Archibald Hyson from Landenberg, PA

Liquid Water-Soluble Insecticidal Concentrates Of S-Methyl N-[(Methylcarbamoyl)-Oxy]Thioacetimidate
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US Patent:

39755185, Aug 17, 1976
Filed:

Apr 10, 1974
Appl. No.:

5/459579
Inventors:

Archibald Miller Hyson - Newark DE
Assignee:

E. I. Du Pont de Nemours and Company - Wilmington DE
International Classification:

A01N 912
A01N 920
US Classification:

424173
Abstract:

Ternary and quaternary solvent systems consisting essentially of 20% to 92% by weight cyclohexanone, 3% to 25% by weight lower alkanol, and at least 5% by weight water, wherein 0-65% of said cyclohexanone can be replaced by an equal quantity of cyclohexanol, such that when sufficient S-methyl N-[(methylcarbamoyl)oxy]thioacetimidate to create a 35% solution of said thioacetimidate is dissolved therein at 25. degree. C. , a single phase results, and single phase, liquid, water-soluble insecticidal concentrates of S-methyl N-[(methylcarbamoyl)oxy]thioacetimidate containing 15% to 35% by weight of said thioacetimidate in such a ternary or quaternary solvent system.

Preparation Of Bromacil/Diuron Complex
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US Patent:

39988309, Dec 21, 1976
Filed:

Apr 1, 1975
Appl. No.:

5/564214
Inventors:

Archibald Miller Hyson - Newark DE
Assignee:

E. I. Du Pont de Nemours and Company - Wilmington DE
International Classification:

C07D23954
US Classification:

260260
Abstract:

A herbicidal complex formed by the reaction of 1 mole of 5-bromo-3-sec-butyl-6-methyluracil with 1 mole of 3-(3,4-dichlorophenyl)-1,1-dimethylurea, and stable herbicidal formulations thereof.

Stabilized Aqueous Formulations Of Sulfonylurea Salts
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US Patent:

49369008, Jun 26, 1990
Filed:

Jan 7, 1987
Appl. No.:

7/001336
Inventors:

Archibald M. Hyson - Landenberg PA
Assignee:

E. I. du Pont de Nemours and Company - Wilmington DE
International Classification:

A01N 4366
A01N 4354
A01N 2502
A01N 2522
US Classification:

71 90
Abstract:

This invention relates to stabilized aqueous compositions consisting essentially of a sulfonylurea or its agriculturally suitable salt with a salt of a carboxylic or an inorganic acid, or with mixtures of such carboxylic or inorganic acid salts, provided that the solubility of carboxylic or inorganic acid salts at 5. degree. C. and a pH of about 6-10 is greater than or equal to 3% and further provided that the pH of a 0. 1 molar solution of the carboxylic or inorganic acid salt is between 6 and 10.

Archibald Hyson