Date published: 2025-10-14

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Cuminaldehyde (CAS 122-03-2)

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Alternate Names:
4-Isopropylbenzaldehyde
CAS Number:
122-03-2
Purity:
≥97%
Molecular Weight:
148.20
Molecular Formula:
C10H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cuminaldehyde (C10H12O) is a colorless liquid with a distinctive aroma, composed of carbon, hydrogen, and oxygen atoms. This organic compound holds significant value in several industries, including perfumes, cosmetics, and food. Also known as cumin aldehyde, it occurs naturally in cumin oil and serves as a vital intermediate in the synthesis of numerous organic compounds. Researchers have extensively explored the diverse applications of cuminaldehyde in scientific research. Additionally, it finds relevance in the production of polymers and pesticides. Although the precise mechanism of action of cuminaldehyde remains incompletely understood, it is believed to operate as an enzyme inhibitor, affecting enzymes like cyclooxygenase and lipoxygenase. Cuminaldehyde′s versatility and beneficial properties have earned it a prominent place in various industries and ongoing scientific investigations.


Cuminaldehyde (CAS 122-03-2) References

  1. Cuminaldehyde: Aldose Reductase and alpha-Glucosidase Inhibitor Derived from Cuminum cyminum L. Seeds.  |  Lee, HS. 2005. J Agric Food Chem. 53: 2446-50. PMID: 15796577
  2. Cuminaldehyde as a lipoxygenase inhibitor: in vitro and in silico validation.  |  Tomy, MJ., et al. 2014. Appl Biochem Biotechnol. 174: 388-97. PMID: 25080377
  3. Cuminaldehyde as the Major Component of Cuminum cyminum, a Natural Aldehyde with Inhibitory Effect on Alpha-Synuclein Fibrillation and Cytotoxicity.  |  Morshedi, D., et al. 2015. J Food Sci. 80: H2336-45. PMID: 26351865
  4. Cuminaldehyde from Cinnamomum verum Induces Cell Death through Targeting Topoisomerase 1 and 2 in Human Colorectal Adenocarcinoma COLO 205 Cells.  |  Tsai, KD., et al. 2016. Nutrients. 8: PMID: 27231935
  5. Aromatic aldehyde compound cuminaldehyde protects nonalcoholic fatty liver disease in rats feeding high fat diet.  |  Haque, MR. and Ansari, SH. 2019. Hum Exp Toxicol. 38: 823-832. PMID: 30974975
  6. Ultrasound processed cuminaldehyde/2-hydroxypropyl-β-cyclodextrin inclusion complex: Preparation, characterization and antibacterial activity.  |  Cui, H., et al. 2019. Ultrason Sonochem. 56: 84-93. PMID: 31101292
  7. Antinociceptive and antineuropathic effects of cuminaldehyde, the major constituent of Cuminum cyminum seeds: Possible mechanisms of action.  |  Koohsari, S., et al. 2020. J Ethnopharmacol. 255: 112786. PMID: 32222574
  8. Cuminaldehyde potentiates the antimicrobial actions of ciprofloxacin against Staphylococcus aureus and Escherichia coli.  |  Monteiro-Neto, V., et al. 2020. PLoS One. 15: e0232987. PMID: 32407399
  9. Cuminaldehyde induces oxidative stress-mediated physical damage and death of Haemonchus contortus.  |  Goel, V., et al. 2020. Biomed Pharmacother. 130: 110411. PMID: 32682984
  10. Dietary administration of cumin-derived cuminaldehyde induce neuroprotective and learning and memory enhancement effects to aging mice.  |  Omari, Z., et al. 2021. Aging (Albany NY). 13: 1671-1685. PMID: 33471781
  11. A novel promising delivery system for cuminaldehyde using gelled lipid nanoparticles: Characterization and anticancer, antioxidant, and antibacterial activities.  |  Ghiasi, F., et al. 2021. Int J Pharm. 610: 121274. PMID: 34752917
  12. Molecular insight into the interactions between starch and cuminaldehyde using relaxation and 2D solid-state NMR spectroscopy.  |  Ma, Y., et al. 2022. Carbohydr Polym. 278: 118932. PMID: 34973750
  13. Transcriptomic and proteomic analysis of Staphylococcus aureus response to cuminaldehyde stress.  |  Li, H., et al. 2022. Int J Food Microbiol. 382: 109930. PMID: 36122481
  14. Synergistic interaction of cuminaldehyde and tobramycin: a potential strategy for the efficient management of biofilm caused by Pseudomonas aeruginosa.  |  Chatterjee, S., et al. 2023. Folia Microbiol (Praha). 68: 151-163. PMID: 36192618
  15. Cuminaldehyde Effects in a MIA-Induced Experimental Model Osteoarthritis in Rat Knees.  |  Morais, SV., et al. 2023. Metabolites. 13: PMID: 36984837

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cuminaldehyde, 5 g

sc-239590
5 g
$23.00