2,4-Dichloro-5-hydroxyaniline

95%

Reagent Code: #176166
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CAS Number 39489-79-7

science Other reagents with same CAS 39489-79-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.016 g/mol
Formula C₆H₅Cl₂NO
badge Registry Numbers
MDL Number MFCD00186187
thermostat Physical Properties
Melting Point 133-137 °C
Boiling Point 292.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.56 g/cm3
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of azo dyes and pigments, this compound contributes to the production of colorants for textiles, inks, and coatings. Its functional groups allow for diazotization and coupling reactions, making it valuable in creating complex dye molecules with specific color properties. Additionally, it serves in the development of certain pharmaceuticals and agrochemicals where chlorinated aniline derivatives are required. Due to its reactivity and structural features, it is also employed in research for designing new organic compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,800.00
inventory 25g
10-20 days ฿13,910.00

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2,4-Dichloro-5-hydroxyaniline
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Used primarily as an intermediate in the synthesis of azo dyes and pigments, this compound contributes to the production of colorants for textiles, inks, and coatings. Its functional groups allow for diazotization and coupling reactions, making it valuable in creating complex dye molecules with specific color properties. Additionally, it serves in the development of certain pharmaceuticals and agrochemicals where chlorinated aniline derivatives are required. Due to its reactivity and structural features,

Used primarily as an intermediate in the synthesis of azo dyes and pigments, this compound contributes to the production of colorants for textiles, inks, and coatings. Its functional groups allow for diazotization and coupling reactions, making it valuable in creating complex dye molecules with specific color properties. Additionally, it serves in the development of certain pharmaceuticals and agrochemicals where chlorinated aniline derivatives are required. Due to its reactivity and structural features, it is also employed in research for designing new organic compounds with potential biological activity.

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