4-Amino-N,N-diethylaniline sulfate salt

for spectrophotometric det. of S2-,Cl2, ≥99%

Reagent Code: #126799
label
Alias CD-1; TSS; p-amino-N,N-diethylaniline sulfate; Diethyl-p-phenylenediamine sulfate, N,N'-diethyl-1,4-phenylenediamine sulfate, N ,N-Diethyl-p-phenylenediamine sulfate, 6065-27-6
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CAS Number 6283-63-2

science Other reagents with same CAS 6283-63-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.33 g/mol
Formula C₁₀H₁₆N₂H₂SO₄
badge Registry Numbers
EC Number 228-500-6
MDL Number MFCD00012993
thermostat Physical Properties
Melting Point 184-186 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in the photographic industry as a developing agent for color films and papers. It plays a crucial role in the formation of dyes during the color development process, enhancing image quality and color accuracy. Additionally, it is employed in certain analytical chemistry applications, such as spectrophotometric detection of sulfide (S2-) and chlorine (Cl2), for detecting and quantifying specific chemical compounds. Its effectiveness in these processes stems from its ability to act as an electron donor, facilitating redox reactions essential for image development and chemical analysis.

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Test Parameter Specification
APPEARANCE White to Light Yellow and Faint Brown to Light Brown and Faint Red to Light Red Powder or Crystals or Granules or Chunks
Purity (%) 98.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿5,990.00

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4-Amino-N,N-diethylaniline sulfate salt
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Used primarily in the photographic industry as a developing agent for color films and papers. It plays a crucial role in the formation of dyes during the color development process, enhancing image quality and color accuracy. Additionally, it is employed in certain analytical chemistry applications, such as spectrophotometric detection of sulfide (S2-) and chlorine (Cl2), for detecting and quantifying specific chemical compounds. Its effectiveness in these processes stems from its abili
Used primarily in the photographic industry as a developing agent for color films and papers. It plays a crucial role in the formation of dyes during the color development process, enhancing image quality and color accuracy. Additionally, it is employed in certain analytical chemistry applications, such as spectrophotometric detection of sulfide (S2-) and chlorine (Cl2), for detecting and quantifying specific chemical compounds. Its effectiveness in these processes stems from its ability to act as an electron donor, facilitating redox reactions essential for image development and chemical analysis.
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