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Trimethylarsine

chemical compound

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJun 2, 2026
Entity authorityQ421500
Source-derived summary

Trimethylarsine (abbreviated TMA or TMAs) is the chemical compound with the formula (CH3)3As, commonly abbreviated AsMe3 or TMAs. This organic derivative of arsine has been used as a source of arsenic in microelectronics industry, a building block to other organoarsenic compounds, and serves as a ligand in coordination chemistry. It has a distinctive garlic-like smell. Trimethylarsine was discovered in 1854.

Structure and preparation

AsMe3 is a pyramidal molecule. The As-C distances average 1.519 Å, and the C-As-C angles are 91.83°

Trimethylarsine can be prepared by treatment of arsenic oxide with trimethylaluminium:

As2O3 + 1.5 [AlMe3]2 → 2 AsMe3 + 3/n (MeAl-O)n

Occurrence and reactions

Trimethylarsine is the volatile byproduct of microbial action on inorganic forms of arsenic which are naturally occurring in rocks and soils at the parts-per-million level. Trimethylarsine has been reported only at trace levels (parts per billion) in landfill gas from Germany, Canada, and the U.S.A., and is the major arsenic-containing compound emitted by landfills.

Trimethylarsine is pyrophoric due to the exothermic nature of the following reaction, which initiates combustion:

AsMe3 + 1/2 O2 → OAsMe3 (TMAO)

History

Poisoning events due to a gas produced by certain microbes was assumed to be associated with the arsenic in paint. In 1893 the Italian physician Bartolomeo Gosio published his results on "Gosio gas" that was subsequently shown to contain trimethylarsine. Under wet conditions, the mold Microascus brevicaulis produces significant amounts of methyl arsines via methylation of arsenic-containing inorganic pigments, especially Paris green and Scheele's Green, which were once used in indoor wallpapers.

Editorial summary

This brief starts where responsible research should: with the source description of “Trimethylarsine” as chemical compound. Everything that follows is an evidence route, not borrowed authority.

Editorial reviewA sound reference starting point where classification, measurement and the date of the underlying evidence remain visible. The current lead gives the account dated anchors—1854, 1893—that can be checked directly. The selected authority fields contribute no independent date. The account is most persuasive where Trimethylarsine, chemical and compound can be independently traced.
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Why this record matters

The subject matters to the science & nature register because the source frames it as chemical compound. Its deeper value depends on whether names, dates, institutions and citations support that framing.

Evidence profile

Stable identifiers, scientific names and standards terminology offer the best bridge between this overview and specialist evidence. The source revision retrieved here is dated Jun 2, 2026. The linked authority identifier is Q421500. None of the 0 selected statements returned an explicit reference. The first chronological checks are 1854 and 1893.

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Current terminology should not be projected backward without checking the classification used when the underlying evidence was created. 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 Trimethylarsine” 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.