56563
Synonym(s):
TBDMS triflate, Trifluoromethanesulfonic acid tert-butyldimethylsilylester
Properties
derivatization grade (GC derivatization)
100
≥98.0% (T)
LiChropur™
reagent type: derivatization reagentreaction type: Silylations
gas chromatography (GC): suitable
n20/D 1.385
65-67 °C/12 mmHg (lit.)
1.151 g/mL at 25 °C (lit.)
2-8°C
CC(C)(C)[Si](C)(C)OS(=O)(=O)C(F)(F)F
1S/C7H15F3O3SSi/c1-6(2,3)15(4,5)13-14(11,12)7(8,9)10/h1-5H3
WLLIXJBWWFGEHT-UHFFFAOYSA-N
Description
Explore all of our products under tert-Butyldimethylsilyl trifluoromethanesulfonate
Danger
Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3
Respiratory system
3 - Flammable liquids
WGK 3
98.6 °F - closed cup
37 °C - closed cup
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Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs
comparable product
226149
tert-Butyldimethylsilyl trifluoromethanesulfonate
reagent grade, 98%
related product
19905
tert-Butyl(chloro)dimethylsilane
≥95.0% (GC)
394882
N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide
>97%
190500
tert-Butyldimethylsilyl chloride
reagent grade, 97%
375934
N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-Butyldimethylchlorosilane
≥95%
473464
tert-Butylchlorodimethylsilane solution
50 wt. % in toluene
384429
tert-Butyldimethylsilyl chloride solution
1.0 M in methylene chloride
372951
1.0 M in THF
250236
1-(tert-Butyldimethylsilyl)imidazole
33092-U
tert-Butyldimethylsilylimidazole solution
TBDMSIM in DMF, pkg of 10 × 1 mL
06735
LiChropur™, ≥99.0% (GC)
77626
derivatization grade (GC derivatization), LiChropur™, ≥98.0% (GC)
00942
LiChropur™, ≥95.0% (GC)
44795
N,O-Bis(tert-butyldimethylsilyl)acetamide