HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioglycolic Acid → Ninhydrin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | L-Methionine | HCID 6137 | — |
| Reactant | O-Methylhomoserine | HCID 18713 | — |
| Reactant | HCID 19391794 | HCID 19391794 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Reactant | HCID 178473673 | HCID 178473673 | — |
| Reactant | HCID 178511840 | HCID 178511840 | — |
| Product | Ninhydrin | HCID 10236 | — |
Reaction Steps
In a manner analogous to that mentioned above, L-methionine, γ-chloro-α-amino butyric acid, and γ-methoxy-α-amino butyric acid were contacted each with thiocysteine, γ-cresol, thioacetic acid, thioglycolic acid and thiolactic acid. Rf of the ninhydrin positive spot of the compounds produced were different from L-methionine, γ-chloro-α-amino butyric acid, and γ-methoxy-α-amino butyric acid, and thus new amino acids were produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04071405 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-2acddceeb7964f28a7b8d77b67c3335e |
| Source note | uspto-grants-1978_01 |