HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Acetyl-L-Cysteine → HCID 22791110, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Acetyl-L-Cysteine | HCID 12035 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22791110 | HCID 22791110 | — |
Reaction Steps
N-acetyl-L-cysteine ammonium salt can also be obtained by modification of the above procedure as follows. About 6.5 ml. of concentrated ammonium hydroxide is added slowly to a stirred mixture of N-acetyl-L-cysteine (16.3 g., 0.1 mole) in 100 ml. of water. The pH of the mixture should be 7 at the end of the addition. The solvent is allowed to evaporate and the white residue thus obtained when dried to constant weight at 45°C. in vacuo over phosphorous pentoxide provides a quantitative yield (18 g.,) of analytically pure ammonium N-acetyl-L-cysteinate, M.P. 148°- 150°C. (dec.), [ α ]D25 + 20.3°(c 5,H2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03965167 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-a22fcff2296d42d5b7419136abac50c2 |
| Source note | uspto-grants-1976_06 |