Interesting facts
Interesting Facts About Quinolin-8-ol
Quinolin-8-ol, often referred to as 8-hydroxyquinoline, is a fascinating compound with a rich history and diverse applications in various fields. Here are some captivating insights:
- Chemical Structure: This compound features a unique bicyclic structure that consists of a quinoline ring fused with a hydroxyl group. This structural arrangement is significant in enhancing its reactivity and interaction with other substances.
- Biological Activity: Quinolin-8-ol exhibits interesting biological properties. It has been studied for its potential as an antimicrobial agent and shows promise in inhibiting various enzymes, which can be beneficial in medicinal chemistry.
- Complexation Potential: One of the remarkable features of quinolin-8-ol is its ability to form stable complexes with metal ions. This property is harnessed in analytical chemistry for the detection of metals such as zinc and copper, serving as an effective chelating agent.
- Applications: This compound is not just limited to research laboratories; it finds its way into practical applications including:
- Use in anti-corrosive coatings, providing protection for various metal surfaces.
- Serving as a fluorescent probe in biological studies, allowing scientists to visualize cellular processes.
- Involvement in the synthesis of pharmaceuticals and other organic compounds.
- Historical Significance: Quinolin-8-ol has a storied past and was first synthesized in the late 19th century. Its discovery opened avenues for the development of countless derivatives that continue to contribute to science and health today.
In summary, quinolin-8-ol is a compound that bridges the realms of chemistry, biology, and material science. Its multifaceted applications and biological relevance make it a noteworthy subject of study for chemists and scientists alike.
Synonyms
8-HYDROXYQUINOLINE
quinolin-8-ol
148-24-3
8-quinolinol
Oxyquinoline
Oxine
Quinophenol
Oxychinolin
8-Quinol
8-Oxyquinoline
Phenopyridine
Oxin
Oxybenzopyridine
Hydroxybenzopyridine
1-Azanaphthalene-8-ol
8-Hydroxychinolin
Bioquin
Tumex
8-Chinolinol
8-Hydroxy-chinolin
Fennosan H 30
8-OQ
Fennosan
Oxyquinol
o-Oxychinolin
Usaf ek-794
8-Oxychinolin
Quinoline, 8-hydroxy-
8 Hydroxyquinoline
Fennosan HF-15
Oxyquinoline [USAN]
Caswell No. 719
NCI-C55298
NSC 2039
MFCD00006807
8-hydroxy-quinoline
CCRIS 340
Oxoquinoline
NSC 615011
HSDB 4073
NSC-2039
EINECS 205-711-1
UNII-5UTX5635HP
8-hydroxy quinoline
EPA Pesticide Chemical Code 059803
NSC-285166
NSC-402623
NSC-615011
BRN 0114512
5UTX5635HP
DTXSID5020730
CHEBI:48981
AI3-00483
NSC-48037
NSC-54230
NSC-82404
NSC-82405
NSC-82409
NSC-82410
NSC-82412
NSC285166
J2.960B
DTXCID30730
MLS002702126
CHEMBL310555
quinoline-8-ol
EC 205-711-1
Oxyquinoline (8-Hydroxyquinoline)
5-21-03-00252 (Beilstein Handbook Reference)
NSC 82404
NSC615011
Oxyquinoline (USAN)
NCGC00090708-03
NCGC00090708-05
OXYQUINOLINE (II)
OXYQUINOLINE [II]
WLN: T66 BNJ JQ
Oxine;8-Hydroxyquinoline;Quinophenol;8-Quinolinone
8-HYDROXYQUINOLINE (IARC)
8-HYDROXYQUINOLINE [IARC]
8-Chinolinol [Czech]
o-Oxychinolin [German]
8 Oxyquinoline
8 Quinolinol
CAS-148-24-3
Manganese, bis(8-quinolinolato)-
SMR000112313
8-Hydroxy-chinolin [German]
Oxychinoline
8-Oxyquinolin
8-Quinolinone
8-Quinolol
8-hydroxiquinoline
8-hydroxychinoline
8-hydroxylquinoline
HQY
UDDER BALM
8-Quinolinol, p.a.
Spectrum_001053
3vh9
8-Hydroxyquinoline Oxine
Spectrum2_000697
Spectrum3_000534
Spectrum4_000465
Spectrum5_001280
8-Hydroxyquinoline, 99%
NCIMech_000694
OXYQUINOLINE [HSDB]
cid_1923
NCIStruc1_000152
NCIStruc2_000240
Oxyquinol Reference Spectrum
NCIOpen2_000962
NCIOpen2_001020
NCIOpen2_001220
NCIOpen2_004264
OXYQUINOLINE [VANDF]
Pesticide Code: 059803
SCHEMBL37189
BSPBio_002147
KBioGR_000910
KBioSS_001533
MLS001055492
BIDD:ER0371
DivK1c_000757
8-Hydroxyquinoline (Standard)
SPBio_000853
8-Hydroxyquinoline, crystalline
HYDROXYQUINOLINE [VANDF]
8-HYDROXYQUINOLINE [MI]
BDBM32203
HMS502F19
HY-B1005R
KBio1_000757
KBio2_001533
KBio2_004101
KBio2_006669
KBio3_001647
HYDROXYQUINOLINE [WHO-DD]
NSC2039
NINDS_000757
8-Quinolinol (7CI,8CI,9CI)
HY-B1005
STR00721
Tox21_113083
Tox21_202986
Tox21_400006
8-Oxychinolin, 8-Quinolinol, Oxine
CCG-35870
NSC 48037
NSC 54230
NSC 82405
NSC 82409
NSC 82410
NSC 82412
NSC402623
s4547
STK943764
8-Hydroxyquinoline ACS Reagent Grade
AKOS001061311
AC-5109
CS-4502
DB11145
FH12040
NSC 285166
NSC 402623
PS-4553
SB40773
8-Hydroxyquinoline, ACS reagent, 99%
IDI1_000757
NCGC00090708-01
NCGC00090708-02
NCGC00090708-04
NCGC00090708-06
NCGC00090708-07
NCGC00090708-08
NCGC00090708-11
NCGC00260531-01
NCI60_001712
NCI60_002335
SBI-0051472.P003
DB-012222
H0305
NS00010316
8-Quinolinol, JIS special grade, >=99.0%
8-Quinolinol, Vetec(TM) reagent grade, 99%
EN300-17403
C19434
D05321
P17615
US9394254, 6
8-Quinolinol, PESTANAL(R), analytical standard
AB00052065_08
8-Quinolinol, >=99% (perchloric acid titration)
AP-065/40180076
Q270162
CU-01000012874-2
BRD-K66808046-065-01-1
BRD-K66808046-065-03-7
Z56926518
F0001-0526
InChI=1/C9H7NO/c11-8-5-1-3-7-4-2-6-10-9(7)8/h1-6,11
205-711-1
8-Quinolinol, puriss. p.a., ACS reagent, for the detection and determination of Al, Mg and others, >=99.0% (NT)
8-Quinolinol, puriss. p.a., ACS reagent, reag. Ph. Eur., >=99% (perchloric acid titration)
Solubility of Quinolin-8-ol (C9H7NO)
Quinolin-8-ol, also known by its IUPAC name 8-hydroxyquinoline, displays a moderate solubility profile that is of particular interest in various applications. When considering its solubility characteristics, several key points can be noted:
In conclusion, while quinolin-8-ol is primarily hydrophobic, its solubility in various organic solvents and the influence of pH on its solubility make it a compound of interest for further studies in chemical formulation and biochemistry. As with many organic compounds, understanding its solubility behavior is crucial for effectively utilizing this compound in diverse chemical contexts.