antidepressants barbiturates hydantoin derivatives iminostilbenes methaqualone compounds neuroleptics psychostimulants succinimides and oxazolidinediones tranquillizers

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IN-CONTEXT TRANSLATIONS

Aldehydes derived from furan, the main one being hydroxymethylfurfural, react with barbituric acid and paratoluidine to give a red compound which is determined by colorimetry at 550 nm.

https://eur-lex.europa.eu/lega (...) (...) [HTML] [2017-12-31]

Furaanaldehyden, waarvan hydroxymethylfurfural de belangrijkste is, reageren met barbituurzuur en para-toluïdine onder vorming van een roodgekleurd complex hetgeen colorimetrisch bij 550 nm wordt bepaald.

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Add 1 ml of distilled water to flask b (control) and 1 ml barbituric acid solution (paragraph 2.2.1) to flask a. Shake to homogenize.

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Voeg aan flesje b (blanco) 1 ml gedistilleerd water toe en aan flesje a 1 ml barbituurzuuroplossing (punt 2.2.1). Schud om te homogeniseren.

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This item also controls products containing one of the anaesthetic agents listed under short or intermediate acting barbiturate anaesthetic agents.

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Dit artikel omvat tevens producten die een of meer van de anesthetica bevatten die zijn vermeld in de lijst van kort en middellang werkende anesthetica op basis van barbituraten.

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Short and intermediate acting barbiturate anaesthetic agents including, but not limited to:

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Kort en middellang werkende anesthetica op basis van barbituraten, zoals onder meer:

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4.1. Short and intermediate acting barbiturate anaesthetic agents including, but not limited to:

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4.1. Kort en middellang werkende anesthetica op basis van barbituraten, zoals onder meer:

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3.3. Solution of 1,3-dimethyl-barbituric acid: dissolve 3,658 g 1,3-dimethyl-barbituric acid (C6H8N2O3) in 15 ml pyridine and 3 ml hydrochloric acid (ρ20=1,19 g/ml) and add 50 ml distilled water

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3.3. 1,3-Dimethylbarbituurzuuroplossing: los 3,658 g 1,3-dimethylbarbituurzuur (C6H8N2O3) op in 15 ml pyridine en 3 ml zoutzuur (ρ20= 1,19 nm/ml) en vul met gedestilleerd water aan tot 50 ml.

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After reacting with chloramine-T and pyridine, the glutaconic dialdehyde formed is determined by colorimetry on the basis of the blue coloration it gives with 1,3-dimethyl-barbituric acid.

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Na reactie met chloramine T en pyridine, wordt het gevormde glutacondialdehyd colorimetrisch bepaald door de blauwkleuring met 1,3-dimethylbarbituurzuur.

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After exactly 60 seconds add 3 ml of 1,3-dimethyl-barbituric acid solution (3.3), seal with stopper and leave for 10 minutes.

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Voeg na precies 60 seconden 3 ml 1,3 dimethyl-barbituurzuuroplossing (3.3) toe, sluit hermetisch af en laat gedurende tien minuten staan.

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Dissolve 500 mg of barbituric acid, C4O3N2H4, in distilled water and heat slightly over a waterbath at 100 °C. Make up to 100 ml with distilled water.

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Los 500 mg barbituurzuur, C4H4O3N2, onder verwarming op een waterbad van 100 °C om het oplossen te vergemakkelijken, op in gedestilleerd water; vul aan tot 100 ml met gedestilleerd water.

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Aldehydes derived from furan, the main one being hydroxymethylfurfural, react with barbituric acid and paratoluidine to give a red compound which is determined by colorimetry at 550 nm.1.2.

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Furaanaldehyden, waarvan hydroxymethylfurfural de belangrijkste is, reageren met barbituurzuur en para-toluïdine onder vorming van een rood gekleurd complex hetgeen colorimetrisch bij 550 nm wordt bepaald.1.2.

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Anderen hebben gezocht naar : barbiturate barbiturate abuse barbiturate allergy barbiturates barbiturate dependence barbiturate intoxication barbiturate type dependence barbituric intoxication sleeping tablet soporific tranquiliser tranquilizer

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Date index: 2021-01-17