water
- N-Glycylglycine + Tetraethylammonium bromide + Water
- Tetraethylammonium bromide + Tetrahydrofuran + 1,3-Dioxolan-2-one
- Acetonitrile + Tetraethylammonium bromide + 1,3-Dioxolan-2-one
- Tetraethylammonium bromide + Ethyl Acetate + 1,3-Dioxolan-2-one
- Tetraethylammonium bromide + Ethane, 1,2-dimethoxy- + 1,3-Dioxolan-2-one
- Tetraethylammonium bromide + dl-Alanine + Water
- Acetonitrile + Tetraethylammonium bromide + Water
- Tetraethylammonium bromide + Formamide + Water
- Propylene Glycol + Tetraethylammonium bromide + Water
- 1,3-Propanediol + Tetraethylammonium bromide + Water
- 1,4-Butanediol + Tetraethylammonium bromide + Water
- Tetraethylammonium bromide + 2,3-Butanediol + Water
- sodium chloride + Tetraethylammonium bromide + Water
- Tetraethylammonium bromide + Sodium nitrate + Water
- Pentanoic acid, 4-oxo- + Tetraethylammonium bromide
- Pentanoic acid, 4-oxo- + Carbon dioxide + Tetraethylammonium bromide
- Ethanol, 2-butoxy- + Tetraethylammonium bromide + Water
Find more mixtures with Tetraethylammonium bromide.
Sources
- Cheméo Relay (1.0, beta) Beta: served but experimental, data-limited and below our cross-validation release bar; the Joback value is recommended where available.
- A model for excess volumes of salty water-acetonitrile mixtures at 298.15 K
- The capability of tetra alkyl ammonium bromides for aqueous biphasic systems formation with both polymers and electrolytes in aqueous solutions
- Standard partial molar volumes of some electrolytes in ethylene carbonate based mixtures
- Effect of tetra-n-alkylammonium bromides on the volumetric properties of glycine, L-alanine and glycylglycine at T = 298:15 K
- Viscometric study of glycine, L-alanine, glycylglycine in aqueous tetra-n-alkylammonium bromide solutions at 298.15 K
- Interactions of some ex-amino acids with tetra-n-alkylammonium bromides in aqueous medium at different temperatures
- Experimental study of the excess molar volume of ternary mixtures containing {water + (1,2-propanediol, or 1,3-propanediol, or 1,2-butanediol, or 1,3-butanediol, or 1,4-butanediol, or 2,3-butanediol) + electrolytes} at a temperature of 298.15 K and atmospheric pressure
- Investigation of solubilities of carbon dioxide in five levulinic acid-based deep eutectic solvents and their thermodynamic properties
- Salting-in and salting-out effects of organic and inorganic ammonium salts on the aqueous polymer solutions
- Temperature dependence of the interaction between two hydrophobic solutes: a calorimetric study
- Temperature dependence of the pair interaction between hydrophobic and hydrophilic solutes: A calorimetric study
- Enthalpies and heat capacities of interaction of tetraalkylammonium bromides with hexamethyl phosphoric triamide in water, methanol and ethylene glycol: the comparative analysis of aqueous and non-aqueous systems
- Densities and Viscosities of Polyhydroxy Solutes in Aqueous Tetraethylammonium Bromide Solutions at Different Temperatures
- Apparent Molar Volumes and Isentropic Compressibilities of Tetraalkylammonium Bromides in Aqueous Propane-1,2-diol. An Attempt to Design Hydraulic Liquids
- Thermodynamic Parameters of Anionic Surfactant-Additive Systems at the Cloud Point
- Electrical Conductivity Studies of Tetraalkylammonium Bromides in Aqueous Solutions at Several Temperatures
- Electrical Conductance of Some Tetraalkylammonium Bromide Salts in 2-Butoxyethanol (1) + Water (2) mixtures at (298.15, 303.15, 308.15, and 313.15) K
- Vapor Pressure Osmometry Determination of the Osmotic and Activity Coefficients of Dilute Aqueous Solutions of Symmetrical Tetraalkyl Ammonium Halides at 308.15 K
- Surface and Micellar Properties of Ionic Liquid 1-Dodecyl-3-methylimidazolium Bromide in Aqueous Solution in the Absence and Presence of a Series of Organic Electrolytes
- Apparent Molal Volumes and Expansibilities of Tetraalkylammonium Bromides in Dilute Aqueous Solutions
- NIST Webbook
Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.