|
|
|
Silylation Reagents  |
 |
|
|
|
BSA is a highly reactive trimethylsilyl donor that forms volatile stable TMS derivatives.
|
|
|
|
|
|
|
|
|
Powerful trimethylsilyl donor with highly volatile by-products for excellent GC separations.
|
|
|
|
|
|
|
|
|
TMCS enhances the reactivity of BSTFA for the silylation of difficult to derivatize compounds.
|
|
|
|
|
|
|
|
|
Useful for preparing oximes of steroids and ketoacids prior to silylation.
|
|
|
|
|
|
|
|
|
The most volatile TMS-amide available, forms volatile and thermally stable derivatives for GC/MS applications. <
|
|
|
|
|
|
|
|
|
Offers stable TBDMS (tert-butyl-dimethylsilyl) derivatization.
|
|
|
|
|
|
|
|
|
An excellent catalyst for difficult to silylate compounds.
|
|
|
|
|
|
|
|
|
The strongest silylation reagent for hydroxyls…reacts quickly and smoothly with hydroxyl and carboxyl groups.
|
|
|
|
|
|
|
|
|
BSA in pyridine (2.5 mEq/ml) for one-step derivatizations.
|
|
|
|
|
|
|
|
|
HMDS/TMCS in pyridine (2:1:10) mixture for one-step derivatization of organic hydroxyl and polyhydroxyl compounds into TMS ethers.
|
|
|
|
|
|
|
|
|
TMSI, BSA, TMCS (3:3:2) catalyzed silylation reagent formulation that converts all classes of hydroxyl groups to TMS ethers.
|
|
|
|
|
|
|
|
|
TMSI in dry pyridine (1.5 mEq/ml) for derivatizing hydroxyl compounds, particularly carbohydrates.
|
|
|
|
|
|
|
|
