a semimetallic chemical element; symbol As; at. no. 33; at. wt. 74.9216; m.p. 817C (at 28 atmospheres pressure); sublimation point 613C; sp. gr. (stable form) 5.73; valence -3, 0, +3, or +5. Arsenic appears in several allotropic forms (see allotropy); the stable form is a silver-gray, brittle crystalline solid that tarnishes rapidly in air, and at high temperatures burns to form a white cloud of arsenic trioxide. A yellow crystalline form and a black amorphous form are also known. Arsenic is a member of group Va of the periodic table. It combines readily with many elements: with hydrogen to form arsine, an extremely poisonous gas; with oxygen to form a pentoxide and the above-mentioned trioxide (As2O3 or As4O6), a deadly poison also called arsenic (III) oxide, arsenious oxide, white arsenic, or, simply, arsenic; with the halogens; and with sulfur. The element is used with other metals to make hard, strong, corrosion-resistant alloys. Its compounds are used in pigments, animal poisons, insecticides (e.g., Paris green), and poison gases (such as lewisite) for chemical warfare. They are also used in glassmaking, in calico and indigo printing, in tanning and taxidermy (as preservatives), and in pyrotechnics. Small quantities of arsenic added to lead in the manufacture of shot assure perfectly spherical pellets by delaying the solidification of the molten lead, and thereby allowing it to flow more readily; the arsenic also contributes hardness. A small amount of arsenic is added to germanium in the production of semiconductor devices such as transistors and integrated circuits. A number of organic compounds of arsenic are used in medicine; the best known is Salvarsan, formerly used extensively in the treatment of syphilis and yaws. On the other hand, many arsenic compounds are strong poisons. One delicate test for the presence of even microscopic quantities of arsenic in compounds is the Marsh test. Arsenic occurs in many ores, including realgar, orpiment, and arsenopyrite, the chief commercial source. When it is prepared commercially from sulfide ores, e.g., arsenical pyrites, the ores are roasted (heated in the absence of air); the arsenic sublimes (passes directly from the solid to the gaseous state) and is condensed. In another method, white arsenic is reduced with carbon. Although realgar, orpiment, and other arsenic minerals were known to the Greeks of Aristotle’s time, the element itself was not. The “arsenic” so called by them and by the later alchemists was not true arsenic, but probably arsenic trioxide. The element was first described by Albertus Magnus in the 13th cent.