Ethyl nitrite
| |||
Names | |||
---|---|---|---|
IUPAC name
1-Nitrosooxyethane | |||
Other names
Ethyl alcohol nitrite; Nitrous acid, ethyl ester; Nitrethyl | |||
Identifiers | |||
109-95-5 | |||
ChEMBL | ChEMBL1551365 | ||
ChemSpider | 7735 | ||
Jmol interactive 3D | Image | ||
PubChem | 8026 | ||
| |||
| |||
Properties | |||
C2H5NO2 | |||
Molar mass | 75.07 g·mol−1 | ||
Boiling point | 17 °C (63 °F; 290 K) | ||
Hazards | |||
Main hazards | [1] | ||
NFPA 704 | |||
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 | |||
The chemical compound ethyl nitrite is an alkyl nitrite. It may be prepared from ethanol.[2]
Ethyl nitrite is the main ingredient in a traditional ethanol-based South African remedy for colds and flu known as Witdulsies and sold in pharmacies. It is known as a traditional Afrikaans remedy and may have Dutch roots, as the same remedy is apparently made by the Germano-Dutch Amish people in the USA. However FDA has blocked over-the-counter sales of this same remedy, known in the USA as sweet nitrite or sweet spirit of nitre since 1980.[3]
References
- ↑ "NFPA 704 Ratings for Common Chemicals".
- ↑ Semon, W. L.; Damerell, V. R. (1943). "Dimethylglyoxime". Org. Synth.; Coll. Vol. 2, p. 204
- ↑ http://www.fda.gov/Drugs/DevelopmentApprovalProcess/DevelopmentResources/Over-the-CounterOTCDrugs/StatusofOTCRulemakings/ucm072140.htm
External links
|
This article is issued from Wikipedia - version of the Thursday, March 24, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.