E363 – SUCCINIC ACID
CAS — · also known as E363 – Aċidu suċċiniku, E363 – Сукцинова киселина, E363 – Bernsteinsäure, E363 – Ηλεκτρικο οξυ, E363 – Kyselina jantárová, E363 – Borostyánkősav, E363 – Jantarna kislina, E363 – Kyselina jantarová, E363 – Ácido succínico, E363 – Gintaro rūgštis, E363 – Kwas bursztynowy, E363 – Ravsyre, E363 – Acido succinico, E363, E363 – Barnsteenzuur, E363 – Dzintarskābe, E363 – Acid succinic, E363 – Merevaikhape, E363 – Bärnstenssyra, E363 – Acide succinique, E363 – Meripihkahappo, E363 – Àcid succínic · other
E363 – SUCCINIC ACID is an other ingredient used in skincare formulations.
Quick facts
Quick Facts:
- Category: other
- Also Known As: E363 – Aċidu suċċiniku, E363 – Сукцинова киселина, E363 – Bernsteinsäure, E363 – Ηλεκτρικο οξυ, E363 – Kyselina jantárová, E363 – Borostyánkősav, E363 – Jantarna kislina, E363 – Kyselina jantarová, E363 – Ácido succínico, E363 – Gintaro rūgštis, E363 – Kwas bursztynowy, E363 – Ravsyre, E363 – Acido succinico, E363, E363 – Barnsteenzuur, E363 – Dzintarskābe, E363 – Acid succinic, E363 – Merevaikhape, E363 – Bärnstenssyra, E363 – Acide succinique, E363 – Meripihkahappo, E363 – Àcid succínic
Chemical Overview
Succinic acid appears as white crystals or shiny white odorless crystalline powder. pH of 0.1 molar solution: 2.7. Very acid taste. (NTP, 1992) Succinic acid is an alpha,-dicarboxylic acid resulting from the formal oxidation of each of the terminal methyl groups of butane to the corresponding carboxy group. It is an intermediate metabolite in the citric acid cycle. It has a role as a micronutrient, an anti-ulcer drug, a nutraceutical, a radiation protective agent and a fundamental metabolite. It is an alpha,omega-dicarboxylic acid and a C4-dicarboxylic acid. It is a conjugate acid of a succinate(1-). A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley’s Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851)
Source(s): CAMEO Chemicals, ChEBI, DrugBank, via PubChem
Comedogenicity
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