Investigations were carried out on the Hinoki Leaf Oil, an essential oil from the leaves of Chamaecyparis obtusa, and a new component, d-terpinyl acetate, was found besides the well-known components of pinene, limonene, bornyl acetate, sesquiterpene and sesquiterpene alcohol. Hinokic acid, m.p. 166°, contained in the acid portion, was founc to correspond to C15H22O2 from its analytical values, rather than the previously proposed C15H24O2. The acid is monobasic, contains two double bonds and gives a tetrahydro compound of m.p. 153°. It was assumed that the chemical structure of hinokid acid would be a bicyclic sesquiterpene-carboxylic acid possessing two double bonds. It was also observed that this acid was effective in inhibiting the growth of Mycobacterium tuberculosis (avian type) in vitro, at about 1:10000 dilution.