HuagongsheHuagongshe Chemistry Print Report · For research reference only
Penicillin G → L-Penicillamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Penicillin G | HCID 5904 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | L-Penicillamine | HCID 92863 | — |
Reaction Steps
N-(2-aminoethyl) carbamylmethylated cellulose was prepared in the manner set forth in Example 1. The amino ethyl derivative was kept at a concentration of 6.5 mg/ml in aqueous solution. Three ml of this solution were diluted to 6 ml with distilled water. The pH was adjusted to 9 with 0.1 N NaOH. One hundred mg of Penicillin G (sodium salt, Sigma Chemicals, St. Louis, U.S.A.) were added at once, and the resulting solution left overnight at room temperature. The solution was then dialyzed in the cold against two daily changes of 2 liters of water for 3 days. The CMC-Pen conjugate thus formed was kept in solution in the cold.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04415552 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-7e3866c4ce434d96a2826866c9c511a0 |
| Source note | uspto-grants-1983_11 |