2,3-Dimethoxyxanthone

98%

Reagent Code: #175225
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CAS Number 42833-49-8

science Other reagents with same CAS 42833-49-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.25 g/mol
Formula C₁₅H₁₂O₄
thermostat Physical Properties
Boiling Point 423.3℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.27g/ml
Storage Room temperature, sealed, ventilated

description Product Description

Used as a photoinitiator in UV-curable systems, enabling rapid polymerization in coatings, inks, and adhesives upon exposure to ultraviolet light. Also investigated for its potential biological activity, including antimicrobial, antioxidant, and anti-inflammatory properties (such as enzyme inhibition related to inflammation), making it relevant in pharmaceutical and agrochemical research. Additionally serves as a building block in organic synthesis for developing more complex xanthone derivatives with tailored functional properties, and as a reference standard in laboratory analysis of plant extracts to identify structurally similar compounds.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿36,340.00

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2,3-Dimethoxyxanthone
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Used as a photoinitiator in UV-curable systems, enabling rapid polymerization in coatings, inks, and adhesives upon exposure to ultraviolet light. Also investigated for its potential biological activity, including antimicrobial, antioxidant, and anti-inflammatory properties (such as enzyme inhibition related to inflammation), making it relevant in pharmaceutical and agrochemical research. Additionally serves as a building block in organic synthesis for developing more complex xanthone derivatives with ta

Used as a photoinitiator in UV-curable systems, enabling rapid polymerization in coatings, inks, and adhesives upon exposure to ultraviolet light. Also investigated for its potential biological activity, including antimicrobial, antioxidant, and anti-inflammatory properties (such as enzyme inhibition related to inflammation), making it relevant in pharmaceutical and agrochemical research. Additionally serves as a building block in organic synthesis for developing more complex xanthone derivatives with tailored functional properties, and as a reference standard in laboratory analysis of plant extracts to identify structurally similar compounds.

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