Dow Global Technolgoies LLC

Alliedsignal Inc.

Angus Chemical Company

Rohm and Haas Company

Other

Microcomputer Doctors, Inc.

Angus Chemical Company and Dow Global Technologies LLC

George David Green

Raymond John Swedo

James R Snyder

Ian A Tomlinson

William B Bedwell

Darryl K Barnes

Daniel M Trauth

Mathias P Koljack

Lidia T Calcaterra

Dale A Hangey

Robert Butterick

Richard L James

Qamardin Farishta

Michael G Koehler

Patrick E Brutto

Stephen A Munk

Zhenwen Fu

Charles Coburn

Andrew Hejl

Eric C Greyson

Raj Madhukar Deshpande

Vandana Neeraj Pandey

Warren E Smith

Jia Tang

Paul Davis

Mrunalini S Dhamdhere

Shao-Ching Hung

Stephen Frederic Yates

Richard E Eibeck

Raymond Hilton Thomas

Asghar Akber Peera

Alfred Karl Schultz

Timothy R Demmin

John J Krajewski

Keith A Horn

Robert Christian Parker

Stephen C Lapin

Gary Michael Knopeck

Willis Hammond

Sheila M Tinetti

Eugene V Sitzmann

John L Pohlman

John C Rohanna

Donna M Ruszaj

Richard J Cook

Ronda L Gras

Jim C Luong

Bonnie A Pyzowski

Bruce T DeBona

Mark A Henning

Lauren M Laboe

Paul M Novy

William C Mullauer

Alan R Whetten

Charles F Marth

Charles R Coburn

Provided is a process for the formation of nitrated compounds by the nitration of hydrocarbon compounds with dilute nitric acid. Also provided are processes for preparing industrially useful downstream derivatives of the nitrated compounds, as well as novel nitrated compounds and derivatives, and methods of using the derivatives in various applications.

Nitrated hydrocarbons, derivatives, and processes for their manufacture

A compound having formula (PhC)Ar(OR), wherein Ph represents a phenyl group, Ar is an aromatic ring system having from six to twenty carbon atoms, R is C-Calkyl or C-Caralkyl, m is one or two, and n is an integer from one to four.

Tritylated ethers

A method for curing an epoxy resin by adding to the epoxy resin a compound having formula (I) wherein X is a difunctional group selected from the group consisting of C-Calkyl, C-Ccycloalkyl, C-Caryl, C-Caryl alkyl, C-Cheteroalkyl or C-Caryl heteroalkyl. 

High performance extended pot life epoxy hardeners

A compound having formula C{Ph(R)(OR)}{Ph(R)(OR)}{Ph(R)(OR)}, wherein Ph represents a benzene ring, R, Rand Rindependently are C-Calkyl; R, Rand Rindependently are C4-C12 alkyl, i, m, n, o, and p independently are zero, one or two; j is one or two.

Tetrarylmethane ethers

Provided are polymeric nitrones comprising polymerized units of (a) acrylates of Formula I: wherein Rand Rare as defined herein; and (b) nitrone-pendant esters of Formula II: wherein Rand Rare as defined herein, and Z is a nitrone substituent of Formula III: wherein R, R, R, R, R, R, R, R, R, and Rare as defined herein, and wherein the sum of m+n is a number from 10 to 50, and the ratio of m to n is from 1:1 to 20:1.

Polymeric nitrones and their use in personal care

Provided is a binder composition and its use in aqueous based paints and coatings and other applications. The binder composition comprises: a polyurethane dispersion containing water and a polyurethane polymer, wherein the polyurethane polymer is prepared by reacting a nitroalcohol compound, a polyol compound, a polyisocyanate compound, and optionally chain extenders, wherein the nitroalcohol compound is of formula I, wherein R, R, and Z are as defined herein. 

Nitrofunctional polyurethane dispersions for binder compositions

A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel by adding to the petroleum hydrocarbon or liquid biologically derived fuel a compound having formula C{Ph(R)(OR)}{Ph(R)(OR)}{Ph(R)(OR)}, wherein Ph represents a benzene ring, R, Rand Rindependently are C-Calkyl or C-Cheteroalkyl; R, Rand Rindependently are C-Calkyl or C-Cheteroalkyl, i, j, m, n, o and p independently are zero, one or two. Each compound having formula C{Ph(R)(OR)}{Ph(R)(OR)}{Ph(R)(OR)} is present at a level from 0.01 ppm to 20 ppm.

Tetrarylmethane ethers as fuel markers

Provided are compounds and compositions thereof that are useful as antioxidants in personal care formulations. The compounds are of the Formula I: wherein R, R, R, R, R, R, R, R, R, and Rare independently H, C-Calkyl, &#x2014;OH, C-Calkoxy, &#x2014;COOH, &#x2014;COOM, or &#x2014;OM, where Mis a sodium, potassium, or ammonium ion, provided that at least one of R, R, R, R, or Ris &#x2014;OH.

Nitrone compounds and their use in personal care

Provided are compounds and compositions thereof that are useful as antioxidants in personal care formulations. The compounds are of the Formula I: wherein R, R, R, R, and Rare independently H, &#x2014;OH, C-Calkoxy, &#x2014;COOH, &#x2014;COOMor &#x2014;OM, where Mis a sodium, potassium, or ammonium ion, wherein at least two of R, R, R, R, or Rare &#x2014;OH, and R, R, R, R, and R, are independently H, &#x2014;OH, C-Calkoxy, &#x2014;COOH, &#x2014;COOMor &#x2014;OMwhere Mis a sodium, potassium, or ammonium ion, or a substituent of Formula II: wherein R, R, R, R,and Rare independently H, &#x2014;OH, C-Calkoxy, &#x2014;COOH, &#x2014;COOMor &#x2014;OM, where Mis a sodium, potassium, or ammonium ion, provided that one of R, R, R, R, and Ris a substituent of Formula II.

Provided are compounds and compositions thereof that are useful as antioxidants in personal care formulations. The compounds are of the Formula I: wherein R, R, R, R, and Rare independently H, &#x2014;OH, C-Calkoxy, &#x2014;COOH, &#x2014;COOMor &#x2014;OM, where Mis a sodium, potassium, or ammonium ion, and R, R, R, R, and R, are independently H, &#x2014;OH, C-Calkoxy, &#x2014;COOH, &#x2014;COOMor &#x2014;OM, where Mis a sodium, potassium, or ammonium ion, or a substituent of Formula II: wherein R, R, R, R, and Rare independently H, &#x2014;OH, C-Calkoxy, &#x2014;COOH, &#x2014;COOMor &#x2014;OM, where Mis a sodium, potassium, or ammonium ion, provided that one of R, R, R, R, and Ris a substituent of Formula II.

A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel by adding to the petroleum hydrocarbon or liquid biologically derived fuel at least one compound having formula Ar(R)(OR), wherein Ar is an aromatic ring system having from six to twenty carbon atoms, Ris C-Calkyl or C-Calkenyl, Ris C-Calkyl or C-Calkenyl, m is an integer from zero to five and n is an integer from one to three; wherein each compound of formula Ar(R)(OR)is present at a level from 0.01 ppm to 100 ppm.

Distillable fuel markers

Provided is a binder composition and its use in aqueous based paints and coatings and other applications. The binder composition comprises: (a) a copolymer formed from one or more esters or amides of acrylic acid or methacrylic acid, or their mixtures, together with a monomer unit of formula I, wherein R, R1 R2, R3, R4, and X are as defined above; and (b) water, wherein the binder composition is an aqueous emulsion. 

Nitrofunctional acrylate copolymers for binder compositions

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Cary, IL, United States of America

George David Green