When ordinary healthy urine is passed through animal charcoal in the manner described in the preceding paper, several organic substances are separated and absorbed by the charcoal in addition to the fatty acid there referred to. The liquid obtained by treating the charcoal with boiling alcohol having been evaporated, the residue is treated with water, which leaves the fatty acid undissolved. The filtered liquid yields on evaporation a quantity of crystals, which, after being purified in the manner described by the author, are found to have the properties and composition of oxalurate of ammonia. The watery solution of the substance gives with acids a white crystalline precipitate of oxaluric acid; with nitrate of silver it produces a precipitate which dissolves without change in boiling water, the solution on cooling depositing white silky needles of oxalurate of silver. The lead compound produced by adding acetate of lead to the watery solution, forms well-defined prismatic crystals. With chloride of calcium the watery solution gives no precipitate, but on adding ammonia and boiling, there is an abundant precipitation of oxalate of lime. By treatment with strong acids the substance is decomposed, yielding oxalic acid and urea. Its composition was found to correspond with the formula C
6
H
7
N
3
O
s
, which is that of oxalurate of ammonia. The author’s experiments were not sufficiently numerous to decide the question whether this salt is a normal constituent of human urine or not. There is no doubt, however, that its presence, whether exceptional or not, affords an easy and satisfactory explanation of a phenomenon which has until now proved very puzzling, viz., the formation of oxalate of lime in urine long after its emission. It is doubtless owing to the decomposition of oxaluric acid, which takes up water and splits up into urea and oxalic acid; the latter then combines with lime, of which there is always a sufficient quantity present to saturate the acid. There can be little doubt also that oxaluric acid is derived in the animal frame, as in the laboratory, from uric acid, the oxidation of which is its only known source.