2,6-Diisopropyl-4-nitroaniline

95%

Reagent Code: #167313
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CAS Number 163704-72-1

science Other reagents with same CAS 163704-72-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.28 g/mol
Formula C₁₂H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD03426208
thermostat Physical Properties
Melting Point 125-126 °C
Boiling Point 333.0±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.091±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of azo dyes and pigments, especially for high-performance colorants in inks, coatings, and plastics. Its structure supports the formation of stable, lightfast dyes with strong chroma. Also employed in the development of agrochemicals and certain pharmaceuticals due to its nitro and amine functionalities, which allow for diverse chemical modifications. Additionally, it serves as a building block in the preparation of specialty chemicals requiring sterically hindered aniline derivatives.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,710.00
inventory 1g
10-20 days ฿26,160.00

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2,6-Diisopropyl-4-nitroaniline
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Used primarily as an intermediate in the synthesis of azo dyes and pigments, especially for high-performance colorants in inks, coatings, and plastics. Its structure supports the formation of stable, lightfast dyes with strong chroma. Also employed in the development of agrochemicals and certain pharmaceuticals due to its nitro and amine functionalities, which allow for diverse chemical modifications. Additionally, it serves as a building block in the preparation of specialty chemicals requiring sterical

Used primarily as an intermediate in the synthesis of azo dyes and pigments, especially for high-performance colorants in inks, coatings, and plastics. Its structure supports the formation of stable, lightfast dyes with strong chroma. Also employed in the development of agrochemicals and certain pharmaceuticals due to its nitro and amine functionalities, which allow for diverse chemical modifications. Additionally, it serves as a building block in the preparation of specialty chemicals requiring sterically hindered aniline derivatives.

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