Names | |
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Preferred IUPAC name Pentyl nitrate | |
Other names
n-Amyl nitrate 1-Nitrooxypentane 1-Pentyl nitrate | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.012.440 |
EC Number |
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PubChem CID | |
UNII | |
UN number | 1112 |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C5H11NO3 |
Molar mass | 133.147 g·mol |
Boiling point | 104 °C (219 °F; 377 K) |
Magnetic susceptibility (χ) | -76.4·10 cm/mol |
Hazards | |
GHS labelling: | |
Pictograms | |
Signal word | Warning |
Hazard statements | H226, H315, H319 |
Precautionary statements | P210, P233, P240, P241, P242, P243, P264, P280, P302+P352, P303+P361+P353, P305+P351+P338, P321, P332+P313, P337+P313, P362, P370+P378, P403+P235, P501 |
Flash point | 47.8 °C (118.0 °F; 320.9 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
Amyl nitrate is the chemical compound with the formula CH3(CH2)4ONO2. This molecule consists of the 5-carbon amyl group attached to a nitrate functional group. It is the ester of amyl alcohol and nitric acid.
Applications
Alkyl nitrates are employed as reagents in organic synthesis. Amyl nitrate is used as an additive in diesel fuel, where it acts as an "ignition improver" (cetane improver) by accelerating the ignition of fuel.
See also
- Amyl nitrite – a similarly named chemical used to treat heart diseases and cyanide poisoning
References
- EPA on Pentyl nitrate
- Zajac, W. W. Jr. (2001). "1-Nitropropane". Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons. doi:10.1002/047084289X.rn051. ISBN 0471936235.
- "Amyl Nitrate | Cameo Chemicals | Noaa". Cameochemicals.noaa.gov. Retrieved 2016-09-22.