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227463

Sigma-Aldrich

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

95%

Synonym(s):

Bismaleimide

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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.)

functional group

imide

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM8133
MKCL8048
MKCK4727
MKCG9474
MKBZ8437V

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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)
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Sanket Patke et al.
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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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