Search results
Results from the WOW.Com Content Network
Arsenobetaine is an organoarsenic compound that is the main source of arsenic found in fish. [1] [2] [3] [4] It is the arsenic analog of trimethylglycine, commonly ...
It is rapidly transformed into grey arsenic by light. The yellow form has a density of 1.97 g/cm 3. [23] Black arsenic is similar in structure to black phosphorus. [23] Black arsenic can also be formed by cooling vapor at around 100–220 °C and by crystallization of amorphous arsenic in the presence of mercury vapors. [26] It is glassy and ...
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 in the gas. [5] [6] [7] Trimethylarsine is pyrophoric due to the exothermic nature of the following reaction, which initiates combustion: AsMe 3 + 1/2 O 2 → OAsMe 3 (TMAO)
When administered intravenously, a steady state is reached after 8–10 days. Arsenic binds to proteins to an insignificant extent. The highest concentrations of arsenic are found in the liver, kidneys, heart, lungs, hair, and nails. Arsenous acid is oxidized to arsenic acid and methylated in the liver, [65] [66] [67] and then excreted 60% in ...
Arsenic forms colorless, odorless, crystalline oxides As 2 O 3 ("white arsenic") and As 2 O 5 which are hygroscopic and readily soluble in water to form acidic solutions. Arsenic(V) acid is a weak acid and the salts are called arsenates , [ 5 ] the most common arsenic contamination of groundwater , and a problem that affects many people.
Arsenic (III) enters the cells though aquaporins 7 and 9, which is a type of aquaglyceroporin. [26] Arsenic (V) compounds use phosphate transporters to enter cells. [26] The arsenic (V) can be converted to arsenic (III) by the enzyme purine nucleoside phosphorylase. [26]
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]
The first breakthrough in the detection of arsenic poisoning was in 1775 when Carl Wilhelm Scheele discovered a way to change arsenic trioxide to garlic-smelling arsine gas (AsH 3), by treating it with nitric acid (HNO 3) and combining it with zinc. [3] As 2 O 3 + 6 Zn + 12 HNO 3 → 2 AsH 3 + 6 Zn(NO 3) 2 + 3 H 2 O