270873
2-Hydroxyquinoline
98%
Synonym(s):
2-Quinolinol, Carbostyril
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C9H7NO
CAS Number:
Molecular Weight:
145.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
200-420-6
MDL number:
Assay:
98%
Form:
crystals
Quality Level
assay
98%
form
crystals
mp
198-199 °C (lit.)
solubility
alcohol: soluble(lit.), diethyl ether: soluble(lit.), dilute HCl: soluble(lit.), water: slightly soluble (1 g/950mL)(lit.)
SMILES string
Oc1ccc2ccccc2n1
InChI
1S/C9H7NO/c11-9-6-5-7-3-1-2-4-8(7)10-9/h1-6H,(H,10,11)
InChI key
LISFMEBWQUVKPJ-UHFFFAOYSA-N
General description
2-Hydroxyquinoline is a specific inhibitor of plaque paraoxonase1 (PON1).
Application
2-Hydroxyquinoline was used to obtain the design of the platinum(IV) complexes with intense bands shifted towards longer wavelengths. The Pt(IV) complexes are inert stable prodrugs that were photoactivated to produce Pt(II) species with promising anticancer activity.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Juan Peris-Vicente et al.
Antibiotics (Basel, Switzerland), 8(4) (2019-11-17)
A method based on micellar liquid chromatography was developed to determine oxolinic acid, ciprofloxacin, enrofloxacin, and sarafloxacin in eggs and egg products. The antimicrobial drugs were obtained in a micellar solution which was directly injected. The analytes were resolved using
Shailesh Kumar Patidar et al.
Biotechnology for biofuels, 11, 102-102 (2018-04-11)
Amelioration of biofuel feedstock of microalgae using sustainable means through synthetic ecology is a promising strategy. The co-cultivation model (Tetraselmis striata and Pelagibaca bermudensis) was evaluated for the robust biofuel production under varying stressors as well as with the selected
Edyta Stec et al.
Chembiochem : a European journal of chemical biology, 12(11), 1724-1730 (2011-06-15)
Aurachins are quinoline alkaloids isolated from the myxobacterium Stigmatella aurantiaca. They are substituted with an isoprenoid side chain and act as potent inhibitors in the electron transport chain. A biosynthetic gene cluster that contains at least five genes (auaA-auaE) has
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 270873-1G | 04061826257630 |
| 270873-5G | 04061833545836 |