Novus International, Inc.

Tracy M Rode

Matthew Mahoney

Stephen J Lorbert

Richard Vonder Embse

James C Peterson

Kevin A Trankler

Dayna L Turner

Graciela Arhancet

Xiaojun Wang

Scott Long

Mercedes Vázquez-Añón

William Scott Hine

Heather A Tucker

Jason Schultz

Cynthia K Snoddy

Chemically modified methionine hydroxy analogs that are protected from degradation by rumen microorganisms. The chemically modified compounds comprise methionine hydroxy analog chemically linked to a fatty acid having at least 12 carbon atoms. Methods for increasing rumen bypass of methionine hydroxy analog and/or providing methionine hydroxy analog to a ruminant's small intestine for absorption, wherein the methods comprise administering to the ruminant a chemically modified methionine hydroxy analog as defined above.

Means for protecting methionine hydroxy analog from rumen degradation

Formulations comprising hydroxy methionine analog and having low levels of sulfate ions and bisulfate salts, processes for preparing the formulations, compositions comprising the formulations, and methods of using the formulations.

Hydroxy methionine analog formulations suitable for specialty chemical applications

Provided herein are processes for the production of methionine or selenomethionine from homoserine. In particular, the processes proceed via the production of 4-substituted 2-aminobutanoic acid intermediates or derivatives thereof.

Preparation of methionine or selenomethionine from homoserine via a 4-substituted 2-aminobutanoic acid intermediate

Provided herein are processes for the production of methionine or selenomethionine from homoserine. In particular, the processes proceed via the production of carbamate intermediates.

Preparation of methionine or selenomethionine from homoserine via a carbamate intermediate

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St. Charles, MO, United States of America

Tracy M Rode