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E8260

Sigma-Aldrich

Ethoxyquin

≥75% (capillary GC)

Sinonimo/i:

1,2-Dihydro-6-ethoxy-2,2,4-trimethylquinoline, 6-Ethoxy-1,2-dihydro-2,2,4-trimethylquinoline

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About This Item

Formula empirica (notazione di Hill):
C14H19NO
Numero CAS:
91-53-2
Peso molecolare:
217.31
Beilstein:
158223
Numero CE:
202-075-7
Numero MDL:
MFCD00023883
Codice UNSPSC:
12352100
ID PubChem:
57654169
NACRES:
NA.22

Saggio

≥75% (capillary GC)

Forma fisica

liquid

Densità

1.03 g/mL at 20 °C (lit.)

Stringa SMILE

CCOc1ccc2NC(C)(C)C=C(C)c2c1

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
DECIPOUIJURFOJ-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
098H0346
013K0628
092H0567
074K0026
064K0023

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Alina Błaszczyk et al.
Chemico-biological interactions, 162(1), 70-80 (2006-06-27)
2,2,4,7-Tetramethyl-1,2,3,4-tetrahydroquinoline (THQ) is a new synthetic compound with potential antioxidant activity. In this study, cytotoxic, genotoxic and antioxidant activities of THQ were studied on human lymphocytes with the use of the trypan blue exclusion assay, the TUNEL method, the comet
Rex Munday et al.
Chemico-biological interactions, 155(3), 140-147 (2005-07-28)
Reduction of naphthoquinones by DT-diaphorase is often described as a detoxification reaction. This is true for some naphthoquinone derivatives, such as alkyl and di-alkyl naphthoquinones, but the situation with other substances, such as 2-hydroxy-1,4-naphthoquinone, is more complex. In the present
Alina Błaszczyk et al.
Acta poloniae pharmaceutica, 62(2), 111-115 (2005-09-16)
In our study ethoxyquin (EQ) and its two complexes with flavonoids were obtained from ethoxyquin (1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline, EQ) and quercetin (EQ-Q, 1:1) or rutin (EQ-R, 1:1). Cytotoxicity of the tested compounds was studied using the trypan blue exclusion method and the
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
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)
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