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5-Aminoquinoline, 99%|182294|611-34-7

5-Aminoquinoline, 99%

Cat. No JK182294_1_G
J&K Chemical

Product Information

Product Name
5-Aminoquinoline, 99%
Brand Name
J&K
Product Number
182294
CAS
611-34-7
Molecular Formula
C9H8N2
Molecular Weight
144.17
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
5-Quinolinamine
PubChem CID
11911
IUPAC Name
quinolin-5-amine
InChI Key
XMIAFAKRAAMSGX-UHFFFAOYSA-N
SMILES
C1=CC(=C2C=CC=NC2=C1)N

Properties

Melting Point
106-109
Boiling Point
310

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
Precautionary Statement
P280
P321
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317

References Data Source From Pubchem

Synthesis, Characterization, Theoretical Analysis, and Solvatochromic Evaluation of Aminoquinoline-Based AIEE-Active Schiff Base, along with its Application as a Probe for Hg2+ and Fe2+ Detection
Publication Name: Journal of Fluorescence
Publication Date: 2026-02-19
DOI: 10.1007/s10895-025-04681-5

Synthesis, Properties, and Applications of Aminoquinoline-Derived Schiff Bases and Their Metal Complexes
Publication Name: Russian Journal of Bioorganic Chemistry
Publication Date: 2026-01-22
DOI: 10.1134/s1068162025601880

Uncovering druggable hotspots on Pin1 via X-ray crystallographic fragment screening
Publication Name: European Journal of Medicinal Chemistry
Publication Date: 2025-12-05
DOI: 10.1016/j.ejmech.2025.118048

Organoselenium-based quinoline sensor for superoxide detection and its antitumor activities
Publication Name: Journal of Chemical Sciences
Publication Date: 2024-06-20
DOI: 10.1007/s12039-024-02276-4

Controllable Ring-opening Polymerization of δ-Valerolactone Catalyzed by Quinolinyl-Urea/MTBD Systems
Publication Name: Chinese Journal of Polymer Science
Publication Date: 2024-04-25
DOI: 10.1007/s10118-024-3127-3

5-Aminoquinoline, 99%

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