Comparing E334 - L(+)-tartaric acid vs E470AI - Sodium salts of fatty acids

Synonyms
E334
L(+)-tartaric acid
tartaric acid
2‚3-dihydroxybutanedioic acid
2‚3-dihydroxysuccinic acid
threaric acid
racemic acid
uvic acid
paratartaric acid
E470ai
Sodium salts of fatty acids
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Found in 2,434 products

Found in 1 products

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Popular questions
  1. Is tartaric acid bad for you?

    No—L(+)-tartaric acid (E334) is approved for use in foods (e.g., EU E-number; FDA GRAS) and is considered safe at typical levels; very high intakes may cause stomach upset, and only the L(+)-form is used as an additive.

  2. What is tartaric acid used for?

    It’s used as an acidulant to add sourness and control pH, and as an antioxidant/sequestrant; it also partners with baking soda in leavening and is added to wine to adjust acidity.

  3. How much tartaric acid to add to wine?

    It depends on your must/wine’s pH and titratable acidity—bench trials are essential; as a rule of thumb, 1 g/L tartaric acid raises TA by about 1 g/L and can lower pH by ~0.1–0.3, with typical adjustments in the 0.5–2 g/L range subject to local regulations.

  4. What does tartaric acid do?

    It provides a sharp, tart flavor while regulating acidity, chelating metals, and limiting oxidation; in baking it reacts with sodium bicarbonate to release CO2, and in wine it helps set acid balance and stability.

  5. What foods have tartaric acid?

    It occurs naturally in grapes, wine, and tamarind (also in smaller amounts in some fruits), and as an additive it’s found in soft drinks, candies, jams/jellies, gelatin desserts, and baking powders/cream of tartar.

  1. Explain why sodium salts of fatty acids, although they are salts, are not very soluble in water?

    Their long hydrophobic hydrocarbon tails outweigh the small ionic (carboxylate) head, so they prefer to aggregate into micelles or lamellar phases rather than disperse as individual ions; solubility decreases with chain length and is generally lower for sodium than potassium salts.

  2. What are sodium or potassium salts of fatty acids?

    They are soaps—anionic surfactants (RCOO− Na+ or RCOO− K+) formed by neutralizing fatty acids with sodium or potassium hydroxide, used in foods as emulsifiers and stabilizers.

  3. What are sodium salts of long chain fatty acids called?

    They are commonly called soaps, for example sodium stearate or sodium palmitate.

  4. What do the sodium salts of fatty acids taste like?

    They have a characteristic soapy, slightly bitter/alkaline taste; at typical food-use levels they contribute little flavor but can cause a soapy off-note if overused.

  5. What is special about sodium salts of fatty acids?

    They are amphiphilic surfactants that lower surface tension and self-assemble (e.g., into micelles), enabling them to emulsify and stabilize fat–water mixtures. They can also form insoluble “soaps” with calcium or magnesium ions.