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W274402

Sigma-Aldrich

6-甲基喹啉

≥98%, FG

别名:

对甲基喹啉

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About This Item

经验公式（希尔记法）:
C10H9N
CAS号:
91-62-3
分子量:
143.19
FEMA號碼:
2744
Beilstein:
110336
EC號碼:
202-084-6
歐洲委員會號碼:
2339
MDL號碼:
MFCD00006804
分類程式碼代碼:
12164502
PubChem物質ID:
24901302
Flavis號碼:
14.042
NACRES:
NA.21
感官的:
leather
等級:
FG
Halal
生物源:
synthetic
agency:
meets purity specifications of JECFA
食物過敏原:
no known allergens

生物源

synthetic

品質等級

400

等級

FG
Halal

agency

meets purity specifications of JECFA

法律遵循

EU Regulation 1334/2008 & 178/2002

蒸汽密度

>1 (vs air)

化驗

≥98%

折射率

n20/D 1.614 (lit.)

bp

256-260 °C (lit.)

密度

1.067 g/mL at 20 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

感官的

leather

SMILES 字串

Cc1ccc2ncccc2c1

InChI

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

InChI 密鑰

LUYISICIYVKBTA-UHFFFAOYSA-N

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相关类别

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H302,H315

危險分類

Acute Tox. 4 Oral - Skin Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

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

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分析证书(COA)

Lot/Batch Number
SHBN9566
SHBL1999
MKCG2161
MKBX1535V
MKBR6074V

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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
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
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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