Ethylammonium nitrate information

Ethylammonium nitrate
Partially condensed, skeletal formula of ethylammonium nitrate with some explicit hydrogens added	Ball and stick model of ethylammonium nitrate
Identifiers
CAS Number	22113-86-6 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:63882;
ChemSpider	4937507 ;
ECHA InfoCard	100.218.244
EC Number	690-858-8;
PubChem CID	6432248;
CompTox Dashboard (EPA)	DTXSID0047901 ;
	InChI InChI=1S/C2H7N.NO3/c1-2-3;2-1(3)4/h2-3H2,1H3;/q;-1/p+1 Key: AHRQMWOXLCFNAV-UHFFFAOYSA-O ; InChI=1/C2H7N.NO3/c1-2-3;2-1(3)4/h2-3H2,1H3;/q;-1/p+1 Key: AHRQMWOXLCFNAV-IKLDFBCSAI;
	SMILES CC[NH3+].[N+](=O)([O-])[O-];
Properties
Chemical formula	[CH3CH2NH3]+[NO3]−
Molar mass	108.0965 g/mol
Appearance	Colorless liquid
Density	1.261 g/ml
Melting point	12 °C (54 °F; 285 K)
Boiling point	240 °C (464 °F; 513 K)
Thermochemistry
Heat capacity (C)	206 J/(mol·K)
Hazards
	Occupational safety and health (OHS/OSH):
Main hazards	Irritant
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P220, P261, P280, P312
Safety data sheet (SDS)	[1]
Related compounds
Other cations	Methylammonium nitrate
	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

Ethylammonium nitrate or ethylamine nitrate^[3] (EAN) is a salt with formula [CH₃CH₂NH₃]⁺[NO₃]⁻. It is an odorless and colorless to slightly yellowish liquid with a melting point of 12 °C.^[4] This compound was described by Paul Walden in 1914,^[5]^[6] and is believed to be the earliest reported example of a room-temperature ionic liquid.^[7]

^ Ionic liquids & ionic liquid acids with high temperature stability for fuel cell and other high temperature applications, method of making and cell employing same United States Patent Application 20070026295, Google patents link
^ "C&L Inventory". echa.europa.eu.
^ Wagaman, Kerry L Liquid monopropellant United States Patent 6001197, Publication Date 12/14/1999
^ Marsh, K.N.; Boxall, J.A.; Lichtenthaler, R. (2004). "Room temperature ionic liquids and their mixtures—a review". Fluid Phase Equilibria. 219: 93–98. doi:10.1016/j.fluid.2004.02.003.
^ P. Walden (1914). Chem. Zentralbl. 85: 1800–1801. {{cite journal}}: Missing or empty |title= (help)
^ P. Walden (1914). "Ueber die Molekulargrösse und elektrische Leitfähigkeit einiger geschmolzenen Salze" (PDF). Bull. Acad. Imper. Sci. St. Pétersbourg. 6. 8: 405–422.
^ Mihkel Koel (2008). Ionic Liquids in Chemical Analysis. CRC Press. p. xxvii. ISBN 978-1-4200-4646-5.

[p1-1] Ionic liquids & ionic liquid acids with high temperature stability for fuel cell and other high temperature applications, method of making and cell employing same United States Patent Application 20070026295, Google patents link

[2] "C&L Inventory". echa.europa.eu.

[3] Wagaman, Kerry L Liquid monopropellant United States Patent 6001197, Publication Date 12/14/1999

[4] Marsh, K.N.; Boxall, J.A.; Lichtenthaler, R. (2004). "Room temperature ionic liquids and their mixtures—a review". Fluid Phase Equilibria. 219: 93–98. doi:10.1016/j.fluid.2004.02.003.

[5] P. Walden (1914). Chem. Zentralbl. 85: 1800–1801. {{cite journal}}: Missing or empty |title= (help)

[walden-6] P. Walden (1914). "Ueber die Molekulargrösse und elektrische Leitfähigkeit einiger geschmolzenen Salze" (PDF). Bull. Acad. Imper. Sci. St. Pétersbourg. 6. 8: 405–422.

[r3-7] Mihkel Koel (2008). Ionic Liquids in Chemical Analysis. CRC Press. p. xxvii. ISBN 978-1-4200-4646-5.

Ethylammonium nitrate information

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