SU535914A3 - Способ обнаружени уробилиногена - Google Patents
Способ обнаружени уробилиногенаInfo
- Publication number
- SU535914A3 SU535914A3 SU1799317A SU1799317A SU535914A3 SU 535914 A3 SU535914 A3 SU 535914A3 SU 1799317 A SU1799317 A SU 1799317A SU 1799317 A SU1799317 A SU 1799317A SU 535914 A3 SU535914 A3 SU 535914A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acid
- groups
- indicator
- urine
- diazonium
- Prior art date
Links
- OBHRVMZSZIDDEK-UHFFFAOYSA-N urobilinogen Chemical compound CCC1=C(C)C(=O)NC1CC1=C(C)C(CCC(O)=O)=C(CC2=C(C(C)=C(CC3C(=C(CC)C(=O)N3)C)N2)CCC(O)=O)N1 OBHRVMZSZIDDEK-UHFFFAOYSA-N 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims 3
- 238000001514 detection method Methods 0.000 title 1
- -1 oxy- Chemical class 0.000 claims description 14
- 210000002700 urine Anatomy 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- BPYKTIZUTYGOLE-IFADSCNNSA-N Bilirubin Chemical compound N1C(=O)C(C)=C(C=C)\C1=C\C1=C(C)C(CCC(O)=O)=C(CC2=C(C(C)=C(\C=C/3C(=C(C=C)C(=O)N\3)C)N2)CCC(O)=O)N1 BPYKTIZUTYGOLE-IFADSCNNSA-N 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 3
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 125000004442 acylamino group Chemical group 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000005228 aryl sulfonate group Chemical group 0.000 claims 1
- CIZVQWNPBGYCGK-UHFFFAOYSA-N benzenediazonium Chemical class N#[N+]C1=CC=CC=C1 CIZVQWNPBGYCGK-UHFFFAOYSA-N 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 claims 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 238000011835 investigation Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 230000035945 sensitivity Effects 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000012954 diazonium Substances 0.000 description 5
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 3
- 235000005811 Viola adunca Nutrition 0.000 description 3
- 240000009038 Viola odorata Species 0.000 description 3
- 235000013487 Viola odorata Nutrition 0.000 description 3
- 235000002254 Viola papilionacea Nutrition 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- DGQLVPJVXFOQEV-JNVSTXMASA-N carminic acid Chemical compound OC1=C2C(=O)C=3C(C)=C(C(O)=O)C(O)=CC=3C(=O)C2=C(O)C(O)=C1[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O DGQLVPJVXFOQEV-JNVSTXMASA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 description 2
- IMPPGHMHELILKG-UHFFFAOYSA-N 4-ethoxyaniline Chemical compound CCOC1=CC=C(N)C=C1 IMPPGHMHELILKG-UHFFFAOYSA-N 0.000 description 2
- 244000172533 Viola sororia Species 0.000 description 2
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 2
- 150000001989 diazonium salts Chemical class 0.000 description 2
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- NCWGZUNGBWYLMS-UHFFFAOYSA-N 2-(4-methoxyanilino)benzenediazonium Chemical compound COC1=CC=C(C=C1)NC1=C(C=CC=C1)[N+]#N NCWGZUNGBWYLMS-UHFFFAOYSA-N 0.000 description 1
- KDVRJBRCHJDVBA-UHFFFAOYSA-N 2-hydroxybenzenediazonium sulfate Chemical compound S(=O)(=O)([O-])[O-].OC1=C(C=CC=C1)[N+]#N.OC1=C(C=CC=C1)[N+]#N KDVRJBRCHJDVBA-UHFFFAOYSA-N 0.000 description 1
- CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 1
- MOMKYJPSVWEWPM-UHFFFAOYSA-N 4-(chloromethyl)-2-(4-methylphenyl)-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=NC(CCl)=CS1 MOMKYJPSVWEWPM-UHFFFAOYSA-N 0.000 description 1
- BAJJCUMRSLDNPB-UHFFFAOYSA-O 4-acetamidobenzenediazonium Chemical compound CC(=O)NC1=CC=C([N+]#N)C=C1 BAJJCUMRSLDNPB-UHFFFAOYSA-O 0.000 description 1
- KBYWCGCRACQITA-UHFFFAOYSA-O 4-benzamido-2,5-dimethoxybenzenediazonium Chemical compound COC1=CC([N+]#N)=C(OC)C=C1NC(=O)C1=CC=CC=C1 KBYWCGCRACQITA-UHFFFAOYSA-O 0.000 description 1
- RBLUJIWKMSZIMK-UHFFFAOYSA-N 4-n-(4-methoxyphenyl)benzene-1,4-diamine Chemical compound C1=CC(OC)=CC=C1NC1=CC=C(N)C=C1 RBLUJIWKMSZIMK-UHFFFAOYSA-N 0.000 description 1
- KLHYPYAETJWSBK-UHFFFAOYSA-J Cl[Zn](Cl)(Cl)Cl Chemical compound Cl[Zn](Cl)(Cl)Cl KLHYPYAETJWSBK-UHFFFAOYSA-J 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
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- HUMHYXGDUOGHTG-HEZXSMHISA-N alpha-D-GalpNAc-(1->3)-[alpha-L-Fucp-(1->2)]-D-Galp Chemical compound O[C@H]1[C@H](O)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](O[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](O)[C@@H](CO)OC1O HUMHYXGDUOGHTG-HEZXSMHISA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- ZBZPTCVJEOXKHK-UHFFFAOYSA-N hydrogen sulfate;4-hydroxybenzenediazonium Chemical compound OS([O-])(=O)=O.OC1=CC=C([N+]#N)C=C1 ZBZPTCVJEOXKHK-UHFFFAOYSA-N 0.000 description 1
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 description 1
- 229960004963 mesalazine Drugs 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000019983 sodium metaphosphate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- PVEFEIWVJKUCLJ-UHFFFAOYSA-N sulfuric acid;toluene Chemical compound OS(O)(=O)=O.CC1=CC=CC=C1 PVEFEIWVJKUCLJ-UHFFFAOYSA-N 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/72—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood pigments, e.g. haemoglobin, bilirubin or other porphyrins; involving occult blood
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/903—Diazo reactions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/14—Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
- Y10T436/145555—Hetero-N
- Y10T436/146666—Bile pigment
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Urology & Nephrology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Cell Biology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2130559A DE2130559C3 (de) | 1971-06-19 | 1971-06-19 | Diagnostisches Mittel zum Nach weis von Urobihnogen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU535914A3 true SU535914A3 (ru) | 1976-11-15 |
Family
ID=5811257
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1799317A SU535914A3 (ru) | 1971-06-19 | 1972-06-16 | Способ обнаружени уробилиногена |
Country Status (18)
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT347600B (de) | 1974-11-11 | 1979-01-10 | Wellcome Found | Testeinrichtungen |
| DE2521402C3 (de) * | 1975-05-14 | 1979-07-26 | Behringwerke Ag, 3550 Marburg | Diagnostisches Mittel zum Nachweis von Urobilinogen |
| US4158546A (en) * | 1978-07-24 | 1979-06-19 | Miles Laboratories, Inc. | Composition, test device and method for determining the presence of urobilinogen in a test sample |
| DE2839931A1 (de) * | 1978-09-14 | 1980-03-27 | Behringwerke Ag | Diagnostisches mittel zum nachweis von urobilinogen |
| US4260579A (en) * | 1979-05-10 | 1981-04-07 | Miles Laboratories, Inc. | Device and method for simulating bilirubin in urine |
| US4311483A (en) * | 1979-06-18 | 1982-01-19 | Beckman Instruments, Inc. | Kinetic method for directly determining total bilirubin |
| US4246133A (en) * | 1979-06-22 | 1981-01-20 | Sherwood Medical Industries Inc. | Stabilized diazotized sulfanilic acid solutions |
| US4405718A (en) * | 1981-07-20 | 1983-09-20 | Miles Laboratories, Inc. | Method and composition for urobilinogen control standard |
| US4468467A (en) * | 1982-02-01 | 1984-08-28 | Eastman Kodak Company | Diazonium salt for bilirubin assay |
| JPS61223651A (ja) * | 1985-03-29 | 1986-10-04 | Kyowa Medetsukusu Kk | ビリルビンの定量方法 |
| US4816415A (en) * | 1987-05-29 | 1989-03-28 | Analytical Innovations, Inc. | Cannabinoid detection method |
| ES2079363T3 (es) * | 1988-06-09 | 1996-01-16 | Abbott Lab | Metodo y dispositivo que emplean colorantes coloreados inmovilizados covalentemente. |
| JPH0270495U (enrdf_load_stackoverflow) * | 1988-11-17 | 1990-05-29 | ||
| US5736408A (en) * | 1994-11-23 | 1998-04-07 | Carter; Jesse M. | Method for the detection of urobilinogen in urine on an automated analyzer |
| US7936505B2 (en) * | 2006-08-28 | 2011-05-03 | Draper, Inc. | Tensioned projection screen |
| US8012761B2 (en) | 2006-12-14 | 2011-09-06 | Kimberly-Clark Worldwide, Inc. | Detection of formaldehyde in urine samples |
| US7846383B2 (en) | 2006-12-15 | 2010-12-07 | Kimberly-Clark Worldwide, Inc. | Lateral flow assay device and absorbent article containing same |
| US9110362B2 (en) | 2009-06-12 | 2015-08-18 | Draper, Inc. | Tensioned projection screen assembly |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2854317A (en) * | 1950-08-08 | 1958-09-30 | Miles Lab | Method and composition for testing bilirubin in urine |
| US3511607A (en) * | 1967-10-06 | 1970-05-12 | Smithkline Corp | Laboratory reagent for assay of total bilirubin |
| DE1767931C3 (de) * | 1967-10-26 | 1973-09-27 | Boehringer Mannheim Gmbh, 6800 Mannheim | Diagnostisches Mittel und Verfahren zum Nachweis von Urobilinogen-Körpern |
| US3585001A (en) * | 1969-02-17 | 1971-06-15 | Miles Lab | Stabilized test device and process for detecting couplable compounds |
| US3585004A (en) * | 1969-03-21 | 1971-06-15 | Miles Lab | Test composition and device for detecting couplable compounds |
| US3652222A (en) * | 1969-04-07 | 1972-03-28 | American Monitor Corp | Bilirubin assay |
-
1971
- 1971-06-19 DE DE2130559A patent/DE2130559C3/de not_active Expired
-
1972
- 1972-05-11 DD DD162894A patent/DD98763A5/xx unknown
- 1972-06-13 HU HUBO1381A patent/HU162948B/hu unknown
- 1972-06-13 FI FI1685/72A patent/FI53508C/fi active
- 1972-06-14 CH CH883772A patent/CH564774A5/xx not_active IP Right Cessation
- 1972-06-14 US US00262923A patent/US3853466A/en not_active Expired - Lifetime
- 1972-06-14 GB GB2781372A patent/GB1343247A/en not_active Expired
- 1972-06-15 FR FR7221551A patent/FR2158791A1/fr active Pending
- 1972-06-15 ES ES403875A patent/ES403875A1/es not_active Expired
- 1972-06-16 NL NLAANVRAGE7208232,A patent/NL170773C/xx not_active IP Right Cessation
- 1972-06-16 CA CA144,993A patent/CA959389A/en not_active Expired
- 1972-06-16 ZA ZA724152A patent/ZA724152B/xx unknown
- 1972-06-16 IT IT25819/72A patent/IT956664B/it active
- 1972-06-16 AT AT841073A patent/AT322116B/de not_active IP Right Cessation
- 1972-06-16 SE SE7207961A patent/SE394328B/xx unknown
- 1972-06-16 AT AT518072A patent/AT317441B/de not_active IP Right Cessation
- 1972-06-16 DK DK303372A patent/DK143147C/da not_active IP Right Cessation
- 1972-06-16 SU SU1799317A patent/SU535914A3/ru active
- 1972-06-19 JP JP47061253A patent/JPS5741693B1/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| SE394328B (sv) | 1977-06-20 |
| DE2130559C3 (de) | 1973-11-22 |
| HU162948B (enrdf_load_stackoverflow) | 1973-05-28 |
| FI53508B (enrdf_load_stackoverflow) | 1978-01-31 |
| ZA724152B (en) | 1973-04-25 |
| DK143147C (da) | 1981-11-09 |
| DK143147B (da) | 1981-06-29 |
| DE2130559B2 (de) | 1973-04-26 |
| DD98763A5 (enrdf_load_stackoverflow) | 1973-07-05 |
| ES403875A1 (es) | 1975-05-16 |
| FR2158791A1 (enrdf_load_stackoverflow) | 1973-06-15 |
| AT317441B (de) | 1974-08-26 |
| AU4354072A (en) | 1973-07-12 |
| JPS5741693B1 (enrdf_load_stackoverflow) | 1982-09-04 |
| NL170773C (nl) | 1982-12-16 |
| NL7208232A (enrdf_load_stackoverflow) | 1972-12-21 |
| DE2130559A1 (de) | 1972-12-21 |
| CH564774A5 (enrdf_load_stackoverflow) | 1975-07-31 |
| GB1343247A (en) | 1974-01-10 |
| US3853466A (en) | 1974-12-10 |
| AT322116B (de) | 1975-05-12 |
| IT956664B (it) | 1973-10-10 |
| CA959389A (en) | 1974-12-17 |
| FI53508C (fi) | 1978-05-10 |
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