p-Dimethylaminobenzaldehyde

Reagent grade, white powder

Reagent Code: #224422
label
Alias p-dimethylaminobenzaldehyde; 4-dimethylaminobenzaldehyde, p-dimethylaminobenzaldehyde, N,N-dimethyl-4-aminobenzaldehyde, p-dimethylaminobenzaldehyde
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CAS Number 100-10-7

science Other reagents with same CAS 100-10-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.19 g/mol
Formula C₉H₁₁NO
badge Registry Numbers
EC Number 200-661-7
MDL Number MFCD00003381
thermostat Physical Properties
Melting Point 72-75 °C(lit.)
Boiling Point 176-177 °C /17 mmHg
inventory_2 Storage & Handling
Density 1.10 g/mL at 20 °C
Storage Room temperature, sealed

description Product Description

Used as a reagent in analytical chemistry for the detection and determination of primary aromatic amines and indoles. It forms intensely colored condensation products, making it valuable in colorimetric assays. Commonly employed in the Ehrlich’s reagent for identifying indoles in urine, drugs, and biological samples. Also applied in the development of dyes and in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its strong electron-donating group enhances reactivity in electrophilic substitution reactions.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 72 - 75
APPEARANCE White powder
Purity (%) 98 - 100
IGNITION RESIDUE (AS SULFATE) 0 - 0.15

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿580.00
25g
10-20 days ฿1,960.00
100g
10-20 days ฿5,880.00
500g
10-20 days ฿18,980.00
p-Dimethylaminobenzaldehyde
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Used as a reagent in analytical chemistry for the detection and determination of primary aromatic amines and indoles. It forms intensely colored condensation products, making it valuable in colorimetric assays. Commonly employed in the Ehrlich’s reagent for identifying indoles in urine, drugs, and biological samples. Also applied in the development of dyes and in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its strong electron-donating group enhances reactivity in electrophilic substitution reactions.
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