SE456370B - Forfarande och detergenthaltigt medel for undanrojande av grumlingar i en prov-reaktionsblandning - Google Patents
Forfarande och detergenthaltigt medel for undanrojande av grumlingar i en prov-reaktionsblandningInfo
- Publication number
- SE456370B SE456370B SE8008598A SE8008598A SE456370B SE 456370 B SE456370 B SE 456370B SE 8008598 A SE8008598 A SE 8008598A SE 8008598 A SE8008598 A SE 8008598A SE 456370 B SE456370 B SE 456370B
- Authority
- SE
- Sweden
- Prior art keywords
- alkyl
- detergents
- detergent
- complex
- soluble
- Prior art date
Links
- 239000003599 detergent Substances 0.000 title claims description 43
- 239000011541 reaction mixture Substances 0.000 title claims description 10
- 238000000034 method Methods 0.000 title claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 239000000654 additive Substances 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 10
- -1 aromatic alcohols Chemical class 0.000 claims description 9
- 230000000996 additive effect Effects 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- 239000000523 sample Substances 0.000 claims description 6
- OUCSIUCEQVCDEL-UHFFFAOYSA-N 2,3,4-tribromophenol Chemical class OC1=CC=C(Br)C(Br)=C1Br OUCSIUCEQVCDEL-UHFFFAOYSA-N 0.000 claims description 5
- HSQFVBWFPBKHEB-UHFFFAOYSA-N 2,3,4-trichlorophenol Chemical class OC1=CC=C(Cl)C(Cl)=C1Cl HSQFVBWFPBKHEB-UHFFFAOYSA-N 0.000 claims description 5
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 claims description 5
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 5
- 150000001896 cresols Chemical class 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- KUDPGZONDFORKU-UHFFFAOYSA-N n-chloroaniline Chemical compound ClNC1=CC=CC=C1 KUDPGZONDFORKU-UHFFFAOYSA-N 0.000 claims description 5
- 150000002894 organic compounds Chemical class 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 125000005012 alkyl thioether group Chemical group 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 230000008030 elimination Effects 0.000 claims description 2
- 238000003379 elimination reaction Methods 0.000 claims description 2
- 150000002334 glycols Chemical class 0.000 claims description 2
- 238000005375 photometry Methods 0.000 claims description 2
- 239000002244 precipitate Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- 125000002091 cationic group Chemical group 0.000 claims 1
- 150000001805 chlorine compounds Chemical class 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 230000001376 precipitating effect Effects 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 239000002671 adjuvant Substances 0.000 description 6
- 229920001213 Polysorbate 20 Polymers 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 5
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 5
- WDNBURPWRNALGP-UHFFFAOYSA-N 3,4-Dichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1 WDNBURPWRNALGP-UHFFFAOYSA-N 0.000 description 4
- RLFWWDJHLFCNIJ-UHFFFAOYSA-N 4-aminoantipyrine Chemical compound CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- 230000008033 biological extinction Effects 0.000 description 4
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- IEQAICDLOKRSRL-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-dodecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO IEQAICDLOKRSRL-UHFFFAOYSA-N 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 229920004890 Triton X-100 Polymers 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000008057 potassium phosphate buffer Substances 0.000 description 3
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 3
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 2
- FAXWFCTVSHEODL-UHFFFAOYSA-N 2,4-dibromophenol Chemical compound OC1=CC=C(Br)C=C1Br FAXWFCTVSHEODL-UHFFFAOYSA-N 0.000 description 2
- URJQSMIFSMHWSP-VVHBOOHCSA-N 2-[[2-[[(4r)-4-[(3r,5s,7r,8r,9s,10s,12s,13r,14s,17r)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]acetyl]amino]ethanesulfonic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCC(=O)NCCS(O)(=O)=O)C)[C@@]2(C)[C@@H](O)C1 URJQSMIFSMHWSP-VVHBOOHCSA-N 0.000 description 2
- 102100035687 Bile salt-activated lipase Human genes 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229940117916 cinnamic aldehyde Drugs 0.000 description 2
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 2
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- NCIAGQNZQHYKGR-UHFFFAOYSA-N naphthalene-1,2,3-triol Chemical class C1=CC=C2C(O)=C(O)C(O)=CC2=C1 NCIAGQNZQHYKGR-UHFFFAOYSA-N 0.000 description 2
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- SLGOCMATMKJJCE-UHFFFAOYSA-N 1,1,1,2-tetrachloro-2,2-difluoroethane Chemical compound FC(F)(Cl)C(Cl)(Cl)Cl SLGOCMATMKJJCE-UHFFFAOYSA-N 0.000 description 1
- UAZUEJTXWAXSMA-UHFFFAOYSA-N 1,1-dichlorobut-1-ene Chemical compound CCC=C(Cl)Cl UAZUEJTXWAXSMA-UHFFFAOYSA-N 0.000 description 1
- UMPSXRYVXUPCOS-UHFFFAOYSA-N 2,3-dichlorophenol Chemical compound OC1=CC=CC(Cl)=C1Cl UMPSXRYVXUPCOS-UHFFFAOYSA-N 0.000 description 1
- LINPIYWFGCPVIE-UHFFFAOYSA-N 2,4,6-trichlorophenol Chemical compound OC1=C(Cl)C=C(Cl)C=C1Cl LINPIYWFGCPVIE-UHFFFAOYSA-N 0.000 description 1
- HFZWRUODUSTPEG-UHFFFAOYSA-N 2,4-dichlorophenol Chemical compound OC1=CC=C(Cl)C=C1Cl HFZWRUODUSTPEG-UHFFFAOYSA-N 0.000 description 1
- BQPYFTUMNBOSNC-UHFFFAOYSA-N 2-(9-ethoxynonyl)phenol Chemical compound CCOCCCCCCCCCC1=CC=CC=C1O BQPYFTUMNBOSNC-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- AKCRQHGQIJBRMN-UHFFFAOYSA-N 2-chloroaniline Chemical compound NC1=CC=CC=C1Cl AKCRQHGQIJBRMN-UHFFFAOYSA-N 0.000 description 1
- BLBSJXNUYKZSAC-UHFFFAOYSA-N 2h-naphthalene-1,1,5-triol Chemical compound C1=CCC(O)(O)C2=C1C(O)=CC=C2 BLBSJXNUYKZSAC-UHFFFAOYSA-N 0.000 description 1
- VEEOFSUIWVGHHJ-UHFFFAOYSA-N 3-ethoxy-2-octylphenol Chemical compound CCCCCCCCC1=C(O)C=CC=C1OCC VEEOFSUIWVGHHJ-UHFFFAOYSA-N 0.000 description 1
- 101100283604 Caenorhabditis elegans pigk-1 gene Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 102100035882 Catalase Human genes 0.000 description 1
- 108010053835 Catalase Proteins 0.000 description 1
- 108010089254 Cholesterol oxidase Proteins 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 241000283073 Equus caballus Species 0.000 description 1
- 108090000371 Esterases Proteins 0.000 description 1
- 108010015776 Glucose oxidase Proteins 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- XJLXINKUBYWONI-NNYOXOHSSA-O NADP(+) Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](OP(O)(O)=O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 XJLXINKUBYWONI-NNYOXOHSSA-O 0.000 description 1
- 239000007832 Na2SO4 Substances 0.000 description 1
- 102000003992 Peroxidases Human genes 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 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
- 108010055297 Sterol Esterase Proteins 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229950005499 carbon tetrachloride Drugs 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 229960003964 deoxycholic acid Drugs 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 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
- 230000035622 drinking Effects 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- SJMLNDPIJZBEKY-UHFFFAOYSA-N ethyl 2,2,2-trichloroacetate Chemical compound CCOC(=O)C(Cl)(Cl)Cl SJMLNDPIJZBEKY-UHFFFAOYSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 229960001867 guaiacol Drugs 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 235000020094 liqueur Nutrition 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- CZVGDZHOGCQXOY-UHFFFAOYSA-N naphthalene-1,2,7-triol Chemical compound C1=CC(O)=C(O)C2=CC(O)=CC=C21 CZVGDZHOGCQXOY-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- FHHPUSMSKHSNKW-SMOYURAASA-M sodium deoxycholate Chemical compound [Na+].C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 FHHPUSMSKHSNKW-SMOYURAASA-M 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 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
- G01N33/96—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood or serum control standard
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/54—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving glucose or galactose
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/60—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving cholesterol
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/62—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving uric acid
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/34—Purifying; Cleaning
-
- 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
- G01N33/02—Food
- G01N33/04—Dairy products
-
- 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
- Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Biomedical Technology (AREA)
- Genetics & Genomics (AREA)
- General Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Pathology (AREA)
- General Physics & Mathematics (AREA)
- Food Science & Technology (AREA)
- Cell Biology (AREA)
- Medicinal Chemistry (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2816229A DE2816229C2 (de) | 1978-04-14 | 1978-04-14 | Verfahren und Mittel zur Beseitigung von Trübungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE8008598L SE8008598L (sv) | 1980-12-08 |
| SE456370B true SE456370B (sv) | 1988-09-26 |
Family
ID=6036990
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8008598A SE456370B (sv) | 1978-04-14 | 1980-12-08 | Forfarande och detergenthaltigt medel for undanrojande av grumlingar i en prov-reaktionsblandning |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US4282001A (fi) |
| EP (1) | EP0004857A3 (fi) |
| JP (2) | JPS54138493A (fi) |
| AT (1) | AT363613B (fi) |
| BE (1) | BE85T1 (fi) |
| CA (1) | CA1131097A (fi) |
| CH (1) | CH651137A5 (fi) |
| DE (1) | DE2816229C2 (fi) |
| FI (1) | FI69929C (fi) |
| FR (1) | FR2473713A1 (fi) |
| GB (1) | GB2055784B (fi) |
| IE (1) | IE48273B1 (fi) |
| IT (1) | IT1148235B (fi) |
| NL (1) | NL184080C (fi) |
| SE (1) | SE456370B (fi) |
| SU (1) | SU1443816A3 (fi) |
| YU (1) | YU87379A (fi) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2816229C2 (de) * | 1978-04-14 | 1983-11-10 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und Mittel zur Beseitigung von Trübungen |
| DE2911284C2 (de) * | 1979-03-22 | 1982-01-28 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und Reagenz zur Aktivierung der Cholesterinesterase |
| US4273867A (en) * | 1979-04-05 | 1981-06-16 | Mallinckrodt, Inc. | Method and reagent for counteracting lipemic interference |
| US4319882A (en) * | 1980-02-21 | 1982-03-16 | Yash Sharma | Method for detecting immunological agglutination and biochemical agent therefor |
| DE3021457A1 (de) * | 1980-06-06 | 1982-01-07 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und mittel zur aufloesung von chylomikronen in waessrigem mediums |
| CA1163908A (en) * | 1980-10-01 | 1984-03-20 | Shyun-Long Yun | Method for eliminating turbidity in a biological fluid and reagent therefor |
| US4503146A (en) * | 1980-10-01 | 1985-03-05 | Technicon Instruments Corporation | Method for eliminating turbidity in a biological fluid and reagent therefor |
| DE3046241A1 (de) * | 1980-12-08 | 1982-07-15 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und reagenz zur bestimmung von cholesterin |
| DE3107060A1 (de) * | 1981-02-25 | 1982-09-09 | Boehringer Mannheim Gmbh, 6800 Mannheim | Kontroll- oder eichserum und verfahren zu seiner herstellung |
| EP0061541A1 (en) * | 1981-03-27 | 1982-10-06 | Biospecia Limited | Immunological analysis and a biochemical agent therefor |
| US5250418A (en) * | 1981-10-06 | 1993-10-05 | Boehringer Mannheim Gmbh | Process and reagent for determining the activity of chymotrypsin and trypsin in feces |
| US4404286A (en) * | 1982-02-22 | 1983-09-13 | The Dow Chemical Company | Bilirubin assay |
| ATE25464T1 (de) * | 1982-04-02 | 1987-02-15 | Ivan Endre Modrovich | Zeitstabile fluessige zusammensetzung fuer den cholesterinnachweis. |
| US5047327A (en) * | 1982-04-02 | 1991-09-10 | Ivan E. Modrovich | Time-stable liquid cholesterol assay compositions |
| DE3374019D1 (en) * | 1982-07-23 | 1987-11-12 | Wako Pure Chem Ind Ltd | Process for quantitative determination of substrate treated with oxidase |
| DE3303098A1 (de) * | 1983-01-31 | 1984-08-02 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und reagenz zur glucosebestimmung im haemolysierten blut |
| JPS59162454A (ja) * | 1983-03-08 | 1984-09-13 | Kainosu:Kk | 体液中の濁りを除去する方法 |
| DE3323949A1 (de) * | 1983-07-02 | 1985-01-03 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und mittel zur raschen und vollstaendigen beseitigung einer truebung in einer biologischen fluessigkeit |
| EP0141879A1 (en) * | 1983-10-18 | 1985-05-22 | Victor A. Bernstam | Surfactant compositions and methods for clarifying and partitioning aqueous lipid-containing specimens |
| US4816411A (en) * | 1984-07-06 | 1989-03-28 | Technicon Instruments Corporation | Method for eliminating turbidity in a biological fluid and reagent therefor |
| JPS6195247A (ja) * | 1984-10-16 | 1986-05-14 | Yatoron:Kk | 血液試料の濁りを減らす方法 |
| FR2599149B1 (fr) * | 1986-05-21 | 1988-08-26 | Univ Nancy | Reactif pour la transparisation de milieux biologiques et ses applications analytiques. |
| DE3620817A1 (de) * | 1986-06-21 | 1987-12-23 | Boehringer Mannheim Gmbh | Verfahren zur spezifischen bestimmung des serumfructosamingehalts sowie hierfuer geeignetes reagenzgemisch |
| DE3743405A1 (de) * | 1987-05-14 | 1988-11-24 | Boehringer Mannheim Gmbh | Verfahren zur bestimmung von fructosamin |
| DE3717402A1 (de) * | 1987-05-23 | 1988-12-08 | Behringwerke Ag | Verfahren zur bestimmung von proteinen und mittel dazu |
| DE3732688A1 (de) * | 1987-09-29 | 1989-04-13 | Boehringer Mannheim Gmbh | Verfahren zur spezifischen bestimmung des serumfructosamingehalts sowie hierfuer geeignetes reagenzgemisch |
| JP2711332B2 (ja) * | 1988-04-15 | 1998-02-10 | 株式会社ヤトロン | 非水溶性物質の透明な水溶液が得られる凍結乾燥品の製造方法 |
| DE3920364A1 (de) * | 1989-06-22 | 1991-01-10 | Technicon Gmbh | Verfahren und reagenz zur verhinderung von truebungen |
| DE4018502A1 (de) * | 1990-06-09 | 1991-12-12 | Merck Patent Gmbh | Verfahren und mittel zur beseitigung von truebungen in biologischen fluessigkeiten |
| US5334503A (en) * | 1991-10-08 | 1994-08-02 | Eastman Kodak Company | Test kit and method for the detection of microorganisms associated with periodontal diseases using surfactant mixture as extraction composition |
| DE4218555A1 (de) * | 1992-06-05 | 1993-12-09 | Elemer Dipl Chem Dr Faltusz | Verfahren zur Solubilisierung der Milch für Untersuchungszwecke |
| DE4228021A1 (de) * | 1992-08-24 | 1994-03-03 | Henkel Kgaa | Waschverfahren |
| DE19850074A1 (de) * | 1998-10-30 | 2000-05-04 | Dade Behring Marburg Gmbh | Stabilisierung von biologischen Flüssigkeiten durch Zusatz von Sterinestern |
| ATE254767T1 (de) | 2001-02-19 | 2003-12-15 | Olympus Diagnostica Gmbh | Mittel zur beseitigung von eintrübungen in biologischen proben |
| US6472216B1 (en) * | 2001-07-24 | 2002-10-29 | Ann-Shyn Chiang | Aqueous tissue clearing solution |
| EP1795605A1 (de) * | 2005-12-12 | 2007-06-13 | Roche Diagnostics GmbH | Chromogene Tests in Gegenwart von Zellen |
| DE102006044795A1 (de) * | 2006-09-13 | 2008-03-27 | Schweigert, Florian, Prof. Dr.med.vet. | Bestimmung von Inhaltsstoffen aus biologischen Materialien |
| FR3019299B1 (fr) * | 2014-03-31 | 2016-05-06 | Spectralys Innovation | Procede d'estimation des proteines seriques denaturees dans un lait. |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3853465A (en) * | 1972-06-09 | 1974-12-10 | Technicon Instr | Turbidity reduction in serum and plasma samples using polyoxyethylated lauric acid compounds |
| US3958939A (en) * | 1975-01-08 | 1976-05-25 | Coulter Electronics, Inc. | Method for clarification of lipemic serum |
| US4148869A (en) * | 1975-03-06 | 1979-04-10 | Baxter Travenol Laboratories, Inc. | Immunological reagent and method of using same |
| US4011045A (en) * | 1975-02-14 | 1977-03-08 | Bonderman Dean P | Turbidity reduction in triglyceride standards |
| DE2612725C3 (de) * | 1976-03-25 | 1979-05-03 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und Reagenz zur Bestimmung von Cholesterin |
| US4154706A (en) * | 1976-07-23 | 1979-05-15 | Colgate-Palmolive Company | Nonionic shampoo |
| DE2724757C2 (de) * | 1977-06-01 | 1979-08-23 | Boehringer Mannheim Gmbh, 6800 Mannheim | Mittel zur Beseitigung von Trübungen in Serum und Verfahren zu seiner Herstellung |
| DE2816229C2 (de) * | 1978-04-14 | 1983-11-10 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und Mittel zur Beseitigung von Trübungen |
-
1978
- 1978-04-14 DE DE2816229A patent/DE2816229C2/de not_active Expired
-
1979
- 1979-02-16 AT AT0122479A patent/AT363613B/de not_active IP Right Cessation
- 1979-02-20 NL NLAANVRAGE7915054,A patent/NL184080C/xx not_active IP Right Cessation
- 1979-02-20 GB GB8032183A patent/GB2055784B/en not_active Expired
- 1979-02-20 CH CH6730/80A patent/CH651137A5/de not_active IP Right Cessation
- 1979-02-20 EP EP79100500A patent/EP0004857A3/de not_active Withdrawn
- 1979-02-20 BE BEBTR85A patent/BE85T1/xx not_active IP Right Cessation
- 1979-03-07 CA CA322,924A patent/CA1131097A/en not_active Expired
- 1979-04-04 US US06/026,851 patent/US4282001A/en not_active Expired - Lifetime
- 1979-04-06 SU SU792746998A patent/SU1443816A3/ru active
- 1979-04-12 FI FI791223A patent/FI69929C/fi not_active IP Right Cessation
- 1979-04-12 YU YU00873/79A patent/YU87379A/xx unknown
- 1979-04-13 JP JP4440979A patent/JPS54138493A/ja active Granted
- 1979-08-08 IE IE779/79A patent/IE48273B1/en not_active IP Right Cessation
-
1980
- 1980-09-03 FR FR8019180A patent/FR2473713A1/fr active Granted
- 1980-10-30 IT IT86284/80A patent/IT1148235B/it active
- 1980-12-08 SE SE8008598A patent/SE456370B/sv not_active IP Right Cessation
-
1986
- 1986-10-06 JP JP61236380A patent/JPS62182651A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE2816229C2 (de) | 1983-11-10 |
| US4282001A (en) | 1981-08-04 |
| JPS6211307B2 (fi) | 1987-03-11 |
| IT8086284A0 (it) | 1980-10-30 |
| ATA122479A (de) | 1981-01-15 |
| IE48273B1 (en) | 1984-11-28 |
| EP0004857A3 (de) | 1980-04-02 |
| AT363613B (de) | 1981-08-25 |
| JPS6345065B2 (fi) | 1988-09-07 |
| BE85T1 (fr) | 1980-11-07 |
| IE790779L (en) | 1979-10-14 |
| NL7915054A (nl) | 1980-11-28 |
| FI69929B (fi) | 1985-12-31 |
| GB2055784A (en) | 1981-03-11 |
| JPS54138493A (en) | 1979-10-26 |
| FI69929C (fi) | 1986-05-26 |
| JPS62182651A (ja) | 1987-08-11 |
| NL184080C (nl) | 1989-04-03 |
| FR2473713A1 (fr) | 1981-07-17 |
| CA1131097A (en) | 1982-09-07 |
| FR2473713B1 (fi) | 1983-11-18 |
| IT1148235B (it) | 1986-11-26 |
| SE8008598L (sv) | 1980-12-08 |
| CH651137A5 (de) | 1985-08-30 |
| DE2816229B1 (de) | 1979-06-28 |
| SU1443816A3 (ru) | 1988-12-07 |
| GB2055784B (en) | 1982-08-25 |
| FI791223A (fi) | 1979-10-15 |
| EP0004857A2 (de) | 1979-10-31 |
| NL184080B (nl) | 1988-11-01 |
| YU87379A (en) | 1983-01-21 |
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