112-54-9
112-54-9
Chemical Structure
Dodecanal
- CAS No.: 112-54-9
- Formula:C12H24O
- Molecular Weight:184.32
IUPAC Name: dodecanal
InChIKey: HFJRKMMYBMWEAD-UHFFFAOYSA-N
SMILES: CCCCCCCCCCCC=O
Biological Activity: Dodecanal is an aliphatic aldehyde and serves as the major volatile metabolite in the leaves, stems and roots of Polygonum minus. Dodecanal acts as a substrate for oxidation reactions and is converted into dodecanoic acid by endogenous ALDH enzymes. Dodecanal is an intermediate in the biological oxidation pathway of n-dodecane and the biotransformation pathway of ω-aminododecane[1][2][3].
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Dodecanal | 99.35% | Dodecanal is an aliphatic aldehyde and serves as the major volatile metabolite in the leaves, stems and roots of Polygonum minus. Dodecanal acts as a substrate for oxidation reactions and is converted into dodecanoic acid by endogenous ALDH enzymes. Dodecanal is an intermediate in the biological oxidation pathway of n-dodecane and the biotransformation pathway of ω-aminododecane. | ||||||||||||||||||||
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Dodecanal-d3 | Dodecanal-d3 is the deuterated-labeled Dodecanal (HY-W004301). Dodecanal is an aliphatic aldehyde and serves as the major volatile metabolite in the leaves, stems and roots of Polygonum minus. Dodecanal acts as a substrate for oxidation reactions and is converted into dodecanoic acid by endogenous ALDH enzymes. Dodecanal is an intermediate in the biological oxidation pathway of n-dodecane and the biotransformation pathway of ω-aminododecane. | |||||||||||||||||||||
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References
- [1]. Ahmad R, et al. Volatile profiling of aromatic traditional medicinal plant, Polygonum minus in different tissues and its biological activities. Molecules (Basel, Switzerland). 2014 Nov 20;19(11):19220-42.
- [2]. Jang J H, et al. Whole Cell Biotransformation of 1‑dodecanol by Escherichia coli by Soluble Expression of ADH Enzyme from Yarrowia lipolytica. Biotechnol Bioproc E, 2021, 26: 247‑255.
- [3]. Grant C, et al. Tools for characterizing the whole-cell bio-oxidation of alkanes at microscale. Biotechnology and bioengineering. 2012 Sep;109(9):2179-89.
