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63179

Sigma-Aldrich

3-（马来酰亚胺基）丙酸 N-羟基琥珀酰亚胺酯

≥98.5% (HPLC)

别名:

3-（马来酰亚胺基）丙酸 N-琥珀酰亚胺酯, BMPS, N-琥珀酰亚胺基 3-马来酰亚胺丙酸酯, N-马来酰基-β-丙氨酸 N'-羟基琥珀酰亚胺酯, N-（3-马来酰亚胺丙酰氧基）琥珀酰亚胺

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About This Item

经验公式（希尔记法）:
C11H10N2O6
CAS号:
55750-62-4
分子量:
266.21
Beilstein:
1492578
MDL编号:
MFCD00043141
UNSPSC代码:
12352106
PubChem化学物质编号:
329759806
NACRES:
NA.25
价格与库存信息目前不能提供

质量水平

200

方案

≥98.5% (HPLC)

表单

solid

反应适用性

reagent type: linker

mp

167-171 °C

官能团

NHS ester

储存温度

2-8°C

SMILES字符串

O=C1CCC(N1OC(CCN2C(C=CC2=O)=O)=O)=O

InChI

1S/C11H10N2O6/c14-7-1-2-8(15)12(7)6-5-11(18)19-13-9(16)3-4-10(13)17/h1-2H,3-6H2

InChI key

JKHVDAUOODACDU-UHFFFAOYSA-N

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应用

琥珀酰亚胺基 3-马来酰亚胺丙酸酯 (SMP，BMPS) 用作脂肪族异双功能交联剂试剂。用于诸如酶免疫测定前半抗原与酶交联或荧光底物与肽抗原交联等技术，用于荧光免疫测定。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCBW7244
SLCK8387
BCBL4586V
BCBR5288V
SLBH7227

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M C Durrieu et al.
Journal of materials science. Materials in medicine, 15(7), 779-786 (2004-09-28)
Ceramics possess osteoconductive properties but exhibit no intrinsic osteoinductive capacity. Consequently, they are unable to induce new bone formation in extra osseous sites. In order to develop bone substitutes with osteogenic properties, one promising approach consists of creating hybrid materials
T. Kitagawa
Enzyme Immunoassay, 81-81 (1981)
S J Xiao et al.
Journal of materials science. Materials in medicine, 8(12), 867-872 (2004-09-07)
Surface modification of acid-pretreated titanium with 3-aminopropyltriethoxylsilane (APTES) in dry toluene resulted in covalently bonded siloxane films with surface coverage that was relatively controllable by regulating the reaction conditions. A hetero-bifunctional cross-linker, N-succinimidyl-3-maleimidopropionate (SMP), reacted with the terminal amino groups
S Heyse et al.
Protein science : a publication of the Protein Society, 4(12), 2532-2544 (1995-12-01)
A new method is presented for measuring sensitively the interactions between ligands and their membrane-bound receptors in situ using integrated optics, thus avoiding the need for additional labels. Phospholipid bilayers were attached covalently to waveguides by a novel protocol, which
Wuensch, E.
Hoppe-Seyler'S Zeitschrift fur Physiologische Chemie, 366, 53-53 (1985)
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