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Names | |
---|---|
Preferred IUPAC name
4-Butylbenzene-1,3-diol | |
Other names
Rucinol, 4-n-Butylresorcinol
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.126.948 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C10H14O2 | |
Molar mass | 166.220 g·mol−1 |
Hazards | |
GHS labelling: | |
![]() ![]() | |
Warning | |
H302, H315, H319, H400 | |
P264, P270, P273, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, P391, P501 | |
Safety data sheet (SDS) | [1] |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
4-Butylresorcinol, sometimes called 4-n-butylresorcinol, is a chemical used to treat hyperpigmentation of the epidermis. Hyperpigmentation is believed to be related to the enzyme tyrosinase which produces melanin. Among several chemicals known to inhibit tyrosinase production, such as hydroquinone, arbutin, and kojic acid, 4-butylresorcinol has been found to be the most powerful inhibitor by a wide margin. [1] 4-Butylresorcinol can be used in the synthesis of Tetrahydrocannabutol.
![]() | |
Names | |
---|---|
Preferred IUPAC name
4-Butylbenzene-1,3-diol | |
Other names
Rucinol, 4-n-Butylresorcinol
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.126.948 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C10H14O2 | |
Molar mass | 166.220 g·mol−1 |
Hazards | |
GHS labelling: | |
![]() ![]() | |
Warning | |
H302, H315, H319, H400 | |
P264, P270, P273, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, P391, P501 | |
Safety data sheet (SDS) | [1] |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
4-Butylresorcinol, sometimes called 4-n-butylresorcinol, is a chemical used to treat hyperpigmentation of the epidermis. Hyperpigmentation is believed to be related to the enzyme tyrosinase which produces melanin. Among several chemicals known to inhibit tyrosinase production, such as hydroquinone, arbutin, and kojic acid, 4-butylresorcinol has been found to be the most powerful inhibitor by a wide margin. [1] 4-Butylresorcinol can be used in the synthesis of Tetrahydrocannabutol.