Comparing E210 - Benzoic acid vs E492 - Sorbitan tristearate
Overview
Synonyms
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Found in 386 products
Found in 447 products
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Search volume over time
Interest over time for 2 keywords in U.S. during the last 10 years.
Interest over time for 2 keywords in U.S. during the last 10 years.
Popular questions
Is benzoic acid soluble in water?
Only sparingly—about 3 g per liter at room temperature; its solubility increases in hot water and it dissolves readily in many organic solvents.
Is benzoic acid polar?
It has a polar carboxyl group but a nonpolar aromatic ring, so overall it’s only weakly polar; its benzoate salt is much more polar and water‑soluble.
Is benzoic acid a strong acid?
No—it's a weak acid, with a pKa of about 4.2.
What is the melting point of benzoic acid?
About 122–123 °C (251–253 °F).
Is benzoic acid bad for you?
At approved food levels it’s considered safe, with an ADI of 0–5 mg/kg body weight/day; some people may experience irritation or hypersensitivity, and benzene formation in certain acidic drinks is monitored and kept very low.
How is sorbitan monostearate and sorbitan tristearate different?
Sorbitan monostearate (E491) has one stearate group, while sorbitan tristearate (E492) has three; this makes E492 more hydrophobic (lower HLB) and better for water‑in‑oil/fat stabilization, whereas E491 has a higher HLB and broader emulsifier uses (e.g., bakery).
What is sorbitan tristearate made from?
It’s produced by esterifying sorbitan (from dehydrated sorbitol) with stearic acid, which is typically sourced from vegetable oils (e.g., palm/soy) and can also be from animal fats.