E8260
エトキシキン
≥75% (capillary GC)
別名:
1,2-ジヒドロ-6-エトキシ-2,2,4-トリメチルキノリン, 6-エトキシ-1,2-ジヒドロ-2,2,4-トリメチルキノリン
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この商品について
実験式（ヒル表記法）:
C14H19NO
CAS番号:
分子量:
217.31
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-075-7
Beilstein/REAXYS Number:
158223
MDL number:
Assay:
≥75% (capillary GC)
Form:
liquid
InChI key
DECIPOUIJURFOJ-UHFFFAOYSA-N
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
SMILES string
CCOc1ccc2NC(C)(C)C=C(C)c2c1
assay
≥75% (capillary GC)
form
liquid
density
1.03 g/mL at 20 °C (lit.)
Quality Level
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関連するカテゴリー
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
保管分類
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
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
第二種指定化学物質
prtr
名称等を表示すべき危険物及び有害物
ishl_indicated
名称等を通知すべき危険物及び有害物
ishl_notified
E8260-VAR: + E8260-BULK: + E8260-100G: + E8260-1KG: + E8260-250G:
jan
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
Victoria J Berdikova Bohne et al.
Toxicological sciences : an official journal of the Society of Toxicology, 93(1), 11-21 (2006-06-23)
The synthetic antioxidant ethoxyquin (EQ) is increasingly used in animal feeds and has been candidate for carcinogenicity testing. EQ has the potential for toxicological and adverse health effects for both fish and fish consumers through "carryover" processes. The toxicological aspects
Anup G Shah et al.
Water research, 39(17), 4251-4263 (2005-10-04)
The potential inhibitory effect of ethoxyquin, an antioxidant commonly used as a preservative in the food processing industry (e.g., for stabilizing dissolved air flotation residuals), was evaluated at concentrations up to 300 mg/L using a mixed, mesophilic (35 degrees C)
Alina Błaszczyk et al.
Cellular & molecular biology letters, 10(1), 15-21 (2005-04-06)
In our study, we analyzed the cytotoxicity of ethoxyquin (EQ) and its two salts, ethoxyquin hydrochloride (EQ-HCL) and ethoxyquin phosphate (EQ-P). It was shown that EQ was the most cytotoxic compound (IC(50) = 0.09 mM), while the lowest cytotoxic effect
Yoichi Aoki et al.
Journal of AOAC International, 93(1), 277-283 (2010-03-26)
An analytical method using HPLC with fluorescence detection (HPLC-FL) has been developed and applied for the survey of residue levels of ethoxyquin in a variety of food products of animal origin. HPLC was performed using a silica octadecylsilane column, butylhydroxytoluene-acetonitrile-water
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