Skip to Content
Merck
All Photos(1)

Key Documents

78485

Sigma-Aldrich

N,N′-(1,4-Phenylene)dimaleimide

≥98.0% (HPLC)

Synonym(s):

1,4-Dimaleimidobenzene, N,N′-(p-Phenylene)dimaleimide

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C14H8N2O4
CAS Number:
Molecular Weight:
268.22
Beilstein:
249631
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:

Assay

≥98.0% (HPLC)

mp

>300 °C (lit.)

SMILES string

O=C1C=CC(=O)N1c2ccc(cc2)N3C(=O)C=CC3=O

InChI

1S/C14H8N2O4/c17-11-5-6-12(18)15(11)9-1-2-10(4-3-9)16-13(19)7-8-14(16)20/h1-8H

InChI key

AQGZJQNZNONGKY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Other Notes

Bifunctional thiol reagent for the cross-linking of proteins; Efficient procedure for the conjugation of an antibody with an enzyme

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support.

Already Own This Product?

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

Visit the Document Library

S Yoshitake et al.
Scandinavian journal of immunology, 10(1), 81-86 (1979-01-01)
An efficient procedure for the conjugation of rabbit Fab' with beta-D-galactosidase from Escherichia coli using N,N-o-phenylenedimaleimide is described. Thiol groups of Fab' were stabilized by the presence of ethylenediaminetetraacetate, and malemide groups were shown to be stable at pH 5
J A Wells et al.
Proceedings of the National Academy of Sciences of the United States of America, 76(10), 4966-4970 (1979-10-01)
Studies with reagents that crosslink two thiol groups have shown that it is possible to trap nucleotides at the active site of myosin chymotryptic subfragment 1. Subfragment 1 incorporates nearly stoichiometric quantities of [14C]ATP or [14C]ADP in a manner that
P Knight
The Biochemical journal, 179(1), 191-197 (1979-04-01)
To understand the extent of the cross-linking of proteins by the bifunctional reagent p-NN'-phenylenebismaleimide, a quantitative study of competing reactions has been undertaken. The two reactive maleimide rings of the bismaleimide are hydrolysed in mildly alkaline aqueous solutions much more
P Knight et al.
Biochemistry, 19(20), 4682-4687 (1980-09-30)
The hypothesis that the subunits of F-actin rotate during interactin with myosin and ATP has been tested by using the specific cross-linking reagent p-phenylene-N,N'-bis(maleimide) (PM). The insertion of cross-links between F-actin subunits does not change the ability of the F-actin

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