GB834308A - Oxazoline and oxazine derivatives, polymers, copolymers thereof and method of preparation - Google Patents
Oxazoline and oxazine derivatives, polymers, copolymers thereof and method of preparationInfo
- Publication number
- GB834308A GB834308A GB14475/57A GB1447557A GB834308A GB 834308 A GB834308 A GB 834308A GB 14475/57 A GB14475/57 A GB 14475/57A GB 1447557 A GB1447557 A GB 1447557A GB 834308 A GB834308 A GB 834308A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compounds
- carbon atoms
- formula
- polymers
- give
- 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
- 229920001577 copolymer Polymers 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 5
- 229920000642 polymer Polymers 0.000 title abstract 5
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 title 1
- 150000004893 oxazines Chemical class 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 13
- -1 alkyl radicals Chemical class 0.000 abstract 9
- 150000001875 compounds Chemical class 0.000 abstract 8
- 125000001931 aliphatic group Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 238000007334 copolymerization reaction Methods 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- 238000006116 polymerization reaction Methods 0.000 abstract 4
- 150000001408 amides Chemical class 0.000 abstract 3
- 239000003112 inhibitor Substances 0.000 abstract 3
- 239000000178 monomer Substances 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 239000013543 active substance Substances 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 abstract 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 239000003995 emulsifying agent Substances 0.000 abstract 2
- 239000000839 emulsion Substances 0.000 abstract 2
- 239000004744 fabric Substances 0.000 abstract 2
- 239000011953 free-radical catalyst Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- WVAFEFUPWRPQSY-UHFFFAOYSA-N 1,2,3-tris(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1C=C WVAFEFUPWRPQSY-UHFFFAOYSA-N 0.000 abstract 1
- FQGJBTLTTWECAR-UHFFFAOYSA-N 1,3-bis(2-ethenoxyethyl)urea Chemical compound C(=C)OCCNC(NCCOC=C)=O FQGJBTLTTWECAR-UHFFFAOYSA-N 0.000 abstract 1
- AKUNSTOMHUXJOZ-UHFFFAOYSA-N 1-hydroperoxybutane Chemical compound CCCCOO AKUNSTOMHUXJOZ-UHFFFAOYSA-N 0.000 abstract 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 abstract 1
- NBTXFNJPFOORGI-UHFFFAOYSA-N 2-ethenoxyethyl prop-2-enoate Chemical compound C=COCCOC(=O)C=C NBTXFNJPFOORGI-UHFFFAOYSA-N 0.000 abstract 1
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical group [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 abstract 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 abstract 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical group [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 150000004703 alkoxides Chemical class 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Chemical group 0.000 abstract 1
- UPIWXMRIPODGLE-UHFFFAOYSA-N butyl benzenecarboperoxoate Chemical compound CCCCOOC(=O)C1=CC=CC=C1 UPIWXMRIPODGLE-UHFFFAOYSA-N 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 239000004495 emulsifiable concentrate Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 abstract 1
- 239000008396 flotation agent Substances 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 229910052733 gallium Inorganic materials 0.000 abstract 1
- 238000010348 incorporation Methods 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 238000005342 ion exchange Methods 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- HNBDRPTVWVGKBR-UHFFFAOYSA-N n-pentanoic acid methyl ester Natural products CCCCC(=O)OC HNBDRPTVWVGKBR-UHFFFAOYSA-N 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- FBGHTANCRDTRCS-UHFFFAOYSA-N octyl 2-[2-(2-phenoxyethoxy)ethoxy]ethanesulfonate Chemical compound C(CCCCCCC)OS(=O)(=O)CCOCCOCCOC1=CC=CC=C1 FBGHTANCRDTRCS-UHFFFAOYSA-N 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 150000002978 peroxides Chemical class 0.000 abstract 1
- 229920000223 polyglycerol Polymers 0.000 abstract 1
- 229920000131 polyvinylidene Polymers 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 239000010936 titanium Chemical group 0.000 abstract 1
- 229910052719 titanium Inorganic materials 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
- 229910052726 zirconium Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/10—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D263/12—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with radicals containing only hydrogen and carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/06—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings
- C07D265/08—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US58417256A | 1956-05-11 | 1956-05-11 | |
| US58417156A | 1956-05-11 | 1956-05-11 | |
| US584173A US2831858A (en) | 1956-05-11 | 1956-05-11 | Oxazine and oxazoline derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB834308A true GB834308A (en) | 1960-05-04 |
Family
ID=27416427
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB14475/57A Expired GB834308A (en) | 1956-05-11 | 1957-05-07 | Oxazoline and oxazine derivatives, polymers, copolymers thereof and method of preparation |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US2831858A (enExample) |
| BE (1) | BE557414A (enExample) |
| CH (1) | CH383971A (enExample) |
| DE (3) | DE1088494B (enExample) |
| FR (1) | FR1180666A (enExample) |
| GB (1) | GB834308A (enExample) |
| NL (2) | NL105271C (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2232547A1 (enExample) * | 1973-06-09 | 1975-01-03 | Bayer Ag |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2897182A (en) * | 1957-09-06 | 1959-07-28 | Rohm & Haas | Oxazine and oxazoline polymers |
| US2993031A (en) * | 1958-05-22 | 1961-07-18 | Dow Chemical Co | Nu-isopropenyl-cyclic carbamate compounds and polymers thereof |
| US2992219A (en) * | 1958-09-19 | 1961-07-11 | Eastman Kodak Co | Phosphorothiolothionates derived from 5, 6-dihydro-4h-1, 3-oxazines and 5, 6-dihydro-4h-1, 3-thiazines |
| US2974140A (en) * | 1959-03-04 | 1961-03-07 | Miles Lab | Substituted 2-alkenyltetrahydro-1, 3-oxazines |
| NL275086A (enExample) * | 1961-02-22 | |||
| DE1261261B (de) | 1966-09-23 | 1968-02-15 | Huels Chemische Werke Ag | Waermehaertbare UEberzugsmittel |
| DE1644760A1 (de) * | 1966-12-24 | 1971-03-04 | Huels Chemische Werke Ag | Verfahren zum Herstellen von UEberzuegen |
| US3687888A (en) * | 1969-10-30 | 1972-08-29 | Commercial Solvents Corp | Terpolymer latex emulsions |
| US3678065A (en) * | 1970-12-09 | 1972-07-18 | Commercial Solvents Corp | Production of hydroxymethyl vinyl oxazoline |
| US3708334A (en) * | 1971-03-22 | 1973-01-02 | Commercial Solvents Corp | Method of marking the skin or fur of animals |
| DE2207576C2 (de) * | 1972-02-18 | 1985-07-25 | Basf Ag, 6700 Ludwigshafen | Oxazolidinderivate |
| US3886128A (en) * | 1973-10-15 | 1975-05-27 | Commercial Solvents Corp | Oxazoline emulsifier in polymerization of styrene and butadiene |
| CA1048507A (en) * | 1974-03-27 | 1979-02-13 | Jack Ryer | Additive useful in oleaginous compositions |
| US4153566A (en) * | 1974-03-27 | 1979-05-08 | Exxon Research & Engineering Co. | Oxazoline additives useful in oleaginous compositions |
| US4157243A (en) * | 1974-12-06 | 1979-06-05 | Exxon Research & Engineering Co. | Additive useful in oleaginous compositions |
| US4178375A (en) * | 1976-08-06 | 1979-12-11 | Sterling Drug Inc. | Preserving and disinfecting method employing certain oxazines |
| DE2704904A1 (de) * | 1977-02-05 | 1978-08-10 | Henkel Kgaa | Kosmetische mittel mit einem gehalt an haut-feuchthaltemitteln |
| US4256592A (en) * | 1979-10-11 | 1981-03-17 | Mobil Oil Corporation | Phosphorus-containing compounds and lubricants containing same |
| US4253973A (en) * | 1979-11-20 | 1981-03-03 | Mobil Oil Corporation | Phosphorus-containing compounds and lubricants containing same |
| US4255271A (en) * | 1979-11-20 | 1981-03-10 | Mobil Oil Corporation | Phosphorus-containing compounds and lubricants containing same |
| US4357464A (en) * | 1981-04-15 | 1982-11-02 | The Dow Chemical Company | Removal of 2-isopropenyl-2-oxazoline monomer |
| US4508869A (en) * | 1983-06-14 | 1985-04-02 | The Dow Chemical Company | Latexes of polymers having pendant coreactive and oxazoline groups |
| DE3824982A1 (de) * | 1987-11-10 | 1989-05-18 | Henkel Kgaa | 2-(11-hydroxy-8-heptadecenyl- oder 11,8- bzw. 11,9-heptadecadienyl)oxazolin, sowie verfahren zur herstellung gegebenenfalls substituierter hoeherer 2-(alkyl- bzw. alkenyl)-oxazoline |
| EP0401286B1 (en) * | 1988-02-25 | 1995-09-13 | The Dow Chemical Company | Process for preparing n-(hydroxyalkyl)-2-unsaturated amides and 2-alkenyl oxazolines |
| DE3914159A1 (de) * | 1989-04-28 | 1990-10-31 | Henkel Kgaa | Verfahren zur herstellung von 2-alkyl- bzw. alkenyl-2-oxazolinen aus fettsaeureglyceriden |
| DE3914133A1 (de) * | 1989-04-28 | 1990-10-31 | Henkel Kgaa | Verfahren zur herstellung von 2-oxazolinen |
| US6063885A (en) * | 1998-03-10 | 2000-05-16 | S. C. Johnson Commercial Markets, Inc. | Oxazoline or oxazine methacrylate aqueous coating compositions |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US913514A (en) * | 1908-11-30 | 1909-02-23 | Farbenfab Vorm Bayer F & Co | Red dye. |
| US2243295A (en) * | 1939-11-15 | 1941-05-27 | Purdue Research Foundation | Process for the production of n-substituted (arylalkyl) amines |
| US2623013A (en) * | 1949-09-24 | 1952-12-23 | Koppers Co Inc | Ion-exchange resins from a vinyl pyridine or a vinyl quinoline and a vinyl ethinyl hydrocarbon |
| US2634259A (en) * | 1951-07-31 | 1953-04-07 | Arnold Hoffman & Co Inc | Polymerization process for n-vinyl pyrrolidone |
| US2665271A (en) * | 1951-10-25 | 1954-01-05 | Gen Aniline & Film Corp | Polymerization of n-vinyl lactams |
| US2739948A (en) * | 1951-11-21 | 1956-03-27 | Koppers Co Inc | Ion-exchange resins from divinyl pyridine |
-
0
- DE DENDAT1067437D patent/DE1067437B/de active Pending
-
1956
- 1956-05-11 US US584173A patent/US2831858A/en not_active Expired - Lifetime
-
1957
- 1957-05-07 GB GB14475/57A patent/GB834308A/en not_active Expired
- 1957-05-10 FR FR1180666D patent/FR1180666A/fr not_active Expired
- 1957-05-10 NL NL217156A patent/NL105271C/xx active
- 1957-05-11 CH CH4596657A patent/CH383971A/fr unknown
- 1957-05-11 DE DER21141A patent/DE1088494B/de active Pending
- 1957-05-11 DE DER21143A patent/DE1094749B/de active Pending
- 1957-05-11 BE BE557414D patent/BE557414A/xx unknown
-
1959
- 1959-11-06 NL NL245078A patent/NL105450C/xx active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2232547A1 (enExample) * | 1973-06-09 | 1975-01-03 | Bayer Ag |
Also Published As
| Publication number | Publication date |
|---|---|
| NL105450C (enExample) | 1963-07-15 |
| FR1180666A (fr) | 1959-06-08 |
| DE1094749B (de) | 1960-12-15 |
| DE1067437B (de) | 1959-10-22 |
| CH383971A (fr) | 1964-11-15 |
| BE557414A (enExample) | 1957-11-12 |
| US2831858A (en) | 1958-04-22 |
| NL105271C (enExample) | 1963-07-15 |
| DE1088494B (de) | 1960-09-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB834308A (en) | Oxazoline and oxazine derivatives, polymers, copolymers thereof and method of preparation | |
| US3983166A (en) | Monomeric emulsion stabilizers | |
| US3265654A (en) | Stable, aqueous dispersions of ethylene copolymers | |
| DE69423653T2 (de) | Verfahren zur radikalischen polymerisation | |
| KR900701714A (ko) | 중합 가능한 계면활성제 | |
| US2686772A (en) | N, n-ethyleneureido esters of acrylic and methacrylic acids | |
| US4064091A (en) | Process of forming a polymeric emulsion which comprises copolymerizing in aqueous dispersion an ethylenically-unsaturated monomer containing quaternary nitrogen | |
| US3386977A (en) | Copolymers of perfuloroalkyl alpha-trifluoromethacrylates | |
| US2694695A (en) | Mjithacrylic acids | |
| US3649581A (en) | Stable polymeric latices of high carboxyl content | |
| US3249595A (en) | Aqueous emulsion polymerization process employing water-soluble peroxides | |
| US3412179A (en) | Polymers of acrylyl perfluorohydroxamates | |
| US3936492A (en) | Monomeric emulsion stabilizers | |
| US4011259A (en) | Monomeric emulsion stabilizers | |
| GB952490A (en) | Hydrocarbontin salts of p-vinylbenzoic acid | |
| GB944266A (en) | Process for the production of acrylonitrile copolymers | |
| DE2430364A1 (de) | Verfahren zur herstellung von amidoalkansulfonsaeureestern | |
| GB1089494A (en) | N,n-bis-acrylamido-acetic compounds, their method of manufacture and their applications | |
| US2675371A (en) | Polymers of alpha-sulfo and sulfonamidomethyl acrylonitriles | |
| US2840546A (en) | Unsaturated quaternary ammonium compounds and polymers | |
| US3372151A (en) | Process for polymerization using salts of alkyl trisulfonylmethanes (tsm's) as emulsifiers | |
| US4029658A (en) | Monomeric morpholinium emulsion stabilizers | |
| GB1004055A (en) | Water-soluble copolymers and process for preparing them | |
| US4451608A (en) | Amphoteric acrylic ester based latexes | |
| US3821299A (en) | Amides and imides of fluorinated alkylamines and maleic and other ethylenically unsaturated dibasic acids and polymers thereof |