Elevance Renewable Sciences, Inc.

Other

Wilmar Trading Pte Ltd.

Schrodi, Yann

Pederson, Richard L.

Tupy, Michael J.

Kaido, Hiroki

Michael John Tupy

Timothy A Murphy

Hiroki Kaido

Richard L Pederson

Yann Schrodi

Timothy Walter Abraham

Scott A Walters

Stephen E Russell

Diza Braksmayer

Choon Woo Lee

Francis Amore

James F Ulrich

Jeffrey R DiMaio

Neal Torrey Jakel

Eugene Joseph Fox

Michael J Beaver

Stephen D Hudson

Joel Ingvalson

Doug C Kotowski

R Trenton Bostic

Baris Kokouz

Andy Shafer

Steven Alan Cohen

Clive P Bosnyak

David E Henton

James C Anderson

Syed Q A Rizvi

William H Sperber

Xiangsheng Meng

Stephen Augustine DiBiase

Mervyn L De Souza

Kevin D Uptain

Monika Mujkic

Garrett Zopp

Jill Louise Zullo

Michelle Morie-Bebel

Benjamin Bergmann

John M Zupfer

Troy Lohrmann

Steve Russell

Alexander Patist

Patrick Adu-Peasah

Alexandre A Pletnev

Patrick Adu-Peashah

Earl H Wagener

Diza Pearl Braksmayer

Stephen A Dibiase

Syed QA Rizvi

Stephen E Russel

Stephen Hudson

Described are methods of making organic compounds by metathesis chemistry. The methods of the invention are particularly useful for making industrially-important organic compounds beginning with starting compositions derived from renewable feedstocks, such as natural oils. The methods make use of a cross-metathesis step with an olefin compound to produce functionalized alkene intermediates having a pre-determined double bond position. Once isolated, the functionalized alkene intermediate can be self-metathesized or cross-metathesized (e.g., with a second functionalized alkene) to produce the desired organic compound or a precursor thereto. The method may be used to make bifunctional organic compounds, such as diacids, diesters, dicarboxylate salts, acid/esters, acid/amines, acid/alcohols, acid/aldehydes, acid/ketones, acid/halides, acid/nitriles, ester/amines, ester/alcohols, ester/aldehydes, ester/ketones, ester/halides, ester/nitriles, and the like.

Methods of making organic compounds by metathesis

Disclosed are petrolatum-like compositions that include metathesized unsaturated polyol esters. Also disclosed are emulsions that include metathesized unsaturated polyol esters. The petrolatum-like compositions may be used as substitutes for petroleum-based petrolatum. The emulsions may be water-in-oil or oil-in-water emulsions and may be suitable for a variety of end uses.

Compositions comprising metathesized unsaturated polyol esters

Natural oil based fatty acid wax compositions and their methods of making are provided. The methods comprise providing a natural oil, and hydrogenating and metathesizing the natural oil, and then converting the hydrogenated metathesized natural oil to obtain a fatty acid wax comprising free fatty acids and/or salts of fatty acids, glycerol and/or alcohol, and paraffin, wherein the fatty acid wax has at least 50 wt % of carbon chain compositions with at least 18 carbon atoms. The compositions may comprise 85-100 wt % long-chain fatty acids, 0-15 wt % esters, wherein the fatty acid comprises between 15-60 wt % long chain di-acids and 40-85 wt % long chain mono-acids. The compositions may comprise about 50-100 wt % long-chain fatty acids and about 0-50 wt % esters, wherein the fatty acid may comprise between about 15-80 wt % long chain di-acids and about 20-85 wt % long chain monoacids.

Renewable fatty acid waxes and methods of making

A wax comprises a metathesis product and/or a product that resembles, at least in part, a product which may be formed from a metathesis reaction. The wax may be used to form articles for example, candles (container candles, votive candles, and/or a pillar candles), crayons, fire logs or tarts. The wax commonly includes other components in addition to the metathesis product.

Candle and candle wax containing metathesis and metathesis-like products

The invention is directed to methods of making organic compounds by metathesis and hydrocyanation. The method of the invention may be used, for example, to make industrial important organic compounds such as diacids, diesters, acid-amines, acid-alcohols, acid-nitriles, ester-amines, ester-alcohols, and ester-nitriles.

Methods of making organic compounds by metathesis and hydrocyanation

Lipid-based wax compositions and their methods of making are provided for compositions substantially free of fat bloom. The compositions comprise approximately 7-80 percent by weight triacylglycerides and approximately 20-93 percent by weight monoacylglycerides and diacylglycerides combined. The methods comprise blending the monoacylglycerides, diacylglycerides, and triacylglycerides in the lipid-based wax composition by heating the lipid-based wax composition at a sufficiently high temperature to destroy substantially all crystal structure within the lipid-based wax composition. The methods further comprise pouring the lipid-based wax composition into a mold or a container having a surface and a core, wherein the pouring is conducted at a temperature at least 15&#xb0; C. greater than the congeal point of the lipid-based wax composition. The methods further comprise cooling the lipid-based wax composition under conditions sufficient to cool the core to at least 5&#xb0; C. below the congeal point of the lipid-based wax composition in approximately 30-90 minutes.

Lipid-based wax compositions substantially free of fat bloom and methods of making

Disclosed are petrolatum-like compositions that comprise metathesized unsaturated polyol esters. Also disclosed are emulsions comprising metathesized unsaturated polyol esters. The petrolatum-like compositions may be used as substitutes for petroleum-based petrolatum. The emulsions may be water-in-oil or oil-in-water emulsions and may be suitable for a variety of end uses.

A wax comprises a metathesis product and/or a product that resembles, at least in part, a product which may be formed from a metathesis reaction. The wax may be used to form articles, for example, candles (container candles, votive candles, and/or a pillar candles), crayons, fire logs, or tarts. The wax commonly includes other components in addition to the metathesis product.

A hybrid wax compositions that are suitable for use in manufacturing wax articles (e.g., candles) by compression molding. The combination of a hydrogenated natural oil-based wax and a paraffin wax having a select distribution of hydrocarbon chain lengths provides the hybrid wax compositions with improved properties, such as improved compressive strength and improved de-molding characteristics, for example, as evidenced by reducing scarring and/or flashing. The hybrid wax compositions comprise: (a) a wax comprising a hydrogenated natural oil; and (b) a paraffin wax, wherein the paraffin wax comprises less than about 50% by weight of the hybrid wax composition, and wherein about 52% or greater of hydrocarbons in the paraffin wax have carbon chain lengths ranging from C25 to C29.

Hybrid wax compositions for use in compression molded wax articles such as candles

Disclosed are improved methods for conducting metathesis utilizing polyunsaturated fatty acid compositions (e.g., polyunsaturated fatty acid polyol esters, polyunsaturated fatty acids, polyunsaturated fatty esters, and mixtures), such as those found in naturally occurring oils and fats, as the starting material. The inventive methods involve hydrogenation of polyunsaturated fatty acid compositions prior to metathesis, thereby providing partially-hydrogenation compositions having a relatively higher amount of monounsaturated fatty acid species. The partially hydrogenated composition can then be subjected to metathesis to provide a metathesis product composition containing industrially useful compounds.

Metathesis methods involving hydrogenation and compositions relating to same

This disclosure relates generally to olefin metathesis, and more particularly relates to the synthesis of terminal alkenes from internal alkenes using a cross-metathesis reaction catalyzed by an olefin metathesis catalyst. According to one aspect, for example, a method is provided for synthesizing a terminal olefin, the method comprising contacting, in the presence of a ruthenium alkylidene metathesis catalyst, an olefinic substrate comprised of at least one internal olefin with a cross metathesis partner comprised of an alpha olefinic reactant, under reaction conditions effective to allow cross-metathesis to occur, wherein the reaction conditions include a reaction temperature of at least 35&#xb0; C. The methods, compositions, reactions and reaction systems herein disclosed have utility in the fields of catalysis, organic synthesis, and industrial chemistry.

Synthesis of terminal alkenes from internal alkenes via olefin metathesis

Growing community of inventors

Crystal, MN, United States of America

Michael John Tupy