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69484

N-Methyl-N-trimethylsilylheptafluorobutyramide

derivatization grade (GC derivatization), LiChropur™, ≥90% (GC)

Synonym(s):

N-Trimethylsilyl-N-methylheptafluorobutyramide, MSHFBA

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Size/SKUAvailabilityPrice
1 mL
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$131.00
5 mL
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$363.00

About This Item

Linear Formula:
CF3CF2CF2CON(CH3)Si(CH3)3
CAS Number:
Molecular Weight:
299.26
UNSPSC Code:
23151817
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6512894
Assay:
≥90% (GC)
Form:
liquid

$131.00


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grade

derivatization grade (GC derivatization)

Quality Segment

assay

≥90% (GC)

form

liquid

quality

LiChropur™

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

technique(s)

HPLC: suitable, LC/MS: suitable, gas chromatography (GC): suitable, ion chromatography: suitable

refractive index

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

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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This Item
394866M789169479
description

derivatization grade (GC derivatization), LiChropur™, ≥90% (GC)

description

synthesis grade

description

BioReagent, for silylations, LiChropur™

description

derivatization grade (GC derivatization), LiChropur™, ≥98.5%

assay

≥90% (GC)

assay

≥98%

assay

-

assay

≥98.5%, ≥98.5% (GC)

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

reaction suitability

reaction type: Silylations, reagent type: derivatization reagent

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

200

bp

148 °C (lit.)

bp

130-132 °C (lit.)

bp

130-132 °C (lit.)

bp

130-132 °C (lit.)

refractive index

n20/D 1.353

refractive index

n20/D 1.38 (lit.)

refractive index

n20/D 1.38 (lit.)

refractive index

n20/D 1.380, n20/D 1.38 (lit.)

form

liquid

form

liquid

form

liquid

form

liquid


Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

91.4 °F - closed cup

Flash Point (°C)

33 °C - closed cup

PPE (personal protective equipment)

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



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