Cas no 547-91-1 (8-Hydroxy-7-iodoquinoline-5-sulfonic acid)

8-Hydroxy-7-iodoquinoline-5-sulfonic acid is a halogenated quinoline derivative with notable applications in analytical chemistry and organic synthesis. Its structure, featuring both hydroxy and sulfonic acid functional groups, enhances its chelating properties, making it useful as a complexing agent for metal ions. The iodine substituent further contributes to its reactivity, particularly in electrophilic substitution reactions. This compound is often employed in spectrophotometric determinations due to its ability to form stable, colored complexes with transition metals. Its water solubility, imparted by the sulfonic acid group, facilitates its use in aqueous systems. The compound’s stability and selectivity make it a valuable reagent in research and industrial processes.
8-Hydroxy-7-iodoquinoline-5-sulfonic acid structure
547-91-1 structure
Product Name:8-Hydroxy-7-iodoquinoline-5-sulfonic acid
CAS No:547-91-1
MF:C9H6INO4S
MW:351.117713451386
MDL:MFCD00006793
CID:38252
PubChem ID:24879346
Update Time:2025-08-02

8-Hydroxy-7-iodoquinoline-5-sulfonic acid Chemical and Physical Properties

Names and Identifiers

    • 8-Hydroxy-7-iodoquinoline-5-sulfonic acid
    • 7-Iodo-8-hydroxyquinoline-5-sulfonic acid
    • Ferron
    • 8-Hydroxy-7-iodo-5-quinolinesulfonic acid
    • Chiniofon
    • 7-Iodo-8-Hydroxychinolin 5-Sulphonic Acid
    • 7-iodo-8-hydroxyquinoline-5-sulphonic acid
    • 8-hydroxy-7-iodoquinoline-5-sulphonic acid
    • 8-hydroxy-7-iodoquinolinium-5-sulphonate
    • CHINIOFON ACID
    • Chinoiodin
    • Chinoiodine
    • Fluorescein sodiuM salt
    • LORETIN
    • Loretin
    • meditrene
    • Quiniofon
    • quiniophen
    • yellon
    • Quinoxyl
    • Anayodin
    • Sefona
    • Yatren
    • Ferron (analytical reagent)
    • 5-Quinolinesulfonic acid, 8-hydroxy-7-iodo-
    • C9H6INO4S
    • 7-Iodooxine-5-sulfonic acid
    • 8-Hydroxy-7-iodoquinolinesulfonic acid
    • 5-Sulfo-7-iodo-8-quinolinol
    • Jod-hydroxychinolin-sulfonsaeure
    • 5-Sulfo-7-iodo-8-hydroxyquinoline
    • NCGC00160410-01
    • BRN 0223832
    • NSC 3784
    • 8-Hydroxy-7-iodoquinoline sulfonate
    • MFCD00006793
    • DS-1838
    • AKOS005203037
    • Cambridge id 5192841
    • FT-0632363
    • 7-Iodo-8-hydroxylquinoline-5-sulfonic acid
    • A830370
    • 2-AMINO-1-MORPHOLIN-4-YL-ETHANONEHCL
    • 7-Iodo-5-sulfonic acid-8-hydroxyquinoline
    • O11676
    • CHEMBL1788402
    • CHEBI:135481
    • BRD-K52284881-236-01-6
    • 8-HYDROXY-7-IODO-5-QUINIOLINE SULFONIC ACID [WHO-DD]
    • SCHEMBL94250
    • Quiniofon; Sefona; Sodium chiniofon; Yatren; Yochinol
    • 8-Hydroxy-7-iod-5-chinolinsulfonsaeure
    • 6E8Y02XFEI
    • m-iodo-o-hydroxyquinolineanasulfonic acid
    • NSC3784
    • NSC-3784
    • SMR001812723
    • SR-01000634736-1
    • 8-Hydroxy-7-iodo-5-quinolinesulfonic acid, for spectrophotometric det. of Fe(III), >=98.5%
    • CAS-547-91-1
    • H0254
    • 8002-90-2
    • NS00016708
    • MLS004774009
    • HY-W103183
    • 8-Hydroxy-7-iodoquinoline-5-sulfonicacid
    • 547-91-1
    • 8-hydroxy-7-iodo-quinoline-5-sulfonic acid;7-Iodo-8-hydroxyquinoline-5-sulfonic acid
    • WLN: T66 BNJ GSWQ II JQ
    • Tox21_111795_1
    • EINECS 208-938-4
    • DTXCID9026136
    • Tox21_111795
    • 5-Iodo-8-quinolinol-5-sulfonic acid
    • DTXSID1046136
    • CCG-44937
    • 8-HYDROXY-7-IODO-5-QUINOLINESULFONIC ACID [MI]
    • 8-hydroxy-7-iodo-quinoline-5-sulfonic acid
    • UNII-6E8Y02XFEI
    • 8-Hydroxy-7-iodo-5-quinoline sulfonic acid
    • CS-0155825
    • Q5101067
    • NCGC00160410-02
    • ZBJWWKFMHOAPNS-UHFFFAOYSA-N
    • 8Hydroxy7iodoquinoline5sulphonic acid
    • 5Quinolinesulfonic acid, 8hydroxy7iodo
    • ALBB-024964
    • 7Iodo5sulfonic acid8hydroxyquinoline
    • STK371235
    • 8-hydroxy-7-iodoquinolin-1-ium-5-sulfonate
    • 7Iodooxine5sulfonic acid
    • AG-664/13101011
    • BRD-K52284881-236-02-4
    • 7Iodo8hydroxylquinoline5sulfonic acid
    • iodoquinoleine
    • 8-HYDROXY-7-IODO-5-QUINIOLINE SULFONIC ACID
    • BBL002814
    • 8Hydroxy7iodoquinolinesulfonic acid
    • 7Iodo8hydroxyquinoline5sulfonic acid
    • quinoline, 8-hydroxy-7-iodo-5-sulpho-
    • 5Sulfo7iodo8quinolinol
    • Jodhydroxychinolinsulfonsaeure
    • DB-052649
    • 8Hydroxy7iod5chinolinsulfonsaeure
    • 5Sulfo7iodo8hydroxyquinoline
    • FH30084
    • HY-W103183R
    • 208-938-4
    • Ferron (Standard)
    • MDL: MFCD00006793
    • Inchi: 1S/C9H6INO4S/c10-6-4-7(16(13,14)15)5-2-1-3-11-8(5)9(6)12/h1-4,12H,(H,13,14,15)
    • InChI Key: ZBJWWKFMHOAPNS-UHFFFAOYSA-N
    • SMILES: IC1=C(C2C(=CC=CN=2)C(=C1)S(=O)(=O)O)O

Computed Properties

  • Exact Mass: 350.90600
  • Monoisotopic Mass: 350.906
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 1
  • Complexity: 355
  • 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: 2
  • XLogP3: 1.2
  • Topological Polar Surface Area: 95.9

Experimental Properties

  • Color/Form: Yellow powder
  • Density: 1.9414 (estimate)
  • Melting Point: 269-270?°C (dec.) (lit.)
  • Refractive Index: 1.776
  • Stability/Shelf Life: Stable.
  • PSA: 95.87000
  • LogP: 2.87250
  • Merck: 4826
  • FEMA: 2694
  • Solubility: It is very slightly soluble in water and ethanol, but practically insoluble in ether, chloroform and benzene. 1g of this product is dissolved in 500ml cold water and 170ml boiling water.

8-Hydroxy-7-iodoquinoline-5-sulfonic acid Security Information

  • Symbol: GHS05
  • Prompt:dangerous
  • Signal Word:Danger
  • Hazard Statement: H314
  • Warning Statement: P280,P305+P351+P338,P310
  • Hazardous Material transportation number:UN 2585 8/PG 3
  • WGK Germany:2
  • Hazard Category Code: 34
  • Safety Instruction: S26; S36/37/39; S45
  • RTECS:VC2800000
  • Hazardous Material Identification: C
  • HazardClass:8
  • PackingGroup:III
  • Storage Condition:Store at room temperature
  • Packing Group:III
  • Risk Phrases:R34
  • Safety Term:S26;S36/37/39;S45
  • Packing Group:III

8-Hydroxy-7-iodoquinoline-5-sulfonic 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%

8-Hydroxy-7-iodoquinoline-5-sulfonic acid Pricemore >>

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Additional information on 8-Hydroxy-7-iodoquinoline-5-sulfonic acid

Introduction to 8-Hydroxy-7-iodoquinoline-5-sulfonic acid (CAS No. 547-91-1)

8-Hydroxy-7-iodoquinoline-5-sulfonic acid (CAS No. 547-91-1) is a versatile compound with significant applications in the fields of medicinal chemistry, biochemistry, and pharmaceutical research. This compound, characterized by its unique molecular structure, has garnered attention for its potential therapeutic properties and its role in various biochemical processes. In this comprehensive introduction, we will delve into the chemical properties, biological activities, and recent research advancements associated with 8-Hydroxy-7-iodoquinoline-5-sulfonic acid.

The chemical structure of 8-Hydroxy-7-iodoquinoline-5-sulfonic acid is composed of a quinoline ring substituted with a hydroxyl group at the 8-position, an iodine atom at the 7-position, and a sulfonic acid group at the 5-position. This intricate arrangement imparts specific physicochemical properties to the molecule, making it suitable for various applications in scientific research and drug development.

In terms of physicochemical properties, 8-Hydroxy-7-iodoquinoline-5-sulfonic acid is a white crystalline solid with a molecular weight of approximately 360.04 g/mol. It is soluble in water and exhibits good stability under standard laboratory conditions. The presence of the sulfonic acid group enhances its solubility in aqueous solutions, which is advantageous for its use in biological assays and pharmaceutical formulations.

The biological activities of 8-Hydroxy-7-iodoquinoline-5-sulfonic acid have been extensively studied in recent years. One of the key areas of interest is its potential as an antimicrobial agent. Research has shown that this compound exhibits broad-spectrum antimicrobial activity against various bacterial strains, including both Gram-positive and Gram-negative bacteria. The mechanism of action is believed to involve the disruption of bacterial cell membranes and the inhibition of essential metabolic pathways.

Beyond its antimicrobial properties, 8-Hydroxy-7-iodoquinoline-5-sulfonic acid has also been investigated for its anti-inflammatory effects. Studies have demonstrated that it can inhibit the production of pro-inflammatory cytokines such as TNF-alpha and IL-6, which are involved in the pathogenesis of inflammatory diseases. This makes it a promising candidate for the development of new anti-inflammatory drugs.

In addition to its direct biological activities, 8-Hydroxy-7-iodoquinoline-5-sulfonic acid has been explored as a lead compound for drug discovery. Its unique structure provides a scaffold for the design and synthesis of novel derivatives with enhanced therapeutic properties. For instance, researchers have synthesized analogs with modified substituents on the quinoline ring to improve their pharmacological profiles and reduce potential side effects.

The use of 8-Hydroxy-7-iodoquinoline-5-sulfonic acid in combination therapies has also been a focus of recent studies. Combining this compound with other antimicrobial or anti-inflammatory agents has shown synergistic effects, leading to improved treatment outcomes. This approach is particularly relevant in addressing multidrug-resistant pathogens and chronic inflammatory conditions.

In the context of drug delivery systems, 8-Hydroxy-7-iodoquinoline-5-sulfonic acid has been incorporated into various formulations to enhance its bioavailability and target specificity. Nanoparticle-based delivery systems have shown promise in improving the pharmacokinetic properties of this compound, allowing for more effective and sustained release at the site of action.

The safety profile of 8-Hydroxy-7-iodoquinoline-5-sulfonic acid has been evaluated through preclinical studies. These studies have indicated that it is generally well-tolerated at therapeutic doses, with minimal toxicity observed in animal models. However, further clinical trials are necessary to fully assess its safety and efficacy in human subjects.

In conclusion, 8-Hydroxy-7-iodoquinoline-5-sulfonic acid (CAS No. 547-91-1) is a multifaceted compound with significant potential in medicinal chemistry and pharmaceutical research. Its unique chemical structure confers specific physicochemical properties that make it suitable for various applications, including antimicrobial and anti-inflammatory therapies. Ongoing research continues to uncover new insights into its biological activities and therapeutic potential, paving the way for innovative drug development strategies.

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