3-Aminoquinoline

97%

Reagent Code: #135336
label
Alias 3-aminoazanaphane; 3-aminoquinoline; aminoquinoline; 3-quinolineamine; 3-aminoquinoline, 98%; Β-aminozanaphane; quinoline-3-amine
fingerprint
CAS Number 580-17-6

science Other reagents with same CAS 580-17-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.17 g/mol
Formula C₉H₈N₂
badge Registry Numbers
EC Number 209-455-1
MDL Number MFCD00006772
thermostat Physical Properties
Melting Point 91-92 °C(lit.)
Boiling Point 137 °C / 1mmHg
inventory_2 Storage & Handling
Density 1.21 g/cm3
Storage Room temperature

description Product Description

Used as a fluorescent derivatization reagent in analytical chemistry, particularly for the detection and quantification of carbonyl compounds such as aldehydes and ketones. Its high sensitivity to fluorescence enables trace analysis in environmental and biological samples. Also employed in the synthesis of pharmaceuticals and agrochemicals due to its nitrogen-containing heterocyclic structure, which serves as a building block in various drug development processes. Additionally, it acts as a ligand in coordination chemistry for metal ion detection and catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿600.00
inventory 5g
10-20 days ฿2,490.00
inventory 25g
10-20 days ฿10,630.00
3-Aminoquinoline
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Used as a fluorescent derivatization reagent in analytical chemistry, particularly for the detection and quantification of carbonyl compounds such as aldehydes and ketones. Its high sensitivity to fluorescence enables trace analysis in environmental and biological samples. Also employed in the synthesis of pharmaceuticals and agrochemicals due to its nitrogen-containing heterocyclic structure, which serves as a building block in various drug development processes. Additionally, it acts as a ligand in coo

Used as a fluorescent derivatization reagent in analytical chemistry, particularly for the detection and quantification of carbonyl compounds such as aldehydes and ketones. Its high sensitivity to fluorescence enables trace analysis in environmental and biological samples. Also employed in the synthesis of pharmaceuticals and agrochemicals due to its nitrogen-containing heterocyclic structure, which serves as a building block in various drug development processes. Additionally, it acts as a ligand in coordination chemistry for metal ion detection and catalysis.

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