N2-[2-(Dimethylamino)phenyl]-N1,N1-dimethyl-1,2-benzenediamine

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Reagent Code: #215385
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CAS Number 1072901-09-7

science Other reagents with same CAS 1072901-09-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.36 g/mol
Formula C₁₆H₂₁N₃
badge Registry Numbers
MDL Number MFCD28556923
thermostat Physical Properties
Boiling Point 356.5±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.103±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used primarily in the synthesis of triarylmethane dyes, this compound acts as a key intermediate in producing vibrant colorants for textiles, inks, and coatings. Its structure supports strong chromophoric properties, making it valuable in developing dyes with high molar absorptivity and lightfastness. Additionally, it finds use in analytical chemistry as a derivatizing agent for detecting specific functional groups in organic molecules. The amine groups enable easy modification for tailored solubility and binding characteristics, expanding its utility in specialty chemical formulations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,010.00
inventory 250mg
10-20 days ฿14,080.00
inventory 1g
10-20 days ฿41,950.00

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N2-[2-(Dimethylamino)phenyl]-N1,N1-dimethyl-1,2-benzenediamine
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Used primarily in the synthesis of triarylmethane dyes, this compound acts as a key intermediate in producing vibrant colorants for textiles, inks, and coatings. Its structure supports strong chromophoric properties, making it valuable in developing dyes with high molar absorptivity and lightfastness. Additionally, it finds use in analytical chemistry as a derivatizing agent for detecting specific functional groups in organic molecules. The amine groups enable easy modification for tailored solubility an

Used primarily in the synthesis of triarylmethane dyes, this compound acts as a key intermediate in producing vibrant colorants for textiles, inks, and coatings. Its structure supports strong chromophoric properties, making it valuable in developing dyes with high molar absorptivity and lightfastness. Additionally, it finds use in analytical chemistry as a derivatizing agent for detecting specific functional groups in organic molecules. The amine groups enable easy modification for tailored solubility and binding characteristics, expanding its utility in specialty chemical formulations.

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