ethyl 2-(2,4,5,7-tetrabromo-3-hydroxy-6-oxo-xanthen-9-yl)benzoate

95%

Reagent Code: #181209
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CAS Number 26799-78-0

science Other reagents with same CAS 26799-78-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 675.9 g/mol
Formula C₂₂H₁₂Br₄O₅
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It efficiently generates free radicals upon exposure to ultraviolet or visible light, making it suitable for initiating polymerization in coatings, inks, and adhesives. Its high bromine content enhances intersystem crossing, improving radical generation efficiency. It is especially effective in radical and hybrid curing systems where deep cure and fast reaction kinetics are required. Due to its xanthene backbone, it also exhibits good thermal stability and light absorption in the near-UV range, allowing for efficient use in layered or pigmented formulations.

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inventory 100g
10-20 days ฿6,030.00

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ethyl 2-(2,4,5,7-tetrabromo-3-hydroxy-6-oxo-xanthen-9-yl)benzoate
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Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It efficiently generates free radicals upon exposure to ultraviolet or visible light, making it suitable for initiating polymerization in coatings, inks, and adhesives. Its high bromine content enhances intersystem crossing, improving radical generation efficiency. It is especially effective in radical and hybrid curing systems where deep cure and fast reaction kinetics are required. Due to its

Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It efficiently generates free radicals upon exposure to ultraviolet or visible light, making it suitable for initiating polymerization in coatings, inks, and adhesives. Its high bromine content enhances intersystem crossing, improving radical generation efficiency. It is especially effective in radical and hybrid curing systems where deep cure and fast reaction kinetics are required. Due to its xanthene backbone, it also exhibits good thermal stability and light absorption in the near-UV range, allowing for efficient use in layered or pigmented formulations.

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