2-Isopropyl-4-nitroaniline

95%

Reagent Code: #200931
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CAS Number 94831-94-4

science Other reagents with same CAS 94831-94-4

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inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. It plays a key role in the production of dinitroaniline-type compounds, which are known for their pre-emergent herbicidal activity. These herbicides inhibit cell division in susceptible weed species, making them effective in crop protection. The compound is also utilized in the development of dyes and pigments due to its aromatic amine structure, which can undergo diazotization and coupling reactions to form colored azo compounds. Its nitro and amine functional groups make it a valuable building block in organic synthesis for pharmaceuticals and specialty chemicals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,960.00
inventory 250mg
10-20 days ฿23,670.00
inventory 1g
10-20 days ฿58,960.00
2-Isopropyl-4-nitroaniline
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Used primarily as an intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. It plays a key role in the production of dinitroaniline-type compounds, which are known for their pre-emergent herbicidal activity. These herbicides inhibit cell division in susceptible weed species, making them effective in crop protection. The compound is also utilized in the development of dyes and pigments due to its aromatic amine structure, which can undergo diazotization and coup

Used primarily as an intermediate in the synthesis of agricultural chemicals, particularly herbicides and insecticides. It plays a key role in the production of dinitroaniline-type compounds, which are known for their pre-emergent herbicidal activity. These herbicides inhibit cell division in susceptible weed species, making them effective in crop protection. The compound is also utilized in the development of dyes and pigments due to its aromatic amine structure, which can undergo diazotization and coupling reactions to form colored azo compounds. Its nitro and amine functional groups make it a valuable building block in organic synthesis for pharmaceuticals and specialty chemicals.

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