55627
7-Hydroxy-4-methyl-2(1H)-quinolone
suitable for fluorescence, ≥97.0% (HPLC)
别名:
7-Hydroxy-4-methylcarbostyryl, 2,7-Dihydroxy-4-methylquinoline
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关于此项目
经验公式（希尔记法）:
C10H9NO2
化学文摘社编号:
分子量:
175.18
UNSPSC Code:
12352202
NACRES:
NA.32
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1528280
InChI
1S/C10H9NO2/c1-6-4-10(13)11-9-5-7(12)2-3-8(6)9/h2-5,12H,1H3,(H,11,13)
SMILES string
Cc1cc(O)nc2cc(O)ccc12
InChI key
MYEVEFULPUKTSZ-UHFFFAOYSA-N
assay
≥97.0% (HPLC)
form
solid
mp
≥250 °C (lit.)
solubility
DMF: soluble, DMSO: soluble, alcohols: soluble
fluorescence
λex 321 nm; λem 357 nm (pH 5.0), λex 351 nm; λem 428 nm in 0.1 M Tris pH 9.0
suitability
suitable for fluorescence
Application
7-Hydroxy-4-methyl-2(1H)-quinolone may be used as a reference material in the study and analysis of quinolone derivatives in research areas such as carcinogenicity and quinolone metabolism.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
E J La Voie et al.
Carcinogenesis, 4(9), 1169-1173 (1983-09-01)
Quinoline is a hepatocarcinogen in mice and rats, a mutagen in Salmonella typhimurium, and induces unscheduled DNA synthesis in primary cultures of rat hepatocytes. In contrast, isoquinoline has not been shown to be genotoxic. The metabolites of quinoline and isoquinoline
A Rüger et al.
Biological chemistry Hoppe-Seyler, 374(7), 479-488 (1993-07-01)
A bacterial strain, designated K1, which utilizes 4-methylquinoline and quinoline as sole source of carbon, nitrogen and energy was isolated from soil. Based on its morphological and physiological characteristics, it was classified as Pseudomonas putida biovar B. Four metabolites of
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