3-Nitrobenzoic acid

99%

Reagent Code: #216745
label
Alias m-nitrobenzoic acid;3-nitrobenzoic acid
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CAS Number 121-92-6

science Other reagents with same CAS 121-92-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.12 g/mol
Formula C₇H₅NO₄
badge Registry Numbers
EC Number 204-508-5
MDL Number MFCD00007251
thermostat Physical Properties
Melting Point 139-141 °C(lit.)
inventory_2 Storage & Handling
Density 1.494 g/cm3
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It plays a key role in the preparation of 3-aminobenzoic acid derivatives via reduction, which are important in the manufacture of certain drugs, fluorescent dyes, and UV-absorbing compounds. Also employed in organic research for nitration and carboxylation studies due to its nitro and carboxylic acid functional groups. Its derivatives are explored in the development of corrosion inhibitors and polymer additives.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿280.00
inventory 100g
10-20 days ฿340.00
inventory 500g
10-20 days ฿930.00
inventory 2.5kg
10-20 days ฿4,000.00
inventory 10kg
10-20 days ฿15,880.00

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3-Nitrobenzoic acid
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Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It plays a key role in the preparation of 3-aminobenzoic acid derivatives via reduction, which are important in the manufacture of certain drugs, fluorescent dyes, and UV-absorbing compounds. Also employed in organic research for nitration and carboxylation studies due to its nitro and carboxylic acid functional groups. Its derivatives are explored in the development of corrosion inhibitors and polymer additives.
Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It plays a key role in the preparation of 3-aminobenzoic acid derivatives via reduction, which are important in the manufacture of certain drugs, fluorescent dyes, and UV-absorbing compounds. Also employed in organic research for nitration and carboxylation studies due to its nitro and carboxylic acid functional groups. Its derivatives are explored in the development of corrosion inhibitors and polymer additives.
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