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Methylpyridinium

chemical compound

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionAug 6, 2026
Entity authorityQ6824050 ↗
Source-derived summary

Methylpyridinium is an ion with the formula C5H5NCH+3. It is the N-methylated derivative of pyridine. It confers no color to its salts. The ion is classified as a quaternary ammonium ion.

Preparation and occurrence

Methylpyridinium is prepared by treating pyridine with dimethylsulfate:

C5H5N + (CH3O)2SO2 → [C5H5NCH3]+CH3OSO−3

It is found in some coffee products as a result of the thermal decarboxylation of trigonelline.

Ionic liquid

The chloride salt of N-methylpyridinium behaves as an ionic liquid. Mixtures of that salt and zinc chloride have been characterised over the temperature range 150–200 °C (423–473 K).

Editorial summary

“Methylpyridinium” enters the record as chemical compound. Crown Archives preserves that source wording while asking what Methylpyridinium, chemical and compound can confirm, complicate or overturn.

Editorial reviewA sound reference starting point where classification, measurement and the date of the underlying evidence remain visible. The current 93-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. Its strongest next move is a source search built around Methylpyridinium, chemical and compound.
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“Methylpyridinium” is worth following because a concise public description often conceals a longer documentary argument. Here, Methylpyridinium, chemical and compound provides the most credible route into that argument.

Evidence profile

Datasets, specimens, observations and peer-reviewed methods provide the appropriate test for the technical claims summarized here. The source revision retrieved here is dated Aug 6, 2026. The linked authority identifier is Q6824050. None of the 0 selected statements returned an explicit reference.

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Scientific names, classifications and consensus can change while older terminology persists in catalogues and historical literature. The lead is largely declarative, so disagreement and counter-evidence require a deliberate search beyond the opening account. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

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Source & attribution

This entry incorporates text from “Methylpyridinium” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.