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Merck
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文件

8.55003

Sigma-Aldrich

Rink Amide MBHA树脂(100-200目)

Novabiochem®

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别名:
Rink Amide MBHA树脂(100-200目)
UNSPSC代码:
12352111
NACRES:
NA.22

质量水平

产品线

Novabiochem®

形式

beads

反应适用性

reaction type: Fmoc solid-phase peptide synthesis

制造商/商品名称

Novabiochem®

应用

peptide synthesis

官能团

amine

储存温度

2-30°C

一般描述

该支持物包括通过正亮氨酸连接至MBHA树脂的修饰的Rink酰胺接头,并且是肽酰胺Fmoc SPP的理想工具。可以通过用95% TFA进行单步处理来实现从该树脂的裂解,从而以高收率和纯度提供肽酰胺。

相关方案和技术文章
肽合成用树脂的上样方案

应用


  • Liquid chromatography-tandem mass spectrometry for forensic analysis: LSD-D₃ is utilized as an internal standard in the liquid chromatography-tandem mass spectrometry determination of LSD and its metabolites in forensic samples, enhancing accuracy and precision in the analytical results (Johansen and Jensen, 2005).

  • Isotope dilution mass spectrometry in urine testing: Employed in the high-performance liquid chromatography-isotope dilution mass spectrometry (IDMS) method, LSD-D₃ serves as a crucial internal standard for the quantification of lysergide (LSD) in urine, aiding in precise and accurate drug testing (White et al., 1999).

  • Automated extraction and LC/MS/MS confirmation: LSD-D₃ is used in the automated extraction of lysergic acid diethylamide from various biological matrices, followed by confirmation using LC/MS/MS. This application highlights its role in improving the efficiency and reliability of toxicological analyses (de Kanel et al., 1998).

联系

替代品:01-64-0037

分析说明

颜色(目测):白色至浅黄色至米黄色
物质外观(目测):微珠
负载量(光度法测定DBU/DMF处理后释放的Fmoc生色团):0.40 - 0.90 mmol/g
TNBS检验:符合检验
溶胀体积(DMF):结果因批次而异
溶胀体积(CH₂Cl₂):结果因批次而异
根据Houben Weyl得到的总溶胀体积(CH2Cl2): ≥ 5.2 ml/g
根据Houben Weyl得到的总溶胀体积(DMF): ≥ 5.2 ml/g
聚合物基质为共聚物(苯乙烯-1% DVB),100 - 200目。

法律信息

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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商品

Novabiochem® offers a wide range of linkers and derivatized resins for Fmoc solid-phase peptide synthesis with specialized protocols.

实验方案

Review various resins like Merrifield, trityl-based, and hydroxymethyl-functionalized for peptide immobilization for diverse applications.

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