| Identification | More | [Name]
6-Methylquinoline | [CAS]
91-62-3 | [Synonyms]
6-METHYLQUINOLINE
FEMA 2744
PARA METHYL QUINOLINE
P-TOLUQUINOLINE
6-methyl-quinolin
p-Methylquinoline
6-METHYLQUINOLINE 98+%
Quinoline, 6-methyl-
3-Chloro-7-methylisoquinoline
4-(Piperidin-1-yl)-8-(trifluoromethyl)quinoline
6,8-Dichloroquinoline
8-Methyl-5-(trifluoromethyl)quinoline
6-methyquinoline
4-Quinoline-carboxamide
4-Quinoline-carboxylic Hydrazide
4-Thioquinoline-carboxamide
Ethyl 4-Quinoline-carboxylate
7-bromo-6-chloroquinazolin-4(3H)-one | [EINECS(EC#)]
202-084-6 | [Molecular Formula]
C10H9N | [MDL Number]
MFCD00006804 | [Molecular Weight]
143.19 | [MOL File]
91-62-3.mol |
| Chemical Properties | Back Directory | [Appearance]
clear light yellow to light orange liquid | [Melting point ]
-22°C | [Boiling point ]
256-260 °C (lit.) | [density ]
1.067 g/mL at 20 °C(lit.)
| [vapor density ]
>1 (vs air)
| [FEMA ]
2744 | [refractive index ]
n20/D 1.614(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Store below +30°C. | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Liquid | [pka]
5.21±0.10(Predicted) | [color ]
green-yellow
| [Odor]
blossom odor, sweet, animalic upon dilution | [Odor Type]
animal | [Water Solubility ]
Not miscible or difficult to mix with water. | [Sensitive ]
Light Sensitive | [JECFA Number]
1302 | [BRN ]
110336 | [LogP]
2.54 | [CAS DataBase Reference]
91-62-3(CAS DataBase Reference) | [NIST Chemistry Reference]
Quinoline, 6-methyl-(91-62-3) | [EPA Substance Registry System]
91-62-3(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed.
R38:Irritating to the skin.
R68:Possible risk of irreversible effects.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
3
| [RTECS ]
VC0550000
| [TSCA ]
Yes | [HS Code ]
29334990 |
| Hazard Information | Back Directory | [General Description]
Clear pale yellow liquid or oil. | [Reactivity Profile]
6-METHYLQUINOLINE(91-62-3) is sensitive to prolonged exposure to light. May react vigorously with strong oxidizing agents and strong acids . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides. | [Air & Water Reactions]
Insoluble in water. | [Fire Hazard]
This chemical is probably combustible. | [Description]
6-Methylquinoline has a quinoline odor. May be synthesized from
p-amino-benzaldehyde and acetone. | [Chemical Properties]
6-Methylquinoline has a pungent, heavy odor. | [Chemical Properties]
clear light yellow to light orange liquid | [Occurrence]
Reported found in Finnish and Japanese whiskey.
| [Application]
6-Methylquinoline, is a building block used for the synthesis of various pharmaceutical compounds, and biologically active compounds. It can be used for the preparation of pyranobenzopyrone compounds, having anti-norovirus activity. | [Uses]
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. | [Definition]
ChEBI: 6-methylquinoline is a member of quinolines. | [Biochem/physiol Actions]
6-Methylquinoline undergoes biodegradation by quinoline-degrading culture of Pseudomonas putida. | [Synthesis]
From coal tar, by synthesis from p-aminobenzaldehyde and acetone. | [Purification Methods]
Reflux it with BaO, then fractionally distil it. Further purified it via its recrystallised ZnCl2 complex (m 190o). [Cumper et al. J Chem Soc 1176 1962, Beilstein 20 III/IV 3498, 20/7 V 400.] |
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