NO752938L - - Google Patents

Info

Publication number: NO752938L
Authority: NO; Norway
Prior art keywords: silanated; antimicrobial; compound; phenol; compound according
Prior art date: 1974-08-28

Application number

NO752938A

Other languages

English (en)

Norwegian (no)

Inventor

M W Brenner

L Laufer

Original Assignee

Schwarz Services Int

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.)

1974-08-28

Filing date

1975-08-27

Publication date

1976-03-02

1974-08-28 Priority claimed from US05/501,058 external-priority patent/US3940430A/en

1975-08-27 Application filed by Schwarz Services Int filed Critical Schwarz Services Int

1976-03-02 Publication of NO752938L publication Critical patent/NO752938L/no

Links

150000001875 compounds Chemical class 0.000 claims description 54
230000000845 anti-microbial effect Effects 0.000 claims description 53
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 51
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 48
ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 claims description 34
229960004068 hexachlorophene Drugs 0.000 claims description 33
150000002989 phenols Chemical class 0.000 claims description 27
239000004599 antimicrobial Substances 0.000 claims description 26
238000006243 chemical reaction Methods 0.000 claims description 23
238000000034 method Methods 0.000 claims description 19
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 claims description 19
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 15
238000010992 reflux Methods 0.000 claims description 14
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 13
125000004432 carbon atom Chemical group C* 0.000 claims description 13
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 12
-1 methoxy, ethoxy Chemical group 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 8
239000000376 reactant Substances 0.000 claims description 8
229910000077 silane Inorganic materials 0.000 claims description 8
238000004519 manufacturing process Methods 0.000 claims description 7
125000005907 alkyl ester group Chemical group 0.000 claims description 5
239000000460 chlorine Substances 0.000 claims description 5
229940090248 4-hydroxybenzoic acid Drugs 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 3
239000004305 biphenyl Substances 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims 3
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
239000012429 reaction media Substances 0.000 claims 2
VXHYVVAUHMGCEX-UHFFFAOYSA-N 2-(2-hydroxyphenoxy)phenol Chemical compound OC1=CC=CC=C1OC1=CC=CC=C1O VXHYVVAUHMGCEX-UHFFFAOYSA-N 0.000 claims 1
150000005166 2-hydroxybenzoic acids Chemical class 0.000 claims 1
150000005168 4-hydroxybenzoic acids Chemical class 0.000 claims 1
239000005711 Benzoic acid Substances 0.000 claims 1
235000010233 benzoic acid Nutrition 0.000 claims 1
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 39
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 36
239000000243 solution Substances 0.000 description 28
239000003208 petroleum Substances 0.000 description 22
238000012360 testing method Methods 0.000 description 17
239000011521 glass Substances 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 13
239000007788 liquid Substances 0.000 description 13
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 12
239000000463 material Substances 0.000 description 12
238000002844 melting Methods 0.000 description 12
230000008018 melting Effects 0.000 description 12
239000000203 mixture Substances 0.000 description 12
238000005406 washing Methods 0.000 description 12
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 11
244000005700 microbiome Species 0.000 description 11
229910052710 silicon Inorganic materials 0.000 description 11
NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 description 10
RIKCMEDSBFQFAL-UHFFFAOYSA-N octyl 4-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=C(O)C=C1 RIKCMEDSBFQFAL-UHFFFAOYSA-N 0.000 description 10
239000002244 precipitate Substances 0.000 description 10
MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
229960003887 dichlorophen Drugs 0.000 description 9
238000002360 preparation method Methods 0.000 description 9
239000010703 silicon Substances 0.000 description 9
WFJIVOKAWHGMBH-UHFFFAOYSA-N 4-hexylbenzene-1,3-diol Chemical compound CCCCCCC1=CC=C(O)C=C1O WFJIVOKAWHGMBH-UHFFFAOYSA-N 0.000 description 8
ZTJORNVITHUQJA-UHFFFAOYSA-N Heptyl p-hydroxybenzoate Chemical compound CCCCCCCOC(=O)C1=CC=C(O)C=C1 ZTJORNVITHUQJA-UHFFFAOYSA-N 0.000 description 8
239000004284 Heptyl p-hydroxybenzoate Substances 0.000 description 8
235000019251 heptyl p-hydroxybenzoate Nutrition 0.000 description 8
229960003258 hexylresorcinol Drugs 0.000 description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
150000003141 primary amines Chemical class 0.000 description 8
239000013078 crystal Substances 0.000 description 7
239000000047 product Substances 0.000 description 7
239000000758 substrate Substances 0.000 description 7
230000015572 biosynthetic process Effects 0.000 description 6
238000011109 contamination Methods 0.000 description 6
150000001412 amines Chemical group 0.000 description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
238000000576 coating method Methods 0.000 description 5
238000002329 infrared spectrum Methods 0.000 description 5
230000000813 microbial effect Effects 0.000 description 5
238000002156 mixing Methods 0.000 description 5
229910052760 oxygen Inorganic materials 0.000 description 5
239000001301 oxygen Substances 0.000 description 5
239000000843 powder Substances 0.000 description 5
229960004889 salicylic acid Drugs 0.000 description 5
239000006228 supernatant Substances 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
238000004458 analytical method Methods 0.000 description 4
239000012736 aqueous medium Substances 0.000 description 4
235000013361 beverage Nutrition 0.000 description 4
238000009835 boiling Methods 0.000 description 4
238000004806 packaging method and process Methods 0.000 description 4
229920001817 Agar Polymers 0.000 description 3
241000894006 Bacteria Species 0.000 description 3
240000004808 Saccharomyces cerevisiae Species 0.000 description 3
239000008272 agar Substances 0.000 description 3
239000011324 bead Substances 0.000 description 3
239000000919 ceramic Substances 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
239000000356 contaminant Substances 0.000 description 3
239000003814 drug Substances 0.000 description 3
235000019441 ethanol Nutrition 0.000 description 3
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
241000195493 Cryptophyta Species 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
239000003513 alkali Substances 0.000 description 2
239000000872 buffer Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
238000000151 deposition Methods 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
230000002070 germicidal effect Effects 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
239000002609 medium Substances 0.000 description 2
239000004570 mortar (masonry) Substances 0.000 description 2
239000012452 mother liquor Substances 0.000 description 2
239000005022 packaging material Substances 0.000 description 2
229910052572 stoneware Inorganic materials 0.000 description 2
239000000725 suspension Substances 0.000 description 2
VHBSECWYEFJRNV-UHFFFAOYSA-N 2-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1O.OC(=O)C1=CC=CC=C1O VHBSECWYEFJRNV-UHFFFAOYSA-N 0.000 description 1
ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
241000233866 Fungi Species 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
239000001888 Peptone Substances 0.000 description 1
108010080698 Peptones Proteins 0.000 description 1
239000006087 Silane Coupling Agent Substances 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
235000012538 ammonium bicarbonate Nutrition 0.000 description 1
239000001099 ammonium carbonate Substances 0.000 description 1
239000003708 ampul Substances 0.000 description 1
150000003931 anilides Chemical class 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
229940088710 antibiotic agent Drugs 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
230000008275 binding mechanism Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
229940041514 candida albicans extract Drugs 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
238000010411 cooking Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
239000006071 cream Substances 0.000 description 1
239000002178 crystalline material Substances 0.000 description 1
230000008021 deposition Effects 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
150000002085 enols Chemical class 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000004403 ethyl p-hydroxybenzoate Substances 0.000 description 1
235000010228 ethyl p-hydroxybenzoate Nutrition 0.000 description 1
229940043351 ethyl-p-hydroxybenzoate Drugs 0.000 description 1
NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012535 impurity Substances 0.000 description 1
230000036512 infertility Effects 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000010985 leather Substances 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
238000004949 mass spectrometry Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
238000006140 methanolysis reaction Methods 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
SVHOVVJFOWGYJO-UHFFFAOYSA-N pentabromophenol Chemical compound OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br SVHOVVJFOWGYJO-UHFFFAOYSA-N 0.000 description 1
235000019319 peptone Nutrition 0.000 description 1
230000002688 persistence Effects 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
239000008055 phosphate buffer solution Substances 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229910052573 porcelain Inorganic materials 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000011084 recovery Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
150000003870 salicylic acids Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
230000007017 scission Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
239000004753 textile Substances 0.000 description 1
239000010409 thin film Substances 0.000 description 1
KVSKGMLNBAPGKH-UHFFFAOYSA-N tribromosalicylanilide Chemical compound OC1=C(Br)C=C(Br)C=C1C(=O)NC1=CC=C(Br)C=C1 KVSKGMLNBAPGKH-UHFFFAOYSA-N 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000012138 yeast extract Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO752938A 1974-08-28 1975-08-27 NO752938L (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US50102274A	1974-08-28	1974-08-28
US05/501,058 US3940430A (en)	1974-08-28	1974-08-28	Silanized antimicrobial compounds

Publications (1)

Publication Number	Publication Date
NO752938L true NO752938L (da)	1976-03-02

Family

ID=27053692

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO752938A NO752938L (da)	1974-08-28	1975-08-27

Country Status (9)

Country	Link
JP (1)	JPS5167731A (da)
AU (1)	AU8433475A (da)
DE (1)	DE2538341A1 (da)
DK (1)	DK384775A (da)
FR (1)	FR2283144A1 (da)
IT (1)	IT1052139B (da)
NL (1)	NL7510170A (da)
NO (1)	NO752938L (da)
SE (1)	SE7509551L (da)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2847400A1 (de) *	1978-11-02	1980-05-08	Dynamit Nobel Ag	Salzartige aminoorganosilanester- phenol-addukte und verfahren zu deren herstellung
EP1285926B1 (de) *	2001-08-06	2004-05-12	Degussa AG	Organosiliciumverbindungen
WO2003017963A1 (en) *	2001-08-24	2003-03-06	Unilever N.V.	Oral composition comprising an alkylhydroxybenzoate
CN106662415B (zh) *	2014-08-07	2018-11-30	夏普株式会社	热交换器、金属构件、电热水器、饮料供应器和饭盒盖

1975
- 1975-08-27 DK DK384775A patent/DK384775A/da unknown
- 1975-08-27 NO NO752938A patent/NO752938L/no unknown
- 1975-08-27 AU AU84334/75A patent/AU8433475A/en not_active Expired
- 1975-08-28 JP JP50104876A patent/JPS5167731A/ja active Pending
- 1975-08-28 FR FR7526554A patent/FR2283144A1/fr not_active Withdrawn
- 1975-08-28 DE DE19752538341 patent/DE2538341A1/de active Pending
- 1975-08-28 NL NL7510170A patent/NL7510170A/xx not_active Application Discontinuation
- 1975-08-28 IT IT51090/75A patent/IT1052139B/it active
- 1975-08-28 SE SE7509551A patent/SE7509551L/xx unknown

Also Published As

Publication number	Publication date
IT1052139B (it)	1981-06-20
AU8433475A (en)	1977-03-03
DK384775A (da)	1976-02-29
SE7509551L (sv)	1976-03-01
NL7510170A (nl)	1976-03-02
FR2283144A1 (fr)	1976-03-26
JPS5167731A (da)	1976-06-11
DE2538341A1 (de)	1976-03-11

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