791571
Isopropyl p-toluenesulfonate
97%
Synonym(e):
Isopropyl p-tosylate
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Alle Fotos(2)
About This Item
Empfohlene Produkte
Assay
97%
Form
liquid
Brechungsindex
n20/D 1.503
Dichte
1.142 g/mL at 25 °C
Lagertemp.
2-8°C
InChI
1S/C10H14O3S/c1-8(2)14(11,12)13-10-6-4-9(3)5-7-10/h4-8H,1-3H3
InChIKey
MUTOLSSCMLECRU-UHFFFAOYSA-N
Anwendung
Isopropyl p-toluenesulfonate can be used as a reactant:
- For the alkylation of amines in the presence of triethylamine.
- For the O-alkylation of cyclic thiohydroxamic acids in the presence of tetrabutylammonium hydroxide.
- To synthesize 3-methyl-2-phenyl-1-butanol by reacting with styrene in the presence of bromo(2-cyclohexylethyl)magnesium and zirconocene dichloride.
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
10 - Combustible liquids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Isopropyl p-toluenesulfonate (IPTS) is a potentially genotoxic by-product formed during the esterification of palm oil-based palmitic and palm kernel oil-based myristic acid with isopropanol to produce isopropyl palmitate or isopropyl myristate. There are no methods described for the analysis of
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[reaction: see structure] The first examples of efficient electrophilic Zr-catalyzed carbomagnesations are disclosed, where in contrast to previous catalytic carbomagnesations the alkyl moiety of the electrophile is transferred (vs that of the Grignard reagent). The identity of the Grignard reagent
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As part of a collaborative study in the Mammalian Mutagenicity Study group of the Japanese Environmental Mutagen Society, we evaluated the in vivo mutagenicity of isopropyl p-toluenesulfonate (IPTS) using a peripheral blood Pig-a assay in rats. Pig-a mutant frequency (MF)
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