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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.)

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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European Journal of Inorganic Chemistry, 2015, 1226-1232 (2015)
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In order to improve the mechanical and dielectric properties of radome cyanate, a synergistic reinforcement method is employed to develop a resin-based ternary-composite with high heat-resistance and preferable radar-band transmission, which is expected to be applied to fabricate radomes capable
Elyse S Fischer et al.
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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)

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