07551
Vanillylidenaceton
≥98.5%
Synonym(e):
4-(4-Hydroxy-3-methoxyphenyl)-3-buten-2-on
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)
About This Item
Empfohlene Produkte
Qualitätsniveau
Assay
≥98.5%
Farbe
yellow
mp (Schmelzpunkt)
125-130 °C
SMILES String
COc1cc(\C=C\C(C)=O)ccc1O
InChI
1S/C11H12O3/c1-8(12)3-4-9-5-6-10(13)11(7-9)14-2/h3-7,13H,1-2H3/b4-3+
InChIKey
AFWKBSMFXWNGRE-ONEGZZNKSA-N
Angaben zum Gen
human ... APP(351)
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Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Journal of food science, 78(1), M64-M69 (2013-01-03)
The efficacy of Dehydrozingerone (DZ; dehydroderivative of zingerone) as an antifungal agent and its mode of action against food spoilage fungal pathogens was studied and presented. DZ is a constituent of ginger (Zingiber officinale rhizomes) and structural half analogue of
Die Pharmazie, 49(7), 516-519 (1994-07-01)
The antioxidant property of dehydrozingerone and its analogs were investigated in the ferric-ascorbate induced lipid peroxidation model in rat brain homogenate. All the non phenolic compounds were either inactive or less active, while phenolic compounds with substitution at both meta
Biochemical pharmacology, 46(11), 2067-2072 (1993-12-03)
The antioxidant properties of three related compounds, dehydrozingerone, isoeugenol and eugenol, were investigated using various models. Isoeugenol was found to be the most active in inhibiting ferrous-ion-, ferric-ion- and cumene-hydroperoxide-induced lipid peroxidation in rat brain homogenates. These compounds also showed
Inhibition of albumin denaturation and antiinflammatory activity of dehydrozingerone and its analogs.
Indian journal of experimental biology, 26(7), 540-542 (1988-07-01)
Journal of cardiovascular pharmacology, 52(5), 422-429 (2008-11-27)
Growth factor and oxidative stress-mediated migration and proliferation of vascular smooth muscle cells (VSMCs) play a key role in the pathogenesis of atherosclerosis. The objective of this study was to assess the ability of dehydrozingerone, a structural analog of curcumin
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