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| Catalog Number | CI-GU-0016 |
| Product Name | Hexylresorcinol |
| CAS | 136-77-6 |
| Structure |  |
| Synonyms | 1,3-Benzenediol, 4-hexyl-;Hexylresorcinol |
| IUPAC Name | 4-hexylbenzene-1,3-diol |
| Molecular Weight | 194.27 g/mol |
| Molecular Formula | C12H18O2 |
| InChI | InChI=1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3 |
| InChI Key | WFJIVOKAWHGMBH-UHFFFAOYSA-N |
| Boiling Point | 333-335 °C |
| Melting Point | 65-67 °C |
| Purity | 95% |
| Density | 1 g/mL |
| Appearance | Solid |
| Highest Usage In Residency Products | 0.01 |
| Isomeric SMILES | CCCCCCC1=C(C=C(C=C1)O)O |
Is Hexylresorcinol safe for use on the skin?
Yes, Hexylresorcinol is considered safe for skin use. It has GRAS (Generally Recognized As Safe) status and has been used historically as a topical skin and mucosal disinfectant for treating superficial wounds. It is a component in various soaps, hand washes, and skin cleaners. Additionally, safety tests conducted by Sytheon, including Human Repeat Insult Patch Tests (HRIPT) and skin scarification tests, indicate that Hexylresorcinol is neither a primary irritant nor a primary sensitizer, even at higher concentrations.
What are the common applications of Hexylresorcinol?
Hexylresorcinol is utilized in several applications. It is effective for use in throat lozenges and as an anti-browning agent, particularly in shrimps. It also appears in various pharmacopeias around the world, including those of Australia, the US, the UK, Finland, the Netherlands, and Ireland, highlighting its antiseptic properties.
Has Hexylresorcinol been approved by regulatory bodies for certain uses?
Yes, the European Commission, Health & Consumer Protection Directorate-General, has found 4-hexylresorcinol toxicologically acceptable for the prevention of melanosis in shrimps.
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