跳转至内容
Merck
CN

12110

Sigma-Aldrich

聚合物键合型二苯甲胺盐酸盐

100-200 mesh, extent of labeling: ~1.5 mmol/g amine loading

别名:

BHA-聚苯乙烯, 聚合物键合型 α-氨基二苯甲烷盐酸盐, 聚苯乙烯交联二乙烯苯,α-氨基苄基化盐酸盐

登录查看公司和协议定价

选择尺寸


关于此项目

MDL编号:
UNSPSC代码:
12352200
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

标记范围

~1.5 mmol/g amine loading

基质

crosslinked with 2% DVB

粒径

100-200 mesh

正在寻找类似产品? 访问 产品对比指南

其他说明

用于固相合成肽的载体;用于制备 NBB-树脂

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助,请联系 客户支持

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

E. Giralt et al.
Tetrahedron, 38, 1193-1193 (1982)
Automated solid phase synthesis of thymosin alpha 1.
S S Wang et al.
International journal of peptide and protein research, 15(1), 1-4 (1980-01-01)
S A Gaehde et al.
International journal of peptide and protein research, 18(5), 451-458 (1981-11-01)
N-tert.-butoxycarbonyl-aminomethyl( alpha-phenyl)phenoxyacetic acid was synthesized and found to be suitable for use as a handle in the solid-phase synthesis of peptide alpha-carboxamides. This handle was prepared with an 82% yield when N-tert.-butoxycarbonyl-( rho-hydroxy)benzhydrylamine was treated with excess sodium iodoacetate under
D H Coy et al.
International journal of peptide and protein research, 15(1), 73-78 (1980-01-01)
The 28-residue sequence of porcine vasoactive peptide (VIP) was assembled on a benzhydrylamine resin support, cleaved by HF treatment, and purified by ion-exchange and partition chromatography. In addition to the normal criteria, the homogeneity of the final material, obtained in

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持