1-Butyl-3-vinyliMidazoliuM broMide - ≥98% , CAS No.1033461-45-8

CAS: 1033461-45-8 Cat. No.: B302110 Peso molecular: 231.13

GRADE & PURITY ≥98%

Synonyms

AS-61646 | SCHEMBL3700399 | 3-Butyl-1-vinyl-1H-imidazol-3-ium bromide | 3-Butyl-1-vinyl-1H-imidazol-3-iumbromide | AKOS025296070 | 3-butyl-1-ethenyl-1H-imidazol-3-ium bromide | 1033461-45-8 | 1-Butyl-3-vinylimidazolium bromide, 98% | AKOS030228737 | 1-vin

Storage

Room temperature,Desiccated

Shipped In

Normal

Specifications

Sinónimos

AS-61646 | SCHEMBL3700399 | 3-Butyl-1-vinyl-1H-imidazol-3-ium bromide | 3-Butyl-1-vinyl-1H-imidazol-3-iumbromide | AKOS025296070 | 3-butyl-1-ethenyl-1H-imidazol-3-ium bromide | 1033461-45-8 | 1-Butyl-3-vinylimidazolium bromide, 98% | AKOS030228737 | 1-vin

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature, Desiccated

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488202441
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488202441
• Sonrisas canónicas: CCCC[N+]1=CN(C=C1)C=C.[Br-]
• IUPAC Name: 1-butyl-3-ethenylimidazol-1-ium;bromide
• InChIKey: XALVOFYVVOAYPO-UHFFFAOYSA-M
• INCHI: 1S/C9H15N2.BrH/c1-3-5-6-11-8-7-10(4-2)9-11;/h4,7-9H,2-3,5-6H2,1H3;1H/q+1;/p-1
• Isómeros SMILES: CCCC[N+]1=CN(C=C1)C=C.[Br-]
• CAS alternativo: 34311-90-5
• Peso molecular: 231.13
• Reaxy-Rn: 4165359
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4165359&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Azoles
      • Subclass Imidazoles
        • Level5 Substituted imidazoles
          • Level6 N-substituted imidazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Azoles
• Subclass: Imidazoles
• Intermediate Tree Nodes: Substituted imidazoles
• Direct Parent: N-substituted imidazoles
• Alternative Parents: Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organic bromide salts Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: N-substituted imidazole - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic bromide salt - Organic salt - Organonitrogen compound - Organic cation - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as n-substituted imidazoles. These are heterocyclic compounds containing an imidazole ring substituted at position 1.
• 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

• Peso molecular: 231.130 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 230.042 Da
• Monoisotopic Mass: 230.042 Da
• Topological Polar Surface Area: 8.800 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 123.000
• 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: 2

XLogP3

Referencias

1. Lifei Liu, Kuntong Song, Tong Feng, Ting Song, Jintong Li, Shangqing Chen, Weizhen Zhao, Suojiang Zhang.  (2023)  Towards environmentally friendly processing of ionic liquid-based photoresists with a boosted lithography performance.  GREEN CHEMISTRY,  25  (15): (5989-5998).  [PMID:] [10.1039/D3GC01520C]

2. Xinping He, Tianyi Zhuang, Shuai Ruan, Xinhui Xia, Yang Xia, Jun Zhang, Hui Huang, Yongping Gan, Wenkui Zhang.  (2023)  An innovative poly(ionic liquid) hydrogel-based anti-freezing electrolyte with high conductivity for supercapacitor.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.143209]

3. Yu-Fen Bao, Yi-Jie Wang, Yu-Chen Wang, Ding-Hua Liu.  (2023)  Homogeneous base catalyst with high activity and stability for synthesis of dimethyl carbonate by transesterification.  RSC Advances,  13  (14): (9347-9352).  [PMID:36959885] [10.1039/D3RA00164D]

4. Mingyuan Gu, Apparao M. Rao, Jiang Zhou, Bingan Lu.  (2023)  In situ formed uniform and elastic SEI for high-performance batteries.  Energy & Environmental Science,  16  (3): (1166-1175).  [PMID:] [10.1039/D2EE04148K]

5. Huiting Wang, Li Dong, Ling Zhang, Xiangxiang Chen, Qian Zhang, Lixin Xia.  (2021)  Thermally responsive reduced graphene oxide with electroactive functionality for controllable electroanalysis.  TALANTA,      [PMID:33965033] [10.1016/j.talanta.2021.122368]

6. Xiao Sha, Xiaoli Sheng, Yuming Zhou, Beibei Wang, Yonghui Liu, Jiehua Bao.  (2019)  High Catalytic Performance of Mesoporous Dual Brønsted Acidic Ternary Poly (Ionic Liquids) for Friedel-Crafts Alkylation.  APPLIED ORGANOMETALLIC CHEMISTRY,  33  (11): (e5180).  [PMID:] [10.1002/aoc.5180]

7. Beibei Wang, Xiaoli Sheng, Yuming Zhou, Huaying Gao, Zhiying Zhu, Saichun Hu, Qiang Liao, Xiao Sha.  (2019)  Synthesis and characterization of a supported ionic-liquid phase catalyst with a dual-mesoporous structure derived from poly(ionic liquids) and P123.  NEW JOURNAL OF CHEMISTRY,  43  (7): (2899-2907).  [PMID:] [10.1039/C8NJ05532G]

8. Yuanhao Shi, Dongxia Li, Xiangfeng Sun, Yuxin Xue, Zhiqi Li, Yulin Fu, Chongxian Luo, Qiong Lin, Xuefeng Gui, Kai Xu.  (2024)  Cationic Polymer Binder for Simultaneously Propelling Ion Transfer and Promoting Polysulfide Conversion in Lithium–Sulfur Batteries.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c00668]

9. Dan Li, Qian Chen, Rui Li, Yaolin Hou, Yulong Liu, Haiming Xie, Jia Liu, Jiefang Zhu.  (2024)  Polymeric Ionic Liquid-Enabled In Situ Protection of Li Anodes for High-Performance Li-O2 Batteries.  ChemSusChem,      [PMID:39536177] [10.1002/cssc.202402102]

10. Shanshan Wang, Chaohu Xiao, Shun Lu, Haijing Lu, Qi-Meige Hasi, Yuhan Zhang, Xingping Luo, Lihua Chen.  (2023)  Integrated Solar Evaporator with Salt Resistance and Lipophobicity Derived from Waste Newspapers for Efficient Desalination.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.2c06869]

11. Shu He, Hongli Fang, Jia Liu, Xing Wu, Zeng Liu, Wen Gu, Wei Shao.  (2024)  Fabrication of anti-freezing and self-healing hydrogel sensors based on carboxymethyl guar gum and poly(ionic liquid).  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39197606] [10.1016/j.ijbiomac.2024.135112]

12. Mei-Qiang Cai, Xiao-Qing Wei, Chun-Hui Du, Xu-Ming Ma, Mi-Cong Jin.  (2014)  Novel amphiphilic polymeric ionic liquid-solid phase micro-extraction membrane for the preconcentration of aniline as degradation product of azo dye Orange G under sonication by liquid chromatography–tandem mass spectrometry.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:24857038] [10.1016/j.chroma.2014.05.008]

13. Tong Hongping, Li Shuangqing, Dong Xiuling, Xing Zheng, Li Haitao, Liu Xiang.  (2025)  Enhanced carbon dispersion of polyacrylamide/sodium alginate hydrogels via irregular copolymerization imidazolyl ionic liquid for flexible sensor.  JOURNAL OF POLYMER RESEARCH,  32  (4): (1-13).  [PMID:] [10.1007/s10965-025-04359-3]

14. Zewei Ye, Haomeng Yu, Hongxia Xie, Wenwen Zhu, Shitao Shi, Chencong Liu, Yuanyuan Wang, Jiaqi Liao, Qingfeng Sun, Dawei Zhao, Xiaoping Shen.  (2025)  Flame-Retardant Ionogel Enabled by Lignin Molecular Networks for Fire Rescue.  Advanced Science,      [PMID:40559707] [10.1002/advs.202506901]

15. Mengyue Chen, Tianqi Huang, Shuang Tong, Chao Wang, Ming Zhang.  (2025)  Heteropolyacid-Based Poly(Ionic Liquid) Catalyst for Ultra-Deep and Recyclable Oxidative Desulfurization of Fuels.  Catalysts,  15  (7): (622).  [PMID:] [10.3390/catal15070622]