Thermo Scientific Chemicals

Potassium phthalimide, 98+%, Thermo Scientific Chemicals

Catalog number: A11134.36
500 g, Each
Thermo Scientific Chemicals

Potassium phthalimide, 98+%, Thermo Scientific Chemicals

Catalog number: A11134.36
500 g, Each
Quantity
Catalog number: A11134.36
also known as A11134-36
Price (USD)
Price: 104.00
Online price: 89.65
Your price:
Quantity
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Chemical Identifiers

CAS
1074-82-4
IUPAC Name
potassium 1,3-dioxo-2,3-dihydro-1H-isoindol-2-ide
Molecular Formula
C8H4KNO2
InChI Key
FYRHIOVKTDQVFC-UHFFFAOYSA-M
SMILES
[K+].O=C1[N-]C(=O)C2=CC=CC=C12
Appearance (Color)
White to cream to yellow to green
Form
Crystalline powder or powder
Assay (Non-aqueous acid-base Titration)
≥98.0 to ≤102.0%
Identification (FTIR)
Conforms
Water Content (Karl Fischer Titration)
≤1%

Description

Potassium phthalimide is used as an intermediate in the synthesis of N-alkylated phthalimides, which is involved in the preparation of primary amines (Gabriel synthesis) by the hydrolysis reaction. It is also used as an intermediate for synthetic indigo, pigments, dyes and pharmaceuticals. Further, it is employed as an organocatalyst for the cyanosilylation of various carbonyl compounds under extremely mild conditions. In addition to this, it serves as a reagent for the transformation of allyl- and alkyl halides into protected primary amines.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Potassium phthalimide is used as an intermediate in the synthesis of N-alkylated phthalimides, which is involved in the preparation of primary amines (Gabriel synthesis) by the hydrolysis reaction. It is also used as an intermediate for synthetic indigo, pigments, dyes and pharmaceuticals. Further, it is employed as an organocatalyst for the cyanosilylation of various carbonyl compounds under extremely mild conditions. In addition to this, it serves as a reagent for the transformation of allyl- and alkyl halides into protected primary amines.

Solubility
Soluble in water.

Notes
Moisture sensitive. Incompatible with strong oxidizing agents and strong acids.
RUO – Research Use Only

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