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341894

Sigma-Aldrich

Cyanogen bromide solution

3.0 M in methylene chloride

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About This Item

Fórmula lineal:
BrCN
Número de CAS:
506-68-3
Peso molecular:
105.92
Beilstein/REAXYS Number:
1697296
MDL number:
MFCD00011597
UNSPSC Code:
12352100
PubChem Substance ID:
24861007
NACRES:
NA.22
form:
liquid

form

liquid

concentration

3.0 M in methylene chloride

solubility

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

density

1.443 g/mL at 25 °C

functional group

bromo

SMILES string

BrC#N

InChI

1S/CBrN/c2-1-3

InChI key

ATDGTVJJHBUTRL-UHFFFAOYSA-N

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General description

Cyanogen bromide solution induces template-guided condensation of oligonucleotides only in the presence of N-substituted morpholines.Mechanism of the phosphomonoester group activation by cyanogen bromide in N-substituted morpholine buffers is investigated.

Application

Cyanogen bromide (CNBr) solution may be used in the cyanogen bromide method for covalent immobilization of trypsin onto poly(2-hydroxyethyl methacrylate)/ polystyrene composite microspheres. It may be used in the preparation of CNBr-activated diol-silica, useful as silica support in HPLC.

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

supp_hazards

EUH032

Storage Class

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
MKCG2197
MKBH9149
MKBG5939
MKBD7228
MKAA2184

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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)
Bart Vanelslander et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(7), 2412-2417 (2012-02-07)
The spatial organization of biofilms is strongly regulated by chemical cues released by settling organisms. However, the exact nature of these interactions and the repertoire of chemical cues and signals that micro-organisms produce and exude in response to the presence
Deborah Negrão-Corrêa et al.
PloS one, 9(2), e88042-e88042 (2014-02-08)
Studies in murine models and human populations have indicated that the collagen-rich granulomatous response against parasite eggs trapped in the liver is associated with the development of severe hepatosplenic schistosomiasis, characterized by periportal fibrosis and portal hypertension. The role of
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