Übersetzung für "Cinnamaldehyde" in Deutsch

1.6 kg of cinnamaldehyde was pumped in over 10 hours.

Another use for cinnamaldehyde is as an antimicrobial.

The most obvious application for Cinnamaldehyde is as flavoring in items like chewing gum.

Cinnamaldehyde has recently been recognized as a very effective insecticide for mosquito larvae.

Cinnamaldehyde is also used as a fungicide.

The additive shall not be used with other sources of carvacrol, cinnamaldehyde, capsaicin and dihydrocapsaicin.

Reduction of the carboxylic acid functional groups in the cinnamic acids provides the corresponding aldehydes, such as cinnamaldehyde.

Explicitly mentioned are, inter alia, cinnamic acid, cinnamaldehyde, benzoic acid, benzalacetone and ethyl benzoylacetate.

The hydrogenation of cinnamaldehyde and derivatives thereof has likewise already been extensively documented in the literature.

Foreign researchers have condition of 22 kinds of pathogenic fungi for cinnamaldehyde antifungal action research.

Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids.

The assessment of the preparation of carvacrol, cinnamaldehyde and capsicum oleoresin shows that the conditions for authorisation, as provided for in Article 5 of Regulation (EC) No 1831/2003, are satisfied.

That application concerns the authorisation of the preparation of carvacrol, cinnamaldehyde and capsicum oleoresin as a feed additive for chickens for fattening, to be classified in the additive category ‘zootechnical additives’.

A process for the manufacture of synthetic strobilurin in the (E) configuration, which comprises condensing a correspondingly substituted cinnamaldehyde with 2-oxo-butyric acid in methanolic KOH to give the correspondingly substituted potassium salt of 3(Z), 5(E)-3-methyl-2-oxo-6-phenyl-3,5-hexadienic acid, converting this potassium salt with methanol/thionyl chloride to the corresponding methyl ester, converting the reaction product with methoxymethylene-triphenylphosphorane to 9(Z) strobilurin, and after chromatographic purification on silica gel irradiating the crude product by means of a mercury vapor lamp in acetone with addition of a small amount of benzene.

It is also stated that, although the odor of cinnamaldehyde was noticed on using phenylethynylcarbinol, the reaction essentially led to tarry products by polymerization.

As brighteners, there have proven useful from group (b), e.g., p-methoxybenzaldehyde (anisaldehyde), 4-hydroxy-3-methoxybenzaldehyde (vanillin) and cinnamaldehyde, from group (c), e.g., butin-2-diol-1,4,butinediolmonopropoxylate, and propargyl alcohol monoethoxylate.

Suitable flavorings are, for example, peppermint oil, curled mint oil, eucalyptus oil, aniseed oil, fennel oil, caraway oil, menthyl acetate, cinnamaldehyde, anethol, vanillin and thymol and also mixtures of these and other natural and synthetic flavorings.

Suitable starting materials of the general formula II are for example: acrolein, methacrolein, ethylacrolein and higher homologs, crotonaldehyde, 2-methylpentenal, tiglinaldehyde, cinnamaldehyde and 2-benzylacrolein.

176 mg of cinnamaldehyde (1.33 mmol) and 3 ml of diisopropyl ether (saturated with 0.02 M histidine buffer, pH 6.8) were then added at room temperature.

The catalysts used for the preparation of the cinnamaldehyde derivatives of the formula I (stage (a)) for the process according to the invention are basic compounds, such as the alkali metal hydroxides NaOH, KOH and LiOH, alkaline earth metal hydroxides, and mixtures thereof, or else compounds of the alkali metal and alkaline earth metals which can liberate the corresponding hydroxides in the presence of water, and also ammonia, amines or alkoxides, such as, for example sodium methoxide or potassium tert-butoxide.