Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

755850

Sigma-Aldrich

11-Maleimidoundecanoic acid

95% (GC)

Synonym(s):

11-Maleimide undecanoic acid, 2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-undecanoic acid, MM-281, MUDA, Maleimidoundecanoic acid

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C15H23NO4
CAS Number:
57079-01-3
Molecular Weight:
281.35
MDL number:
MFCD00941279
UNSPSC Code:
12162002
PubChem Substance ID:
329766146
NACRES:
NA.23

Quality Level

100

Assay

95% (GC)

form

powder

mp

94-98 °C

SMILES string

OC(=O)CCCCCCCCCCN1C(=O)C=CC1=O

InChI

1S/C15H23NO4/c17-13-10-11-14(18)16(13)12-8-6-4-2-1-3-5-7-9-15(19)20/h10-11H,1-9,12H2,(H,19,20)

InChI key

UVZTZBRGZXIBLZ-UHFFFAOYSA-N

Related Categories

General description

Intermediate for ester and amide linked maleimide monomers, can be used to generate liquid crystal copolymers

Application

The maleimide functional group can be used to conjugate a variety of biomolecules such as enzymes and DNA to the polymer chain.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

Safak, M.; Alemdaroglu, F. E.; Li, Y.; Ergen, E.; Hernnann, A.
Advanced Materials, 19, 1499-1499 (2007)
Karina L Heredia et al.
Macromolecules, 42(7), 2360-2367 (2009-01-01)
In this report we describe a straightforward approach to synthesize polymers with end-groups that bind site-specifically to two different proteins. Telechelic biotin, maleimide poly(N-isopropylacrylamide) (pNIPAAm) was synthesized for the formation of streptavidin (SAv)-bovine serum albumin (BSA) polymer conjugates. Reversible addition-fragmentation
Pietro Buono et al.
ChemSusChem, 10(5), 984-992 (2017-01-04)
In the present report an environmentally friendly approach to transforming renewable feedstocks into value-added materials is proposed. This transformation pathway was conducted under green conditions, without the use of solvents or catalyst. First, controlled modification of lignin, a major biopolymer

Articles

Recent Trends in Self-Healing Soft Electronics

Self-healing soft electronic materials enable autonomous repair, reducing waste and costs in electronic devices.

Recent Trends in Self-Healing Soft Electronics

Self-healing soft electronic materials enable autonomous repair, reducing waste and costs in electronic devices.

Recent Trends in Self-Healing Soft Electronics

Self-healing soft electronic materials enable autonomous repair, reducing waste and costs in electronic devices.

Recent Trends in Self-Healing Soft Electronics

Self-healing soft electronic materials enable autonomous repair, reducing waste and costs in electronic devices.

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