1-Hexyl-3-methylimidazolium tetrafluoroborate(HMIMBF4) - ≥97% , CAS No.244193-50-8

CAS: 244193-50-8 Cat. No.: H101525 Peso molecular: 254.08 Beilstein Registry Number: 8366236 Número EC: 680-100-4 PubChem CID: 2734179

GRADE & PURITY ≥97%

Synonyms

ZB1666 | 1-Hexyl-3-methylimidazolium tetrafluoroborate [HMIm]BF4 | C10H19BF4N2 | 1-n-Hexyl-3-methylimidazolium tetrafluoroborate | 1-Hexyl-3-methylimidazolium tetrafluoroborate [HMIM] [BF4] | SY015054 | 1-hexyl-3-methyl-1H-imidazol-3-ium tetrafluoroborate

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

ZB1666 | 1-Hexyl-3-methylimidazolium tetrafluoroborate [HMIm]BF4 | C10H19BF4N2 | 1-n-Hexyl-3-methylimidazolium tetrafluoroborate | 1-Hexyl-3-methylimidazolium tetrafluoroborate [HMIM] [BF4] | SY015054 | 1-hexyl-3-methyl-1H-imidazol-3-ium tetrafluoroborate

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 488192499
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488192499
• Sonrisas canónicas: [B-](F)(F)(F)F.CCCCCCN1C=C[N+](=C1)C
• IUPAC Name: 1-hexyl-3-methylimidazol-3-ium;tetrafluoroborate
• InChIKey: MFXLOVLEQJRXFP-UHFFFAOYSA-N
• INCHI: 1S/C10H19N2.BF4/c1-3-4-5-6-7-12-9-8-11(2)10-12;2-1(3,4)5/h8-10H,3-7H2,1-2H3;/q+1;-1
• Isómeros SMILES: [B-](F)(F)(F)F.CCCCCCN1C=C[N+](=C1)C
• WGK Alemania: 3
• PubChem CID: 2734179
• Peso molecular: 254.08
• Beilstein: 8366236
• Reaxy-Rn: 8366236

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 Organic metalloid salts Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: N-substituted imidazole - Heteroaromatic compound - Azacycle - Organic metalloid salt - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organonitrogen compound - 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

• Sensibilidad: Moisture sensitive.
• Índice de refracción: 1.43
• Punto de fusión (°C): -82°C
• Peso molecular: 254.080 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 254.158 Da
• Monoisotopic Mass: 254.158 Da
• Topological Polar Surface Area: 8.800 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 134.000
• 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. Ju Wang, Jun-Qin Qiao, Wei-Juan Zheng, Hong-Zhen Lian.  (2023)  Effect of ionic liquids as mobile phase additives on retention behaviors of G-quadruplexes in reversed-phase high performance liquid chromatography.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38176351] [10.1016/j.chroma.2023.464604]

2. Zidan Luo, Mengfei Tian, Naveed Ahmad, Wu Qiu, Yu Zhang, Chunying Li, Chunjian Zhao.  (2022)  A switchable temperature-responsive ionic liquid-based surfactant-free microemulsion for extraction and separation of hydrophilic and lipophilic compounds from Camptotheca acuminata and extraction mechanism.  COLLOIDS AND SURFACES B-BIOINTERFACES,      [PMID:36469979] [10.1016/j.colsurfb.2022.113067]

3. Guoqiang Lu, Hengda Yuan, Jiulei Zhou, Fuping Chen, Chao Li, Tanlong Xue, Xin Shu, Yingying Zhao, Jun Nie, Xiaoqun Zhu.  (2022)  Patterned Magnetofluids via Magnetic Printing and Photopolymerization for Multifunctional Flexible Electronic Sensors.  ACS Applied Materials & Interfaces,      [PMID:35730674] [10.1021/acsami.2c04755]

4. Xiaofeng Li, Maohua Ma, Xuan Xin, Yuqian Tang, Guanglei Zhao, Xinglong Xiao.  (2019)  Efficient acylation of gastrodin by Aspergillus oryzae whole-cells in non-aqueous media.  RSC Advances,  9  (29): (16701-16712).  [PMID:35516375] [10.1039/C9RA01605H]

5. Xiaopo Wang, Yao Zhang, Dongbo Wang, Yanjun Sun.  (2017)  Phase Equilibria of trans-1,3,3,3-Tetrafluoropropene with Three Imidazolium Ionic Liquids.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/acs.jced.7b00047]

6. Shun Lu, Chaohu Xiao, Min Yin, Yang Jin, Shuqin Xu, Qi-Meige Hasi, Yuhan Zhang, Lihua Chen.  (2024)  Double-layered solar evaporator based on polymeric ionic liquid grafted attapulgite and MXene/PPy for efficient desalination and photodegradation.  Surfaces and Interfaces,      [PMID:] [10.1016/j.surfin.2024.104191]

7. Shichen Mao, Baogang Wang, Shanshan Dai, Hongsheng Lu.  (2024)  Synthesizing Benzotriazole Group-Terminated Carbon Dots as Multifunctional Additives of Poly(ethylene glycol).  LANGMUIR,      [PMID:38211333] [10.1021/acs.langmuir.3c03492]

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