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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617113Generated: October 29, 2026

Formaldehyde → N,N-Bis(carboxymethyl)-L-glutamic acid

https://huagongshe.com/reaction/617113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantHydrogen CyanideHCID 768—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantL-Glutamic AcidHCID 33032—
SolventWaterHCID 962—
ProductN,N-Bis(carboxymethyl)-L-glutamic acidHCID 18711581—

Reaction Conditions

Temperature90 °C

Reaction Steps

A reactor was charged with 314.0 g of L-glutamic acid, 350.0 g of a 40% aqueous solution of sodium hydroxide and 200.0 g of water. The temperature of the contents was raised to 90° C., followed by the addition of 110.6 g of prussic acid, 405.4 g of 30% formalin and 450.0 g of a 40% aqueous solution of sodium hydroxide. The resulting mixture was stirred at 105° C. for 2 hours. After the completion of the reaction, the residual prussic acid was decomposed by the addition of 30.0 g of 10% formalin. 1000.0 g of a 40% aqueous solution of sulfuric acid was added to the resulting mixture to conduct crystallization. The crystalline product thus deposited was recovered by filtration to obtain 441.8 g of N,N-bis(carboxymethyl)glutamic acid as a crude crystal. This crude crystal was recrystallized from water/methanol to give 411.9 g of purified N,N-bis(carboxymethyl)glutamic acid (yield: 75.5%). This acid was neutralized with 40% aqueous sodium hydroxide to give a tetrasodium N,N-bis(carboxymethyl)-glutamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948748
Source datasetuspto-grants-1999_09
ORD IDord-22478715fdc34e9cbd227f98d6325260
Source noteuspto-grants-1999_09