DMAB-OH

98%

Reagent Code: #177588
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CAS Number 172611-73-3

science Other reagents with same CAS 172611-73-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.43 g/mol
Formula C₂₀H₂₇NO₃
badge Registry Numbers
MDL Number MFCD01075006
thermostat Physical Properties
Boiling Point 482.9 °C
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of azo dyes and pigments, providing vibrant coloration in textile and printing industries. Also employed in the preparation of functional organic materials for electrochemical sensors due to its redox-active aromatic amine structure. Its hydroxyl and amine groups allow for easy chemical modification, making it valuable in developing photoresists and specialty polymers. Additionally, it serves as a derivatizing agent in analytical chemistry to enhance detection of carbonyl compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,750.00
inventory 250mg
10-20 days ฿2,710.00
inventory 500mg
10-20 days ฿5,280.00
inventory 1g
10-20 days ฿9,600.00
inventory 5g
10-20 days ฿38,400.00
inventory 10g
10-20 days ฿64,000.00

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DMAB-OH
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Used as a key intermediate in the synthesis of azo dyes and pigments, providing vibrant coloration in textile and printing industries. Also employed in the preparation of functional organic materials for electrochemical sensors due to its redox-active aromatic amine structure. Its hydroxyl and amine groups allow for easy chemical modification, making it valuable in developing photoresists and specialty polymers. Additionally, it serves as a derivatizing agent in analytical chemistry to enhance detection

Used as a key intermediate in the synthesis of azo dyes and pigments, providing vibrant coloration in textile and printing industries. Also employed in the preparation of functional organic materials for electrochemical sensors due to its redox-active aromatic amine structure. Its hydroxyl and amine groups allow for easy chemical modification, making it valuable in developing photoresists and specialty polymers. Additionally, it serves as a derivatizing agent in analytical chemistry to enhance detection of carbonyl compounds.

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