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  2. Dehydroacetic acid - Wikipedia

    en.wikipedia.org/wiki/Dehydroacetic_acid

    Dehydroacetic acid is an organic compound which has several industrial applications. The compound is classified as a pyrone derivative. It presents as an odorless, colorless to white crystalline powder, almost insoluble in water and moderately soluble in most organic solvents.

  3. Sodium dehydroacetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_dehydroacetate

    Sodium dehydroacetate is a compound with the formula Na(CH 3 C 5 HO(O 2)(CH 3)CO).It is the sodium salt of dehydroacetic acid.It is used as a preservative in food, [1] cosmetics and personal care products such as shower gels, which is highly effective against a broad range of bacteria even at low concentrations such as 0.075 g/kg in meat.

  4. DHA - Wikipedia

    en.wikipedia.org/wiki/DHA

    Docosahexaenoic acid, a 22:6 omega-3 fatty acid; Dehydroandrosterone, an endogenous androgenic steroid; Dehydroascorbic acid, an oxidized form of ascorbic acid; Dehydroacetic acid, a pyrone derivative used as a plasticiser, as a fungicide, as a bactericide, and as a food preservative

  5. E265 - Wikipedia

    en.wikipedia.org/wiki/E265

    Dehydroacetic acid, a chemical compound Topics referred to by the same term This disambiguation page lists articles associated with the same title formed as a letter–number combination.

  6. Dehydroascorbic acid - Wikipedia

    en.wikipedia.org/wiki/Dehydroascorbic_acid

    Dehydroascorbic acid (DHA) is an oxidized form of ascorbic acid (vitamin C). It is actively imported into the endoplasmic reticulum of cells via glucose transporters. [ 1 ] It is trapped therein by reduction back to ascorbic acid by glutathione and other thiols . [ 2 ]

  7. Triacetic acid lactone - Wikipedia

    en.wikipedia.org/wiki/Triacetic_acid_lactone

    Triacetic acid lactone is synthesized either from dehydroacetic acid, another 2-pyrone derivative, or from glucose by enzymatic catalysis. In its original synthesis, triacetic acid lactone was obtained by treatment of dehydroacetic acid with sulfuric acid at 135 °C. Dehydroacetic acid undergoes ring-opening and hydration to form "tetracetic ...

  8. Haloacetic acids - Wikipedia

    en.wikipedia.org/wiki/Haloacetic_acids

    Dichloroacetic acid (Cl 2 CH−CO 2 H) Trichloroacetic acid (Cl 3 C−CO 2 H) Bromoacetic acid (BrCH 2 −CO 2 H) Dibromoacetic acid (Br 2 CH−CO 2 H) The regulation limit for these five acids combined is 60 parts per billion (ppb). [5] The sum of bromodichloroacetic acid, dibromochloroacetic acid and tribromoacetic acid concentrations is ...

  9. E number - Wikipedia

    en.wikipedia.org/wiki/E_number

    A solution of E101 riboflavin (also known as vitamin B2) Crystals of E621 monosodium glutamate (MSG), a flavour enhancer. E numbers, short for Europe numbers, are codes for substances used as food additives, including those found naturally in many foods, such as vitamin C, for use within the European Union (EU) [1]: 27 and European Free Trade Association (EFTA). [2]