31519
乙氧基喹啉
PESTANAL®, analytical standard
别名:
1,2-二氢-6-乙氧基-2,2,4-三甲基喹啉, 6-乙氧基-1,2-二氢-2,2,4-三甲基喹啉
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关于此项目
经验公式（希尔记法）:
C14H19NO
化学文摘社编号:
分子量:
217.31
Beilstein/REAXYS Number:
158223
NACRES:
NA.24
E Number:
E324
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
202-075-7
MDL number:
InChI
1S/C14H19NO/c1-5-16-11-6-7-13-12(8-11)10(2)9-14(3,4)15-13/h6-9,15H,5H2,1-4H3
InChI key
DECIPOUIJURFOJ-UHFFFAOYSA-N
SMILES string
CCOc1ccc2NC(C)(C)C=C(C)c2c1
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
density
1.03 g/mL at 20 °C (lit.)
application(s)
cleaning products
cosmetics
food and beverages
personal care
format
neat
shipped in
wet ice
storage temp.
2-8°C
Quality Level
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General description
乙氧基喹 (EQ)，一种芳香化合物，是一种抗氧化剂，主要用于动物和鱼类饲料。可见抑制多环芳烃的致癌作用。不饱和脂肪中空气、光或转换金属引发的氧化可通过 EQ 停止传播。
Application
有关合适仪器技术的更多信息，请参考产品分析证书。如需进一步支持，请联系技术服务部门。
采用高效液相色谱-荧光检测器测定大西洋鲑鱼组织中的 EQ 及其主要代谢物。
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
光敏：敏感
空气敏感：氩气下手柄
空气敏感：氩气下手柄
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
The inhibitory effects of ethoxyquin on the carcinogenic action of aflatoxin B1 in rats.
Cabral JR, Neal GE.
Cancer Letters, 19(2), 125-132 (1983)
Laia Sanchez Costa et al.
Analytical methods : advancing methods and applications, 12(32), 4080-4088 (2020-08-08)
Ethoxyquin (EQ) is a quinolone commonly used as an antioxidant additive and a fungicide. However, Regulation (EU) 2017/962 suspended its authorisation as a feed additive for all animal species and categories. The aim of this study is thus to ensure
Sangit Kumar et al.
The Journal of organic chemistry, 72(16), 6046-6055 (2007-07-03)
6-(Ethylthio)-, 6-(ethylseleno)-, and 6-(ethyltelluro)-2,2,4-trimethyl-1,2-dihydroquinoline-three heavier chalcogen analogues of ethoxyquin-were prepared by dilithiation of the corresponding 6-bromodihydroquinoline followed either by treatment with the corresponding diethyl dichalcogenide (sulfur derivative) or by insertion of selenium/tellurium into the carbon-lithium bond, oxidation to a diaryl
J Andrew Keightley et al.
Molecular & cellular proteomics : MCP, 3(2), 167-175 (2003-12-17)
We are using a proteomic approach that combines two-dimensional electrophoresis and tandem mass spectrometry to detect and identify proteins that are differentially expressed in a cell line that is resistant to oxidative stress. The resistant cell line (OC14 cells) was
Alina Błaszczyk
Toxicology letters, 163(1), 77-83 (2005-11-04)
Ethoxyquin (1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline, EQ) is widely used in various food products and in animal feeds because of its powerful antioxidant activity. This compound was recently found to cause not only many unfavourable side-effects in animals fed with feeds containing it, but
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