2, 3-Dichlorobenzenesulfonic acid

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Reagent Code: #177991
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CAS Number 93648-06-7

science Other reagents with same CAS 93648-06-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.07 g/mol
Formula C₆H₄Cl₂O₃S
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly for azo dyes that require chlorinated aromatic backbones for enhanced stability and color fastness. Also employed in the production of certain pharmaceuticals where the sulfonic acid group aids in solubility and bioavailability. Its chlorinated structure makes it valuable in agrochemical formulations, especially in herbicides and fungicides, where it contributes to the molecule’s reactivity and target specificity. Additionally, it serves as a building block in the preparation of sulfonamide-based compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,900.00
inventory 250mg
10-20 days ฿7,820.00

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2, 3-Dichlorobenzenesulfonic acid
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Used as an intermediate in the synthesis of dyes and pigments, particularly for azo dyes that require chlorinated aromatic backbones for enhanced stability and color fastness. Also employed in the production of certain pharmaceuticals where the sulfonic acid group aids in solubility and bioavailability. Its chlorinated structure makes it valuable in agrochemical formulations, especially in herbicides and fungicides, where it contributes to the molecule’s reactivity and target specificity. Additionally, i

Used as an intermediate in the synthesis of dyes and pigments, particularly for azo dyes that require chlorinated aromatic backbones for enhanced stability and color fastness. Also employed in the production of certain pharmaceuticals where the sulfonic acid group aids in solubility and bioavailability. Its chlorinated structure makes it valuable in agrochemical formulations, especially in herbicides and fungicides, where it contributes to the molecule’s reactivity and target specificity. Additionally, it serves as a building block in the preparation of sulfonamide-based compounds with potential biological activity.

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