Cyanogen bromide - ≥97% , CAS No.506-68-3

CAS: 506-68-3 Cat. No.: C106913 Peso molecular: 105.92 Beilstein Registry Number: 1697296 Número EC: 208-051-2

GRADE & PURITY ≥97%

Synonyms

CYANOGEN BROMIDE [HSDB] | FT-0665252 | NCGC00356964-01 | UN1889 | RCRA waste number U246 | Bromine cyanide (BrCN) | AI3-28715 | Bromocyanogen | Bromine cyanide | Cyanogen bromide, reagent grade, 97% | Q420258 | Bromine cyanide(BrCN) | DTXCID601550 | UN 18

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads,FedEx DG Service

Descripción general

Cyanogen bromide has been used in protein immobilization procedures, and to cleave peptides to find the low resolution structure of a protein. This product is also used dissolved in acetonitrile (sc-207252) to activate agarose (sc-280594) for affinity chromatography
Used For peptide cleavage and use in protein immobilization procedures.

Specifications

Sinónimos

CYANOGEN BROMIDE [HSDB] | FT-0665252 | NCGC00356964-01 | UN1889 | RCRA waste number U246 | Bromine cyanide (BrCN) | AI3-28715 | Bromocyanogen | Bromine cyanide | Cyanogen bromide, reagent grade, 97% | Q420258 | Bromine cyanide(BrCN) | DTXCID601550 | UN 18

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Argon charged

Enviado en

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Pureza

≥97%

Nombres e identificadores

• Sonrisas canónicas: C(#N)Br
• IUPAC Name: carbononitridic bromide
• InChIKey: ATDGTVJJHBUTRL-UHFFFAOYSA-N
• INCHI: 1S/CBrN/c2-1-3
• Isómeros SMILES: C(#N)Br
• WGK Alemania: 3
• Número ONU: 1889
• Grupo de embalaje: I
• Peso molecular: 105.92
• Beilstein: 1697296
• Reaxy-Rn: 1697296
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697296&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Organic cyanides
        • Level5 Nitriles
          • Level6 Cyanogens

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Organic cyanides
• Intermediate Tree Nodes: Nitriles
• Direct Parent: Cyanogens
• Alternative Parents: Organopnictogen compounds Organobromides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Cyanogen - Organopnictogen compound - Hydrocarbon derivative - Organobromide - Organohalogen compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as cyanogens. These are organonitrogen compounds of the form NC-CN or X-CN, where X is a halogen.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: Soluble in water (slightly with decomposition and release of toxic gases), chloroform, dichloromethane, ethanol (readily), and acetonitrile
• Sensibilidad: light and Moisture sensitive
• Punto de ebullición (°C): 61.5°C
• Punto de fusión (°C): 52°C
• Peso molecular: 105.920 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 104.921 Da
• Monoisotopic Mass: 104.921 Da
• Topological Polar Surface Area: 23.800 Ų
• Heavy Atom Count: 3
• Formal Charge: 0
• Complexity: 31.300
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Wei Liu, Yongan Feng, Yapeng Yao, Zihang Liang, Fei Xiao, Zhongliang Ma.  (2023)  In situ synthesis of [Cu(BODN)·5H2O]n@nano-Al composite energetic films with tunable properties in pyro-MEMS.  LAB ON A CHIP,  23  (20): (4493-4503).  [PMID:37753862] [10.1039/D3LC00282A]

2. Linze Liu, Yiqinq Xia, Lian Wang, Rui Shi, Shuai Yan, Xingyu Zhao, Yongzhong Jin, Yuping Sheng.  (2022)  Cyanate Ester Resin with High Heat-Resistance and Degradable Diacetal Structure: Synthesis, Polymerization, and Properties.  MACROMOLECULAR MATERIALS AND ENGINEERING,  307  (11): (2200423).  [PMID:] [10.1002/mame.202200423]

3. Qinglei Wang, Xiaochen Liu, Zili Cui, Xuehui Shangguan, Huanrui Zhang, Jianjun Zhang, Kun Tang, Longshan Li, Xinhong Zhou, Guanglei Cui.  (2020)  A fluorinated polycarbonate based all solid state polymer electrolyte for lithium metal batteries.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2020.135843]

4. Wei Xu, Ran Guan, Fushan Shi, Aifang Du, Songhua Hu.  (2017)  Structural analysis and immunomodulatory effect of polysaccharide from Atractylodis macrocephalae Koidz. on bovine lymphocytes.  CARBOHYDRATE POLYMERS,      [PMID:28821047] [10.1016/j.carbpol.2017.07.041]

5. Ruyun Lou, Weiting Yu, Yizhe Song, Ying Ren, Huizhen Zheng, Xin Guo, Yunfei Lin, Guoyu Pan, Xiuli Wang, Xiaojun Ma.  (2016)  Fabrication of stable galactosylated alginate microcapsules via covalent coupling onto hydroxyl groups for hepatocytes applications.  CARBOHYDRATE POLYMERS,      [PMID:27702535] [10.1016/j.carbpol.2016.08.098]

6. Hao Wang, Xiaohui Zhang, Cunlong Yin, Lu Liu, Liang Chen, Hengfang Tang, Bo Wu, Junfeng Wang.  (2025)  High-purity preparation and biophysical characterization of OX40-TC in lipid nanodiscs.  PROTEIN EXPRESSION AND PURIFICATION,      [PMID:40049376] [10.1016/j.pep.2025.106697]

7. Dongkun Yu, Tiancheng Mu.  (2019)  Strategy To Form Eutectic Molecular Liquids Based on Noncovalent Interactions.  JOURNAL OF PHYSICAL CHEMISTRY B,      [PMID:31117609] [10.1021/acs.jpcb.9b02891]