4-tert-butyl-N,N-dimethylaniline

97%

Reagent Code: #218393
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CAS Number 2909-79-7

science Other reagents with same CAS 2909-79-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.286 g/mol
Formula C₁₂H₁₉N
badge Registry Numbers
MDL Number MFCD00008833
thermostat Physical Properties
Melting Point -45 °C(estimate)
Boiling Point 250-253 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of azo dyes and pigments, particularly for high-performance colorants in inks and coatings. Acts as a coupling component in the formation of thermochromic and photochromic materials, making it valuable in smart dyes and sensors. Employed in organic synthesis for its electron-rich aromatic structure, facilitating electrophilic substitution reactions. Also utilized in the preparation of functional polymers and as a building block in pharmaceuticals and agrochemicals. Its tert-butyl group enhances steric stability and solubility in nonpolar systems, improving performance in specialty applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,550.00
inventory 5g
10-20 days ฿4,770.00
inventory 25g
10-20 days ฿18,980.00
4-tert-butyl-N,N-dimethylaniline
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Used as a key intermediate in the synthesis of azo dyes and pigments, particularly for high-performance colorants in inks and coatings. Acts as a coupling component in the formation of thermochromic and photochromic materials, making it valuable in smart dyes and sensors. Employed in organic synthesis for its electron-rich aromatic structure, facilitating electrophilic substitution reactions. Also utilized in the preparation of functional polymers and as a building block in pharmaceuticals and agrochemic

Used as a key intermediate in the synthesis of azo dyes and pigments, particularly for high-performance colorants in inks and coatings. Acts as a coupling component in the formation of thermochromic and photochromic materials, making it valuable in smart dyes and sensors. Employed in organic synthesis for its electron-rich aromatic structure, facilitating electrophilic substitution reactions. Also utilized in the preparation of functional polymers and as a building block in pharmaceuticals and agrochemicals. Its tert-butyl group enhances steric stability and solubility in nonpolar systems, improving performance in specialty applications.

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