Date published: 2025-11-20

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1-Nonadecanol (CAS 1454-84-8)

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Alternate Names:
Nonadecyl alcohol; Nonadecan-1-ol; N-NONADECANOL
Application:
1-Nonadecanol is an internal standard used in the study of coprostanol in sediment
CAS Number:
1454-84-8
Molecular Weight:
284.52
Molecular Formula:
C19H40O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1-Nonadecanol, a long-chain fatty alcohol with 19 carbon atoms, has gained significant attention in research related to material science and surface chemistry. It serves as a model compound in studies involving self-assembled monolayers (SAMs) on metal or silica surfaces due to its ability to form organized, densely packed films. These monolayers are widely used to investigate surface interactions, adhesion, and lubrication, providing valuable insights into surface functionalization and the design of hydrophobic and oleophobic coatings. In addition, 1-nonadecanol is used in the development and study of surfactants and emulsifiers. It is valuable in exploring the structure-activity relationship of fatty alcohol-based surfactants due to its hydrophobic properties and long-chain structure, which influence micelle formation and emulsification behavior. Research involving emulsions and phase behavior often uses 1-nonadecanol as a model to understand the influence of fatty alcohols on the stability and characteristics of colloidal systems. Furthermore, in polymer science, 1-nonadecanol is utilized to synthesize and modify long-chain esters, which can then be studied for their melting points, crystallization, and phase behavior. This aids in the exploration of materials that have potential in coatings, lubricants, and biodegradable plastics. Its role in modifying the mechanical and thermal properties of polymers has proven crucial in the search for innovative, sustainable materials.


1-Nonadecanol (CAS 1454-84-8) References

  1. Freezing of water and aqueous NaCl droplets coated by organic monolayers as a function of surfactant properties and water activity.  |  Knopf, DA. and Forrester, SM. 2011. J Phys Chem A. 115: 5579-91. PMID: 21568271
  2. Composition and antimicrobial activity of the essential oil of Heracleum thomsonii (Clarke) from the cold desert of the western Himalayas.  |  Guleria, S., et al. 2011. Nat Prod Res. 25: 1250-60. PMID: 21854172
  3. Antifeedant activity of long-chain alcohols, and fungal and plant metabolites against pea aphid (Acyrthosiphon pisum) as potential biocontrol strategy.  |  Aznar-Fernández, T., et al. 2019. Nat Prod Res. 33: 2471-2479. PMID: 29595339
  4. The scent of Neotinea orchids from Basilicata (Southern Italy).  |  D'auria, M., et al. 2022. Nat Prod Res. 36: 3741-3743. PMID: 33461336
  5. Investigation of the potential anti-urolithiatic activity of Alhagi maurorum (Boiss.) grown wild in Al-Ahsa (Eastern Province), Saudi Arabia.  |  Ammar, RB., et al. 2022. Braz J Biol. 84: e259100. PMID: 35588519
  6. Phytochemical Analysis, GC-MS Profiling, and In Vitro Evaluation of Biological Applications of Different Solvent Extracts of Leonotis nepetifolia (L.) R.Br. Flower Buds.  |  Nagaraja, SK., et al. 2023. Appl Biochem Biotechnol. 195: 1197-1215. PMID: 36342622
  7. A New Essential Oil from the Leaves of Gynoxys rugulosa Muschl. (Asteraceae) Growing in Southern Ecuador: Chemical and Enantioselective Analyses.  |  Maldonado, YE., et al. 2023. Plants (Basel). 12: PMID: 36840197

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Nonadecanol, 500 mg

sc-208669
500 mg
$75.00