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  2. Red Dye 3 Just Got Banned. These Are the Foods to Avoid If ...

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    The FDA’s recent ban on Red Dye No. 3, set to take effect by 2027 for foods and 2028 for drugs, marks a significant step in addressing safety concerns over artificial food dyes in the U.S. food ...

  3. How to Make Natural Food Coloring Using Everyday Ingredients

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  4. Everything You Need To Know about Tyrosine - AOL

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    Tyrosine is an amino acid made by the body. It may boost cognitive function, especially during periods of stress. Many foods contain tyrosine. Skip to main content. 24/7 Help. For premium support ...

  5. Betalain - Wikipedia

    en.wikipedia.org/wiki/Betalain

    Betalains are a class of red and yellow tyrosine-derived pigments found in plants of the order Caryophyllales, where they replace anthocyanin pigments. Betalains also occur in some higher order fungi. [1] They are most often noticeable in the petals of flowers, but may color the fruits, leaves, stems, and roots of plants that contain them.

  6. Tyrosinase - Wikipedia

    en.wikipedia.org/wiki/Tyrosinase

    In the food industry, tyrosinase inhibition is desired as tyrosinase catalyzes the oxidation of phenolic compounds found in fruits and vegetables into quinones, which gives an undesirable taste and color and also decreases the availability of certain essential amino acids as well as the digestibility of the products.

  7. Erythrosine - Wikipedia

    en.wikipedia.org/wiki/Erythrosine

    Its use as a food dye was legalized in the US by the Pure Food and Drug Act of 1906. [6] By early 1920s, it was produced mainly for the food industry, [ 7 ] with 2,170 pounds (0.98 t) made in America in 1924, [ 8 ] rising to 9,468 pounds (4.29 t) in 1938 [ 9 ] and approximately 50 tons in 1967.

  8. 4 Valentine's Day candy options free of dyes and chemicals - AOL

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    Nutritionists Robin DeCicco of the New York area and Ilana Muhlstein of Los Angeles shared nutritious alternatives to typical Valentine's Day sweets such as chocolate, gummy candies and baked goods.

  9. Dityrosine - Wikipedia

    en.wikipedia.org/wiki/Dityrosine

    The tyrosinetyrosine crosslink can form by ultraviolet irradiation and other conditions that induce radical formation. [4] Proteins with calcium binding sites consisting of two tyrosine residues, such as calmodulin and troponin C, are especially prone to this reaction as a result of coordination of their phenol groups to a calcium ion.