Date published: 2025-10-2

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12-Methyltridecanal (CAS 75853-49-5)

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CAS Number:
75853-49-5
Molecular Weight:
212.37
Molecular Formula:
C14H28O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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12-Methyltridecanal is primarily utilized in the field of organic chemistry and materials science research due to its properties as a long-chain aldehyde. It is of interest in the study of pheromone analogs and the synthesis of complex organic molecules, where researchers explore its reactivity and potential as a building block in the creation of larger, more complex structures. In the area of materials science, 12-Methyltridecanal is investigated for its potential use in the development of organic polymers and fragrance materials, due to its ability to undergo various chemical reactions that can lead to new compounds with desirable physical and chemical properties. Additionally, it is used in the field of analytical chemistry as a standard for the calibration of detection instruments, such as gas chromatography-mass spectrometry (GC-MS), aimed at identifying and quantifying volatile compounds within complex mixtures. Its role in the synthesis of surface-active agents is another area of application, contributing to research on substances that alter the surface tension of liquids.


12-Methyltridecanal (CAS 75853-49-5) References

  1. Occurrence of 12-methyltridecanal in microorganisms and physiological samples isolated from beef.  |  Kerscher, R., et al. 2000. J Agric Food Chem. 48: 2387-90. PMID: 10888555
  2. Analysis of fatty aldehyde composition, including 12-methyltridecanal, in plasmalogens from longissimus muscle of concentrate- and pasture-fed bulls.  |  Dannenberger, D., et al. 2006. J Agric Food Chem. 54: 182-8. PMID: 16390197
  3. (1S)-1-ethyl-2-methylpropyl 3,13-dimethylpentadecanoate: major sex pheromone component of Paulownia bagworm, Clania variegata.  |  Gries, R., et al. 2006. J Chem Ecol. 32: 1673-85. PMID: 16900424
  4. Studies on catalytic enantioselective total synthesis of caprazamycin B: construction of the western zone.  |  Gopinath, P., et al. 2012. J Org Chem. 77: 9260-7. PMID: 23020577
  5. Identification of the possible new odor-active compounds '12-methyltridecanal and its analogs' responsible for the characteristic aroma of ripe Gouda-type cheese.  |  Inagaki, S., et al. 2015. Biosci Biotechnol Biochem. 79: 2050-6. PMID: 26223460
  6. Biotechnological Production of Methyl-Branched Aldehydes.  |  Fraatz, MA., et al. 2018. J Agric Food Chem. 66: 2387-2392. PMID: 29534574
  7. Higher Straight-Chain Aliphatic Aldehydes: Importance as Odor-Active Volatiles in Human Foods and Issues for Future Research.  |  Tsuzuki, S. 2019. J Agric Food Chem. 67: 4720-4725. PMID: 30945546
  8. Key Male Glandular Odorants Attracting Female Ring-Tailed Lemurs.  |  Shirasu, M., et al. 2020. Curr Biol. 30: 2131-2138.e4. PMID: 32302584
  9. Lack of evidence for pheromones in lemurs.  |  Drea, CM., et al. 2020. Curr Biol. 30: R1355-R1357. PMID: 33202228
  10. Key Odorants of Raw and Cooked Green Kohlrabi (Brassica oleracea var. gongylodes L.).  |  Marcinkowska, M., et al. 2021. J Agric Food Chem. 69: 12270-12277. PMID: 34609877
  11. α-Dioxygenases (α-DOXs): Promising Biocatalysts for the Environmentally Friendly Production of Aroma Compounds.  |  Kim, IJ., et al. 2022. Chembiochem. 23: e202100693. PMID: 35107200
  12. Comparison of Odorants in Beef and Chicken Broth-Focus on Thiazoles and Thiazolines.  |  Yeo, H., et al. 2022. Molecules. 27: PMID: 36235248
  13. Dependence of the 12-methyltridecanal concentration in beef on the age of the animal.  |  Guth, H. and Grosch, W. 1995. Z Lebensm Unters Forsch. 201: 25-6. PMID: 7571862

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

12-Methyltridecanal, 1 g

sc-484580
1 g
$316.00