p-Nitrobenzaldehyde

Reagent grade, 97.0% (GC)

Reagent Code: #216668
label
Alias p-nitrobenzaldehyde;4-nitrobenzaldehyde
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CAS Number 555-16-8

science Other reagents with same CAS 555-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.13 g/mol
Formula C₇H₅NO₃
badge Registry Numbers
MDL Number MFCD00007346
thermostat Physical Properties
Melting Point 103-106 °C(lit.)
inventory_2 Storage & Handling
Density 1.496 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 production of certain antibiotics and antipyretic drugs. Also employed in the preparation of nonlinear optical materials and as a precursor in the manufacture of pigments and corrosion inhibitors. Its electrophilic nature makes it valuable in organic transformations such as condensation reactions and the formation of Schiff bases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿360.00
inventory 100g
10-20 days ฿1,100.00
inventory 500g
10-20 days ฿4,580.00
inventory 2.5kg
10-20 days ฿22,890.00
p-Nitrobenzaldehyde
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Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It plays a key role in the production of certain antibiotics and antipyretic drugs. Also employed in the preparation of nonlinear optical materials and as a precursor in the manufacture of pigments and corrosion inhibitors. Its electrophilic nature makes it valuable in organic transformations such as condensation reactions and the formation of Schiff bases.

Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It plays a key role in the production of certain antibiotics and antipyretic drugs. Also employed in the preparation of nonlinear optical materials and as a precursor in the manufacture of pigments and corrosion inhibitors. Its electrophilic nature makes it valuable in organic transformations such as condensation reactions and the formation of Schiff bases.

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