HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Aspartic Acid → L-Aspartic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Aspartic Acid | HCID 5960 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Product | L-Aspartic Acid | HCID 5960 | — |
| Product | L-Aspartic acid, sodium salt (1:2) | HCID 21806 | — |
| Product | Ammonium Aspartate | HCID 86590683 | — |
Reaction Steps
A sample of 13.3 g (100 mmol) of aspartic acid was slurried in 100 ml distilled water with stirring, and the aspartic acid was partially neutralized with 5 ml of 10 N NaOH (50 mmol). Conc. NH4OH (3.38 ml, 14.8 N, 50 mmol) was pipetted into the beaker, fully neutralizing and solubilizing the aspartic acid. The beaker was placed in a drying oven at 120° C. overnight, producing a clear, slightly yellowish glass of the comonomers, aspartic acid (plus residual ammonium aspartate) and sodium aspartate. The beaker was then heated in a vacuum oven at 200° C., 25 mm Hg, for 4 hours, to convert the material to a copolymer of sodium aspartate and succinimide. Titration data confirmed the 1:1 residue ratio.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091305B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-e9f0bef708674089b4baba65dc3ddbb7 |
| Source note | uspto-grants-2006_08 |