CH421928A - Verfahren zur Herstellung neuer Dijodbenzoylverbindungen - Google Patents

Verfahren zur Herstellung neuer Dijodbenzoylverbindungen

Info

Publication number: CH421928A
Authority: CH; Switzerland
Prior art keywords: weight; percent; compounds; ester; acid
Prior art date: 1961-07-21

Application number

CH876462A

Other languages

German (de)

English (en)

Inventor

Archer Sydney

Jerome Flynn Vincent

Original Assignee

Sterling Drug Inc

Priority date (The priority date 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 date listed.)

1961-07-21

Filing date

1962-07-20

Publication date

1966-10-15

1962-07-20 Application filed by Sterling Drug Inc filed Critical Sterling Drug Inc

1966-10-15 Publication of CH421928A publication Critical patent/CH421928A/de

Links

-1 diiodobenzoyl compounds Chemical class 0.000 title claims description 15
238000002360 preparation method Methods 0.000 title claims description 10
238000000034 method Methods 0.000 title claims description 8
239000004014 plasticizer Substances 0.000 claims description 23
229920005989 resin Polymers 0.000 claims description 16
239000011347 resin Substances 0.000 claims description 16
150000001875 compounds Chemical class 0.000 claims description 12
NWLCZLDFMGINSB-UHFFFAOYSA-N 2-ethoxyethyl 2,5-diiodobenzoate Chemical compound CCOCCOC(=O)C1=CC(I)=CC=C1I NWLCZLDFMGINSB-UHFFFAOYSA-N 0.000 claims description 7
229920003023 plastic Polymers 0.000 claims description 7
239000004033 plastic Substances 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 6
229920000915 polyvinyl chloride Polymers 0.000 claims description 6
239000004800 polyvinyl chloride Substances 0.000 claims description 6
239000011342 resin composition Substances 0.000 claims description 6
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
229920002554 vinyl polymer Polymers 0.000 claims description 4
125000002947 alkylene group Chemical group 0.000 claims description 3
239000000203 mixture Substances 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
150000002148 esters Chemical class 0.000 description 7
239000000047 product Substances 0.000 description 7
239000000126 substance Substances 0.000 description 7
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
HFTLDTOPQGFMBS-UHFFFAOYSA-N 2,5-diiodobenzoyl chloride Chemical compound ClC(=O)C1=CC(I)=CC=C1I HFTLDTOPQGFMBS-UHFFFAOYSA-N 0.000 description 5
238000009835 boiling Methods 0.000 description 5
239000003381 stabilizer Substances 0.000 description 5
IHBCFWWEZXPPLG-UHFFFAOYSA-N [Ca].[Zn] Chemical compound [Ca].[Zn] IHBCFWWEZXPPLG-UHFFFAOYSA-N 0.000 description 4
230000005855 radiation Effects 0.000 description 4
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
239000004593 Epoxy Substances 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
239000002253 acid Substances 0.000 description 3
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 3
229910052797 bismuth Inorganic materials 0.000 description 3
JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
239000003814 drug Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
NSKPFWAAYDFCFS-UHFFFAOYSA-N 2,5-diiodobenzoic acid Chemical compound OC(=O)C1=CC(I)=CC=C1I NSKPFWAAYDFCFS-UHFFFAOYSA-N 0.000 description 2
SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
229940093475 2-ethoxyethanol Drugs 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
239000002026 chloroform extract Substances 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
230000002496 gastric effect Effects 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
239000000049 pigment Substances 0.000 description 2
230000019612 pigmentation Effects 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000002627 tracheal intubation Methods 0.000 description 2
230000002485 urinary effect Effects 0.000 description 2
210000003462 vein Anatomy 0.000 description 2
QGNWXTKXVFUTFK-UHFFFAOYSA-N 2,3-diiodobenzoic acid Chemical compound OC(=O)C1=CC=CC(I)=C1I QGNWXTKXVFUTFK-UHFFFAOYSA-N 0.000 description 1
QGSVMKAGSSPCIW-UHFFFAOYSA-N 2,3-diiodobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC(I)=C1I QGSVMKAGSSPCIW-UHFFFAOYSA-N 0.000 description 1
LWLHVWSQNTYSSG-UHFFFAOYSA-N 2,4-diiodobenzoic acid Chemical compound OC(=O)C1=CC=C(I)C=C1I LWLHVWSQNTYSSG-UHFFFAOYSA-N 0.000 description 1
QJASZQLQPXQBAR-UHFFFAOYSA-N 2,6-diiodobenzoic acid Chemical compound OC(=O)C1=C(I)C=CC=C1I QJASZQLQPXQBAR-UHFFFAOYSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
YTAFOWSVLBCZFU-UHFFFAOYSA-N 2-ethoxyethyl 2,4-diiodobenzoate Chemical compound CCOCCOC(=O)C1=CC=C(I)C=C1I YTAFOWSVLBCZFU-UHFFFAOYSA-N 0.000 description 1
DEDUBNVYPMOFDR-UHFFFAOYSA-N 2-ethoxypropan-1-ol Chemical compound CCOC(C)CO DEDUBNVYPMOFDR-UHFFFAOYSA-N 0.000 description 1
UPGSWASWQBLSKZ-UHFFFAOYSA-N 2-hexoxyethanol Chemical compound CCCCCCOCCO UPGSWASWQBLSKZ-UHFFFAOYSA-N 0.000 description 1
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
HCGFUIQPSOCUHI-UHFFFAOYSA-N 2-propan-2-yloxyethanol Chemical compound CC(C)OCCO HCGFUIQPSOCUHI-UHFFFAOYSA-N 0.000 description 1
DFYULHRIYLAUJM-UHFFFAOYSA-N 3,4-diiodobenzoic acid Chemical compound OC(=O)C1=CC=C(I)C(I)=C1 DFYULHRIYLAUJM-UHFFFAOYSA-N 0.000 description 1
FHTJRJBWLBXVPO-UHFFFAOYSA-N 3,5-diiodobenzoic acid Chemical compound OC(=O)C1=CC(I)=CC(I)=C1 FHTJRJBWLBXVPO-UHFFFAOYSA-N 0.000 description 1
AZMINPXWCSBLGV-UHFFFAOYSA-N 3,5-diiodobenzoyl chloride Chemical compound ClC(=O)C1=CC(I)=CC(I)=C1 AZMINPXWCSBLGV-UHFFFAOYSA-N 0.000 description 1
XHMWPVBQGARKQM-UHFFFAOYSA-N 3-ethoxy-1-propanol Chemical compound CCOCCCO XHMWPVBQGARKQM-UHFFFAOYSA-N 0.000 description 1
SFFDJWPLFTUFQC-UHFFFAOYSA-N 3-ethoxybutan-2-ol Chemical compound CCOC(C)C(C)O SFFDJWPLFTUFQC-UHFFFAOYSA-N 0.000 description 1
QRUOTIJTSNETKW-UHFFFAOYSA-N 4-ethoxybutan-1-ol Chemical compound CCOCCCCO QRUOTIJTSNETKW-UHFFFAOYSA-N 0.000 description 1
206010002091 Anaesthesia Diseases 0.000 description 1
229920001342 Bakelite® Polymers 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
239000004803 Di-2ethylhexylphthalate Substances 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical group CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
RTTLIGUVNXGNJB-UHFFFAOYSA-N IC=1C=C(C(=O)Cl)C=CC1I Chemical compound IC=1C=C(C(=O)Cl)C=CC1I RTTLIGUVNXGNJB-UHFFFAOYSA-N 0.000 description 1
208000000913 Kidney Calculi Diseases 0.000 description 1
206010029148 Nephrolithiasis Diseases 0.000 description 1
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
208000007536 Thrombosis Diseases 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000037005 anaesthesia Effects 0.000 description 1
239000004637 bakelite Substances 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
210000001124 body fluid Anatomy 0.000 description 1
239000010839 body fluid Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
230000000747 cardiac effect Effects 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229920006037 cross link polymer Polymers 0.000 description 1
238000004042 decolorization Methods 0.000 description 1
238000001514 detection method Methods 0.000 description 1
229940079593 drug Drugs 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
239000012259 ether extract Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000011888 foil Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
230000002262 irrigation Effects 0.000 description 1
238000003973 irrigation Methods 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical class [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000000178 monomer Substances 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003973 paint Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
239000004634 thermosetting polymer Substances 0.000 description 1
238000012800 visualization Methods 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/14—Materials characterised by their function or physical properties, e.g. lubricating compositions
- A61L29/18—Materials at least partially X-ray or laser opaque
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/14—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L31/18—Materials at least partially X-ray or laser opaque
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M29/00—Dilators with or without means for introducing media, e.g. remedies
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
- C07C51/60—Preparation of carboxylic acid halides by conversion of carboxylic acids or their anhydrides or esters, lactones, salts into halides with the same carboxylic acid part
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Animal Behavior & Ethology (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Heart & Thoracic Surgery (AREA)
Physics & Mathematics (AREA)
Anesthesiology (AREA)
Optics & Photonics (AREA)
Hematology (AREA)
Epidemiology (AREA)
Biomedical Technology (AREA)
Vascular Medicine (AREA)
Medicinal Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Surgery (AREA)
Polymers & Plastics (AREA)
Oil, Petroleum & Natural Gas (AREA)
Materials For Medical Uses (AREA)
Compositions Of Macromolecular Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH876462A 1961-07-21 1962-07-20 Verfahren zur Herstellung neuer Dijodbenzoylverbindungen CH421928A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US12564161A	1961-07-21	1961-07-21

Publications (1)

Publication Number	Publication Date
CH421928A true CH421928A (de)	1966-10-15

Family

ID=22420713

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH876462A CH421928A (de)	1961-07-21	1962-07-20	Verfahren zur Herstellung neuer Dijodbenzoylverbindungen

Country Status (4)

Country	Link
CH (1)	CH421928A (fr)
DE (1)	DE1270807B (fr)
FR (2)	FR1336758A (fr)
GB (1)	GB961902A (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4225725A (en)	1975-10-20	1980-09-30	Mallinckrodt, Inc.	Lower alkoxymethyl esters of 2,4,6-triiodobenzoic acid derivatives
US4581390A (en) *	1984-06-29	1986-04-08	Flynn Vincent J	Catheters comprising radiopaque polyurethane-silicone network resin compositions
US4584326A (en) *	1984-06-29	1986-04-22	Flynn Vincent J	Radiopaque polyvinyl-silicone network resin compositions and medical-surgical tubings prepared therefrom
US4579879A (en) *	1984-06-29	1986-04-01	Flynn Vincent J	Radiopaque polyurethane-silicone network resin compositions and medical-surgical tubings prepared therefrom

1961
- 1961-07-13 GB GB26991/62A patent/GB961902A/en not_active Expired
1962
- 1962-07-20 FR FR904671A patent/FR1336758A/fr not_active Expired
- 1962-07-20 DE DEP1270807A patent/DE1270807B/de active Pending
- 1962-07-20 CH CH876462A patent/CH421928A/de unknown
- 1962-10-19 FR FR912763A patent/FR2066M/fr active Active

Also Published As

Publication number	Publication date
DE1270807B (de)	1968-06-20
FR1336758A (fr)	1963-09-06
GB961902A (en)	1964-06-24
FR2066M (fr)	1963-10-07

Publication	Publication Date	Title
US3361700A (en)	1968-01-02	Iodinated esters and resin compositions containing same
EP0023686B1 (fr)	1984-10-31	Esters (méth)acryliques de décandiols tricycliques contenant des groupes éthers, procédé de préparation et utilisation pour la fabrication de mélanges adhésifs et de jointoyage
DE1929832C3 (de)	1973-12-06	Zahnfüllmassen
DE2816823C2 (de)	1982-04-29	Verwendung von Diacrylsäure- oder Dimethacrylsäureester zur Herstellung von polymerisierbaren Dentalmassen
US3645955A (en)	1972-02-29	Plasticized radiopaque vinyl resin compositions
CH626873A5 (fr)	1981-12-15
DE1921870A1 (de)	1969-12-18	Diacrylsaeureester von bifunktionellen Alkoholverbindungen
DE2660982C2 (de)	1986-07-17	Verwendung von Esterderivaten von Cumylphenol als nichtreaktive Weichmacher für Polyurethan- und Polyvinylchloridharze
DD207917A5 (de)	1984-03-21	Verfahren zum stabilisieren von polymerisaten auf der basis von vinylchlorid
DE1295820B (de)	1969-05-22	Weichmacher fuer Vinylhalogenidpolymerisate
CH421928A (de)	1966-10-15	Verfahren zur Herstellung neuer Dijodbenzoylverbindungen
DE3106071C2 (fr)	1988-12-15
DE1569407B2 (de)	1971-09-02	Stabilisatorgemische fuer vinylchloridpolymerisate
DE2509552C2 (de)	1984-08-09	Terephthalat von 2,2'-Methylen-bis(4-methyl-6-tert.-butylphenol) sowie dessen Verwendung
DE2939453A1 (de)	1981-04-30	Verfahren zur herstellung von durch innere weichmachung weichgemachten polyvinylchlorid
EP0164663B1 (fr)	1990-01-10	Matière plastique de grande transparence aux ultraviolets et son procédé de préparation
DE3520750A1 (de)	1986-02-06	Verfahren zur herstellung von citratestern und deren verwendung fuer medizinische artikel
DE2645870C3 (de)	1978-11-23	Stabilisierte Polyvinylchlorid-Formmassen
DE1768208A1 (de)	1971-11-11	Hochmolekulare organische Zinnverbindungen
DE1694894B2 (de)	1978-04-13	Massen auf der Grundlage von Polymerisaten und Mischpolymerisaten der Vinylester mit Phenoxarsinverbindungen als mikrobizide Zusätze
DE3504981A1 (de)	1986-08-14	Stabilisatoren
DE667863C (de)	1938-11-22	Verfahren zur Herstellung unloeslicher Stoffe aus Polymerisaten von aliphatischen Verbindungen
DE1227656C2 (de)	1973-09-20	Verfahren zur herstellung von mischpolymerisaten des vinylchlorids
DE934500C (de)	1955-10-27	Loesungs-, Weichmachungs- und Gelatinierungsmittel
AT211484B (de)	1960-10-10	Masse zur Füllung von Hohlräumen in Zähnen und zur Befestigung von Zahnersatzteilen