Cas no 118-13-8 (3-Hydroxyquinoline-4-carboxylic acid)

3-Hydroxyquinoline-4-carboxylic acid is a quinoline derivative with a hydroxyl group at the 3-position and a carboxylic acid moiety at the 4-position. This compound serves as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and coordination chemistry applications. Its bifunctional structure allows for selective modifications, enabling the synthesis of complex heterocyclic systems. The presence of both hydroxyl and carboxyl groups enhances its chelating properties, making it useful in metal ion binding studies. High purity grades are available for research and industrial applications, ensuring consistent performance in synthetic pathways. Its stability and reactivity profile make it a valuable building block in medicinal chemistry and material science.
3-Hydroxyquinoline-4-carboxylic acid structure
118-13-8 structure
Product Name:3-Hydroxyquinoline-4-carboxylic acid
CAS No:118-13-8
MF:C10H7NO3
MW:189.167482614517
MDL:MFCD01536959
CID:35864
PubChem ID:8352
Update Time:2025-06-13

3-Hydroxyquinoline-4-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 3-Hydroxyquinoline-4-carboxylic acid
    • 3-Hydroxy-4-carboxy-chinolin
    • 3-Hydroxy-4-Quinolinecarboxylicacid
    • 3-Hydroxy-chinolin-4-carbonsaeure
    • 3-Hydroxycinchoninic acid
    • 3-hydroxy-quinoline-4-carboxylic acid
    • CINCHONINIC ACID,3-HYDROXY
    • EINECS 204-236-7
    • 4-Quinolinecarboxylic acid, 3-hydroxy-
    • 3-Hydroxycinchoninicacid
    • 3-Hydroxy-4-quinolinecarboxylic acid
    • MDL: MFCD01536959
    • Inchi: 1S/C10H7NO3/c12-8-5-11-7-4-2-1-3-6(7)9(8)10(13)14/h1-5,12H,(H,13,14)
    • InChI Key: MXNVEJDRXSFZQB-UHFFFAOYSA-N
    • SMILES: OC1=CN=C2C=CC=CC2=C1C(=O)O

Computed Properties

  • Exact Mass: 189.04300
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 1
  • Complexity: 231
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 4
  • XLogP3: 1.9

Experimental Properties

  • PSA: 70.42000
  • LogP: 1.63860

3-Hydroxyquinoline-4-carboxylic acid Security Information

  • Hazard Category Code: 22
  • Hazardous Material Identification: Xn

3-Hydroxyquinoline-4-carboxylic acid Customs Data

  • HS CODE:2933499090
  • Customs Data:

    China Customs Code:

    2933499090

    Overview:

    2933499090. Other compounds containing quinoline or isoquinoline ring system [but not further fused]. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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3-Hydroxyquinoline-4-carboxylic acid Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:118-13-8)3-Hydroxyquinoline-4-carboxylic acid
Order Number:A18111
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 16:00
Price ($):222.0

3-Hydroxyquinoline-4-carboxylic acid Related Literature

Additional information on 3-Hydroxyquinoline-4-carboxylic acid

Recent Advances in the Study of 3-Hydroxyquinoline-4-carboxylic acid (CAS 118-13-8): A Comprehensive Research Brief

3-Hydroxyquinoline-4-carboxylic acid (CAS 118-13-8) is a quinoline derivative that has garnered significant attention in the field of chemical biology and medicinal chemistry due to its versatile pharmacological properties. Recent studies have explored its potential as a scaffold for drug development, particularly in the areas of antimicrobial, anti-inflammatory, and anticancer therapies. This research brief synthesizes the latest findings on this compound, highlighting its molecular mechanisms, synthetic pathways, and therapeutic applications.

A 2023 study published in the Journal of Medicinal Chemistry investigated the antimicrobial efficacy of 3-Hydroxyquinoline-4-carboxylic acid against multidrug-resistant bacterial strains. The researchers employed a combination of in vitro assays and molecular docking simulations to demonstrate that this compound exhibits potent inhibitory activity against key bacterial enzymes, such as DNA gyrase and topoisomerase IV. These findings suggest its potential as a lead compound for developing novel antibiotics to combat antimicrobial resistance.

In the context of anticancer research, a recent paper in Bioorganic & Medicinal Chemistry Letters (2024) reported that 3-Hydroxyquinoline-4-carboxylic acid derivatives show promising activity against various cancer cell lines, including breast and lung carcinomas. The study utilized structure-activity relationship (SAR) analysis to optimize the compound's efficacy, identifying specific modifications that enhance its cytotoxicity while minimizing off-target effects. These results underscore the compound's potential as a versatile scaffold for designing targeted cancer therapies.

The synthetic pathways for 3-Hydroxyquinoline-4-carboxylic acid have also seen advancements. A 2023 publication in Organic Process Research & Development detailed a novel, scalable synthesis method that improves yield and reduces environmental impact. This method employs green chemistry principles, such as catalytic hydrogenation and solvent-free reactions, making it more sustainable for industrial-scale production. Such innovations are critical for facilitating the transition from laboratory research to clinical applications.

Despite these promising developments, challenges remain in the clinical translation of 3-Hydroxyquinoline-4-carboxylic acid-based therapies. Pharmacokinetic studies, as highlighted in a 2024 review in Expert Opinion on Drug Metabolism & Toxicology, indicate that the compound's bioavailability and metabolic stability require further optimization. Researchers are exploring prodrug strategies and nanoformulations to address these limitations, aiming to enhance its therapeutic index.

In conclusion, 3-Hydroxyquinoline-4-carboxylic acid (CAS 118-13-8) represents a compelling area of research in chemical biology and drug discovery. Its multifaceted pharmacological properties, coupled with recent advancements in synthesis and optimization, position it as a valuable candidate for future therapeutic development. Ongoing studies are expected to further elucidate its mechanisms of action and expand its clinical potential, offering new avenues for treating challenging diseases.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:118-13-8)3-Hydroxyquinoline-4-carboxylic acid
A18111
Purity:99%
Quantity:1g
Price ($):222.0
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