Adipaldehyde
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| Names | |
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| IUPAC name
hexanedial
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| Other names
1,4-Butane dicarboxaldehyde, 1,6-hexanedial
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
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| EC Number |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C6H10O2 | |
| Molar mass | 114.144 g·mol−1 |
| Appearance | colorless liquid |
| Density | 1.003 g/cm3 |
| Melting point | −8 °C (18 °F; 265 K) |
| Boiling point | 68–70 °C (154–158 °F; 341–343 K) 3 mm Hg |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Adipaldehyde is the organic compound with the formula (CH2)4(CHO)2. It is a colorless oil that is usually encountered as an aqueous solution because it is highly reactive like many dialdehydes.[1] The compound has attracted interest as a precursor to nylon-related polymers. It can be produced by double hydroformylation of 1,3-butadiene, but this methodology has not achieved commercialization.[2] It has been prepared by oxidation of 1,6-hexanediol with pyridinium chlorochromate.[3]
References
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