4-Iodophenyl isothiocyanate

98%

Reagent Code: #84002
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CAS Number 2059-76-9

science Other reagents with same CAS 2059-76-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.09 g/mol
Formula C₇H₄INS
badge Registry Numbers
MDL Number MFCD00041091
thermostat Physical Properties
Melting Point 70-76 °C
Boiling Point 299.5°C
inventory_2 Storage & Handling
Density 1.76 g/mL
Storage room temperature, dry

description Product Description

Used primarily as a derivatizing agent in analytical chemistry, it reacts with amines, amino acids, and peptides to form stable thiourea derivatives, aiding in their identification and quantification via techniques like HPLC or mass spectrometry. It is also employed in the synthesis of heterocyclic compounds and in the preparation of biologically active molecules for pharmaceutical research. Additionally, it serves as a labeling reagent in proteomics for studying protein interactions and modifications.

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Test Parameter Specification
APPEARANCE White to Cream to Yellow to Red to Brown Crystals or Powder or Crystalline powder or Lumps or Fused solid
Purity (%) 97.5-100
Melting Point (C) 72.0-82.0
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿76,230.00

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4-Iodophenyl isothiocyanate
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Used primarily as a derivatizing agent in analytical chemistry, it reacts with amines, amino acids, and peptides to form stable thiourea derivatives, aiding in their identification and quantification via techniques like HPLC or mass spectrometry. It is also employed in the synthesis of heterocyclic compounds and in the preparation of biologically active molecules for pharmaceutical research. Additionally, it serves as a labeling reagent in proteomics for studying protein interactions and modifications.

Used primarily as a derivatizing agent in analytical chemistry, it reacts with amines, amino acids, and peptides to form stable thiourea derivatives, aiding in their identification and quantification via techniques like HPLC or mass spectrometry. It is also employed in the synthesis of heterocyclic compounds and in the preparation of biologically active molecules for pharmaceutical research. Additionally, it serves as a labeling reagent in proteomics for studying protein interactions and modifications.

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