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CAS RN: 484-20-8 | Product Number: B2840

Bergapten


Purity: >98.0%(GC)
Synonyms:
  • 4-Methoxyfuro[3,2-g]benzopyran-7-one
  • 5-Methoxypsoralen
Product Documents:
1G
€107.00
Contact Us 30  
5G
€343.00
6   2  

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Product Number B2840
Purity / Analysis Method >98.0%(GC)
Molecular Formula / Molecular Weight C__1__2H__8O__4 = 216.19 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
Condition to Avoid Light Sensitive
CAS RN 484-20-8
Reaxys Registry Number 19560
PubChem Substance ID 87558737
Merck Index (14) 1157
Specifications
Appearance White to Light yellow powder to crystal
Purity(GC) min. 98.0 %
Melting point 189.0 to 193.0 °C
NMR confirm to structure
Properties (reference)
Melting Point 191 °C
Maximum Absorption Wavelength 480(MeOH) nm
Solubility (soluble in) Ether
Solubility (slightly sol. in) Alcohol, Benzene, Chloroform
GHS
Pictogram Pictogram Pictogram
Signal Word Danger
Hazard Statements H317 : May cause an allergic skin reaction.
H350 : May cause cancer.
Precautionary Statements P261 : Avoid breathing dust.
P201 : Obtain special instructions before use.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P308 + P313 : IF exposed or concerned: Get medical advice/ attention.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P333 + P313 : If skin irritation or rash occurs: Get medical advice/ attention.
Related Laws:
EC Number 207-604-5
RTECS# LV1300000
Transport Information:
HS Number 2932209090
Application
5-Methoxypsoralen (5-MOP): A Photosensitizer in Combination with UV-A irradiation, called PUVA

5-Methoxypsoralen (5-MOP), 8-methoxypsoralen (8-MOP) [X0009] and 4,5',8-trimethylpsoralen [T2267] are naturally occurring linear psoralens (furocoumarins). They have been successfully used as photosensitizers in combination with UV-A irradiation which is called the psoralen-based PUVA (psoralen + UV-A) to manage dermatological diseases, such as psoriasis, vitiligo and cancer. Reportedly, the most important mechanism implies the [2 + 2] cycloaddition photoreaction of psoralen and a DNA pyrimidine nucleobase. The formation of psoralen-pyrimidine adducts prevents the division of the injured cells. In another photoreaction, the activated psoralen can transfer energy to molecular oxygen to generate reactive radicals or excited singlet oxygen which becomes prone to damage the membrane of the harmed cell. In addition, 5-MOP and 8-MOP work as Cytochrome P450 inhibitors. (The product is for research purpose only.)

References


PubMed Literature


TCIMAIL
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