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Silylation is the most widely used derivatization procedure for sample analysis by GC. In silylation, an active hydrogen is replaced by an alkylsilyl group such as trimethylsilyl (TMS) or tert-butyldimethylsilyl (tert-BDMS). Silyl derivatives are more volatile, less polar, and more thermally stable. As a result, GC separation is improved and detection is enhanced.
Both TMS and tert-BDMS reagents are suitable for a wide variety of compounds and can be used for many GC applications. Note that silylation reagents are generally moisture sensitive and must be sealed to prevent deactivation.
Description | CAS # | qty. | Cat.# | ||||
MSTFA (N-methyl-N-trimethylsilytrifluoroacetamide) | 24589-78-4 | 10-pk. (10x1g) | 35600 | ||||
MSTFA (N-methyl-N-trimethylsilytrifluoroacetamide) | 24589-78-4 | 25g vial | 35601 | ||||
MSTFA w/1% TMCS (N-methyl-N-trimethylsilytrifluoroacetamide w/1% trimethylchlorosilane) | 24589-78-4 | 10-pk. (10x1g) | 35602 | ||||
MSTFA w/1% TMCS (N-methyl-N-trimethylsilytrifluoroacetamide w/1% trimethylchlorosilane) | 24589-78-4 | 25g vial | 35603 | ||||
BSTFA (N,O-bis[trimethylsilyl]trifluoroacetamide) | 25561-30-2 | 10-pk. (10x1g) | 35604 | ||||
BSTFA (N,O-bis[trimethylsilyl]trifluoroacetamide) | 25561-30-2 | 25g vial | 35605 | ||||
BSTFA w/1% TMCS (N,O-bis[trimethylsilyltrifluoroacetamide] w/1% trimethylchlorosilane) | 25561-30-2 | 10-pk. (10x1g) | 35606 | ||||
BSTFA w/1% TMCS (N,O-bis[trimethylsilyltrifluoroacetamide] w/1% trimethylchlorosilane) | 25561-30-2 | 25g vial | 35607 | ||||
MTBSTFA w/1% TBDMCS (N-methyl-N[tert-butyldimethylsilyl trifluoroacetamide] w/1% tert-butyldimethylchlorosilane) | 77377-52-7 | 10-pk. (10x1g) | 35608 | ||||
MTBSTFA w/1% TBDMCS (N-methyl-N[tert-butyldimethylsilyl trifluoroacetamide] w/1% tert-butyldimethylchlorosilane) | 77377-52-7 | 25g vial | 35610 | ||||
TMCS (trimethylchlorosilane) | 75-77-4 | 10-pk. (10x1g) | 35611 | ||||
TMCS (trimethylchlorosilane) | 75-77-4 | 25g vial | 35612 | ||||