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Merck

755850

Sigma-Aldrich

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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About This Item

经验公式(希尔记法):
C15H23NO4
CAS号:
分子量:
281.35
MDL號碼:
分類程式碼代碼:
12162002
PubChem物質ID:
NACRES:
NA.23

品質等級

化驗

95% (GC)

形狀

powder

mp

94-98 °C

SMILES 字串

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 密鑰

UVZTZBRGZXIBLZ-UHFFFAOYSA-N

一般說明

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

應用

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析证书(COA)

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访问文档库

Safak, M.; Alemdaroglu, F. E.; Li, Y.; Ergen, E.; Hernnann, A.
Advanced Materials, 19, 1499-1499 (2007)
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
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(

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