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Stauffer Chemical Company Patents
Assignee:
Stauffer Chemical Company
Address:
Westport, CT
No. of patents:
1251
Patents:












Patent Number Title Of Patent Date Issued
RE31300 Process for preparing alkyl- or arylphosphonothioic dihalides July 5, 1983
Alkyl- or arylphosphonothioic dihalides are prepared by contacting an alkyl or aryl halide with a trivalent phosphorus compound having three halogens attached thereto or a pentavalent thiophosphorus halide having three halogens attached thereto or mixtures of the trivalent and pentavalen
RE30495 Meta-thiocarbamyl phenylene ureas January 27, 1981
Meta-thiocarbamyl phenylene amides and ureas having the formula ##STR1## in which R' is alkyl or benzyl and R is alkyl, monoalkylamino, N,N-di-substituted amino wherein said substituents are independently selected from the group consisting of alkyl, alkoxy, furfuryl and cycloalke
RE30284 Polymeric alkoxysilanes May 27, 1980
Polymeric alkoxysilanes which comprise a polymer network of the average formula ##STR1## wherein each R is an independently selected hydrocarbon or hydrocarbon ether radical, each .[.R'.]..Iadd.R.sup.1 .Iaddend. is an independently selected hydrocarbon radical, all of said radica
RE30279 Process for preparing alkyl or aryl phosphorus halides and mixed isomers thereof May 20, 1980
Alkyl or aryl phosphonic or phosphonothioic dihalides and phosphinic or phosphinothioic monohalides are prepared by reacting an alkyl halide or aryl halide respectively with a tri-valent phosphorus compound having at least two halogens attached thereto, and preferably three two halogens
RE30097 Control injection system for drycleaning apparatus in systems September 18, 1979
This invention provides a control injection system for adding a chemical and/or water from a metering device to a programmed drycleaning machine for a predetermined time interval. The control injection system comprises an automatic reset electrical timer having a dial which is setable fo
RE29675 O-(Halophenylcarbamyl)-N-(halophenyl) glycolamides June 20, 1978
5247349 Passivation and insulation of III-V devices with pnictides, particularly amorphous pnictides hav September 21, 1993
Pnictide thin films, particularly phosphorus, grown on III-V semiconductors, particularly InP, GaP, and GaAs, are amorphous and have a novel layer-like, puckered sheet-like local order. The thin films are typically 400 Angstroms thick and grown preferably by molecular beam deposition
5032472 Films of catenated phosphorus materials, their preparation and use, and semiconductor and other July 16, 1991
High phosphorus polyphosphides, namely MP.sub.x, where M is an alkali metal (Li, Na, K, Rb, and Cs) or metals mimicking the bonding behavior of an alkali metal, and x=7 to 15 or very much greater than 15 (new forms of phosphorus) are useful semiconductors in their crystalline, polycr
4999066 Process for bonding tiles to substrate using magnesium phosphate comprising activator prepared b March 12, 1991
A fast-setting magnesium phosphate one-component adhesive/grout is used to bond tiles, e.g. ceramic tiles, to a substrate, e.g. sheet-rock. The grout comprises an activator prepared by e.g., mixing diatomaceous earth with at least a sufficient amount of an ammonium phosphate solution to
4880831 Fungicidal carbanilates November 14, 1989
Novel fungicidal carbanilates having the general structural formula ##STR1## wherein R is methoxy or allyloxy; R.sub.1 is selected from the group consisting of hydrogen, C.sub.2 -C.sub.4 alkoxyalkyl and formyl; and R.sub.2 is C.sub.1 -C.sub.6 alkyl, preferably C.sub.2 -C.sub.3 alkyl
4874593 Conversion of pyrophoric P.sub.4 -containing material to P.sub.2 O.sub.5 material October 17, 1989
A process for treating a pyrophoric P.sub.4 -containing material to convert it to a substantially non-pyrophoric P.sub.2 O.sub.5 material is described. The process comprises supplying streams of fluid P.sub.4 -containing material and an oxygen-containing gas to a reactor filled with
4871856 Certain 3-benzoyl-4-oxolactams October 3, 1989
Compounds having the formula ##STR1## wherein R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.n --wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl; R.sup.1 is hydrogen or C.sub.1 -C.sub.4 alkyl; R
4855477 Ester intermediates for 2-benzoyl-4-phenyl-1,3-cyclohexanediones August 8, 1989
Compounds of the formula ##STR1## wherein R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; trifluoromethoxy or difluoromethoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; R.sup.a SO.sub.n --wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl, trifluoromethyl or
4854966 Method of controlling undesirable vegetation utilizing certain 3-(substituted thio)-2-benzoyl-cy August 8, 1989
A compound of the formula ##STR1## wherein R is halogen, C.sub.1 -C.sub.2 alkyl, C.sub.1 -C.sub.2 alkoxy, nitro; cyano; C.sub.1 -C.sub.2 haloalkyl, or R.sup.a SO.sub.n - wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl; R.sup.1 is hydrogen or C.sub.1 -C.sub.4 alkyl; R.su
4853028 Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones August 1, 1989
Compounds of the formula ##STR1## wherein R is halogen, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, cyano, nitro, (S(O).sub.n R wherein R is C.sub.1 -C.sub.4 alkyl and n is the integer 0, 1 or 2; and R.sup.2 through R.sup.8 are hydrogen or certain
4838932 Certain 2-(2-substituted benzoyl)-4-(substituted imino, oximino or carbonyl)-1,3-cyclohexanedion June 13, 1989
A method of controlling undesirable vegetation utilizing an herbicidal compounds of the formula ##STR1## wherein X NR.sup.9 wherein R.sup.9 is hydrogen, C.sub.1 -C.sub.4 alkyl or C.sub.1 -C.sub.4 alkoxy;R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; trifluorometho
4837352 3-chloro-2-(2'-substituted benzoyl)-cyclohex-2-enone intermediate compounds June 6, 1989
An intermediate compound having the structural formula ##STR1## wherein R is halogen, C.sub.1 -C.sub.2 alkyl, C.sub.1 -C.sub.2 alkoxy, nitro; cyano; C.sub.1 -C.sub.2 haloalkyl, or R.sup.a SO.sub.n - wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl; R.sup.1 is hydrogen or
4837209 S-cycloalkylmethyl trithiophosphonate insecticides June 6, 1989
Compounds and compositions containing them, for insecticidal control, particularly for use as soil and/or foliar insecticides, have the formula ##STR1## in which R.sub.1 is methyl or ethyl;R.sub.2 is C.sub.1 -C.sub.6 alkyl; andR.sub.3 is C.sub.3 -C.sub.6 cycloakyl.
4828823 Dicalcium phosphate dihydrate for fluoride dentifrice compositions May 9, 1989
The monofluorophosphate compatibility of dicalcium phosphate dihydrate can be improved in processes in which a slaked lime slurry is reacted with phosphoric acid to form a monocalcium phosphate solution to which is added magnesium oxide, additional lime slurry and pyrophosphoric acid wit
4824649 High viscosity potassium metaphosphate April 25, 1989
An improved process for preparing potassium metaphosphate is provided which comprises reacting potassium ions, preferably from the carbonate or bicarbonate, with phosphare ions in an amount sufficient to provide a K/P molar ratio ranging from about 0.85 to about 0.95 substantially in the
4822906 Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones April 18, 1989
Intermediate compounds of the structural formula ##STR1## wherein R.sup.60 is hydrogen; halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.n -- wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl, trifluorom
4822905 Certain 2-(2-(substituted phenyl)acetyl)-1,3-cyclohexanediones April 18, 1989
Compounds having the structural formula ##STR1## wherein R.sub.1, R.sub.2 R.sub.3, R.sub.4 and R.sup.5 are the same or different and are selected from the group consisting of hydrogen, chlorine, bromine, iodine, nitro, alkyl having from 1 to 4 carbon atoms, alkoxy having from 1 t
4822581 Catenated phosphorus materials and their preparation April 18, 1989
High phosphorus polyphosphides, namely MP.sub.x, where M is an alkali metal (Li, Na, K, Rb, and Cs) or metals mimicking the bonding behavior of an alkali metal, and x=7 to 15 or very much greater than 15 (new forms of phosphorus) are useful semiconducutors in their crystalline, polyc
4820325 Treatment of toxicant-impregnated filter cake April 11, 1989
A filter cake formed of a glass precursor material and impregnated with a normally leachable toxicant can be heated, preferably with at least one other glass precursor material, at a sufficiently high temperature to form a molten composition which solidifies, upon cooling, to form a glas
4818636 Films of catenated phosphorus materials, their preparation and use, and semiconductor and other April 4, 1989
High phosphorus polyphosphides, namely MP.sub.x, where M is an alkali metal (Li, Na, K, Rb, and Cs) or metals mimicking the bonding behavior of an alkali metal, and x=7 to 15 or very much greater than 15 (new forms of phosphorus) are useful semiconductors in their crystalline, polycr
4816066 Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones March 28, 1989
Compounds of the formula ##STR1## wherein R is halogen, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkyl, cyano, nitro, S(O).sub.n R wherein R is C.sub.1 -C.sub.4 alkyl and n is the integer 0, 1 or 2; and R.sup.2 through R.sup.8 are hydrogen or certain substituents, their salt
4816059 Method of controlling undesirable vegetation with certain 2-phenylacetyl-1,3,5-cyclohexanetrione March 28, 1989
Compounds of the formula ##STR1## wherein R is hydrogen; halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.m -- wherein m is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl;R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are meth
4814151 Soda ash manufacture March 21, 1989
An improved process for the manufacture of soda ash from trona by the sodium carbonate monohydrate method utilizing an activated carbon treatment of evaporator fines bleed.
4810507 Production of fermented vegetable oil products containing an emulsifier March 7, 1989
A vegetable oil and mineral salts broth is fermented with an organism to produce a vegetable oil product containing an emulsifier. Fermentation is carried out by forming a fermentation broth of vegetable oil and mineral salts, and optionally yeast extract and then fermenting the broth wi
4808733 Certain 4-oxo-3-benzoylvalerolactones and thiolactones February 28, 1989
An intermediate compound having the structural formula ##STR1## wherein X is oxygen or sulfur;R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.n --wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl;R.sup
4808720 Certain 3-benzoyl-4-oxolactams February 28, 1989
Compounds having the formula ##STR1## wherein R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.n -- wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl; R.sup.1 is hydrogen or C.sub.1 -C.sub.4 alkyl;
4808338 Certain 3-oxo-4-(substituted oxy or substituted thio)cyclohex-1-enyl-2-substituted benzoate inte February 28, 1989
Intermediate compounds of the formula ##STR1## wherein X is oxy, thio, sulfinyl or sulfonyl; R is halogen; C.sub.1 C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; trifluoromethoxy; difluoromethoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; R.sup.a SO.sub.n -- wherein n is 0 or 2 and R.su
4808214 Certain 2-(2-substituted benzoyl)-4-(substituted oxy or substituted thio)-1,3-cyclohexanediones February 28, 1989
Compounds of the formula ##STR1## wherein X is oxy, thio, sulfinyl or sulfonyl;R is hydrogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; trifluoromethyoxy; difluoromethoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; R.sup.a SO.sub.n --wherein n is 0 or 2 and R.sup.a is C.sub.1
4806653 Process for preparation of iminooxazolidines February 21, 1989
A process of the preparation of iminooxazolidines which comprises (a) reacting a urea alcohol of the formula ##STR1## X, Y, n and R are as defined, with a dehydrating agent to form an intermediate salt compound of the formula ##STR2## wherein X, Y, n and R are as previously d
4806165 Preparation of activators for fast-setting cements February 21, 1989
A particulate solid activator comprising a porous material containing absorbed P.sub.2 O.sub.5 values can be prepared by a process which comprises spray drying a slurry of a liquid P.sub.2 O.sub.5 material and the porous material to obtain the particulate solid. The P.sub.2 O.sub.5 m
4806152 Certain 2-(substituted benzoyl)-5-(substituted or unsubstituted phenyl)-1,3-cyclohexanediones as February 21, 1989
Compounds of the formula ##STR1## wherein R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; trifluoromethoxy or difluoromethoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; R.sup.a SO.sub.n -- wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl, trifluoromethyl o
4806146 Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones February 21, 1989
Compounds of the formula ##STR1## wherein R is halogen, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, cyano, nitro, S(O).sub.n R wherein R is C.sub.1 -C.sub.4 alkyl and n is the integer 0, 1 or 2; and R.sup.2 through R.sup.8 are hydrogen or certain
4797150 Certain 2-(2-substituted benzoyl)-1,3,5-cyclohexanetriones January 10, 1989
Compounds of the formula ##STR1## wherein R.sup.60 is halogen, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, cyano, nitro, S(O).sub.n R wherein R is C.sub.1 -C.sub.4 alkyl and n is the integer 0, 1 or 2; and R.sup.61 through R.sup.66 are hydrogen or
4797147 Herbicidal method and composition utilizing certain 5-(2-substituted benzoyl)-barbituric acids January 10, 1989
Herbicidal compositions and method of controlling undesirable vegetation utilizing compounds of the formula ##STR1## wherein R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.m -- wherein m is 0 or 2 and R.s
4795489 Certain 1,3-diphenyl-1,3-propanediones January 3, 1989
Compounds of the formula ##STR1## wherein R is hydrogen; halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.n -- wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl;R.sup.1 is C.sub.1 -C.sub.4 alkyl or C.sub.1 -
4795488 2-(Substituted benzoyl)-4-(substituted or unsubstituted phenyl)-1,3-cyclohexanediones as herbici January 3, 1989
Compounds of the formula ##STR1## wherein R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; trifluoromethoxy or difluoromethoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; R.sup.a SO.sub.n --wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl, trifluoromethyl or
4786309 Certain substituted 4-benzoyl-3,5-dioxotetrahydropyrans and thiopyrans November 22, 1988
Compounds of the formula ##STR1## wherein X is oxygen, sulfur or sulfonyl;R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.m -- wherein m is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl;R.sup.1 is hydrogen or C
4785121 Preparation of halophthalic anhydrides November 15, 1988
A process for selectively substituting an aromatic nitro group of a nitrophthalic anhydride with a halo group which comprises contacting the nitroaromatic-containing compound with a phosphorus halide of formula:wherein n is selected from 0, 1, 2 and 3; R is selected from the group consis
4785120 Process for preparing substituted phthalic anhydrides November 15, 1988
Yield and assay (purity) improvements in the reaction of bromine and the Diels-Alder addition product of maleic anhydride and a conjugated diene in the presence of a nitrogenous acid acceptor are realized in the instant process. The heating time after completion of bromine addition is
4783213 Certain 2-(2-substituted benzoyl)-4-(substituted oxy or substituted thio)-1,3-cyclohexanediones November 8, 1988
Compounds of the formula ##STR1## wherein X is oxy, thio, sulfinyl or sulfonyl;R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; trifluoromethoxy; difluoromethoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; R.sup.a SO.sub.n -- wherein n is 0 or 2 and R.sup.a is C.sub.1
4781752 Haloacetamidines compositions and the herbicidal use thereof November 1, 1988
Dichloroacetamidines having the formula ##STR1## in which A and B are independently selected from hydrogen, fluorine, chlorine, bromine and methyl, provided that at least one of A or B is other than hydrogen;M is hydrogen or methyl;X is selected from the group consisting of trifluoro
4781751 Certain 2-(2-substituted benzoyl)-4-(substituted)-1,3-cyclohexanediones November 1, 1988
Compounds of the formula ##STR1## wherein R is halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; trifluoromethoxy; difluoromethoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; R.sup.a SO.sub.n -- wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl; trifluoromethyl or
4780569 Certain 1,3-diphenyl-1,3-propanediones October 25, 1988
Compounds of the formula ##STR1## wherein R is hydrogen; halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.n - wherein n is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl;R.sup.1 is C.sub.1 -C.sub.4 alkyl or C.sub.1 -C
4780550 Certain 2-phenylacetyl-1,3,5-cyclohexanetriones October 25, 1988
Compounds of the formula ##STR1## wherein R is hydrogen; halogen; C.sub.1 -C.sub.2 alkyl; C.sub.1 -C.sub.2 alkoxy; nitro; cyano; C.sub.1 -C.sub.2 haloalkyl; or R.sup.a SO.sub.m -- wherein m is 0 or 2 and R.sup.a is C.sub.1 -C.sub.2 alkyl;R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are meth
4780127 Certain 2-(substituted benzoyl)-1,3-cyclohexanediones and their use as herbicides October 25, 1988
Compounds of the formula ##STR1## wherein R is halogen, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, cyano, nitro, S(O).sub.n R wherein R is C.sub.1 -C.sub.4 alkyl and n is the integer 0, 1 or 2; and R.sup.2 through R.sup.8 are hydrogen or certain

 
 
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