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Psoralen

CAS No.
66-97-7
Chemical Name:
Psoralen
Synonyms
FICUSIN;Furocoumarin;Psoralene;Psoralea extract;7H-Furo[3,2-g]chromen-7-one;7H-FURO[3,2-G][1]BENZOPYRAN-7-ONE;PSORALEN;Prosuler;Psorline-P;NSC 404562
CBNumber:
CB3181900
Molecular Formula:
C11H6O3
Molecular Weight:
186.16
MDL Number:
MFCD00010520
MOL File:
66-97-7.mol
MSDS File:
SDS
Last updated:2024-11-20 11:41:24

Psoralen Properties

Melting point 160-162 °C
Boiling point 280.64°C (rough estimate)
Density 1.2477 (rough estimate)
refractive index 1.6310 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Solid
color White to Off-White
Water Solubility 65.16mg/L(25 ºC)
λmax 328nm(EtOH)(lit.)
Merck 14,7928
BRN 152784
InChIKey ZCCUUQDIBDJBTK-UHFFFAOYSA-N
LogP 1.670
CAS DataBase Reference 66-97-7(CAS DataBase Reference)
NCI Dictionary of Cancer Terms psoralen
FDA UNII KTZ7ZCN2EX
NIST Chemistry Reference 7H-furo[3,2-g][1]benzopyran-7-one(66-97-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H317
Precautionary statements  P280-P301+P312+P330-P302+P352
Hazard Codes  Xn
Risk Statements  22-36/37/38
Safety Statements  26
WGK Germany  3
RTECS  LV0944000
8-10
HS Code  29339900
NFPA 704
0
2 0

Psoralen price More Price(55)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P8399 Psoralen ≥99% (HPLC) 66-97-7 10mg $129 2024-03-01 Buy
Sigma-Aldrich 73633 Psoralen analytical standard 66-97-7 10mg $508 2022-05-15 Buy
TCI Chemical P2077 Psoralen >99.0%(GC) 66-97-7 20mg $70 2024-03-01 Buy
TCI Chemical P2077 Psoralen >99.0%(GC) 66-97-7 100mg $209 2024-03-01 Buy
Alfa Aesar J60042 Psoralen, 97% 66-97-7 100mg $241.65 2024-03-01 Buy
Product number Packaging Price Buy
P8399 10mg $129 Buy
73633 10mg $508 Buy
P2077 20mg $70 Buy
P2077 100mg $209 Buy
J60042 100mg $241.65 Buy

Psoralen Chemical Properties,Uses,Production

Description

Psoralen is a kind of naturally occurring furocoumarin. It is naturally occurred in the seeds of Psoralea corylifolia as well as in the common fig, celery, parsley, West Indian Satinwood and all citrus fruits. It is capable of binding to DNA via single- and double-strand cross-linking upon photoactivation with UV radiation. It can intercalate with DNA, blocking its synthesis and cell division. For this reason, it is an important mutagen and can be used in related molecular biology studies. It also exhibits anti- proliferative, anti-allergenic and anti-histamine functions. It can also be used in PUVA treatment for skin diseases such as psoriasis, eczema and vitiligo. It is also effective tanning activator in sunscreens. Some of its derivatives, e.g. amino-psoralen, amotosalen HCl, can even inactivate pathogens in blood products.

References

https://en.wikipedia.org/wiki/Psoralen
https://pubchem.ncbi.nlm.nih.gov/compound/Psoralen#section=Top

Chemical Properties

Crystalline Solid

Uses

Use as photochemical probe in biological systems

Uses

Psoralens are phytoalexins; they are used by plants in a defensive response to attacks by fungi and insects. They have also shown photosensitizing and phototoxic effects in animals and humans and have been used in photochemotherapy for management of vitiligo, psoriasis, and mycosis fungoides. Used as photochemical probe in biological systems.

Uses

As photochemical probe in biological systems: P.-S. Song, C.-N. Ou, Ann. N.Y. Acad. Sci. 346, 355 (1980).

Definition

ChEBI: The simplest member of the class of psoralens that is 7H-furo[3,2-g]chromene having a keto group at position 7. It has been found in plants like Psoralea corylifolia and Ficus salicifolia.

Synthesis Reference(s)

Journal of the American Chemical Society, 106, p. 6735, 1984 DOI: 10.1021/ja00334a044
Synthetic Communications, 37, p. 63, 2007 DOI: 10.1080/00397910600978093

Biochem/physiol Actions

Psoralen belongs to the linear type furanocoumarins. It intercalates and induces interstrand cross-links in DNA. On UV exposure psoralen is excited leading to irreversible intercalation with DNA by covalent bond formation. This property of psoralen ultraviolet A light (PUVA) is exploited in treating skin diseases and cutaneous T-cell lymphoma. However, usage psoralen also leads to hepatotoxicity and cytotoxicity by the generation of psoralen photoproducts (POPs). It may be useful in treating osteoporosis

87725-60-8
66-97-7
Synthesis of Psoralen from 7H-Furo[3,2-g][1]benzopyran-7-one, 2,3-dihydro-3-hydroxy-2-(1-hydroxy-1-methylethyl)-, (2S,3R)-
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View Lastest Price from Psoralen manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Psoralen pictures 2024-11-28 Psoralen
66-97-7
US $0.00 / kg 1kg 99.8% 1000 kg BINBO BIOLOGICAL CO.,LTD
Psoralen pictures 2024-11-19 Psoralen
66-97-7
US $50.00 / mg 99.30% 10g TargetMol Chemicals Inc.
Psoralen pictures 2024-11-06 Psoralen
66-97-7
US $0.00-0.00 / kg 0.10000000149011612kg ≥98% 20tons Chongqing Zhihe Biopharmaceutical Co., Ltd.
  • Psoralen pictures
  • Psoralen
    66-97-7
  • US $0.00 / kg
  • 99.8%
  • BINBO BIOLOGICAL CO.,LTD
  • Psoralen pictures
  • Psoralen
    66-97-7
  • US $50.00 / mg
  • 99.30%
  • TargetMol Chemicals Inc.
  • Psoralen pictures
  • Psoralen
    66-97-7
  • US $0.00-0.00 / kg
  • ≥98%
  • Chongqing Zhihe Biopharmaceutical Co., Ltd.

Psoralen Spectrum

PSORALEN Fructus Psoraleae extract Psoralen, >=99% TGRRRRRRRRRRRRRRRRRRRRRRRRRRRRRRRRRRRY MJJNNNNNNN Psoralea corylifolia Linn. Extract furo(2’,3’,7,6)coumarin furo(2’,3’:7’,6)coumarin Furo(4',5',6,7)coumarin furo(4’,5’,6,7)coumarin furo(4’,5’:6,7)coumarin Furo[2',3':7,6]coumarin Furo[2'.3':7.6]coumarin Furo[2’,3’:7,6]coumarin furo[3,2-g]chromen-2-one Furo[3,2-g]chromen-7-one Psoralen, froM Psoralea corylifolia L. PSORALEN, FOR FLUORESCENCE 6-Hydroxy-5-benzofuranacrylic acid γ-lactone PSORALEN90% PSORALEN(SH) PSORALEN hplc PSORALEN WITH HPLC 7H-Furo[3,2-γ],[1]benzopyran-7-one Furo[3,2-γ],coumarin 7H-Furo[3,2-g]benzopyran-7-one, Furo[3,2-g]coumarin 7h-furo[3,2-g]benzopyran-7-one FURO[3,2-G]BENZOPYRAN-7-ONE FURO[3,2-G]COUMARIN 2-Propenoic acid, 3-(6-hydroxy-5-benzofuranyl)-, delta-lactone 2-Propenoicacid,3-(6-hydroxy-5-benzofuranyl)-,δ-lactone 3-(6-hydroxy-5-benzofuranyl)-2-propenoicacidelta-lactone 5-Benzofuranacrylic acid, 6-hydroxy-, delta-lactone 6,7-Furanocoumarin 6-hydroxy-5-benzofuranacrylicacidbeta-lactone 6-hydroxy-5-benzofuranacrylicacidelta-lactone Furo(2',3',7,6)coumarin Furo[4',5':6,7]coumarin Furo[4’,5’:6,7]coumarin Psorline-P Psoralen,7H-Furo[3,2-g]benzopyran-7-one, Furo[3,2-g]coumarin Psoralen (Ficusin) 3-(6-Hydroxy-5-benzofuranyl)-2-propenoic Acid δ-Lactone NSC 404562 Prosuler Psoralen, 99%, from Psoralea corylifolia L. 7-furo[3,2-g][1]benzopyranone Extract psoralen extract in stock Psoralen 66-97-7 PSORALEAE FRUCTUS Psoralen> Psoralen USP/EP/BP Psoralen (psoralene, Ficusin, Furocoumarin) Psoralen brass 7H-FURO[3,2-G][1]BENZOPYRAN-7-ONE FICUSIN 7H-Furo[3,2-g]chromen-7-one Furocoumarin Psoralene