ES404187A1 - Sulfosuccinic acid semi-esters of oxyalkylated polynuclear alkyl-phenols - Google Patents
Sulfosuccinic acid semi-esters of oxyalkylated polynuclear alkyl-phenolsInfo
- Publication number
- ES404187A1 ES404187A1 ES404187A ES404187A ES404187A1 ES 404187 A1 ES404187 A1 ES 404187A1 ES 404187 A ES404187 A ES 404187A ES 404187 A ES404187 A ES 404187A ES 404187 A1 ES404187 A1 ES 404187A1
- Authority
- ES
- Spain
- Prior art keywords
- formula
- see formula
- esters
- polynuclear
- sulfosuccinic acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 title abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 230000001476 alcoholic effect Effects 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 abstract 1
- 239000003377 acid catalyst Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 239000008346 aqueous phase Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- 239000011976 maleic acid Substances 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229920003986 novolac Polymers 0.000 abstract 1
- 125000006353 oxyethylene group Chemical group 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
Landscapes
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Procedure for the preparation of semi-esters of sulfosuccinic acid of oxalkoxylated polynuclear alcoholic phenols of the formula I ** (See formula) ** in which R means a radical (see formula) or ** (See formula) ** - (OX) means oxyalkohylene radicals, namely oxyethylene and/or oxypropylene, and R1 means a branched or straight chain saturated alcohol radical with 6 to 14 carbon atoms, and in which Y represents hydrogen or has the same meanings as R, and n represents numbers from 2 to 25 and z represents numbers from 1 to 9 and Me means hydrogen or an alkali metal, characterized in that monoalcohilphenols are condensed ** (See formula) ** with formaldehyde in the molar ratio of 2: 1 to 10: 9 in the presence of acid catalysts to form polynuclear novolak resins, these are reacted in the presence of alkaline catalysts with 2 to 25 moles of alcoholic oxide for each mole of monoalcohilphenol used, and the free hydroxyl groups of the oxalkoxylates obtained totally or partially are esterified with maleic acid anhydride, and after this, the maleic acid half esters obtained in the aqueous phase are reacted with salts of the sulfurous acid to form the sulfosuccinic acid half esters of formula I. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712132405 DE2132405C3 (en) | 1971-06-30 | Process for the preparation of sulfobernstelic acid half-esters of oxyalkylated polynuclear alkylphenols, use of these compounds and dispersants containing these compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES404187A1 true ES404187A1 (en) | 1975-11-16 |
Family
ID=5812173
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES404187A Expired ES404187A1 (en) | 1971-06-30 | 1972-06-23 | Sulfosuccinic acid semi-esters of oxyalkylated polynuclear alkyl-phenols |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US3888828A (en) |
| JP (2) | JPS5617339B1 (en) |
| AT (1) | AT325021B (en) |
| AU (1) | AU473171B2 (en) |
| BE (1) | BE785711A (en) |
| BR (1) | BR7204257D0 (en) |
| CA (1) | CA1015767A (en) |
| CH (1) | CH583183A5 (en) |
| DD (1) | DD99987A5 (en) |
| ES (1) | ES404187A1 (en) |
| FR (1) | FR2144415A5 (en) |
| GB (1) | GB1391358A (en) |
| HU (1) | HU165058B (en) |
| IL (1) | IL39778A (en) |
| IT (1) | IT956933B (en) |
| NL (1) | NL177686C (en) |
| YU (1) | YU36923B (en) |
| ZA (1) | ZA724139B (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2759203C2 (en) * | 1977-12-31 | 1985-10-31 | Hoechst Ag, 6230 Frankfurt | Pigment dispersions and their use for pigmenting hydrophilic and hydrophobic media |
| DE2901461A1 (en) * | 1979-01-16 | 1980-07-24 | Hoechst Ag | USE OF OXALKYLATED NOVOLAC RESIN AS A PREPARATION AGENT FOR DISPERSION DYES AND PREPARATIONS THEREFORE |
| DE3026823A1 (en) * | 1980-07-16 | 1982-02-18 | Basf Ag, 6700 Ludwigshafen | NITROGEN-BASED GROUPS CARRYING POLYADDITIONS / POLYCONDENSATION PRODUCT, METHOD FOR THE PRODUCTION AND USE THEREOF |
| DE3104991A1 (en) * | 1981-02-12 | 1982-08-19 | Hoechst Ag, 6000 Frankfurt | ANIONIC INTERFACE-ACTIVE COMPOUNDS BASED ON OXALKYLATED NAPHTHOL NOVOLAKES AND THEIR USE |
| DE3120697A1 (en) * | 1981-05-23 | 1982-12-09 | Hoechst Ag, 6000 Frankfurt | ANIONIC COMPOUNDS BASED ON MODIFIED NOVOLACK OXALKYLATES, THEIR PRODUCTION AND THEIR USE AS A FOAM-FREE INTERFACE ACTIVE AGENT |
| DE3240862A1 (en) * | 1982-11-05 | 1984-05-10 | Hoechst Ag, 6230 Frankfurt | LIQUID PESTICIDES IN THE FORM OF SUSPENSION CONCENTRATES |
| JP2515537B2 (en) * | 1986-04-02 | 1996-07-10 | 武田薬品工業株式会社 | Pesticide powder |
| DE59108019D1 (en) * | 1990-10-18 | 1996-08-29 | Hoechst Schering Agrevo Gmbh | Aqueous herbicidal dispersion concentrate containing linuron and monolinuron as active ingredients |
| ATE348518T1 (en) * | 1996-10-25 | 2007-01-15 | Monsanto Technology Llc | COMPOSITION AND METHOD FOR TREATING PLANTS WITH EXOGENOUS CHEMICALS |
| DE102005060947A1 (en) * | 2005-12-20 | 2007-06-28 | Construction Research & Technology Gmbh | Powdered polycondensation products |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2454542A (en) * | 1948-11-23 | Polymeric detergents | ||
| US2663698A (en) * | 1950-04-11 | 1953-12-22 | Monsanto Chemicals | Process for producing synthetic tannins by dehydrating and sulfonating a novolak resin in a vacuum |
| US3210291A (en) * | 1959-06-08 | 1965-10-05 | Nalco Chemical Co | Processes for breaking petroleum emulsions with dicarboxy acid esters of sulfated oxyalkylated alkyl phenolformaldehyde resins |
| US3137713A (en) * | 1962-05-03 | 1964-06-16 | Petrolite Corp | Fluorine-containing alpha-sulfocarboxylic esters |
| US3293214A (en) * | 1962-05-15 | 1966-12-20 | Crompton & Knowles Corp | Preparation of a sulfomethylated bisphenol-formaldehyde composition for treating wool |
| US3442859A (en) * | 1965-08-30 | 1969-05-06 | Diamond Shamrock Corp | Condensates of sulfonated formaldehyde-mixed phenols condensates with formaldehyde and a phenol |
-
0
- BE BE785711D patent/BE785711A/en not_active IP Right Cessation
-
1972
- 1972-06-15 ZA ZA724139A patent/ZA724139B/en unknown
- 1972-06-23 NL NLAANVRAGE7208668,A patent/NL177686C/en not_active IP Right Cessation
- 1972-06-23 ES ES404187A patent/ES404187A1/en not_active Expired
- 1972-06-27 CH CH962972A patent/CH583183A5/xx not_active IP Right Cessation
- 1972-06-28 IL IL39778A patent/IL39778A/en unknown
- 1972-06-28 AT AT556372A patent/AT325021B/en not_active IP Right Cessation
- 1972-06-28 IT IT26371/72A patent/IT956933B/en active
- 1972-06-28 JP JP6418572A patent/JPS5617339B1/ja active Pending
- 1972-06-28 DD DD164020A patent/DD99987A5/xx unknown
- 1972-06-28 AU AU43978/72A patent/AU473171B2/en not_active Expired
- 1972-06-29 CA CA146,011A patent/CA1015767A/en not_active Expired
- 1972-06-29 HU HUHO1494A patent/HU165058B/hu unknown
- 1972-06-29 US US267512A patent/US3888828A/en not_active Expired - Lifetime
- 1972-06-29 BR BR4257/72A patent/BR7204257D0/en unknown
- 1972-06-29 YU YU1722/72A patent/YU36923B/en unknown
- 1972-06-29 GB GB3051372A patent/GB1391358A/en not_active Expired
- 1972-06-30 FR FR7223801A patent/FR2144415A5/fr not_active Expired
-
1980
- 1980-07-15 JP JP55095778A patent/JPS5812241B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IL39778A (en) | 1975-03-13 |
| DE2132405B2 (en) | 1976-01-02 |
| ZA724139B (en) | 1973-03-28 |
| BE785711A (en) | 1973-01-02 |
| GB1391358A (en) | 1975-04-23 |
| BR7204257D0 (en) | 1973-06-14 |
| FR2144415A5 (en) | 1973-02-09 |
| YU172272A (en) | 1982-06-18 |
| AU4397872A (en) | 1974-01-03 |
| DD99987A5 (en) | 1973-09-05 |
| NL7208668A (en) | 1973-01-03 |
| JPS5812241B2 (en) | 1983-03-07 |
| AU473171B2 (en) | 1976-06-17 |
| NL177686B (en) | 1985-06-03 |
| CH583183A5 (en) | 1976-12-31 |
| CA1015767A (en) | 1977-08-16 |
| IL39778A0 (en) | 1972-08-30 |
| JPS5639001A (en) | 1981-04-14 |
| YU36923B (en) | 1984-08-31 |
| DE2132405A1 (en) | 1973-01-18 |
| AT325021B (en) | 1975-09-25 |
| NL177686C (en) | 1985-11-01 |
| IT956933B (en) | 1973-10-10 |
| US3888828A (en) | 1975-06-10 |
| JPS5617339B1 (en) | 1981-04-22 |
| HU165058B (en) | 1974-06-28 |
| SU439970A3 (en) | 1974-08-15 |
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