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Maleimide, 98+%, Thermo Scientific Chemicals
製品番号（カタログ番号）： A13135.14
25 g, Each
化学物質識別子
CAS
541-59-3
IUPAC Name
potassium silver(1+) bis(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-ide)
Molecular Formula
C8H4AgKN2O4
InChI Key
KWLWLQRUFFGWNG-UHFFFAOYSA-L
SMILES
[K+].[Ag+].O=C1[N-]C(=O)C=C1.O=C1[N-]C(=O)C=C1
仕様
スペックシートAppearance (Color)
White to pale yellow
Form
Crystals or powder or crystalline powder or granules
Assay (GC)
≥98.0%
Identification (FTIR)
Conforms
Solution Test
2.5% Ethanol: clear to faintly turbid
概要
Reacts quantitatively with sulfhydryl groups.Maleimide is used to immobilize the bovine serum albumin-boronic acid conjugates in association with silica beads. Its nanoparticle surface favors the conjugation with cell penetration peptides. It is involved in Rhodium-catalyzed conjugate arylation with arylboronic acids. It is actively involved in Michael additions and Diels-Alder reactions by the addition across the double bond. It acts as crosslinking reagents in polymer chemistry.
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
Reacts quantitatively with sulfhydryl groups.Maleimide is used to immobilize the bovine serum albumin-boronic acid conjugates in association with silica beads. Its nanoparticle surface favors the conjugation with cell penetration peptides. It is involved in Rhodium-catalyzed conjugate arylation with arylboronic acids. It is actively involved in Michael additions and Diels-Alder reactions by the addition across the double bond. It acts as crosslinking reagents in polymer chemistry.
Solubility
Soluble in water.
Notes
Store in a cool place. Incompatible with strong oxidizing agents, strong acids, strong bases and strong reducing agents.
Reacts quantitatively with sulfhydryl groups.Maleimide is used to immobilize the bovine serum albumin-boronic acid conjugates in association with silica beads. Its nanoparticle surface favors the conjugation with cell penetration peptides. It is involved in Rhodium-catalyzed conjugate arylation with arylboronic acids. It is actively involved in Michael additions and Diels-Alder reactions by the addition across the double bond. It acts as crosslinking reagents in polymer chemistry.
Solubility
Soluble in water.
Notes
Store in a cool place. Incompatible with strong oxidizing agents, strong acids, strong bases and strong reducing agents.
RUO – Research Use Only
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