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:
产品名称
11-马来酰亚胺基癸酸, 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
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
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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