| Catalog | Description | Size | Price (USD) | Qty |
|---|---|---|---|---|
| 786-061 | Sodium Cyanoborohydride | 0.5g | $33.00 | |
| 786-062 | Sodium Cyanoborohydride | 4 x 0.5g | $65.00 |
Carbonyl groups, including aldehydes, ketones and glyoxals, react with amines to form Schiff base intermediates that are in equilibrium with their free forms. The labile Schiff’s base interaction can be stabilized by chemical reduction. If the Schiff’s base is formed between an aldehyde and an amine then sodium cyanoborohydride is routinely used for the reduction of the Schiff’s base to a covalent bond1 .
Features
Applications
Carbonyl groups, including aldehydes, ketones and glyoxals, react with amines to form Schiff base intermediates that are in equilibrium with their free forms. The labile Schiff’s base interaction can be stabilized by chemical reduction. If the Schiff’s base is formed between an aldehyde and an amine then sodium cyanoborohydride is routinely used for the reduction of the Schiff’s base to a covalent bond1 .
Features
Applications
