348 
Wisconsin Academy of Sciences , Arts and Letters . 
product crystallizes from an ethyl-alcoholic solution with a molecule of 
C 3 H 5 O H, from a methyl-alcholic solution wit a molecule of C H 3 
OH. 
Hydrochlor-nitrolbenzylamine , 34 C 10 H 17 Cl 
The Zimonewe-derivatives were obtained in white filty needles, which 
melt at 103-104.° They turn the plane of polarized light as do the 
underlying hydrocarbons: [n] = +•149.6° resp. —147.4.° 
The chlorhydrates crystallize from alcohol in small needles which 
melt and decompose at 163-164. ° The action upon polarized light cor¬ 
responds to that of the free bases though weakened: [a] = + 46.97° 
resp. — 50.9. ° 
The dipentene-hydrochlor-nitrol-benzylamine crstallizes better than 
its optically active components, melts at 150° and is but difficultly solu¬ 
ble. Its hydrochlorate, however, is more soluble than its components, 
but possesses the same melting point. 
HydrocTilor-nitrolanilids , 35 C 10 H 17 Cl 
The limonene-derivatives crystallize from ether in handsome colorless 
flat prisms. Melting point 117-118° [n]^ = +126.95,° resp. —122.34.° 
DipewZewe-hydrochlor-nitrolanilid, prepared synthetically is colorless and 
melts at 140-141.° When hydrogen-chloride is split off a- and ft- nitrol 
anilids apparently result. 36 
