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Tetrapropylammonium perruthenate

330744 -

97%

DOWNLOAD MSDS (PDF)

Synonym: TPAP

Properties

Related CategoriesMicro/NanoElectronics, Others, Oxidation, Ruthenium, Solution Deposition Precursors,
assay97%
mp~160 °C (dec.)(lit.)

Description

Application

A soluble, nonvolatile, air-stable, mild oxidant which can be used either stoichiometrically or catalytically with a suitable co-oxidant.

Oxidant used to convert N,N′-dihydroxyimidazolidines to nitronyl nitroxide free radicals.1 Oxidation of hydroxyl-substituted tri-n-butylammonium trifluoroborates to aldehydes and ketones without concomitant cleavage of the carbon-boron bond.2,3

Packaging

1 g in glass btl

250 mg in glass btl

Price and Availability

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Documents

Certificate of Analysis

Certificate of Origin

Structure Search
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Safety Information

SymbolGHS03GHS07  GHS03, GHS07
Signal wordDanger
Hazard statementsH272-H315-H319-H335
Precautionary statementsP220-P261-P305 + P351 + P338
Personal Protective EquipmentEyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
Hazard CodesO,Xi
Risk Statements5-8-36/37/38
Safety Statements17-26-36
RIDADRUN 1479 5.1/PG 2
WGK Germany3
Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Articles

Oxidizing and Reducing Agents

Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis, and are some of the organic chemist’s most powerful tools for creating novel products. ...
ChemFiles Volume 1 Article 3
Keywords: Organic synthesis, Oxidations, Reductions

References

1. Synlett, 948, (2006)

2. J. Am. Chem. Soc. 128, 9634, (2006) Abstract

3. Synthesis 7, 639-666, (1994)

Synthesis, 639, (1994)

Aldrichimica Acta 23, 13, (1990)

Tetrahedron Lett. 45, 303-308, (2004)

Merck 14,10463

Fieser 14,302 / Fieser 16,325

Structure Index 1, 60:B:1


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