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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736271Generated: October 30, 2026

Maleic Acid → Ammonium Aspartate

https://huagongshe.com/reaction/1736271

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 410 g of maleic acid at 30° C., to precipitate crystals of L-aspartic acid. After the addition, a temperature of the solution was 34.5° C., and pH value thereof was 3.8. L-aspartic acid crystals were separated by filtration, so as to recover 1.6 L of mother liquors. The crude crystals was 502 g (Excluding water) (89.1 wt % aspartic acid, 10.2 wt % malic acid, 250 μm average crystal size). The crystals were washed with 300 ml of water and dried so as to obtain 447 g of L-aspartic acid crystals (99.0 wt % aspartic acid, 0.62 wt % maleic acid, 100 μm average crystal size).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541090
Source datasetuspto-grants-1996_07
ORD IDord-028b46b42fe94d90913a93411b486536
Source noteuspto-grants-1996_07