NO122701B - - Google Patents
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- Publication number
- NO122701B NO122701B NO167038A NO16703867A NO122701B NO 122701 B NO122701 B NO 122701B NO 167038 A NO167038 A NO 167038A NO 16703867 A NO16703867 A NO 16703867A NO 122701 B NO122701 B NO 122701B
- Authority
- NO
- Norway
- Prior art keywords
- peroxydicarbonate
- peroxydicarbonates
- bis
- cycloalkyl
- dicyclohexyl
- Prior art date
Links
- BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical class C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 239000007800 oxidant agent Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 239000003505 polymerization initiator Substances 0.000 claims description 2
- -1 N-substituted methacrylamides Chemical class 0.000 description 7
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 2
- JHQVCQDWGSXTFE-UHFFFAOYSA-N 2-(2-prop-2-enoxycarbonyloxyethoxy)ethyl prop-2-enyl carbonate Chemical compound C=CCOC(=O)OCCOCCOC(=O)OCC=C JHQVCQDWGSXTFE-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000007306 turnover Effects 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- IWVJLGPDBXCTDA-UHFFFAOYSA-N cyclohexyl carbonochloridate Chemical compound ClC(=O)OC1CCCCC1 IWVJLGPDBXCTDA-UHFFFAOYSA-N 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/28—Oxygen or compounds releasing free oxygen
- C08F4/32—Organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/32—Peroxy compounds the —O—O— group being bound between two >C=O groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8714/66A GB1107956A (en) | 1966-02-28 | 1966-02-28 | Improvements in or relating to organic peroxydicarbonates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO122701B true NO122701B (US07488766-20090210-C00029.png) | 1971-08-02 |
Family
ID=9857830
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO167038A NO122701B (US07488766-20090210-C00029.png) | 1966-02-28 | 1967-02-27 |
Country Status (13)
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2151142A5 (US07488766-20090210-C00029.png) * | 1970-08-21 | 1973-04-13 | Pennwalt Corp | |
| US3879353A (en) * | 1971-09-01 | 1975-04-22 | Owens Illinois Inc | Linear copolymers having pendant peroxycarbonate ester functionality, their synthesis and use |
| FR2439794A1 (fr) * | 1978-10-26 | 1980-05-23 | Oreal | Procede de preparation de copolymeres pour laques aerosols et laques aerosols les contenant |
| US4285877A (en) * | 1980-01-17 | 1981-08-25 | Argus Chemical Corporation | Di(2-methyl-2-phenyl propyl) peroxy dicarbonate and other novel (2-alkyl-2-phenyl) substituted peroxy dicarbonates |
| FR2475558A1 (fr) * | 1980-02-07 | 1981-08-14 | Poudres & Explosifs Ste Nale | Procede de synthese de polymeres et de copolymeres a base de chloroformiate de vinyle |
| DE3038164A1 (de) * | 1980-10-09 | 1982-05-06 | Peroxid-Chemie GmbH, 8023 Höllriegelskreuth | Verfahren zur kontinuierlichen herstellung von dialkylperoxydicarbonaten |
| US4372877A (en) * | 1981-11-05 | 1983-02-08 | U.S. Peroxygen Company | Di(acylperoxy)-1,4-cyclohexane dimethanol-bis-carbonates |
| BE1009969A3 (fr) | 1996-01-25 | 1997-11-04 | Solvay | Procede pour la polymerisation en suspension aqueuse du chlorure de vinyle a l'intervention de peroxydicarbonates de dialkyle. |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2370588A (en) * | 1942-10-22 | 1945-02-27 | Pittsburgh Plate Glass Co | Organic percarbonates |
| US2517164A (en) * | 1947-02-19 | 1950-08-01 | Bruno F Arps | Two-speed hydraulic ram |
| US2464062A (en) * | 1947-11-26 | 1949-03-08 | Pittsburgh Plate Glass Co | Polymerization with a peroxydicar-bonate catalyst |
| NL247429A (US07488766-20090210-C00029.png) * | 1959-01-16 | |||
| DE1259325B (de) * | 1964-05-22 | 1968-01-25 | Hoechst Ag | Verfahren zur kontinuierlichen Herstellung von Loesungen von Peroxydikohlensaeureestern |
-
1966
- 1966-02-28 GB GB8714/66A patent/GB1107956A/en not_active Expired
-
1967
- 1967-01-16 NL NL6700636A patent/NL6700636A/xx unknown
- 1967-02-01 BE BE693478D patent/BE693478A/xx not_active IP Right Cessation
- 1967-02-01 IL IL27376A patent/IL27376A/en unknown
- 1967-02-10 CH CH198467A patent/CH481865A/de not_active IP Right Cessation
- 1967-02-11 DE DE19671618578D patent/DE1618578B1/de active Pending
- 1967-02-15 ES ES336866A patent/ES336866A1/es not_active Expired
- 1967-02-17 US US616775A patent/US3499919A/en not_active Expired - Lifetime
- 1967-02-23 AT AT180967A patent/AT272302B/de active
- 1967-02-27 SE SE02668/67A patent/SE339940B/xx unknown
- 1967-02-27 DK DK104167AA patent/DK120635B/da not_active IP Right Cessation
- 1967-02-27 NO NO167038A patent/NO122701B/no unknown
- 1967-02-27 SE SE14414/69A patent/SE361669B/xx unknown
- 1967-02-28 FR FR96769A patent/FR1512825A/fr not_active Expired
-
1969
- 1969-04-01 US US833229*A patent/US3528956A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AT272302B (de) | 1969-07-10 |
| GB1107956A (en) | 1968-03-27 |
| SE339940B (US07488766-20090210-C00029.png) | 1971-11-01 |
| ES336866A1 (es) | 1968-01-01 |
| US3528956A (en) | 1970-09-15 |
| NL6700636A (US07488766-20090210-C00029.png) | 1967-08-29 |
| FR1512825A (fr) | 1968-02-09 |
| DE1618578B1 (de) | 1971-01-21 |
| US3499919A (en) | 1970-03-10 |
| BE693478A (US07488766-20090210-C00029.png) | 1967-07-17 |
| CH481865A (de) | 1969-11-30 |
| DK120635B (da) | 1971-06-28 |
| SE361669B (US07488766-20090210-C00029.png) | 1973-11-12 |
| IL27376A (en) | 1970-09-17 |
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