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375934

Sigma-Aldrich

N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide

≥95%, with 1% tert-Butyldimethylchlorosilane

Sinonimo/i:

MTBSTFA+TBDMSCl, 99:1, N-Methyl-N-tert-butyldimethylsilyltrifluoroacetamide, MTBSTFA + 1% TBDMSCl, Silylating mixture VI

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About This Item

Formula empirica (notazione di Hill):
C9H18F3NOSi
Numero CAS:
77377-52-7
Peso molecolare:
241.33
Beilstein:
3606546
Numero MDL:
MFCD00009671
Codice UNSPSC:
12352001
ID PubChem:
24863412
NACRES:
NA.22

Nome del prodotto

N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-Butyldimethylchlorosilane, ≥95%

Livello qualitativo

100

Saggio

≥95%

Stato

liquid

contiene

1% TBDMSCl

Gruppo funzionale

amine
fluoro

Temperatura di conservazione

−20°C

Stringa SMILE

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
QRKUHYFDBWGLHJ-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-butyldimethylchlorosilane is commonly used for the preparation of N-tert-butyldimethylsilyl ethanolamines resulting from the hydrolysis of nitrogen mustards. It is also used for selective O-silylation of N,O-diacylhydroxyl amines.

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Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H226,H315,H319

Classi di pericolo

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

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

113.0 °F - closed cup

Punto d’infiammabilità (°C)

45 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG3071
BCCB0590
BCBX5506
BCBW0512
BCBV7472

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tert-Butyldimethylsilyl chloride reagent grade, 97%

Sigma-Aldrich

190500

tert-Butyldimethylsilyl chloride

Organometallics, 23, 2157-2161 (2004)
Xiaodong Huang et al.
Analytical chemistry, 80(1), 107-114 (2007-12-07)
This work describes an approach to differential metabolomics that involves stable isotope labeling for relative quantification as part of sample analysis by two-dimensional gas chromatography/mass spectrometry (GCxGC/MS). The polar metabolome in control and experimental samples was extracted and differentially derivatized
Claude Schummer et al.
Talanta, 77(4), 1473-1482 (2008-12-17)
In this study, MTBSTFA and BSTFA, which are among the preferred derivatization reagents for silylation were both tested on derivatization of six different groups of polar chemicals to get information about usefulness in terms of sensitivity and specificity of both
A Royer et al.
Journal of chromatography. A, 1108(1), 129-135 (2006-01-31)
An analytical method has been developed for the determination of residues of ethephon (2-chloroethyl phosphonic acid) in drinking and surface water. The procedure is based on de-ionisation with an anion/cation-exchange resin, solid phase extraction by means of anion-exchange polystyrene-divinylbenzene extraction
Xiaowei Wang et al.
Analytica chimica acta, 753, 57-63 (2012-10-31)
A sample preparation method for the determination of hydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) in sediment samples was developed using gas chromatography-mass spectrometry (GC-MS). Dispersive liquid-liquid microextraction (DLLME) with derivatization was performed following the subcritical water extraction (SWE) that provided which
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Silylation of Non-Steroidal Anti-Inflammatory Drugs

Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs

Global Trade Item Number

SKUGTIN
375934-1G
375934-250MG
375934-10X1ML4061837790256
375934-10ML
375934-1ML4061837790263
375934-25ML4061831835106
375934-5ML4061831835113

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