Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

227463

Sigma-Aldrich

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

95%

Synonym(s):

Bismaleimide

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C21H14N2O4
CAS Number:
13676-54-5
Molecular Weight:
358.35
EC Number:
237-163-4
MDL number:
MFCD00005507
UNSPSC Code:
12352100
PubChem Substance ID:
24853634
NACRES:
NA.22

Assay

95%

form

powder

mp

156-158 °C (lit.)

SMILES string

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

InChI key

XQUPVDVFXZDTLT-UHFFFAOYSA-N

Related Categories

General description

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).

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H315,H319,H330,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

N,N'-(1,3-PHENYLENE)DIMALEIMIDE AldrichCPR

S375055

N,N'-(1,3-PHENYLENE)DIMALEIMIDE

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
Furan-Modified Spherosilicates as Building Blocks for Self-Healing Materials
T Engel, et al.
European Journal of Inorganic Chemistry, 2015, 1226-1232 (2015)
Hou-Yu Li et al.
Molecules (Basel, Switzerland), 25(14) (2020-07-12)
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.
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
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)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service