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Merck

M-108

Supelco

MTBSTFA

with 1% t-BDMCS, ampule of 5 × 1 mL, analytical standard, Cerilliant®

Synonym(e):

N-Methyl-N-tert-butyldimethylsilyltrifluoracetamid, MTBSTFA + 1 % TBDMSCl, Silylierungsmischung VI

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About This Item

Empirische Formel (Hill-System):
C9H18F3NOSi
CAS-Nummer:
Molekulargewicht:
241.33
Beilstein:
3606546
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:

product name

N-tert-Butyldimethylsilyl-N-methyltrifluoracetamid mit 1% tert-Butyldimethylchlorsilan, (with 1% t-BDMCS), ampule of 5 × 1 mL, analytical standard, Cerilliant®

Qualität

analytical standard

Eignung der Reaktion

reagent type: derivatization reagent
reaction type: Acylations

Verpackung

ampule of 5 × 1 mL

Hersteller/Markenname

Cerilliant®

Methode(n)

gas chromatography (GC): suitable

Anwendung(en)

forensics and toxicology

Format

neat

Lagertemp.

−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

InChIKey

QRKUHYFDBWGLHJ-UHFFFAOYSA-N

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Anwendung


  • 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).


Rechtliche Hinweise

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany

Piktogramme

FlameExclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

113.0 °F - closed cup

Flammpunkt (°C)

45 °C - closed cup


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Kunden haben sich ebenfalls angesehen

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.
Clayton B'Hymer et al.
Analytical and bioanalytical chemistry, 383(2), 201-209 (2005-09-15)
Several extraction and derivatization procedures were evaluated for the quantification of (2-methoxyethoxy)acetic acid (MEAA) in urine. MEAA is a metabolite and a biomarker for exposure to 2-(2-methoxyethoxy)ethanol, a glycol ether with widespread use in various industrial applications and the specific
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
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
Xiaowei Wang et al.
Journal of chromatography. A, 1216(35), 6267-6273 (2009-07-31)
A sample pretreatment method for the determination of 18 chlorophenols (CPs) in aqueous samples by derivatization liquid-phase microextraction (LPME) was investigated using gas chromatography-mass spectrometry. Derivatization reagent was spiked into the extraction solvent to combine derivatization and extraction into one

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