Chemistry:Propionic anhydride
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| Names | |
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| Preferred IUPAC name
Propanoic anhydride | |
| Other names
Propionic anhydride
Propanoyl propanoate | |
| Identifiers | |
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| UNII | |
| UN number | 2496 |
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| Properties | |
| C6H10O3 | |
| Molar mass | 130.14 g/mol |
| Appearance | Clear liquid, with a strong smell similar to vinegar |
| Density | 1.015 g/cm3, liquid |
| Melting point | −42 °C (−44 °F; 231 K) |
| Boiling point | 167 to 170 °C (333 to 338 °F; 440 to 443 K) |
| Reacts to give propanoic acid | |
| Viscosity | 1.144 cP at ?°C |
| Hazards | |
| Main hazards | flammable |
| Safety data sheet | External MSDS |
| GHS pictograms | 
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| GHS Signal word | Danger |
| H314 | |
| P260, P264, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P405, P501 | |
| Flash point | 63 °C (145 °F; 336 K) |
| Related compounds | |
Related compounds
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Acetic anhydride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Propionic anhydride is an organic compound with the formula (CH3CH2CO)2O. This simple acid anhydride is a colourless liquid. It is a widely used reagent in organic synthesis as well as for producing specialty derivatives of cellulose.[1]
Synthesis
Industrial route to propionic anhydride involves thermal dehydration of propionic acid, driving off the water by distillation:
- 2 CH3CH2CO2H → (CH3CH2CO)2O + H2O
Another routes is the Reppe carbonylation of ethylene with propionic acid and nickel carbonyl as the catalyst:[1]
- CH2=CH2 + CH3CH2CO2H + CO → (CH3CH2CO)2O
Propionic anhydride has also been prepared by dehydration of propionic acid using ketene:[2]
- 2 CH3CH2CO2H + CH2=C=O → (CH3CH2CO)2O + CH3CO2H
Safety
Propanoic anhydride is strong smelling and corrosive, and will cause burns on contact with skin. Vapour can burn eyes and lungs.
Legal Status
Due to its potential use as a precursor in the synthesis of fentanyl and fentanyl analogs, propanoic anhydride is regulated by the United States Drug Enforcement Administration as a List I chemical under the Controlled Substances Act.[3]
References
- ↑ 1.0 1.1 Samel, Ulf-Rainer; Kohler, Walter; Gamer, Armin Otto; Keuser, Ullrich (2005). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_223.
- ↑ Williams, J. W. Krynitsky, J. A. (1941). "n-Caproic Anhydride". Organic Syntheses 21: 13. doi:10.15227/orgsyn.021.0013.
- ↑ Drugs of Abuse Publication, Chapter 2
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