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N-Methyl-N-trimethylsilylheptafluorobutyramide

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

Synonym(s):

N-Trimethylsilyl-N-methylheptafluorobutyramide, MSHFBA

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About This Item

Linear Formula:
CF3CF2CF2CON(CH3)Si(CH3)3
CAS Number:
Molecular Weight:
299.26
Beilstein:
6512894
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NA.22

grade

for GC derivatization

Quality Level

Assay

≥90% (GC)

form

liquid

quality

LiChropur

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

technique(s)

gas chromatography (GC): suitable

refractive index

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

bp

148 °C (lit.)

density

1.254 g/mL at 25 °C (lit.)

SMILES string

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

InChI key

CMXKINNDZCNCEI-UHFFFAOYSA-N

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Application


  • 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).

Other Notes

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

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

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Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

91.4 °F - closed cup

Flash Point(C)

33 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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

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