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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Hydrogen Cyanide | HCID 768 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Glutamic Acid | HCID 33032 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-Bis(carboxymethyl)-L-glutamic acid | HCID 18711581 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05948748 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-22478715fdc34e9cbd227f98d6325260 |
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| Source note | uspto-grants-1999_09 |
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