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Merck
CN

382493

3-Methylquinoline

99%

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About This Item

Empirical Formula (Hill Notation):
C10H9N
CAS Number:
612-58-8
Molecular Weight:
143.19
NACRES:
NA.22
PubChem Substance ID:
24863900
UNSPSC Code:
12352100
EC Number:
210-315-7
MDL number:
MFCD00014661
Assay:
99%
Form:
liquid

Key Documents

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Product Name

3-Methylquinoline, 99%

InChI key

DTBDAFLSBDGPEA-UHFFFAOYSA-N

InChI

1S/C10H9N/c1-8-6-9-4-2-3-5-10(9)11-7-8/h2-7H,1H3

SMILES string

Cc1cnc2ccccc2c1

assay

99%

form

liquid

refractive index

n20/D 1.615 (lit.)

bp

252-253 °C (lit.)

mp

16-17 °C (lit.)

density

1.069 g/mL at 25 °C (lit.)

Quality Level

100

Gene Information

human ... CYP1A2(1544)

Related Categories

Application

3-Methylquinoline may be used as carbon, nitrogen and energy supplement to investigate its degradation by Comamonas testosteroni 63. It may be used as ligand in the preparation of tetra-μ-benzoato-bis[(3-methylquinoline)copper(II)], a paddle-wheel-type dinuclear complex.

General description

3-Methylquinoline is a quinoline derivative. It is widely employed for the synthesis of dyes, food coloring agents, pharmaceutical reagents, pH indicators and in various industrial processes. It has been synthesized by the methylation of quinoline with methanol in the presence of various zeolites in a fixed-bed reactor.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Carc. 2 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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

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Certificates of Analysis (COA)

Lot/Batch Number
06426HE
S36696
02314HE
16729TD
S31314

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S Schach et al.
European journal of biochemistry, 232(2), 536-544 (1995-09-01)
The enzymes catalysing the first two steps of quinoline and 3-methylquinoline degradation by Comamonas testosteroni 63 were investigated. Quinoline 2-oxidoreductase, which catalyses the hydroxylation of (3-methyl-)quinoline to (3-methyl-)2-oxo-1,2-dihydroquinoline, was purified to apparent homogeneity. The native enzyme, with a molecular mass
S Schach et al.
Biological chemistry Hoppe-Seyler, 374(3), 175-181 (1993-03-01)
A bacterial strain which utilizes 3-methylquinoline as sole source of carbon, nitrogen and energy was isolated from activated sludge. On the basis of its morphological and physiological characteristics, this isolate was classified as Comamonas testosteroni. Four metabolites of 3-methylquinoline degradation
Byeong Kwon Park et al.
Acta crystallographica. Section E, Structure reports online, 64(Pt 9), m1141-m1141 (2008-01-01)
In the title compound, [Cu(2)(C(7)H(5)O(2))(4)(C(10)H(9)N)(2)], the paddle-wheel-type dinuclear complex mol-ecule contains four bridging benzoate groups and two terminal 3-methyl-quinoline ligands. The asymmetric unit contains one and a half mol-ecules with a total of three independent Cu atoms; there is an
Selective synthesis of 2-methylquinoline over zeolites.
Reddy PR, et al.
Catalysis Letters, 56(2-3), 155-158 (1998)
Tamara Rodríguez-Cabo et al.
Analytical and bioanalytical chemistry, 407(20), 6159-6170 (2015-06-05)
Time-of-flight accurate mass spectrometry (TOF-MS), following a previous chromatographic (gas or liquid chromatography) separation step, is applied to the identification and structural elucidation of quinoline-like alkaloids in honey. Both electron ionization (EI) MS and positive electrospray (ESI+) MS spectra afforded

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