![]() | |
![]() | |
Names | |
---|---|
IUPAC name
hexanedial
| |
Other names
1,4-Butane dicarboxaldehyde, 1,6-hexanedial
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.012.731 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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).
|
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]
![]() | |
![]() | |
Names | |
---|---|
IUPAC name
hexanedial
| |
Other names
1,4-Butane dicarboxaldehyde, 1,6-hexanedial
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.012.731 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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).
|
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]