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Merck

M-132

Supelco

N-Methyl-N-trimethylsilyltrifluoracetamid

ampule of 10 × 1.2 mL, analytical standard, Cerilliant®

Synonym(e):

N-Trimethylsilyl-N-methyltrifluoracetamid, MSTFA

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About This Item

Lineare Formel:
CF3CON(CH3)Si(CH3)3
CAS-Nummer:
Molekulargewicht:
199.25
Beilstein:
1941550
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Dampfdichte

>1 (vs air)

Dampfdruck

8.8 mmHg ( 27 °C)

Eignung der Reaktion

reagent type: derivatization reagent
reaction type: Acylations

Verpackung

ampule of 10 × 1.2 mL

Hersteller/Markenname

Cerilliant®

Methode(n)

gas chromatography (GC): suitable

Brechungsindex

n20/D 1.38 (lit.)

bp

130-132 °C (lit.)

Dichte

1.075 g/mL at 25 °C (lit.)

Anwendung(en)

forensics and toxicology

Format

neat

Lagertemp.

−20°C

SMILES String

CN(C(=O)C(F)(F)F)[Si](C)(C)C

InChI

1S/C6H12F3NOSi/c1-10(12(2,3)4)5(11)6(7,8)9/h1-4H3

InChIKey

MSPCIZMDDUQPGJ-UHFFFAOYSA-N

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Allgemeine Beschreibung

MSTFA (N-Methyl-N-trimethylsilylfluoroacetamide) is an important trimethylsilyl reagent, and a commonly applied reagent since it is highly reactive towards a broad range of compound classes. GC-MS optimization studies reveal the use of this reagent either alone or in combination with 1% of trimethylchlorosilane as a catalyst for silylation of complex mixtures. It has similar reactivity as BSA and BSTFA.

Anwendung

MSTFA reagent may be used as a derivatizing agent in the following:
  • Analysis of estrogen steroids such as estrone (E1), 17α-ethinylestradiol (EE2), and trenbolone acetate metabolites, melengestrol in environmental matrices using gas chromatography coupled to mass spectrometry (GC-MS).
  • Quantification of ibuprofen, naproxen, ketoprofen, and diclofenac in wastewater samples using gas chromatography coupled to mass spectrometry (GC-MS).

Leistungsmerkmale und Vorteile

  • Very volatile of TMS-acetamides.
  • More volatile than BSA or BSTFA but with similar silylation strength.
  • Useful in the analysis of volatile trace materials.
  • Used in the preparation of volatile and thermally stable derivatives for GC and MS analysis.

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 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

78.8 °F - closed cup

Flammpunkt (°C)

26 °C - closed cup


Analysenzertifikate (COA)

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

The use of trimethylsilyl cyanide derivatization for robust and broad-spectrum high-throughput gas chromatography?mass spectrometry based metabolomics
Khakimov B, et al.
Analytical and Bioanalytical Chemistry, 405(3), 9193-9205 (2013)
Identification and quantification of ibuprofen, naproxen, ketoprofen and diclofenac present in waste-waters, as their trimethylsilyl derivatives, by gas chromatography mass spectrometry
Sebok A, et al.
Talanta, 76(3), 642-650 (2008)
Analysis of trenbolone acetate metabolites and melengestrol in environmental matrices using gas chromatography--tandem mass spectrometry
Parker AJ, et al.
Talanta, 99(3), 238-246 (2012)
Harin Kanani et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 871(2), 191-201 (2008-06-10)
Metabolomics being the most recently introduced "omic" analytical platform is currently at its development phase. For the metabolomics to be broadly deployed to biological and clinical research and practice, issues regarding data validation and reproducibility need to be resolved. Gas
Sumandeep Rana et al.
Journal of analytical toxicology, 32(5), 355-363 (2008-06-12)
A method for the simultaneous determination of six commonly prescribed cyclic antidepressants and their major metabolites in urine is presented. This method can be used for quantitation of amitriptyline, nortriptyline, imipramine, desipramine, doxepin, desmethyldoxepin, and maprotiline in human urine, in

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