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Merck
CN

755850

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

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About This Item

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

Key Documents

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Product Name

11-Maleimidoundecanoic acid, 95% (GC)

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)

SMILES string

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

InChI key

UVZTZBRGZXIBLZ-UHFFFAOYSA-N

assay

95% (GC)

form

powder

mp

94-98 °C

Quality Level

100

Related Categories

Application

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

General description

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ2069
MKCW6997
MKCP5105
MKCJ3121
MKCC1045

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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

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