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4-Methoxybenzyl alcohol (CAS 105-13-5)

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Alternate Names:
p-Anisyl alcohol; Anis alcohol; Anise alcohol
CAS Number:
105-13-5
Purity:
≥98%
Molecular Weight:
138.16
Molecular Formula:
C8H10O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Methoxybenzyl alcohol is a compound that functions as a precursor in organic synthesis, particularly in the production of fragrances, and other fine chemicals. It acts as a reagent in various chemical reactions, including esterification, etherification, and oxidation processes. At the molecular level, 4-Methoxybenzyl alcohol undergoes specific chemical transformations, such as nucleophilic substitution and oxidation-reduction reactions, to facilitate the formation of desired products. Its mechanism of action involves participating in the formation of new chemical bonds and functional groups, contributing to the synthesis of complex organic molecules. In experimental applications, 4-Methoxybenzyl alcohol serves as a building block for the creation of diverse chemical compounds, enabling the development of novel materials and substances. Its role in chemical synthesis involves specific interactions with other reagents and substrates, leading to the production of target molecules with defined structures and properties.


4-Methoxybenzyl alcohol (CAS 105-13-5) References

  1. Thiourea-enhanced flavin photooxidation of benzyl alcohol.  |  Svoboda, J., et al. 2008. Chemistry. 14: 1854-65. PMID: 18058784
  2. Anomalous reactivity of radical cations produced by photosensitized oxidation of 4-methoxybenzyl alcohol derivatives: role of the sensitizer.  |  Del Giacco, T., et al. 2008. Phys Chem Chem Phys. 10: 200-10. PMID: 18075700
  3. Home-prepared anatase, rutile, and brookite TiO(2) for selective photocatalytic oxidation of 4-methoxybenzyl alcohol in water: reactivity and ATR-FTIR study.  |  Augugliaro, V., et al. 2009. Photochem Photobiol Sci. 8: 663-9. PMID: 19424540
  4. Triplet state of 4-methoxybenzyl alcohol chemisorbed on silica nanoparticles.  |  Arce, VB., et al. 2012. Photochem Photobiol Sci. 11: 1032-40. PMID: 22421904
  5. Aerobic oxidation reactions catalyzed by vanadium complexes of bis(phenolate) ligands.  |  Zhang, G., et al. 2012. Inorg Chem. 51: 7354-61. PMID: 22708725
  6. Molecular characterization and expression of a novel alcohol oxidase from Aspergillus terreus MTCC6324.  |  Chakraborty, M., et al. 2014. PLoS One. 9: e95368. PMID: 24752075
  7. Vasodilatory effects and underlying mechanisms of the ethyl acetate extracts from Gastrodia elata.  |  Dai, R., et al. 2017. Can J Physiol Pharmacol. 95: 564-571. PMID: 28177685
  8. Single-Atom-Based Vanadium Oxide Catalysts Supported on Metal-Organic Frameworks: Selective Alcohol Oxidation and Structure-Activity Relationship.  |  Otake, KI., et al. 2018. J Am Chem Soc. 140: 8652-8656. PMID: 29950097
  9. Water-Soluble Polymeric Carbon Nitride Colloidal Nanoparticles for Highly Selective Quasi-Homogeneous Photocatalysis.  |  Krivtsov, I., et al. 2020. Angew Chem Int Ed Engl. 59: 487-495. PMID: 31659848
  10. Investigation of lipoic acid - 4-methoxybenzyl alcohol reaction and evaluation of its analytical usefulness.  |  Turkowicz, M., et al. 2020. Food Chem. 309: 125750. PMID: 31704079
  11. 4-Methoxybenzylalcohol protects brain microvascular endothelial cells against oxygen-glucose deprivation/reperfusion-induced injury via activation of the PI3K/AKT signaling pathway.  |  Lin, Q., et al. 2021. Exp Ther Med. 21: 252. PMID: 33613705
  12. The Phenolic Antioxidant 3,5-dihydroxy-4-methoxybenzyl Alcohol (DHMBA) Prevents Enterocyte Cell Death under Oxygen-Dissolving Cold Conditions through Polyphyletic Antioxidant Actions.  |  Fukai, M., et al. 2021. J Clin Med. 10: PMID: 34064340
  13. The marine factor 3,5-dihydroxy-4-methoxybenzyl alcohol suppresses growth, migration and invasion and stimulates death of metastatic human prostate cancer cells: targeting diverse signaling processes.  |  Yamaguchi, M., et al. 2022. Anticancer Drugs. 33: 424-436. PMID: 35324521
  14. Chloroperoxidase-catalyzed benzylic hydroxylation.  |  Miller, VP., et al. 1995. Arch Biochem Biophys. 319: 333-40. PMID: 7786013
  15. Chemical synthesis of 15 beta-hydroxytestosterone and its derivatives using a (4-methoxyphenyl)methyl protecting group.  |  Cerný, I., et al. 1996. Steroids. 61: 58-64. PMID: 8750433

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Methoxybenzyl alcohol, 5 g

sc-232831
5 g
$23.00

4-Methoxybenzyl alcohol, 100 g

sc-232831A
100 g
$32.00