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W274402

Sigma-Aldrich

6-Methylquinoline

≥98%, FG

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Synonym(s):
p-Toluquinoline, NSC 4152
Empirical Formula (Hill Notation):
C10H9N
CAS Number:
Molecular Weight:
143.19
FEMA Number:
2744
Beilstein/REAXYS Number:
110336
EC Number:
Council of Europe no.:
2339
MDL number:
PubChem Substance ID:
Flavis number:
14.042
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

FG
Halal

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002

vapor density

>1 (vs air)

assay

≥98%

refractive index

n20/D 1.614 (lit.)

bp

256-260 °C (lit.)

density

1.067 g/mL at 20 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

leather

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

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This Item
Q2626108928Q2125
6-Methylquinoline ≥98%, FG

W274402

6-Methylquinoline

Quinaldine phosphate salt analytical standard

Q2626

Quinaldine phosphate salt

6-Methylquinoline 98%

108928

6-Methylquinoline

Quinaldine analytical standard, ≥90% (GC)

Q2125

Quinaldine

organoleptic

leather

organoleptic

-

organoleptic

-

organoleptic

-

biological source

synthetic

biological source

-

biological source

-

biological source

-

food allergen

no known allergens

food allergen

-

food allergen

-

food allergen

-

assay

≥98%

assay

-

assay

98%

assay

≥90% (GC)

documentation

see Safety & Documentation for available documents

documentation

-

documentation

-

documentation

-

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

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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Umar Farooq Rizvi et al.
Acta crystallographica. Section C, Crystal structure communications, 64(Pt 10), o547-o549 (2008-10-08)
Molecules of (E)-3-(2-chloro-6-methylquinolin-3-yl)-1-(5-iodo-2-thienyl)prop-2-en-1-one, C(17)H(11)ClINOS, (I), and (E)-3-(2-chloro-6-methylquinolin-3-yl)-1-(5-methyl-2-furyl)prop-2-en-1-one, C(18)H(14)ClNO(2), (II), adopt conformations slightly twisted from coplanarity. Both structures are devoid of classical hydrogen bonds. However, nonclassical C-H...O/N interactions [with C...O = 3.146 (5) A and C...N = 3.487 (3) A] link
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%

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