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

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Identification
Molecular formula
C9H6I NO4S
CAS number
1248-33-5
IUPAC name
8-hydroxy-7-iodo-quinoline-5-sulfonic acid
State
State

At room temperature, 8-Hydroxy-7-iodoquinoline-5-sulfonic acid is in a solid state. It remains stable under normal storage conditions, which include shielding from moisture and excessive heat.

Melting point (Celsius)
260.00
Melting point (Kelvin)
533.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
364.20g/mol
Molar mass
364.1970g/mol
Density
2.5400g/cm3
Appearence

8-Hydroxy-7-iodoquinoline-5-sulfonic acid is typically a light yellow crystalline solid. It can appear as a powder or finely divided crystals. The color variation may depend on the purity and the specific form of the sample.

Comment on solubility

Solubility of 8-Hydroxy-7-iodo-quinoline-5-sulfonic Acid

8-hydroxy-7-iodo-quinoline-5-sulfonic acid is a fascinating compound known for its distinctive chemical properties, particularly in relation to solubility. Here are some important points regarding its solubility:

  • Solvent Dependence: This compound exhibits varying solubility when exposed to different solvents. Generally, it is considered soluble in water, which is a significant property for its applications in biological and chemical research.
  • pH Sensitivity: The solubility may also be influenced by the pH of the solution. It tends to be more soluble in acidic conditions, allowing for better interaction in various experimental setups.
  • Complex Formation: In certain conditions, the compound can form complexes with metal ions, further enhancing its solubility profile in those specific environments.

Overall, the solubility of 8-hydroxy-7-iodo-quinoline-5-sulfonic acid highlights its versatility in various chemical contexts and underscores its utility as a reagent in synthetic and analytical chemistry.

Interesting facts

Interesting Facts about 8-hydroxy-7-iodo-quinoline-5-sulfonic acid

8-hydroxy-7-iodo-quinoline-5-sulfonic acid, often abbreviated as a complex chemical name, belongs to the class of quinoline derivatives which are widely studied due to their diverse biological properties. This compound is particularly noted for its role in various chemical and biological applications. Here are some fascinating insights:

  • Fluorescent Properties: One of the remarkable features of this compound is its fluorescent capability, which makes it useful in several analytical chemistry applications, including fluorescence microscopy and as a marker in biological assays.
  • Biological Activity: The quinoline structure is renowned for its involvement in medicinal chemistry. Many quinoline derivatives exhibit significant antibacterial and antimalarial activities, contributing to their exploration in drug development.
  • Research Importance: The intricate structure of 8-hydroxy-7-iodo-quinoline-5-sulfonic acid opens doors for chemical modifications that could lead to novel therapeutic agents. Scientists are constantly investigating such derivatives for potential uses in treating various diseases.
  • Analytical Applications: In laboratory settings, this compound may be employed as a reagent for the detection of metals or in titration processes due to its specific reactivity and ability to form stable complexes with metal ions.

As a compound featuring both iodine and sulfonic acid functional groups, 8-hydroxy-7-iodo-quinoline-5-sulfonic acid illustrates the intricate relationship between structure and function in chemistry. Its multifaceted applications underscore the importance of studying such compounds, as they may lead to groundbreaking discoveries in both academia and industry. The versatility and reactivity of this molecule indeed make it a topic of ongoing research and interest.

Synonyms
547-91-1
Ferron
Loretin
8-Hydroxy-7-iodo-5-quinolinesulfonic acid
Meditrene
Quiniophen
Yatren
Anayodin
Quinoxyl
Sefona
Yellon
5-Quinolinesulfonic acid, 8-hydroxy-7-iodo-
Ferron (analytical reagent)
7-Iodooxine-5-sulfonic acid
5-Sulfo-7-iodo-8-quinolinol
Jod-hydroxychinolin-sulfonsaeure
8-Hydroxy-7-iodoquinolinesulfonic acid
UNII-6E8Y02XFEI
5-Sulfo-7-iodo-8-hydroxyquinoline
NSC 3784
EINECS 208-938-4
6E8Y02XFEI
5-Iodo-8-quinolinol-5-sulfonic acid
8-Hydroxy-7-iod-5-chinolinsulfonsaeure
BRN 0223832
DTXSID1046136
7-Iodo-5-sulfonic acid-8-hydroxyquinoline
7-Iodo-8-hydroxylquinoline-5-sulfonic acid
NSC-3784
m-iodo-o-hydroxyquinolineanasulfonic acid
DTXCID9026136
8-HYDROXY-7-IODO-5-QUINOLINESULFONIC ACID [MI]
8-HYDROXY-7-IODO-5-QUINIOLINE SULFONIC ACID [WHO-DD]
iodoquinoleine
5Sulfo7iodo8quinolinol
7Iodooxine5sulfonic acid
5Sulfo7iodo8hydroxyquinoline
Jodhydroxychinolinsulfonsaeure
8Hydroxy7iod5chinolinsulfonsaeure
8Hydroxy7iodoquinolinesulfonic acid
7Iodo5sulfonic acid8hydroxyquinoline
7Iodo8hydroxyquinoline5sulfonic acid
7Iodo8hydroxylquinoline5sulfonic acid
8Hydroxy7iodoquinoline5sulphonic acid
5Quinolinesulfonic acid, 8hydroxy7iodo
8-hydroxy-7-iodoquinolin-1-ium-5-sulfonate
8-HYDROXY-7-IODO-5-QUINIOLINE SULFONIC ACID
208-938-4
5-22-07-00582 (beilstein handbook reference)
8-Hydroxy-7-iodoquinoline-5-sulfonic acid
CHINIOFON
7-Iodo-8-hydroxyquinoline-5-sulfonic acid
8-Hydroxy-7-iodoquinoline-5-sulphonic acid
NCGC00160410-01
C9H6INO4S
Quiniofon; Sefona; Sodium chiniofon; Yatren; Yochinol
CAS-547-91-1
Ferron (Standard)
MFCD00006793
8-hydroxy-7-iodo-quinoline-5-sulfonic acid
Cambridge id 5192841
SCHEMBL94250
MLS004774009
CHEMBL1788402
NSC3784
CHEBI:135481
ZBJWWKFMHOAPNS-UHFFFAOYSA-N
WLN: T66 BNJ GSWQ II JQ
ALBB-024964
HY-W103183R
8-Hydroxy-7-iodoquinoline sulfonate
Tox21_111795
BBL002814
CCG-44937
STK371235
AKOS005203037
Tox21_111795_1
DS-1838
FH30084
HY-W103183
quinoline, 8-hydroxy-7-iodo-5-sulpho-
NCGC00160410-02
8-Hydroxy-7-iodoquinoline-5-sulfonicacid
SMR001812723
DB-052649
8-Hydroxy-7-iodo-5-quinoline sulfonic acid
CS-0155825
H0254
NS00016708
O11676
AG-664/13101011
Q5101067
SR-01000634736-1
BRD-K52284881-236-01-6
BRD-K52284881-236-02-4
8-Hydroxy-7-iodo-5-quinolinesulfonic acid, for spectrophotometric det. of Fe(III), >=98.5%