BSTFA Silylation Reagent
Description
BSTFA is a powerful thrimethylsilyl donor, with donor strength that is comparable to its unfluorinated analog BSA [N,O-Bis(trimethylsilyl)acetamide]. BSTFA reacts to replace labile hydrogens on a wide range of polar compounds with a -Si(CH3)3 group. This physical characteristic is particularly useful in the gas chromatography of some lower boiling TMS-amino acids and TMS Krebs cycle acids.
Increased volatility of reaction byproducts mono(trimethylsilyl)trifluoroacetamide and trifluoroacetamide over corresponding nonfluorinated compounds from BSA
Increased volatility makes it possible to derivatize smaller molecules with which the TMS derivatives elute with the byproducts from BSA
Limited warranty period: Subject to all warranty requirements and exclusions set out in our Terms and Conditions of Sale, this product is warranted from the date we ship the product and for ninety (90) days thereafter. Disclaimer to internal research use restriction: Any restrictions on the purchaser to utilize the product(s) for internal research purposes only does not apply to the product(s) on the web pages associated with this statement.
General References:
- Her, G.R., et al. (1985). Anal. Biochem. 151, 292-298.
- Shanchun, J., et al. (1994). Org. Geochem. 21, 415-422.
Note:
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