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Psoralen

7H-Furo[3,2-g][1]benzopyran-7-one

Ficusin · Furo[3,2-g]coumarin

Tricyclic benzofuranoid lactone · C₁₁H₆O₃

Chemical structure of Psoralen
2D structure PubChem / NCI CIR

Chemical info

CAS number CAS
66-97-7
Molecular formula
C₁₁H₆O₃
Molecular weight
186.16 g/mol
Aroma
Essentially odorless, a hidden phototoxic constituent in citrus and umbelliferous oils.

Safety

Phototoxic · Mutagenic · IFRA + EU prohibited

Psoralen is one of a group of furanocoumarins causing significant photosensitization and phototoxicity in animals and humans. The European Union and SCCP impose strict limits in cosmetics.

Phototoxicity. In combination with UVA, psoralen causes DNA damage and persistent skin darkening. It is the constituent that makes rue, bitter orange and non-FCF bergamot oils highly phototoxic.

Mutagenicity. Psoralen was positive in the SOS chromotest and genotoxic in human lymphocytes and HepG2 hepatoma cells. It was mutagenic in HPRT assay and photogenotoxic in a micronucleus assay above 5 µg/mL.

CYP interaction. Psoralen is a potent inhibitor of microsomal CYP3A with an IC50 of 5.1 µM. It inhibits CYP3A4 more weakly with IC50 of 116 to 257 µM in human liver.


Usage guidelines

Concern level
High · phototoxic and mutagenic
EU SCCNFP limit
1 ppm for furocoumarin-like substances in all cosmetics
Oils with high content
Rue 0.015 percent · Angelica root 0.011 percent

Found in essential oils

Principal sources
Rue0.015 %
Angelica root0.0112 %
Taget0.011 %
Orange (bitter)0.007 %
Bergamot0 – 0.0026 %

Notes

Psoralen is used medically alongside UVA in PUVA therapy for psoriasis and vitiligo under strict supervision. In cosmetics and fragrance, psoralen and related furanocoumarins are limited to 1 ppm.