33059-U
Rejuv-8™
pkg of 25 mL, Silylating reagent
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 Statements
Precautionary Statements
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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