Passa al contenuto
Merck
Tutte le immagini(1)

Key Documents

69484

Supelco

N-Methyl-N-trimethylsilylheptafluorobutyramide

for GC derivatization, LiChropur, ≥90% (GC)

Sinonimo/i:

N-Trimethylsilyl-N-methylheptafluorobutyramide, MSHFBA

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Formula condensata:
CF3CF2CF2CON(CH3)Si(CH3)3
Numero CAS:
Peso molecolare:
299.26
Beilstein:
6512894
Numero MDL:
Codice UNSPSC:
12000000
ID PubChem:
NACRES:
NA.22

Grado

for GC derivatization

Livello qualitativo

Saggio

≥90% (GC)

Forma fisica

liquid

Qualità

LiChropur

Impiego in reazioni chimiche

reagent type: derivatization reagent
reaction type: Silylations

tecniche

gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.353 (lit.)
n20/D 1.353

P. eboll.

148 °C (lit.)

Densità

1.254 g/mL at 25 °C (lit.)

Stringa SMILE

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

InChI

1S/C8H12F7NOSi/c1-16(18(2,3)4)5(17)6(9,10)7(11,12)8(13,14)15/h1-4H3
CMXKINNDZCNCEI-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Applicazioni


  • Simultaneous quantitation of cocaine, opiates, and their metabolites in human hair by positive ion chemical ionization gas chromatography-mass spectrometry: This study demonstrates the application of N-Methyl-N-trimethylsilylheptafluorobutyramide in forensic toxicology to analyze drug residues in human hair, providing a robust method for detecting such compounds at trace levels (Höld KM, Wilkins DG, Rollins DE, Joseph RE Jr, Cone EJ, 1998).

  • Detection of stanozolol in hair by negative ion chemical ionization mass spectrometry: The research utilizes N-Methyl-N-trimethylsilylheptafluorobutyramide for the sensitive detection of stanozolol, a performance-enhancing steroid, in hair samples. This method is particularly useful in sports doping analyses to ensure fair play (Höld KM, Wilkins DG, Crouch DJ, Rollins DE, Maes RA, 1996).

Altre note

N-methyl-N-trimethylsilylheptafluorobutyramide (MSHFBA) has been used in the silylation reaction during GC analysis of samples containing 1-monoolein, 2-monoolein, 1,2-diolein, 1,3-diolein, ethyl oleate, oleic acid and triolein.
Silylating agent for use in GC-analyses. It interferes least with flame-ionization detectors

Note legali

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Pittogrammi

FlameExclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

91.4 °F - closed cup

Punto d’infiammabilità (°C)

33 °C - closed cup

Dispositivi di protezione individuale

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


Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

J. Heberle et al.
Silylating Agents, 2nd ed. (1995)
Effects of regioselectivity and lipid class specificity of lipases on transesterification, exemplified by biodiesel production.
Sinkuniene, Dovile, and Patrick Adlercreutz
Journal of the American Oil Chemists' Society, 97 (1), 1283-1290 (2014)
Matthias Zielonka et al.
Experimental neurology, 314, 91-99 (2019-01-18)
Acute hyperammonemic encephalopathy is a life-threatening manifestation of individuals with urea cycle disorders, which is associated with high mortality rates and severe neurological sequelae in survivors. Cerebral bioenergetic failure has been proposed as one of the key mechanisms underlying hyperammonemia-induced
Tobias Kieliba et al.
Drug testing and analysis, 11(2), 267-278 (2018-08-26)
The detection of Δ9 -tetrahydrocannabinol (THC), cannabidiol (CBD) and cannabinol (CBN) in hair, for the purpose of identifying cannabis consumption, is conducted in many forensic laboratories. Since external contamination of hair with these cannabis components cannot be excluded, even after
Bing Fang et al.
Journal of food science and technology, 54(7), 1938-1944 (2017-07-20)
Tocopherols and sterols were lost considerably during the refining process of vegetable oils, resulting in a dramatic decrease in the oxidation stability. However, the oxidation stability of vegetable oils was not directly proportional to tocopherol content, not mention to its

Articoli

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

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.