AROMATIC CHEMICAL FOR USE IN

Brand Owner (click to sort) Address Description
CALONE FIRMENICH SA Case postale 239 1 route des Jeunes Geneve 8 CH-1211 Switzerland Aromatic Chemical for Use in the Perfume Industry;
CETONAL GIVAUDAN SA Chemin de la Parfumerie 5 1214 Vernier 0 Switzerland AROMATIC CHEMICAL FOR USE IN THE MANUFACTURE OF PERFUMES AND SOAPS;
CYCLOTENE DOW CHEMICAL COMPANY, THE 2211 H.H. Dow Way MIDLAND MI 48674 AROMATIC CHEMICAL FOR USE IN SOAPS, COSMETICS, PERFUME EXTRACTS, AND FLAVORING EXTRACTS;
FIXOLIDE Givaudan Corporation Clifton NJ AROMATIC CHEMICAL FOR USE IN THE MANUFACTURE OF PERFUMES, SOAPS, AND COSMETICS;
IRONAL Givaudan Corporation Clifton NJ AROMATIC CHEMICAL FOR USE IN THE MANUFACTURE OF PERFUME, SOAPS, AND COSMETICS;
LAVONE GIVAUDAN-DELAWANNA, INC. 330 WEST 42ND ST. NEW YORK NY AROMATIC CHEMICAL FOR USE IN THE PREPARATION OF PERFUME, SOAPS AND COSMETICS;
OZMALDEHYDE GIVAUDAN-DELAWANNA, INC. 330 WEST 42ND ST. NEW YORK NY AROMATIC CHEMICAL FOR USE IN THE PREPARATION OF PERFUME, SOAPS AND COSMETICS;
PALATONE DOW CHEMICAL COMPANY, THE 2211 H.H. Dow Way MIDLAND MI 48674 AROMATIC CHEMICAL FOR USE IN SOAPS, COSMETICS, PERFUME EXTRACTS, AND FLAVORING EXTRACTS;
VERDYL ACETATE Givaudan Corporation Clifton NJ Aromatic Chemical for Use in the Preparation of Perfume, Soaps and Cosmetics;The word Acetate is disclaimed apart from the mark as used.;
VERDYL PROPIONATE Givaudan Corporation Clifton NJ AROMATIC CHEMICAL FOR USE IN THE PREPARATION OF PERFUME, SOAPS, AND COSMETICS;THE WORD PROPIONATE IS DISCLAIMED APART FROM THE MARK AS USED.;
VERNALDEHYDE GIVAUDAN SA Chemin de la Parfumerie 5 1214 Vernier 0 Switzerland AROMATIC CHEMICAL FOR USE IN THE PREPARATION OF PERFUME, SOAPS AND COSMETICS;
 

Where the owner name is not linked, that owner no longer owns the brand

    
Technical Examples
  1. Nonmetallic, chiral organic catalysts are used to catalyze the 1,4-addition of an aromatic nucleophile to an ?,?-unsaturated aldehyde. The aromatic nucleophile may be an N,N-disubstituted aniline compound, or an analog thereof. The reaction is efficient and enantioselective, and proceeds with a variety of substituted and unsubstituted aromatic nucleophiles and aldehydes. The invention also provides a method for the deamination of aromatic N,N-disubstituted amines such as those resulting from the 1,4-addition of an aromatic nucleophile to an ?,?-unsaturated aldehyde.