This is a demo store. No orders will be fulfilled.

4-Quinolinol - >98.0%(HPLC), high purity , CAS No.611-36-9

    Grade & Purity:
  • ≥98%(HPLC)
In stock
Item Number
Q160821
Grouped product items
SKU Size
Availability
Price Qty
Q160821-1g
1g
10
$9.90
Q160821-5g
5g
4
$16.90
Q160821-10g
10g
4
$29.90
Q160821-25g
25g
2
$49.90
Q160821-50g
50g
1
$79.90
Q160821-100g
100g
2
$139.90

Basic Description

Synonyms KUC100207 | STL129466 | 4(1H)-Quinolinone | AKOS005738113 | PB43148 | 4-Quinolinol, 98% | SY002846 | 1,4-dihydroquinolin-4-one | HYDROXYQUINOLINE, 4- | Q0029 | SCHEMBL10031 | 4-OXO-1,4-DIHYDROQUINOLINE | MFCD00006777 | BDBM14321 | EN300-54449 | Z818727120
Specifications & Purity ≥98%(HPLC)
Storage Temp Argon charged
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Quinolines and derivatives
Subclass Quinolones and derivatives
Intermediate Tree Nodes Not available
Direct Parent Hydroquinolones
Alternative Parents Hydroquinolines  Pyridines and derivatives  Benzenoids  Vinylogous amides  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Dihydroquinolone - Dihydroquinoline - Benzenoid - Pyridine - Heteroaromatic compound - Vinylogous amide - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as hydroquinolones. These are compounds containing a hydrogenated quinoline bearing a ketone group.
External Descriptors a small molecule

Associated Targets(Human)

ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EP300 Tchem Histone acetyltransferase p300 (1259 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KAT2B Tchem Histone acetyltransferase PCAF (884 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (221 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

BCHE Cholinesterase (8742 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Brain (1 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488184235
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488184235
IUPAC Name 1H-quinolin-4-one
INCHI InChI=1S/C9H7NO/c11-9-5-6-10-8-4-2-1-3-7(8)9/h1-6H,(H,10,11)
InChIKey PMZDQRJGMBOQBF-UHFFFAOYSA-N
Smiles C1=CC=C2C(=C1)C(=O)C=CN2
Isomeric SMILES C1=CC=C2C(=C1)C(=O)C=CN2
WGK Germany 3
RTECS VC4070000
PubChem CID 69141
Molecular Weight 145.16
Beilstein 2900
Reaxy-Rn 1524969

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

14 results found

Lot Number Certificate Type Date Item
D2423339 Certificate of Analysis Mar 25, 2024 Q160821
K2317154 Certificate of Analysis Oct 30, 2023 Q160821
K2317155 Certificate of Analysis Oct 30, 2023 Q160821
K2317156 Certificate of Analysis Oct 30, 2023 Q160821
K2317157 Certificate of Analysis Oct 30, 2023 Q160821
J1822065 Certificate of Analysis Aug 11, 2022 Q160821
J1822062 Certificate of Analysis Aug 11, 2022 Q160821
B2211172 Certificate of Analysis Jan 12, 2022 Q160821
B2211171 Certificate of Analysis Jan 12, 2022 Q160821
B2211174 Certificate of Analysis Jan 12, 2022 Q160821
B2211173 Certificate of Analysis Jan 12, 2022 Q160821
B2211124 Certificate of Analysis Jan 12, 2022 Q160821
B2211197 Certificate of Analysis Jan 12, 2022 Q160821
D23261191 Certificate of Analysis Jan 12, 2022 Q160821

Show more⌵

Chemical and Physical Properties

Solubility Soluble in methanol
Sensitivity Light and air sensitive
Melt Point(°C) 200-206℃
Molecular Weight 145.160 g/mol
XLogP3 0.600
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 145.053 Da
Monoisotopic Mass 145.053 Da
Topological Polar Surface Area 29.100 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 198.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Shengxiang Yi, Gaowei Zhang, Mingyan Liu, Wenjie Yu, Guohua Cheng, Liping Luo, Fangjian Ning.  (2023)  Citrus Honey Ameliorates Liver Disease and Restores Gut Microbiota in Alcohol–Feeding Mice.  Nutrients,  15  (5): (1078). 
2. Gui-Fang Wu, Xiao-Lan Jiang, Yu-Zhou Gong, Ya-Dong Hu, Xiao-Lin Bai, Xun Liao.  (2019)  Ligand fishing of anti-neurodegenerative components from Lonicera japonica using magnetic nanoparticles immobilised with monoamine oxidase B.  JOURNAL OF SEPARATION SCIENCE,  42  (6): (1289-1298). 

Solution Calculators

Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.