4-Chloro-4'-hydroxydiphenyl Ether

≥95.0%(GC)

Reagent Code: #159664
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CAS Number 21567-18-0

science Other reagents with same CAS 21567-18-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.65 g/mol
Formula C₁₂H₉ClO₂
badge Registry Numbers
MDL Number MFCD00125839
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Widely used as an intermediate in the synthesis of triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol), a broad-spectrum antimicrobial agent. Triclosan is incorporated into personal care products, cosmetics, soaps, toothpastes, and medical devices to inhibit the growth of bacteria and fungi. The compound's diphenyl ether structure with chloro and hydroxyl groups facilitates further halogenation and modifications for biocide production. It is also employed in research for developing novel antimicrobials and as a component in the synthesis of heat- and chemical-resistant polymers for plastics and fibers.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿500.00
5g
10-20 days ฿1,380.00
25g
10-20 days ฿6,900.00
4-Chloro-4'-hydroxydiphenyl Ether
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Widely used as an intermediate in the synthesis of triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol), a broad-spectrum antimicrobial agent. Triclosan is incorporated into personal care products, cosmetics, soaps, toothpastes, and medical devices to inhibit the growth of bacteria and fungi. The compound's diphenyl ether structure with chloro and hydroxyl groups facilitates further halogenation and modifications for biocide production. It is also employed in research for developing novel antimicrobials an

Widely used as an intermediate in the synthesis of triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol), a broad-spectrum antimicrobial agent. Triclosan is incorporated into personal care products, cosmetics, soaps, toothpastes, and medical devices to inhibit the growth of bacteria and fungi. The compound's diphenyl ether structure with chloro and hydroxyl groups facilitates further halogenation and modifications for biocide production. It is also employed in research for developing novel antimicrobials and as a component in the synthesis of heat- and chemical-resistant polymers for plastics and fibers.

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