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Inventor:
Sanders; James Milton
Address:
Eatontown, NJ
No. of patents:
12
Patents:












Patent Number Title Of Patent Date Issued
4122120 Derivatives of 1-acetyl-3,3-dimethylcyclohexane October 24, 1978
Described is a mixture of 1-(3,3-dimethylcyclohexyl)-4-methyl-cis-2-pentene-1-one, 1-(3,3-dimethylcyclohexyl)-4-methyl-trans-2-pentene-1-one, and 1-(3,3-dimethylcyclohexyl)-4-methyl-3-pentene-1-one and a mixture of 1-(3,3-dimethylcyclohexyl)-cis-2-pentene-1-one, 1-(3,3-dimethylcycloh
4120308 Substituted norbornane derivatives used in the process of flavoring tobacco and the product ther October 17, 1978
The use of substituted norbornane derivatives used in the process of flavoring tobacco and the product thereof.
4119577 Substituted-norbornane perfumes compositions October 10, 1978
Substituted-norbornane derivatives are described for use as perfumes, colognes and in perfume aroma augmenting, modifying, enhancing, and imparting compositions. The substituted norbornane derivatives having the following structure: ##STR1## wherein R is C.sub.3 or C.sub.4 alkeny
4119576 Perfume compositions and colognes containing 1-butanoyl-3,3-dimethylcyclohexane October 10, 1978
Processes and compositions are described for the use in perfume and perfumed article aroma augmenting, enhancing and imparting compositions and as perfume and perfumed article aroma imparting materials of 1-butanoyl-3,3-dimethylcyclohexane having the formula: ##STR1## Addition of
4107093 3,3-Dimethyl-1-(4-methylvaleryl)-cyclohexane perfume compositions August 15, 1978
Compositions are described for the use in perfume and cologne of the compound ##STR1## or of mixtures of the compounds ##STR2## to produce fruity, woody, piney aromas with armoise and floral nuances and slight chocolate undertones.
4103036 Flavoring with derivatives of 1-acetyl-3,3-dimethylcyclohexane, and processes for using same and July 25, 1978
Processes and compositions are described for the use in foodstuff, chewing gum, toothpaste and medicinal product flavor and aroma, tobacco flavor and aroma, perfume and perfumed article aroma augmenting, enhancing and imparting compositions and as foodstuff, chewing gum, toothpaste,
4081481 1-Butanoyl-3,3-dimethylcyclohexane March 28, 1978
Processes and compositions are described for the use in perfume and perfumed article aroma augmenting, enhancing and imparting compositions and as perfume and perfumed article aroma imparting materials of 1-butanoyl-3,3-dimethylcyclohexane having the formula: ##STR1## produced ac
4076853 Flavoring with substituted norbornane derivatives February 28, 1978
Norbornane derivatives are used in foodstuffs and flavorings. Specifically, alpha-allyl-3, 3-dimethyl-2-norbornanemethanol, alpha-methallyl-3,3-dimethyl-2-norbornanemethanol, and alpha-allyl-alpha-3,3-trimethyl-2-norbornanemethanol are used.
4062894 Derivatives of 1-acetyl-3,3-dimethylcyclohexane December 13, 1977
Processes and compositions are described for the use in foodstuff, chewing gum, toothpaste and medicinal product flavor and aroma, tobacco flavor and aroma, perfume and perfumed article aroma augmenting, enhancing and imparting compositions and as foodstuff, chewing gum, toothpaste,
4031161 Process for producing mixture containing 4-(4'-methyl-4'-hydroxyamyl)-.DELTA..sup.3 -cyclohexene June 21, 1977
A process is described for reacting "myrac aldehyde" having the structure: ##STR1## (which structure is representative of a mixture of two compounds, one where the carboxaldehyde is in the "4" position and the other wherein the carboxaldehyde is in the "5" position) with an acid hydr
4007137 Process for producing mixture containing 4-(4-methyl-4-hydroxyamyl).DELTA..sup.3 -cyclohexenecar February 8, 1977
A process is described for reacting acrolein having the structure: ##STR1## with myrcenol having the structure: ##STR2## in the presence of a Lewis acid catalyst which is one of zinc chloride, zinc bromide or stannic chloride or mixtures thereof to produce a mixture containin
3978090 Process for production of isochromans August 31, 1976
Process for producing isochromans having the structure: ##SPC1##Wherein R.sub.1 and R.sub.2 are each (i) separately selected from the group consisting of hydrogen, lower alkoxyl, lower alkyl, and, (ii) taken together, selected from the group consisting of benzo, cyclopentano, cyclohe










 
 
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