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65943

N-Methyl-bis-trifluoracetamid

derivatization grade (GC derivatization), LiChropur, ≥99.0% (GC)

Synonym(e):

MBTFA

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Über diesen Artikel

Lineare Formel:
CF3CON(CH3)COCF3
CAS-Nummer:
Molekulargewicht:
223.07
UNSPSC Code:
23151817
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-680-5
Beilstein/REAXYS Number:
1878402
MDL number:
Assay:
≥99.0% (GC)
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grade

derivatization grade (GC derivatization)

Quality Segment

assay

≥99.0% (GC)

quality

LiChropur

reaction suitability

reagent type: derivatization reagent
reaction type: Acylations, reagent type: derivatization reagent
reaction type: Silylations

technique(s)

gas chromatography (GC): suitable

refractive index

n20/D 1.346

bp

121-122 °C (lit.)

density

1.547 g/mL at 25 °C

SMILES string

CN(C(=O)C(F)(F)F)C(=O)C(F)(F)F

InChI

1S/C5H3F6NO2/c1-12(2(13)4(6,7)8)3(14)5(9,10)11/h1H3

InChI key

AWGBWLXGUPTXHF-UHFFFAOYSA-N

General description

N-Methyl-bis(trifluoroacetamide) is a common reagent used in the alkylation process, which targets highly polar, multi-functional compounds such as carbohydrates and amino acids.

Application

Reagenz für das Einführen einer Trifluoracetyl-Gruppe
N-Methyl-bis(trifluoroacetamide) may be used as an on-column derivatization agent for the determination of amphetamine-type stimulants in biological samples, and ketamine, norketamine, dehydronorketamine in urine samples using gas chromatography coupled to mass spectrometry technique.
It is a derivatization agent in GC-MS technique used as an alternative to trifluoroacetyl anhydride (TFAA) for trifluoroacylating primary and secondary amines, and the hydroxyl group under mild non-acidic conditions.
Reagent for introducing trifluoroacetyl group. Suitable for the derivatization of alcohols, amines, amino acids, carbohydrates(mono-,di-,tri- and tetrasaccharides, carboxylic acids, hydroxyamines, 3-hydroxy-1-nitrosopyrrolidine, indolalkylamine, phenolalkylamines, pyridoxal (and other B6 vitamers), and thiols.

Other Notes

Reagens für Trifluoracetylierungen unter milden Bedingungen[1]
Reagent for trifluoroacetyl, N-trimethylsilyl-N-tifluoroacetyl and trimethylsilyl.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

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Dieser Artikel
M07891522269479
assay

≥99.0% (GC)

assay

≥97.0% (GC)

assay

≥99.0% (GC)

assay

≥98.5% (GC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

200

reaction suitability

reagent type: derivatization reagent
reaction type: Acylations, reagent type: derivatization reagent
reaction type: Silylations

reaction suitability

reagent type: derivatization reagent
reaction type: Acylations

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

refractive index

n20/D 1.346

refractive index

n20/D 1.346 (lit.)

refractive index

n20/D 1.384 (lit.)

refractive index

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

bp

121-122 °C (lit.)

bp

121-122 °C (lit.)

bp

45-50 °C/14 mmHg (lit.)

bp

130-132 °C (lit.)

density

1.547 g/mL at 25 °C

density

1.547 g/mL at 25 °C

density

0.969 g/mL at 25 °C (lit.)

density

1.075 g/mL at 25 °C (lit.)


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pictograms

FlameCorrosion

signalword

Danger

hcodes

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Lagerklasse

3 - Flammable liquids

wgk

WGK 3

flash_point_f

113.0 °F - closed cup

flash_point_c

45 °C - closed cup

ppe

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



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K. Blau et al.
Handbook of Derivatives for Chromatography, 131-131 (1977)
Derivatization reactions and reagents for gas chromatography analysis
Advanced Gas Chromatography: Progress in Agricultural, Biomedical and Industrial Applications, 83-108 (2012)
Development of a two-step injector for GC?MS with on-column derivatization, and its application to the determination of amphetamine-type stimulants (ATS) in biological specimens
Miki A, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 865(1-2), 25-32 (2008)



Global Trade Item Number

SKUGTIN
65943-5ML04061832733791
65943-25ML04061837811173

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