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227463

Sigma-Aldrich

1,1′-(Methylenedi-4,1-phenylene)bismaleimide

95%

Synonyme(s) :

Bismaleimide

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About This Item

Formule empirique (notation de Hill):
C21H14N2O4
Numéro CAS:
Poids moléculaire :
358.35
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Pureté

95%

Forme

powder

Pf

156-158 °C (lit.)

Groupe fonctionnel

imide

Chaîne SMILES 

O=C1C=CC(=O)N1c2ccc(Cc3ccc(cc3)N4C(=O)C=CC4=O)cc2

InChI

1S/C21H14N2O4/c24-18-9-10-19(25)22(18)16-5-1-14(2-6-16)13-15-3-7-17(8-4-15)23-20(26)11-12-21(23)27/h1-12H,13H2

Clé InChI

XQUPVDVFXZDTLT-UHFFFAOYSA-N

Description générale

The thermal and mechanical properties of GEEA cured by 1,1′-(methylenedi-4,1-phenylene)bismaleimide were studied. MDP-BMI is a cross-linking agent widely used in the synthesis of thermosetting polymers and flame retardant resins.

Application

1,1′-(Methylenedi-4,1-phenylene)bismaleimide was used to cure glycidyl ester of eleostearic acid (GEEA).

Pictogrammes

Skull and crossbones

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 2 Inhalation - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Consulter la Bibliothèque de documents

Seon Min Woo et al.
Chemico-biological interactions, 260, 168-175 (2016-10-13)
Jaceosidin is a flavonoid isolated from Artemisia vestita that has been reported to possess anti-tumor and anti-proliferative activities in many cancer cells. In this study, we investigated the anti-tumor activity of jaceosodin in renal carcinoma cells. Jaceosidin induced apoptosis in
Kun Huang et al.
Biomacromolecules, 15(3), 837-843 (2014-02-04)
A novel biobased epoxy monomer with conjugated double bonds, glycidyl ester of eleostearic acid (GEEA) was synthesized from tung oil fatty acids and characterized by (1)H and (13)C NMR. Differential scanning calorimeter analysis (DSC) and Fourier transform infrared spectroscopy (FT-IR)
Elyse S Fischer et al.
Protein science : a publication of the Protein Society, 28(6), 1059-1070 (2019-04-04)
In recent years, anthrax toxin has been reengineered to act as a highly specific antiangiogenic cancer therapeutic, shown to kill tumors in animal models. This has been achieved by modifying protective antigen (PA) so that its activation and toxicity require
Sanket Patke et al.
mAbs, 9(3), 430-437 (2017-01-27)
Bispecific antibodies are a growing class of therapeutic molecules. Many of the current bispecific formats require DNA engineering to convert the parental monoclonal antibodies into the final bispecific molecules. We describe here a method to generate bispecific molecules from hybridoma
Shin Kim et al.
International journal of oncology, 49(6), 2620-2628 (2016-11-15)
Previous studies have demonstrated the anticancer effects of the newly developed cyclin-dependent kinase inhibitor BAI in various cancer cells. However, the molecular mechanisms of the cellular effects induced by BAI have not been fully elucidated. The objective of this study

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