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Merck
CN

33059-U

Supelco

Rejuv-8

pkg of 25 mL, Silylating reagent

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About This Item

UNSPSC Code:
12352200
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packaging

pkg of 25 mL

General description

Rejuv-8 is a commercially available resilylating mixture of N,O-bis(trimethylsilyl)acetamide, hexamethyldisilazane and 1-(trimethylsilyl)imidazole.

Application

Rejuv-8 was used as resilylating reagent during:
  • postcoating treatment performed for the GC column in fast separation of organophosphonate and organosulfur compounds.
  • pre-reduction and cryotrapping for speciation analysis of pentavalent arsenicals by thioglycolic acid using selective hydride generation-cryotrapping-atomic absorption spectrometry.
  • studying GC models for separation optimization in pressure-tunable tandem capillary columns using new capillary column interface.

Legal Information

Rejuv-8 is a trademark of Sigma-Aldrich Co. LLC

Analyte

Description

    N,O-Bis(trimethylsilyl)acetamide
    Hexamethyldisilazane
    1-(Trimethylsilyl)imidazole

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

41.0 °F - closed cup

Flash Point(C)

5 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Stanislav Musil et al.
Spectrochimica acta. Part B, Atomic spectroscopy, 63(6), 685-691 (2009-06-06)
An improvement of current method of selective hydride generation based on pre-reduction for differentiation of tri- and pentavalent arsenicals is described, applied for the oxidation state specific speciation analysis of inorganic, mono-, di- and trimethylated arsenicals with minimum sample pretreatment
Enrico Veschetti et al.
Journal of separation science, 37(4), 412-418 (2013-12-03)
In the previous part of this study, a significant improvement of the fundamental relationships that control GC resolution in a pressure-tunable assembly operating in isothermal conditions inside a single oven was made. A theoretical approach for the correct choice of
Adarsh D Radadia et al.
Analytical chemistry, 80(11), 4087-4094 (2008-04-30)
This article demonstrates how to prepare microfabricated columns (microcolumns) for organophosphonate and organosulfur compound separation that rival the performance of commercial capillary columns. Approximately 16,500 theoretical plates were generated with a 3 m long OV-5-coated microcolumn with a 0.25 microm

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