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Safety Information

44156

Supelco

N-Methyl-N-trimethylsilyltrifluoroacetamide activated II

for GC derivatization, LiChropur, activated with 2-(Trimethylsilyl)ethanethiol

Synonym(s):

MSTFA activated II

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About This Item

EC Number:
UNSPSC Code:
41116105
NACRES:
NA.22

grade

for GC derivatization

Quality Level

form

liquid

quality

LiChropur

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

technique(s)

gas chromatography (GC): suitable

refractive index

n20/D 1.380

storage temp.

2-8°C

Application

  • Derivatizing agent for the trimethylsilylation of -OH and -NH groups for GC and GC-MS
  • Suitable for the silylation of testosterone, tested by GCMS

Features and Benefits

  • Activated with trimethylsily-ethanethiol.       
  • This mixture is equivalent to a 1000:2 mixture of MSTFA and iodotrimethylsilane.       

Other Notes

This mixture is equivalent to a 1000 : 2 mixture of MSTFA and iodotrimethylsilane.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

related product

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)

78.8 °F

Flash Point(C)

26 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

44156-BULK-F:
44156-VAR-F:
44156-5ML-F:4548173994086
44156-25ML-F:
44156-100ML-F:


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W. Schanzer et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 687, 93-93 (1996)

Articles

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

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