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A substance is pyrophoric (from Ancient Greek: πυροφόρος, pyrophoros, 'fire-bearing') if it ignites spontaneously in air at or below 54 °C (129 °F) (for gases) or within 5 minutes after coming into contact with air (for liquids and solids). [1] Examples are organolithium compounds and triethylborane.
Germane is a highly flammable, potentially pyrophoric, [11] and a highly toxic gas. In 1970, the American Conference of Governmental Industrial Hygienists (ACGIH) published the latest changes and set the occupational exposure threshold limit value at 0.2 ppm for an 8-hour time weighted average. [ 12 ]
Diborane is a pyrophoric gas. Commercially available adducts are typically used instead, at least for applications in organic chemistry. These adducts include borane-tetrahydrofuran (borane-THF) and borane-dimethylsulfide. [16] The toxic effects of diborane are mitigated because the compound is so unstable in air.
Triethylborane is strongly pyrophoric, with an autoignition temperature of −20 °C (−4 °F), [13] burning with an apple-green flame characteristic for boron compounds. Thus, it is typically handled and stored using air-free techniques.
It is a colorless, pyrophoric gas with a sharp, repulsive, pungent smell, somewhat similar to that of acetic acid. [6] Silane is of practical interest as a precursor to elemental silicon . Silanes with alkyl groups are effective water repellents for mineral surfaces such as concrete and masonry.
Gaseous signaling molecules are gaseous molecules that are either synthesized internally (endogenously) in the organism, tissue or cell or are received by the organism, tissue or cell from outside (say, from the atmosphere or hydrosphere, as in the case of oxygen) and that are used to transmit chemical signals which induce certain physiological or biochemical changes in the organism, tissue or ...
In its standard state arsine is a colorless, denser-than-air gas that is slightly soluble in water (2% at 20 °C) [1] and in many organic solvents as well. [citation needed] Arsine itself is odorless, [5] but it oxidizes in air and this creates a slight garlic or fish-like scent when the compound is present above 0.5 ppm. [6]
For example, LiBF 4 can tolerate a moisture content up to 620 ppm at room temperature whereas LiPF 6 readily hydrolyzes into toxic POF 3 and HF gases, often destroying the battery's electrode materials.