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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736272Generated: November 2, 2026

Maleic Acid → Ammonium Aspartate

https://huagongshe.com/reaction/1736272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AcidHCID 444266—
ReactantDiammonium maleateHCID 10997209—
ProductAmmonium AspartateHCID 8659068399%

Reaction Conditions

Temperature30 °C

Reaction Steps

According to the same procedure of Example 1, cells of Alcaligenes faecalis ATCC 8750 was added to 2 L of an ammonium maleate substrate solution containing 400 g of maleic acid, and the substrate solution was gently stirred at 30° C. for 24 hours. After the reaction, ammonium L-aspartate was formed with a molar yield of 99.0% based on maleic acid. To the reaction solution from which the cells had been removed by centrifugation, was added 1.23 kg of 33.3 wt % maleic acid aqueous solution at 30° C. After the addition, a temperature of the solution was 38.5° C., and pH value of thereof was 3.7. L-aspartic acid crystals were separated by filtration, so as to recover 2.37 L of mother liquors. The crude crystals were 481 g (excluding water) (93.6 wt % aspartic acid, 6.0 wt % maleic acid, 250 μm average crystal size). The crystals were washed with about 300 ml of water and dried so as to obtain 448 g (excluding water) of L-aspartic acid crystals (99.1 wt % aspartic acid weight, 0.50 wt % maleic acid, 200 μm average crystal size).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541090
Source datasetuspto-grants-1996_07
ORD IDord-0b3154c644174968a509e8847b67b9f7
Source noteuspto-grants-1996_07