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Fórmula empírica (notación de Hill):
C9H18F3NOSi
Número CAS:
Peso molecular:
241.33
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
Beilstein/REAXYS Number:
3606546
Servicio técnico
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Permítanos ayudarleNombre del producto
N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-Butyldimethylchlorosilane, ampule of 5 × 1 mL, (with 1% t-BDMCS), analytical standard, Cerilliant®
grade
analytical standard
Quality Level
reaction suitability
reagent type: derivatization reagent
reaction type: Acylations
packaging
ampule of 5 × 1 mL
manufacturer/tradename
Cerilliant®
technique(s)
gas chromatography (GC): suitable
application(s)
forensics and toxicology
format
neat
storage temp.
−20°C
SMILES string
CN(C(=O)C(F)(F)F)[Si](C)(C)C(C)(C)C
InChI
1S/C9H18F3NOSi/c1-8(2,3)15(5,6)13(4)7(14)9(10,11)12/h1-6H3
InChI key
QRKUHYFDBWGLHJ-UHFFFAOYSA-N
Application
- Pharmaceutical substances in ambient particulates: A preliminary assessment.: This study explores the presence of pharmaceutical compounds in environmental particulate matter, using analytical methods that could involve derivatization agents like MTBSTFA. The detection of these substances in air samples suggests potential health impacts and environmental persistence (Cecinato et al., 2017) (Cecinato et al., 2017).
Legal Information
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 3
flash_point_f
113.0 °F - closed cup
flash_point_c
45 °C - closed cup
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P Canosa et al.
Journal of chromatography. A, 1072(1), 107-115 (2005-05-11)
A solid-phase microextraction (SPME) method for the determination of triclosan, methyl triclosan, 2,4-dichlorophenol and 2,3,4-trichlorophenol (considered as possible triclosan metabolites) in water samples was optimised. Analytes were first concentrated on a SPME fibre, directly exposed to the sample, and then
José Angel Prieto et al.
Clinical biochemistry, 42(1-2), 125-128 (2008-11-11)
Evaluation of a GC-MS method using N-tert-butyldimethylsilyl-N-methyltrifluoroacetamide (MTBSTFA) as the silylating agent for GC-MS. Study of the stability of creatine and guanidinoacetate in urine. 22 urines were kept at RT, 4 degrees C and -30 degrees C for 15 days.
Paul L Wood et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 831(1-2), 313-319 (2006-01-13)
The GC-MS quantitation of a large number of neurochemicals utilizing a single derivatization step is not common but is provided by the reagent N-(tert-butyldimethylsilyl)-N-methyltrifluro-acetamide (MTBSTFA). Previous workers have utilized this derivative for GC-MS analyses of amino acids, carboxylic acids and

