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About This Item
Empirical Formula (Hill Notation):
C14H19NO
CAS Number:
Molecular Weight:
217.31
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-075-7
Beilstein/REAXYS Number:
158223
MDL number:
Product Name
Ethoxyquin, ≥75% (capillary GC)
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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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
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
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Victoria J Berdikova Bohne et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46(5), 1834-1843 (2008-03-11)
The biological fate of the fish feed additive, ethoxyquin (EQ) was examined in the muscle of Atlantic salmon during 12 weeks of feeding followed by a 2 weeks depuration period. Parent EQ (1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline), quinone imine (2,6-dihydro-2,2,4-trimethyl-6-quinolone), de-ethylated EQ (6-hydroxy-2,2,4-trimethyl-1,2-dihydroquinoline) and
R Ørnsrud et al.
Journal of food protection, 74(9), 1574-1580 (2011-09-10)
The feed additive ethoxyquin (EQ) is a commonly used synthetic antioxidant preservative in animal feeds. In farmed Atlantic salmon fillets, EQ residues are present, both as the parent compound and as EQ derivatives. One of the main EQ derivates in
A Błaszczyk et al.
Food additives and contaminants, 24(6), 553-560 (2007-05-10)
The complexes of antioxidant ethoxyquin (1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline; EQ) with rutin or quercetin (EQ-R and EQ-Q, respectively) were studied in human lymphocytes for genotoxic and antioxidant activities with the use of the comet assay and micronucleus test. The study was undertaken to
Ronald A Lubet et al.
Chemico-biological interactions, 182(1), 22-28 (2009-08-22)
Identifying agents that block tumor initiation is a goal of cancer prevention. The ability of a chemically varied group of agents to induce various drug metabolizing genes in livers of rats was examined. Sprague-Dawley rats were treated for 7 days
Regulation of aldo-keto reductase AKR1B10 gene expression: involvement of transcription factor Nrf2.
Toru Nishinaka et al.
Chemico-biological interactions, 191(1-3), 185-191 (2011-02-01)
Aldo-keto reductase 1B10 (AKR1B10) is an aldose reductase-like oxidoreductase of human origin. The expression of AKR1B10 is highly induced in the cells of various cancers such as lung non-small-cell carcinoma and hepatocellular carcinoma. Since the enzyme exhibits broad substrate specificities
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