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Methoxsalen

Base Information Edit
  • Chemical Name:Methoxsalen
  • CAS No.:298-81-7
  • Deprecated CAS:12692-94-3
  • Molecular Formula:C12H8O4
  • Molecular Weight:216.193
  • Hs Code.:29322090
  • European Community (EC) Number:206-066-9
  • NSC Number:757114,45923
  • UN Number:1759
  • UNII:U4VJ29L7BQ
  • DSSTox Substance ID:DTXSID8020830
  • Nikkaji Number:J2.983A
  • Wikipedia:Methoxsalen
  • Wikidata:Q408570
  • NCI Thesaurus Code:C643
  • RXCUI:6854
  • Pharos Ligand ID:X7VNVLGFGBAW
  • Metabolomics Workbench ID:42889
  • ChEMBL ID:CHEMBL416
  • Mol file:298-81-7.mol
Methoxsalen

Synonyms:8 Methoxypsoralen;8 MOP;8-Methoxypsoralen;8-MOP;8MOP;Ammoidin;Deltasoralen;Dermox;Geroxalen;Méladinine;Meladinina;Meladinine;Meloxine;Methoxa Dome;Methoxa-Dome;Methoxsalen;Oxsoralen;Oxsoralen Ultra;Oxsoralen-Ultra;Puvalen;Ultramop;Xanthotoxin

Suppliers and Price of Methoxsalen
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Xanthotoxin
  • 20mg
  • $ 297.00
  • TRC
  • 8-MethoxyPsoralen
  • 50mg
  • $ 65.00
  • TCI Chemical
  • Xanthotoxin >98.0%(GC)
  • 100mg
  • $ 14.00
  • TCI Chemical
  • Xanthotoxin >98.0%(GC)
  • 1g
  • $ 43.00
  • Sigma-Aldrich
  • Xanthotoxin analytical standard
  • 50mg
  • $ 102.00
  • Sigma-Aldrich
  • 8-Methoxypsoralen analytical standard
  • 5g
  • $ 206.00
  • Sigma-Aldrich
  • 8-Methoxypsoralen analytical standard
  • 1g
  • $ 43.10
  • Sigma-Aldrich
  • Methoxsalen United States Pharmacopeia (USP) Reference Standard
  • 200mg
  • $ 366.00
  • Medical Isotopes, Inc.
  • Methoxsalen
  • 10 mg
  • $ 890.00
  • Labseeker
  • 8-METHOXYPSORALEN 99
  • 1kg
  • $ 7170.00
Total 153 raw suppliers
Chemical Property of Methoxsalen Edit
Chemical Property:
  • Appearance/Colour:Crystalline Solid 
  • Vapor Pressure:4.33E-07mmHg at 25°C 
  • Melting Point:148-150 °C(lit.) 
  • Refractive Index:1.635 
  • Boiling Point:414.795 °C at 760 mmHg 
  • Flash Point:204.661 °C 
  • PSA:52.58000 
  • Density:1.368 g/cm3 
  • LogP:2.54780 
  • Storage Temp.:-20°C Freezer, Under Inert Atmosphere 
  • Solubility.:H2O: slightly soluble 
  • Water Solubility.:PRACTICALLY INSOLUBLE 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:216.04225873
  • Heavy Atom Count:16
  • Complexity:325
  • Transport DOT Label:Corrosive
Purity/Quality:

more than 98% *data from raw suppliers

Xanthotoxin *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn, Toxic
  • Hazard Codes:Xn,T 
  • Statements: 22-43-46-45-34 
  • Safety Statements: 36/37-53-45-36/37/39-26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Other Organic Compounds
  • Canonical SMILES:COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2
  • Recent ClinicalTrials:Extracorporeal Photopheresis in Sezary Syndrome
  • Recent EU Clinical Trials:Phase II multicenter study of extracorporeal photopheresis with UvadexTM plus standard steroid treatment for high risk acute Graft-versus-Host Disease
  • Description 8-methoxypsoralen (also known as methoxsalen) is a naturally occurring furocoumarin compound existing in several species of plants such as Psoralea corylifolia. It is a photoactive substance that can form DNA adducts upon UVA irradiation. It is a drug used for the treatment of psoriasis, eczema, vitiligo, and some kinds of cutaneous lymphomas associated with the exposure of skin to the UVA or light from lamps or sunlight. Its mechanism of action is through inhibiting the synthesis of the deoxyribonucleic acid (DNA). After the activation, it can preferentially bind to the guanine and cytosine molecules of DNA, further leading to the cross-linking of DNA, thus inhibiting the DNA synthesis. It can further inhibit the RNA and protein synthesis at high concentration. It is extracted from Ammi majus. 8-Methoxypsoralen (8-MOP) and other psoralens are naturally found in plants, including common fruit and vegetable crops.
  • Uses 8-Methoxypsoralen, is used in Photochemotherapy (methoxsalen with long wave ultraviolet radiation) is indicated for the repigmentation of idiopathic vitiligo. It is also used in Photopheresis (methoxsalen with long wave ultraviolet radiation of white blood cells) is indicated for use with the UVAR* System in the palliative treatment of the skin manifestations of cutaneous T-cell lymphoma. antipsoriatic, pigmentation agent Naturally occurring analog of Psoralen (P839800). Use in treatment of psoriasis and mycosis fungoides. For the treatment of psoriasis and vitiligo A potent suicide inhibitor of cytochrome P-450. Naturally occurring analog of psoralen. Use in treatment of psoriasis and mycosis fungoides
  • Indications Methoxsalen has effects similar to those of trioxsalen. Methoxsalen is superior to trioxsalen in producing erythema and tanning and is the drug used in PUVA therapy. Methoxsalen is also available as a 1% lotion.
  • Therapeutic Function Dermal pigmentation enhancer
Technology Process of Methoxsalen

There total 48 articles about Methoxsalen which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With potassium carbonate; In acetone; Reflux; Inert atmosphere;
DOI:10.1007/s00044-014-1312-6
Guidance literature:
With sodium tetrahydroborate; sodium carbonate; In toluene; Heating;
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