108928
6-Methylquinoline
98%
Synonym(s):
p-Toluquinoline, NSC 4152
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About This Item
Empirical Formula (Hill Notation):
C10H9N
CAS Number:
Molecular Weight:
143.19
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39180204
UNSPSC Code:
12352100
EC Number:
202-084-6
MDL number:
Beilstein/REAXYS Number:
110336
Assay:
98%
vapor density
>1 (vs air)
Quality Level
assay
98%
refractive index
n20/D 1.614 (lit.)
bp
256-260 °C (lit.)
density
1.067 g/mL at 20 °C (lit.)
SMILES string
Cc1ccc2ncccc2c1
InChI
1S/C10H9N/c1-8-4-5-10-9(7-8)3-2-6-11-10/h2-7H,1H3
InChI key
LUYISICIYVKBTA-UHFFFAOYSA-N
Application
6-Methylquinoline can be used as primary carbon source in culture of Pseudomonas putida QP1. 6-Methylquinoline was used in the synthesis of fluorescent halide-sensitive quinolinium dyes and fluorescent probes for determination of chloride in biological systems.
Biochem/physiol Actions
6-Methylquinoline undergoes biodegradation by quinoline-degrading culture of Pseudomonas putida.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Chloride sensitive probes for biological applications.
Geddes CD, et al.
Dyes and Pigments, 48(3), 227-231 (2001)
S Rothenburger et al.
Applied and environmental microbiology, 59(7), 2139-2144 (1993-07-01)
Selective culturing of pseudomonads that could degrade quinoline led to enrichment cultures and pure cultures with expanded substrate utilization and transformation capabilities for substituted quinolines in immobilized and batch cultures. Immobilized cells of the pseudomonad cultures rapidly transformed quinolines to
C E Scharping et al.
Carcinogenesis, 14(5), 1041-1047 (1993-05-01)
The hepatic microsomal metabolism of the carcinogenic 8-methylquinoline (8MQ) and its noncarcinogenic isomer, 6-methylquinoline (6MQ), were compared for preparations from control rats and rats pretreated with phenobarbital or 3-methylcholanthrene. For each compound the alcohol was the major metabolite, constituting 50-75%
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 108928-25G | 04061838687685 |
| 108928-100G | 04061838687678 |