6-Hydroxyquinolin-2(1H)-one
Names
[ CAS No. ]:
19315-93-6
[ Name ]:
6-Hydroxyquinolin-2(1H)-one
[Synonym ]:
6-Hydroxy-2(H)-quinolinone
2,6-dihydroxyquinoline
EINECS 209-454-6
2(1H)-Quinolinone, 6-hydroxy-
6-hydroxy-quinolone
2,6-Dihydroxyquinoline 6-Hydroxycarbostyril
6-Hydroxy-2(1H)-quinolinone
6-hydroxyquinoline-2-one
6-HYDROXYQUINOLINE
6-hydroxyquinolin-2(1H)-one
quinoline-2,6-diol
6-hydroxy-2-quinolinone
2,6-quinolinediol
6-hydroxycarbostyril
6-hydroxy-1H-quinolin-2-one
MFCD00047611
6-Hydroxyquinolin-2-one
Chemical & Physical Properties
[ Density]:
1.4±0.1 g/cm3
[ Boiling Point ]:
441.7±25.0 °C at 760 mmHg
[ Melting Point ]:
188-190 °C(lit.)
[ Molecular Formula ]:
C9H7NO2
[ Molecular Weight ]:
161.157
[ Flash Point ]:
220.9±23.2 °C
[ Exact Mass ]:
161.047684
[ PSA ]:
53.35000
[ LogP ]:
1.59
[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C
[ Index of Refraction ]:
1.743
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ RTECS ]:
VC4130000
[ HS Code ]:
2933499090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2933499090
[ 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%
Articles
Food Chem. 141(3) , 1888-94, (2013)
The aim of this work was to characterise new UV-absorbing compounds (UAC) in cow milk in order to gain an overview of the molecular diversity of the minor bioactive constituents, that could be used to...
In vivo elution of tryptophan metabolites and other aromatic nitrogen compounds from cholesterol pellets implanted into mouse bladders. Bryan GT, et al.Cancer Res. 24(4) , 586-595, (1964)
Mouse bladder carcinogenicity of certain tryptophan metabolites and other aromatic nitrogen compounds suspended in cholesterol. Bryan GT, et al.
Cancer Res. 24(4) , 596-602, (1964)