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382493

Sigma-Aldrich

3-Methylquinoline

99%

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About This Item

Fórmula empírica (Notação de Hill):
C10H9N
Número CAS:
612-58-8
Peso molecular:
143.19
Número CE:
210-315-7
Número MDL:
MFCD00014661
Código UNSPSC:
12352100
ID de substância PubChem:
24863900
NACRES:
NA.22

Ensaio

99%

Formulário

liquid

índice de refração

n20/D 1.615 (lit.)

p.e.

252-253 °C (lit.)

pf

16-17 °C (lit.)

densidade

1.069 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

Cc1cnc2ccccc2c1

InChI

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

chave InChI

DTBDAFLSBDGPEA-UHFFFAOYSA-N

Informações sobre genes

human ... CYP1A2(1544)

Descrição geral

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.

Aplicação

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.

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

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

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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)
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
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
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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