713112
1-丁基-4-甲基碘化吡啶
99%
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关于此项目
经验公式（希尔记法）:
C10H16IN
化学文摘社编号:
分子量:
277.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3731243
InChI
1S/C10H16N.HI/c1-3-4-7-11-8-5-10(2)6-9-11;/h5-6,8-9H,3-4,7H2,1-2H3;1H/q+1;/p-1
SMILES string
[I-].CCCC[n+]1ccc(C)cc1
InChI key
RSJCFBORABJFGA-UHFFFAOYSA-M
assay
≥98.5% (HPLC/T), 99%
form
powder
impurities
≤0.5% water
anion traces
bromide (Br-): ≤25 mg/kg, chloride (Cl-): ≤25 mg/kg, fluoride (F-): ≤10 mg/kg, nitrate (NO3-): ≤25 mg/kg, phosphate (PO43-): ≤10 mg/kg, sulfate (SO42-): ≤10 mg/kg
Application
1-Butyl-4-methylpyridinium iodide can be used:
- To prepare host-guest inclusion complexes of α- and β-cyclodextrins in an aqueous medium.
- As a halogen source in the preparation of bismuth oxyhalide semiconductors for photocatalysis applications.
- As a catalyst in the synthesis of allyl glycidyl carbonates by cycloaddition of epoxides with CO2.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Self-assembly inclusion of green solvent with oligosaccharides
Roy MN, et al.
Journal of Molecular Liquids, 216, 132-136 (2016)
Microwave-assisted, rapid cycloaddition of allyl glycidyl ether and CO2 by employing pyridinium-based ionic liquid catalysts
Tharun J, et al.
Catalysis Communications, 54, 31-34 (2014)
Morphology, surface properties and photocatalytic activity of the bismuth oxyhalides semiconductors prepared by ionic liquid assisted solvothermal method
Bielicka-Gieldo'n A, et al.
Separation and Purification Technology, 217, 164-173 (2019)
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