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Merck
CN

341894

Sigma-Aldrich

溴化氰 溶液

3.0 M in methylene chloride

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线性分子式:
BrCN
CAS号:
分子量:
105.92
Beilstein:
1697296
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

形式

liquid

浓度

3.0 M in methylene chloride

溶解性

alcohol: freely soluble
diethyl ether: freely soluble
water: freely soluble

密度

1.443 g/mL at 25 °C

SMILES字符串

BrC#N

InChI

1S/CBrN/c2-1-3

InChI key

ATDGTVJJHBUTRL-UHFFFAOYSA-N

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一般描述

溴化氰溶液仅在N-取代吗啉存在下诱导模板引导的寡核苷酸缩合。研究了N-取代吗啉缓冲液中溴化氰激活磷酸单酯基团的机理。

应用

溴化氰(CNBr)溶液可用于溴化氰法将胰蛋白酶共价固定在聚(2-羟乙基甲基丙烯酸酯)/聚苯乙烯复合微球上。它可用于制备CNBr活化的二醇二氧化硅,可用作HPLC中的二氧化硅载体。

警示用语:

Danger

危险分类

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

靶器官

Central nervous system

补充剂危害

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品

分析证书(COA)

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Luis A Jurado et al.
Journal of chromatography. A, 971(1-2), 95-104 (2002-09-28)
To obtain silica supports for high-performance affinity chromatography, a method of preparing CNBr-activated diol-silica under anhydrous conditions was developed. Activation of the silane-derived hydroxyls with cyanogen bromide and triethylamine was optimized and demonstrated to efficiently couple several amino ligands (tryptophan
Z A Shabarova et al.
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 27(5-6), 555-566 (2001-09-07)
Cyanogen bromide has been found to induce the template-guided condensation of oligonucleotides only in the presence of N-substituted morpholines. Based on 31P, 1H and 13C NMR spectroscopy data, the mechanism of the phosphomonoester group activation by cyanogen bromide in N-substituted
Covalent immobilization of trypsin onto poly (2-hydroxyethyl methacrylate)/polystyrene composite microspheres by cyanogen bromide method and its enzymatic activity.
Okubo M, et al.
Colloid and Polymer Science, 265(11), 957-964 (1987)
Arthur T Kopylov et al.
Proteomics, 13(5), 727-742 (2013-01-03)
In this paper, we present a method for the determination of low- and ultralow copy-number proteins in biomaterials based on a combination of concentrating the protein from the sample onto cyanogen bromide-activated Sepharose 4B (via nonspecific binding of free amino
P P Moerman et al.
Journal of proteomics, 73(8), 1454-1460 (2010-02-16)
We present a novel approach to perform C-terminal sequence analysis by discriminating the C-terminal peptide in a mass spectral analysis of a CNBr digest. During CNBr cleavage, all Met-Xxx peptide bonds are cleaved and the generated internal peptides all end

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