1-Butyl-4-methylpyridinium iodide
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- $97 - $2670.48
- Product name: 1-Butyl-4-methylpyridinium iodide
- CAS: 32353-64-3
- MF: C10H16IN
- MW: 277.14521
- EINECS:
- MDL Number:MFCD15143656
- Synonyms:1-butyl-4-methylpyridin-1-ium iodide;1-Butyl-4-methylpyridinium iodide 99%;1-Butyl-4-methylpyridinium iodide
3 prices
Selected condition:
Brand
- aablocks
- American Custom Chemicals Corporation
Package
- 5g
- 50G
- Manufactureraablocks
- Product numberAA00CSRM
- Product description1-butyl-4-methylpyridin-1-ium iodide ≥98%
- Packaging5g
- Price$97
- Updated2026-05-28
- Buy
- ManufacturerAmerican Custom Chemicals Corporation
- Product numberCHM0115535
- Product description1-BUTYL-4-METHYLPYRIDINIUM IODIDE 95.00%
- Packaging5G
- Price$849.53
- Updated2021-12-16
- Buy
- ManufacturerAmerican Custom Chemicals Corporation
- Product numberCHM0115535
- Product description1-BUTYL-4-METHYLPYRIDINIUM IODIDE 95.00%
- Packaging50G
- Price$2670.48
- Updated2021-12-16
- Buy
| Manufacturer | Product number | Product description | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|
| aablocks | AA00CSRM | 1-butyl-4-methylpyridin-1-ium iodide ≥98% | 5g | $97 | 2026-05-28 | Buy |
| American Custom Chemicals Corporation | CHM0115535 | 1-BUTYL-4-METHYLPYRIDINIUM IODIDE 95.00% | 5G | $849.53 | 2021-12-16 | Buy |
| American Custom Chemicals Corporation | CHM0115535 | 1-BUTYL-4-METHYLPYRIDINIUM IODIDE 95.00% | 50G | $2670.48 | 2021-12-16 | Buy |
Properties
form :powder
BRN :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
InChIKey :RSJCFBORABJFGA-UHFFFAOYSA-M
SMILES :[I-].CCCC[n+]1ccc(C)cc1
BRN :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
InChIKey :RSJCFBORABJFGA-UHFFFAOYSA-M
SMILES :[I-].CCCC[n+]1ccc(C)cc1
Safety Information
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| Signal word: | Warning | ||||||||||||||||||||||||||||
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Description
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.
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