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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736274Generated: November 1, 2026

Ammonia → Ammonium Aspartate

https://huagongshe.com/reaction/1736274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMaleic AcidHCID 444266—
ReactantDiammonium maleateHCID 10997209—
SolventWaterHCID 962—
ProductAmmonium AspartateHCID 8659068398.8%

Reaction Conditions

Temperature30 °C

Reaction Steps

According to the same procedure of Example 1, 600 g maleic acid was dissolved in deionized water, and 705 g of 25 wt % aqueous ammonia solution (molar ratio to maleic acid was about 2.0) was added thereon. The cells of Alcaligenes faecalis ATCC 8750 were added to 2 L of an ammonium maleate substrate solution (pH 8.4) containing 600 g maleic acid, and the substrate solution were gently stirred at 30° C. for 72 hours. After the reaction, ammonium L-aspartate was formed with a molar yield of 98.8% based on maleic acid. To the reaction solution from which the cells had been removed by centrifugation, was added 610 g maleic acid at 30° C. After the addition, a temperature of the solution was 37.0° C., and pH value thereof was 3.8. L-aspartic acid crystals were separated by filtration, so as to recover 1.5 L of mother liquors. The crude crystals was 769 g (excluding water) (88.0 wt % aspartic acid, 11.4 wt % maleic acid, 250 μm average crystal size). The crystals were washed with about 600 ml of water and dried so as to obtain 675 g of L-aspartic acid crystals (98.8 wt % aspartic acid, 0.77 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-3ae3bf38ed6642a7987f13ef3f67673a
Source noteuspto-grants-1996_07