Acetyl nitrate

Acetyl nitrate
Names
	Preferred IUPAC name Acetic nitric anhydride
	Other names Acetyl nitrate
Identifiers
CAS Number	591-09-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	11069;
PubChem CID	11557;
UNII	79CY6496CR ;
CompTox Dashboard (EPA)	DTXSID40207839 ;
	InChI InChI=1S/C2H3NO4/c1-2(4)7-3(5)6/h1H3 Key: JCZMXVGQBBATMY-UHFFFAOYSA-N;
	SMILES CC(=O)O[N+](=O)[O-];
Properties
Chemical formula	C2H3NO4
Molar mass	105.049 g·mol−1
Appearance	colorless liquid
Density	1.24 g/cm3 (15 °C)
Boiling point	22 °C at 70 Torr
Hazards
	Occupational safety and health (OHS/OSH):
Main hazards	explosion
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Acetyl nitrate is the organic compound with the formula CH₃C(O)ONO₂. It is classified as the mixed anhydride of nitric and acetic acids. It is a colorless explosive liquid that fumes in moist air.

Synthesis and reactions[edit]

It was first prepared in 1907 by Amé Pictet and E. Khotynsky from acetic anhydride and dinitrogen pentoxide, fuming nitric acid can also be used:

(CH₃CO)₂O + HNO₃ → CH₃C(O)ONO₂ + CH₃COOH

It hydrolyzes in moist air to acetic acid and nitric acid. Alternatively, nitric acid adds to ketene.

It is used for some nitrations and nitrolysis reactions.^[2] It acetylates amines, akin to the behavior of acetyl chloride:

{\ce {2NH3 + CH3C(O)ONO2 -> NH4NO3 + CH3CONH2}}

References[edit]

^ A. Pictet, E. Khotinsky: Über Acetylnitrat. in Chem. Ber. 40, 1907, S. 1163–1166, doi:10.1002/cber.190704001172.
^ Louw, Robert "Acetyl nitrate" e-EROS Encyclopedia of Reagents for Organic Synthesis 2001, 1-2. doi:10.1002/047084289X.ra032

[Pictet-1] A. Pictet, E. Khotinsky: Über Acetylnitrat. in Chem. Ber. 40, 1907, S. 1163–1166, doi:10.1002/cber.190704001172.

[2] Louw, Robert "Acetyl nitrate" e-EROS Encyclopedia of Reagents for Organic Synthesis 2001, 1-2. doi:10.1002/047084289X.ra032

[1]

[2]