Quinoline-8-sulfonic acid

98%

Reagent Code: #228461
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CAS Number 85-48-3

science Other reagents with same CAS 85-48-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.23 g/mol
Formula C₉H₇NO₃S
badge Registry Numbers
MDL Number MFCD00024037
thermostat Physical Properties
Melting Point >300°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of dyes and fluorescent whiteners due to its sulfonic acid group enhancing water solubility and binding to substrates. Employed in coordination chemistry to form metal complexes with catalytic or luminescent properties. Acts as a derivatizing agent for detecting amines and amino acids in analytical methods. Also explored in the development of photoactive compounds and sensors owing to the quinoline ring’s favorable photophysical traits.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿350.00
inventory 10g
10-20 days ฿600.00
inventory 25g
10-20 days ฿1,400.00
inventory 100g
10-20 days ฿5,540.00
Quinoline-8-sulfonic acid
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Used as an intermediate in the synthesis of dyes and fluorescent whiteners due to its sulfonic acid group enhancing water solubility and binding to substrates. Employed in coordination chemistry to form metal complexes with catalytic or luminescent properties. Acts as a derivatizing agent for detecting amines and amino acids in analytical methods. Also explored in the development of photoactive compounds and sensors owing to the quinoline ring’s favorable photophysical traits.

Used as an intermediate in the synthesis of dyes and fluorescent whiteners due to its sulfonic acid group enhancing water solubility and binding to substrates. Employed in coordination chemistry to form metal complexes with catalytic or luminescent properties. Acts as a derivatizing agent for detecting amines and amino acids in analytical methods. Also explored in the development of photoactive compounds and sensors owing to the quinoline ring’s favorable photophysical traits.

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