|AHFS/Drugs.com||International Drug Names|
|CompTox Dashboard (EPA)|
|Chemical and physical data|
|Molar mass||194.27 g·mol−1|
|3D model (JSmol)|
It is available for use topically on small skin infections, or as an ingredient in throat lozenges. Johnson & Johnson markets hexylresorcinol in its Neutrogena and RoC skincare products as an anti-aging cream. It is marketed as S.T. 37 by Numark Laboratories, Inc. (in a 0.1% solution) for oral pain relief and as an antiseptic.
A study published in Chemical Research in Toxicology  shows that 4-hexylresorcinol used as a food additive (E-586) exhibits some estrogenic activity, i.e. resembles action of the female sex hormone estrogen.
- O. Gisvold (1966). C. O. Wilson, O. Gisvold and R. F. Doerge (eds.). Textbook of Organic Medicinal and Pharmaceutical Chemistry (5th ed.). Philadelphia: Lippincott. pp. 237–262.CS1 maint: Uses editors parameter (link)
- Amadasi, A; Mozzarelli, A; Meda, C; Maggi, A; Cozzini, P (2009). "Identification of xenoestrogens in food additives by an integrated in silico and in vitro approach". Chem. Res. Toxicol. 22 (1): 52–63. doi:10.1021/tx800048m. PMC 2758355. PMID 19063592.
- Montero, P. (2006). "Parapenaeus longirostris
- Kim, Seong-Gon (2011). "4-hexylresorcinol inhibits NF-κB phosphorylation and has a synergistic effect with cisplatin in KB cells". Oncology Reports. doi:10.3892/or.2011.1436.