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Merck
CN

803332

Sigma-Aldrich

磺基-SANPAH(磺基琥珀酰亚胺基6(4′-叠氮基-2′-硝基苯氨基)己酸酯

别名:

(sulfosuccinimidyl 6-(4′-azido-2′-nitrophenylamino)hexanoate), 1-[[6-[(4-azido-2-nitrophenyl)amino]-1-oxohexyl]oxy]-2,5-dioxo-3-pyrrolidinesulfonic acid monosodium salt, Sulfo-SANPAH

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About This Item

经验公式(希尔记法):
C16H17O9N6NaS
分子量:
492.40
UNSPSC代码:
12352102
PubChem化学物质编号:
NACRES:
NA.22

形式

powder

质量水平

分子量

492.4

反应适用性

reagent type: cross-linking reagent

储存条件

desiccated

溶解性

water: soluble

官能团

azide

运输

ambient

储存温度

−20°C

SMILES字符串

O=C1CC(S(=O)([O-])=O)C(N1OC(CCCCCNC2=CC=C(N=[N+]=[N-])C=C2[N+]([O-])=O)=O)=O.[Na+]

InChI

1S/C16H18N6O9S.Na/c17-20-19-10-5-6-11(12(8-10)22(26)27)18-7-3-1-2-4-15(24)31-21-14(23)9-13(16(21)25)32(28,29)30;/h5-6,8,13,18H,1-4,7,9H2,(H,28,29,30);/q;+1/p-1

InChI key

XXUXLXCHYVHAOD-UHFFFAOYSA-M

一般描述

ANB-NOS和磺基-SANBAH是异双官能交联剂,含有胺反应性的N-羟基琥珀酰亚胺酯和光活化的硝基苯叠氮化物。NHS酯在pH 7-9缓冲液中与伯氨基(-NH2)有效反应,形成稳定的酰胺键。当暴露在紫外光下时,硝基苯叠氮化合物形成氮烯基团,该基团可以引发双键的加成反应,插入碳氢和氮氢位点,或随后与亲核体(例如伯胺)发生扩环反应。

应用


  • Dynamic Control of Cell Adhesion on a Stiffness-Tunable Substrate for Analyzing the Mechanobiology of Collective Cell Migration: This study uses Sulfo-SANPAH for photochemical cross-linking in cell adhesion research (Kamimura et al., 2017).

  • Evaluation of L929 fibroblast attachment and proliferation on ArgGlyAspSer (RGDS) immobilized chitosan: This paper investigates the use of Sulfo-SANPAH to enhance fibroblast attachment on chitosan substrates (Karakecili et al., 2016).

特点和优势

  • 反应基团:磺基氨基磺酸酯和硝基苯叠氮化物
  • 对氨基和任何亲核物质有反应
  • 不可切割
  • n-磺基琥珀酰亚胺基-6-(4′-叠氮基-2′-硝基苯氨基)己酸酯
  • 最佳光解发生在320-350纳米;将辐射对生物分子的损害降至最低
  • 水溶性;不可切割

注意

这种产品对湿气很敏感。小瓶包装在带有干燥剂的可再密封袋中,以减少湿气接触。冷藏后,打开前将小瓶平衡至室温,以减少小瓶内的冷凝。制备新的溶液。不建议储存原液。使用后,将小瓶放回可重新密封的袋子中。封闭袋子,在推荐的温度下储存产品。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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