Abstract:
Hydrolyzed Diels-Alder adducts of ocimenol have been synthesized and found to have good olfactory and perfumery properties. The hydrolyzed adducts are made by reacting ocimenol and an Alpha , Beta - unsaturated carbonyl compound, preferably acrolein, methacrolein or crotonaldehyde, in a Diels-Alder reaction, followed by hydrolysis.
Abstract:
CRUDE SULFATE TURPENTINE OR DISTILLATE FRACTION THEREOF IS DESULFURIZED WHILE SIMULTANEOUSLY RETARDING CHLORINATION OF THE ORGANIC COMPONENTS THEREIN. THE STOCK FOR TREATMENT IS MIXED WITH AN AQUEOUS DISPERSION OF HYPOCHLORITE CONTAINING NOT SUBSTANTIALLY MORE THAN ABOUT 10% AVAILABLE CHLORINE AND HAVING A PH FROM 10.1 TO 10.6 UNTIL MAXIMUM DESULFURIZATION HAS OCCURRED CONSISTENT WITH ACCEPTABLE LIMITED INCREASE IN ORGANIC CHLORIDE. THE RESULTING DESULFURIZED RAFFINATE PHASE IS SEPARATED FROM THE AQUEOUS PHASE, WASHED WITH WATER, AND RECOVERED.
Abstract:
NOVEL INSECTIPHOBIC COMPOSITIONS COMPRISING BETA-DIALKYLAMINOALKYL ETHERS AND THIO-ETHERS OF DEFINED NONTERPENOID ORGANIC ALCHOLS AND MERCAPTANS ARE DESCRIBED. THE COMPOSITIONS COMPRISE THE COMPOUNDS WHICH ARE USED IN CONJUNCTION WITH CONVENTIONAL INSECTIPHOBIC CARRIERS. THE COMPOSITIONS HAVE BEEN FOUND TO BE EFFECTIVE INSECTICIDES AND INSECT REPELLENTS AND IN CERTAIN INSTANCES HAVE BEEN FOUND TO BE SYNERGIZERS FOR CONVENTIONAL INSECTICIDES SUCH AS THE PYRETHRINS AND ALLERTHRIN.