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Psoralen (also called psoralene) is the parent compound in a family of natural products known as furocoumarins. It is structurally related to coumarin by the addition of a fused furan ring, and may be considered as a derivative of umbelliferone. Psoralen occurs naturally in the seeds of Psoralea corylifolia, as well as in the common fig, celery, parsley, West Indian satinwood and in all citrus fruits. It is widely used in PUVA (psoralen + UVA) treatment for psoriasis, eczema, vitiligo, and cutaneous T-cell lymphoma. Many furocoumarins are extremely toxic to fish, and some are deposited in streams in Indonesia to catch fish.

Product Details:

Name:Psoralen

Synonyms: 

FICUSIN;

Psoralene;

Furocoumarin (Psoralen);

7H-furo[3,2-g]chromen-7-one;

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

6,7-Furanocoumarin;

Psorline-P;

Prosuler;

CAS:66-97-7

EINECS:200-639-7

MF:C11H6O3

MW: 186.16400

Density: 1.389 g/cm3

BP: 362.6?C at 760 mmHg

MP: 160-162 °C

FP: 173.1?C

Purity: 97%+

Refractive index: 1.667

Storage condition: 2-8?C

Stability:Stable under normal temperature and pressure

Appearance:crystalline solid

Package: 5g, 25g, 100g, 500g, 1kg, 25kg

Application: Phototoxic plant antitoxin; It has the effect of increasing skin melanin and is suitable for vitiligo.

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