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Merck
모든 사진(1)

주요 문서

69484

Supelco

N-Methyl-N-trimethylsilylheptafluorobutyramide

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

동의어(들):

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 코드:
12000000
PubChem Substance ID:
NACRES:
NA.22

Grade

for GC derivatization

Quality Level

분석

≥90% (GC)

양식

liquid

품질

LiChropur

반응 적합성

reagent type: derivatization reagent
reaction type: Silylations

기술

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션


  • 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).

기타 정보

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

법적 정보

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

관련 제품

픽토그램

FlameExclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

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

개인 보호 장비

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


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시험 성적서(COA)

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문서 라이브러리 방문

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

문서

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

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