反応式
Cl.Cl.[CH2:3]([S:9][S:10][CH2:11][C@H:12]([NH2:16])[C:13]([OH:15])=[O:14])[C@H:4]([NH2:8])[C:5]([OH:7])=[O:6].[OH-].[Na+]>O>[CH2:3]([S:9][S:10][CH2:11][C@H:12]([NH2:16])[C:13]([OH:15])=[O:14])[C@H:4]([NH2:8])[C:5]([OH:7])=[O:6]参加物
4
実験手順
100 grams of L-cystine dihydrochloride were dissolved in 500 ml of water. The solution was adjusted to pH 3 by the addition of a concentrated aqueous solution of sodium hydroxide. As a result of this, the L-cystine separated out. The yield was 74 grams, corresponding to 94% based on the L-cystine dihydrochloride added. The L-cystine in a 5 percent solution in 1 N aqueous hydrochloric acid had a specific rotation of -217°. According to thin layer chromatography and column chromatography examination it was free from impurities.
出典と根拠
- ORDレコード
- ord-8639b9d8e332499b9f823fd2b498e86b
- 出典データセット
- uspto-grants-1981_01
- 特許番号
- US04245117
関連ノート
読み込み中…