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Potassium phthalimide, 98+%, Thermo Scientific Chemicals

33.90 € - 354.00 €

Chemical Identifiers

CAS 1074-82-4
Molecular Formula C8H4KNO2
Molecular Weight (g/mol) 185.22
MDL Number MFCD00005887
InChI Key FYRHIOVKTDQVFC-UHFFFAOYSA-M
Synonym potassium phthalimide, potassium 1,3-dioxoisoindolin-2-ide, n-potassiophthalimide, phthalimide potassium salt, n-potassium phthalimide, unii-x6kka27dil, phthalimide, potassium salt, potassium phthalamide, 1h-isoindole-1,3 2h-dione, potassium salt, x6kka27dil
PubChem CID 3356745
IUPAC Name potassium;isoindol-2-ide-1,3-dione
SMILES [K+].O=C1[N-]C(=O)C2=CC=CC=C12
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Thermo Scientific Alfa Aesar
A11134.22
100 g
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Thermo Scientific Alfa Aesar
A11134.36
500 g
90.20 €
500g
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Thermo Scientific Alfa Aesar
A11134.0E
2500 g
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Description

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.
Specifications

Chemical Identifiers

1074-82-4
185.22
FYRHIOVKTDQVFC-UHFFFAOYSA-M
3356745
[K+].O=C1[N-]C(=O)C2=CC=CC=C12
C8H4KNO2
MFCD00005887
potassium phthalimide, potassium 1,3-dioxoisoindolin-2-ide, n-potassiophthalimide, phthalimide potassium salt, n-potassium phthalimide, unii-x6kka27dil, phthalimide, potassium salt, potassium phthalamide, 1h-isoindole-1,3 2h-dione, potassium salt, x6kka27dil
potassium;isoindol-2-ide-1,3-dione

Specifications

1074-82-4
1.63
MFCD00005887
Moisture sensitive
Soluble in water.
[K+].O=C1[N-]C(=O)C2=CC=CC=C12
185.22
185.23
Potassium phthalimide
>300°C
C8H4KNO2
3598719
potassium phthalimide, potassium 1,3-dioxoisoindolin-2-ide, n-potassiophthalimide, phthalimide potassium salt, n-potassium phthalimide, unii-x6kka27dil, phthalimide, potassium salt, potassium phthalamide, 1h-isoindole-1,3 2h-dione, potassium salt, x6kka27dil
FYRHIOVKTDQVFC-UHFFFAOYSA-M
potassium;isoindol-2-ide-1,3-dione
3356745
≥98%
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Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

GHS P Statement
P261-P280-P305+P351+P338-P304+P340-P405-P501a
Avoid breathing dust/fume/gas/mist/vapors/spray.
Wear protective gloves/protective clothing/eye protection/face protection.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do.
Continue rinsing.
IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing.
Store locked up.
Dispose of contents/container in accordance with local/regional/national/international regulations.

Warning

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Recommended Storage : Ambient temperatures

SDS
Documents

Documents

Product Certifications

RUO – Research Use Only