755850
11-马来酰亚胺基癸酸
95% (GC)
别名:
11-Maleimide undecanoic acid, 2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-undecanoic acid, MM-281, MUDA, Maleimidoundecanoic acid
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关于此项目
经验公式（希尔记法）:
C15H23NO4
化学文摘社编号:
分子量:
281.35
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
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
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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