FuMaric Acid Monoethyl Ester MagnesiuM Salt is the magnesium salt of fumaric acid monoethyl ester, with two monoethyl fumarate anions coordinating to one Mg²⁺ cation. The molecular formula is C₁₂H₁₄MgO₈, and the molecular weight is 310.54 g/mol. The compound appears as a white to off‑white crystalline powder and decomposes at 169 °C (characteristic of many metal carboxylates). The InChI key is ZHLRSUSHKGQBNV-SYWGCQIGSA-L, and the SMILES representation CCOC(=O)\C=C\C(=O)O[Mg]OC(=O)\C=C\C(=O)OCC clearly shows the symmetric structure with magnesium bridging two monoester units via the carboxylate oxygens.
Calcium and magnesium are the two most common physiologically benign counterions for carboxylic acids. FuMaric Acid Monoethyl Ester MagnesiuM Salt offers distinct advantages over its calcium counterpart: lower molecular weight (310.54 vs. 326.31 for the calcium salt), meaning a higher loading of the active monoester per gram. While the calcium salt (CAS 62008‑22‑4) is widely used as a stable, crystalline form of the monoester, FuMaric Acid Monoethyl Ester MagnesiuM Salt is particularly valuable because magnesium is an essential mineral involved in hundreds of enzymatic reactions. Magnesium salts are often preferred in nutritional supplements and certain pharmaceutical formulations where calcium might interfere (e.g., in patients with hypercalcemia or on calcium‑channel blockers). FuMaric Acid Monoethyl Ester MagnesiuM Salt can be used interchangeably with the calcium salt in most synthetic applications, but its different solubility and thermal behavior (lower decomposition temperature, 169 °C vs. 285 °C) may offer processing benefits in specific formulations. For these reasons, FuMaric Acid Monoethyl Ester MagnesiuM Salt is a compelling choice for both process chemistry and nutritional product development.
Lower molecular weight means more monoethyl fumarate per gram — more efficient for large-scale reactions.
Physiologically benign counterion
Magnesium is an essential nutrient, making this salt suitable for nutritional supplements and certain pharmaceutical formulations.
Crystalline solid
Easy to weigh, handle, and store — no sticky oils or waxy residues.
Controlled release of monoester
Upon acidification, the free monoester is generated in situ, ideal for one-pot reactions.
Scalable and economical
Manufactured from cheap starting materials (fumaric acid, ethanol, magnesium base).
Reduced irritation
Less irritating than the free monoester acid; dust is the main concern.
Safety & Handling – What You Need to Know
This compound carries multiple hazard classifications:
Hazard Category
Classification
Eye irritation
Category 2 (causes serious eye irritation)
Skin irritation
Category 2 (causes skin irritation)
Skin sensitization
Category 1 (may cause allergic skin reaction)
STOT-SE
Category 3 (may cause respiratory irritation)
Storage class
11 – Combustible solid
Required Protective Measures:
● Eyes: Safety goggles (mandatory).
● Skin: Chemical-resistant gloves (nitrile). If you have a history of skin allergies, take extra precautions due to skin sensitizer classification.
● Respiratory: Use in a fume hood. Avoid breathing dust.
● First aid:
1. Eye contact – rinse with water for 15 min (S26).
2. Skin contact – wash with soap and water. If rash or irritation develops, seek medical advice (skin sensitizer).
3. Inhalation – move to fresh air.
● Storage: Keep container tightly sealed in a dry place at room temperature. Store away from ignition sources (combustible solid). Avoid contact with strong mineral acids (releases irritating free monoester).
● Disposal: Collect as chemical waste. WGK 1 indicates low water hazard, but best practice is not to flush down drains.
Frequently Asked Questions (FAQ)
Q1: How does the magnesium salt differ from the calcium salt in terms of handling?
A: Both are free‑flowing crystalline powders. The magnesium salt has a lower decomposition temperature (169 °C vs. 285 °C) , so avoid heating above 150 °C. It also has a slightly lower molecular weight, giving higher active content per gram. The main difference is the counterion – choose based on your formulation or biological requirements.
Q2: Can I use this salt directly in amide coupling reactions?
A: It is possible but not ideal. The magnesium salt has low solubility in organic solvents. The preferred method is to liberate the free monoester by suspending the salt in ethyl acetate/water and adding dilute HCl (2 eq relative to Mg). Extract the free monoester into the organic layer, dry, and concentrate. Then activate the carboxylic acid with HATU/EDC as usual.
Contact Cosperpharm – Get Your Magnesium Monoester Salt Today
Looking for a magnesium‑based alternative to the standard calcium fumarate salt? Cosperpharm supplies CAS 83918‑60‑9 with verified purity, full safety documentation, and flexible packaging options. Whether you need 5 grams for a formulation pilot or 5 kilograms for production, we deliver consistent quality and responsive support.
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