Article · Wikipedia archive · Last revised Aug 11, 2026

Ethyl nitrite

The chemical compound ethyl nitrite is an alkyl nitrite with a chemical formula C2H5NO2. It may be prepared from ethanol.

Last revised
Aug 11, 2026
Read time
≈ 2 min
Length
404 w
Citations
6
Source
Ethyl nitrite
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Names
Preferred IUPAC name
Ethyl nitrite
Other names
1-Nitrosooxyethane
Ethyl alcohol nitrite
Nitrous acid
Nitrous ether
Ethyl ester
Nitrethyl
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.003.385
UNII
  • InChI=1S/C2H5NO2/c1-2-5-3-4/h2H2,1H3 checkY
    Key: QQZWEECEMNQSTG-UHFFFAOYSA-N checkY
  • InChI=1/C2H5NO2/c1-2-5-3-4/h2H2,1H3
    Key: QQZWEECEMNQSTG-UHFFFAOYAU
  • O=NOCC
Properties
C2H5NO2
Molar mass 75.067 g·mol−1
Boiling point 17 °C (63 °F; 290 K)
5.07 g/100 ml
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
1
NFPA 704 (fire diamond)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X markN verify (what is checkYX markN ?)

The chemical compound ethyl nitrite is an alkyl nitrite with a chemical formula C2H5NO2. It may be prepared from ethanol.2

Uses

It is used as a reagent with butanone to yield the dimethylglyoxime end product.

Ethyl nitrite is the main ingredient in a traditional ethanol-based South African remedy for colds and flu known as Witdulsies, which is sold in pharmacies. It is known as a traditional Afrikaans remedy; the same remedy is apparently made by the Amish in the US. However, FDA has blocked over-the-counter sales of this same remedy, known in the US as sweet nitrite or sweet spirit of nitre, since 1980.3 Its use has been associated with fatal methemoglobinemia.4

Methemoglobinemia is the primary toxic effect of ethyl nitrite.5 Due to ethyl nitrite's high volatility and faint smell, in the presence of ethyl nitrite vapors, it is easy to breathe a high dose of it without realizing, resulting in methemoglobinemia,6 which may or may not be severe, or even fatal.

References

References

  1. "NFPA 704 Ratings for Common Chemicals".
  2. Semon, W. L.; Damerell, V. R. (1943). "Dimethylglyoxime". Organic Syntheses; Collected Volumes, vol. 2, p. 204.
  3. "Rulemaking History for OTC Sweet Spirits of Nitre Drug Products". fda.gov. Archived from the original on July 9, 2009. Retrieved 2016-12-26.
  4. "ETHYL NITRITE - National Library of Medicine HSDB Database". toxnet.nlm.nih.gov. Retrieved 2017-11-18. "ETHYL NITRITE - National Library of Medicine HSDB Database". Archived from the original on 2017-12-01. Retrieved 2017-11-18.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  5. "Ethyl nitrite". Haz-Map. Retrieved 2020-08-08.
  6. Titov, V Yu; Petrenko, Yu M (2005). "Proposed mechanism of nitrite-induced methemoglobinemia". Biochemistry (Moscow). 70 (4): 473–83. doi:10.1007/s10541-005-0139-7. PMID 15892615. S2CID 22906218.
External links