Nowadays, Dodecanal has become a topic of interest to many people around the world. From its impact on society to its implications in science and technology, Dodecanal has captured the attention of academics, researchers and professionals from various areas. As we continue to explore the dimensions of Dodecanal, we encounter endless possibilities and challenges that invite us to reflect on its importance in our daily lives. In this article, we will take a closer look at Dodecanal and its impact on our daily lives, as well as the opportunities it offers for the future.
![]() | |
Names | |
---|---|
Preferred IUPAC name
Dodecanal | |
Other names
Lauraldehyde; Dodecyl aldehyde
| |
Identifiers | |
3D model (JSmol)
|
|
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.003.621 |
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C12H24O | |
Molar mass | 184.323 g·mol−1 |
Appearance | Colorless liquid[1] |
Density | 0.83 g cm−3[1] |
Melting point | 12 °C (54 °F; 285 K)[1] |
Boiling point | 257 °C (495 °F; 530 K)[1] |
Hazards | |
GHS labelling:[1] | |
![]() ![]() | |
Warning | |
H315, H411 | |
P273, P302+P352 | |
Flash point | 114 °C (237 °F; 387 K)[1] |
Related compounds | |
Related
|
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
|
Dodecanal, also known as lauraldehyde or dodecyl aldehyde, is an organic compound with the chemical formula CH3(CH2)10CHO. This colourless liquid is a component of many fragrances. It occurs naturally in citrus oils, but commercial samples are usually produced from dodecanol by dehydrogenation.[2]