3-Methoxy-o-Phenylenediamine

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Reagent Code: #207780
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CAS Number 37466-89-0

science Other reagents with same CAS 37466-89-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.17 g/mol
Formula C₇H₁₀N₂O
badge Registry Numbers
MDL Number MFCD08276903
thermostat Physical Properties
Melting Point 39-40 °C
Boiling Point 114-116 °C
inventory_2 Storage & Handling
Density 1.170±0.06 g/cm3
Storage 2-8°C

description Product Description

Used in the synthesis of dyes and pigments, particularly for azo dyes which are widely applied in the textile, printing, and coloring industries. It serves as a key intermediate in the production of functional organic compounds, including pharmaceuticals and agrochemicals, due to its amine and methoxy functional groups that facilitate coupling reactions. Also employed in the development of specialty polymers and photochemicals where aromatic amines enhance stability and reactivity. Its structure supports use in research for new heterocyclic compounds with potential biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿790.00
inventory 1g
10-20 days ฿2,230.00
inventory 5g
10-20 days ฿8,900.00
inventory 25g
10-20 days ฿41,200.00

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3-Methoxy-o-Phenylenediamine
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Used in the synthesis of dyes and pigments, particularly for azo dyes which are widely applied in the textile, printing, and coloring industries. It serves as a key intermediate in the production of functional organic compounds, including pharmaceuticals and agrochemicals, due to its amine and methoxy functional groups that facilitate coupling reactions. Also employed in the development of specialty polymers and photochemicals where aromatic amines enhance stability and reactivity. Its structure supports

Used in the synthesis of dyes and pigments, particularly for azo dyes which are widely applied in the textile, printing, and coloring industries. It serves as a key intermediate in the production of functional organic compounds, including pharmaceuticals and agrochemicals, due to its amine and methoxy functional groups that facilitate coupling reactions. Also employed in the development of specialty polymers and photochemicals where aromatic amines enhance stability and reactivity. Its structure supports use in research for new heterocyclic compounds with potential biological activity.

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