CA2497322A1 - Urea-, glycerate- and , hydroxyamide-headed hydrocarbon chain lyotropic phase forming surfactants - Google Patents
Urea-, glycerate- and , hydroxyamide-headed hydrocarbon chain lyotropic phase forming surfactants Download PDFInfo
- Publication number
- CA2497322A1 CA2497322A1 CA002497322A CA2497322A CA2497322A1 CA 2497322 A1 CA2497322 A1 CA 2497322A1 CA 002497322 A CA002497322 A CA 002497322A CA 2497322 A CA2497322 A CA 2497322A CA 2497322 A1 CA2497322 A1 CA 2497322A1
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- CA
- Canada
- Prior art keywords
- phase
- surfactant
- integer
- lyotropic
- group
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
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- 239000004094 surface-active agent Substances 0.000 title claims abstract description 126
- 230000002535 lyotropic effect Effects 0.000 title claims abstract description 94
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title abstract description 11
- 125000001183 hydrocarbyl group Chemical group 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 32
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 116
- 239000000203 mixture Substances 0.000 claims description 27
- 239000000463 material Substances 0.000 claims description 26
- 239000007788 liquid Substances 0.000 claims description 23
- 239000002245 particle Substances 0.000 claims description 23
- -1 octadec-9,12-dienyl chains Chemical group 0.000 claims description 8
- 125000001117 oleyl 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])/C([H])=C([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])[H] 0.000 claims description 7
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- 239000002360 explosive Substances 0.000 claims description 6
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 claims description 6
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- 229940124597 therapeutic agent Drugs 0.000 claims description 4
- YFHFHLSMISYUAQ-UHFFFAOYSA-N farnesane Chemical compound CCC(C)CCCC(C)CCCC(C)C YFHFHLSMISYUAQ-UHFFFAOYSA-N 0.000 claims description 3
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- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims 8
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 230000002496 gastric effect Effects 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract description 22
- 239000004202 carbamide Substances 0.000 abstract description 9
- RBNPOMFGQQGHHO-UWTATZPHSA-N D-glyceric acid Chemical compound OC[C@@H](O)C(O)=O RBNPOMFGQQGHHO-UWTATZPHSA-N 0.000 abstract description 4
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- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 11
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- 238000000921 elemental analysis Methods 0.000 description 6
- RBNPOMFGQQGHHO-UHFFFAOYSA-N glyceric acid Chemical compound OCC(O)C(O)=O RBNPOMFGQQGHHO-UHFFFAOYSA-N 0.000 description 6
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 6
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
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- 239000003381 stabilizer Substances 0.000 description 5
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 4
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 4
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- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 description 4
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- 230000003993 interaction Effects 0.000 description 1
- 230000006525 intracellular process Effects 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 125000005645 linoleyl group Chemical group 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 229940029985 mineral supplement Drugs 0.000 description 1
- 235000020786 mineral supplement Nutrition 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 231100000418 oral toxicity Toxicity 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
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- 239000000575 pesticide Substances 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- CGIHFIDULQUVJG-UHFFFAOYSA-N phytantriol Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)(O)C(O)CO CGIHFIDULQUVJG-UHFFFAOYSA-N 0.000 description 1
- CGIHFIDULQUVJG-VNTMZGSJSA-N phytantriol Natural products CC(C)CCC[C@H](C)CCC[C@H](C)CCC[C@@](C)(O)[C@H](O)CO CGIHFIDULQUVJG-VNTMZGSJSA-N 0.000 description 1
- AJAKLDUGVSKVDG-UHFFFAOYSA-N phytanyl alcohol Natural products CC(C)CCCC(C)CCCC(C)CCCC(C)CCO AJAKLDUGVSKVDG-UHFFFAOYSA-N 0.000 description 1
- BOTWFXYSPFMFNR-PYDDKJGSSA-N phytol Chemical compound CC(C)CCC[C@@H](C)CCC[C@@H](C)CCC\C(C)=C\CO BOTWFXYSPFMFNR-PYDDKJGSSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004007 reversed phase HPLC Methods 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
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- 238000010561 standard procedure Methods 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/17—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/18—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/04—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms
- C07C275/06—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an acyclic and saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/04—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms
- C07C275/06—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an acyclic and saturated carbon skeleton
- C07C275/10—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an acyclic and saturated carbon skeleton being further substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/04—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms
- C07C275/20—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/58—Y being a hetero atom
- C07C275/62—Y being a nitrogen atom, e.g. biuret
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/675—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Dermatology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2002951216A AU2002951216A0 (en) | 2002-09-05 | 2002-09-05 | Surfactants and lyotropic phases formed therefrom |
| AU2002951216 | 2002-09-05 | ||
| PCT/AU2003/001139 WO2004022530A1 (en) | 2002-09-05 | 2003-09-04 | Urea-, glycerate- and, hydroxyamide-headed hydrocarbon chain lyotropic phases forming surfactants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2497322A1 true CA2497322A1 (en) | 2004-03-18 |
Family
ID=27671538
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002497322A Abandoned CA2497322A1 (en) | 2002-09-05 | 2003-09-04 | Urea-, glycerate- and , hydroxyamide-headed hydrocarbon chain lyotropic phase forming surfactants |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20050249665A1 (enExample) |
| EP (1) | EP1534669A4 (enExample) |
| JP (2) | JP2005538151A (enExample) |
| KR (1) | KR100948890B1 (enExample) |
| CN (2) | CN101538200A (enExample) |
| AU (2) | AU2002951216A0 (enExample) |
| CA (1) | CA2497322A1 (enExample) |
| NO (1) | NO20051142L (enExample) |
| WO (1) | WO2004022530A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1667656A4 (en) * | 2003-09-01 | 2011-12-28 | Mayne Pharma Int Pty Ltd | COMPOSITIONS AND METHODS OF DISTRIBUTING BIOLOGICALLY ACTIVE AGENTS |
| WO2006043705A1 (ja) * | 2004-10-19 | 2006-04-27 | National Institute Of Advanced Industrial Scienceand Technology | Ｉｉ型キュービック液晶組成物 |
| IL187247A0 (en) | 2007-11-08 | 2008-12-29 | Hadasit Med Res Service | Novel synthetic analogs of sphingolipids |
| EP2393472B1 (en) | 2008-12-05 | 2019-06-05 | NanoMed Holdings Pty Ltd | Amphiphile prodrugs |
| WO2012119838A1 (en) * | 2011-03-04 | 2012-09-13 | Unilever Nv | Self-adhesive hard surface cleaning composition |
| JP7730760B2 (ja) * | 2019-08-19 | 2025-08-28 | Jsr株式会社 | 分散組成物、分散剤、異方性膜及びその製造方法、並びに異方性膜形成装置 |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2813783A (en) * | 1953-05-18 | 1957-11-19 | Universal Oil Prod Co | Stabilization of organic compounds |
| GB818864A (en) * | 1956-05-15 | 1959-08-26 | Monsanto Chemicals | Process for the production of ureas |
| US3157477A (en) * | 1961-10-03 | 1964-11-17 | Standard Oil Co | Nu-acylated aminohydroxy compound as a multi-functional gasoline additive |
| US3211692A (en) * | 1961-11-06 | 1965-10-12 | Gulf Oil Corp | Ethylene polymeric compositions containing substituted ureas |
| US3161676A (en) * | 1962-05-21 | 1964-12-15 | Berkeley Chemical Corp | Preparation of substituted alkyl ureas |
| US3956366A (en) * | 1967-11-21 | 1976-05-11 | Pennwalt Corporation | N-monohalomonosubstituted ureas |
| US3706667A (en) * | 1970-08-03 | 1972-12-19 | Monsanto Co | Monosubstituted ureas in lubricating compositions |
| US4039576A (en) * | 1972-03-28 | 1977-08-02 | Ciba-Geigy Corporation | Process for the manufacture of alkoxylated N-methylol ureas |
| US4081386A (en) * | 1976-10-01 | 1978-03-28 | The Lubrizol Corporation | Reaction mixtures from reacting di- and triazines with sulfur-containing compounds and lubricants and fuels containing the same |
| JPS5695108A (en) * | 1979-12-28 | 1981-08-01 | Kao Corp | Water-in-oil cosmetic |
| JPS56133281A (en) * | 1980-03-21 | 1981-10-19 | Kao Corp | Preparation of glyceryl ether |
| DE3239858A1 (de) * | 1982-07-06 | 1984-01-12 | Max Planck Gesellschaft zur Förderung der Wissenschaften e.V., 3400 Göttingen | Neue d-mannitderivate als ausgangsprodukte zur synthese von phospholipiden |
| CA1264162A (en) * | 1984-03-15 | 1990-01-02 | Manfred Breuninger | Glycerol ether phosphatides |
| DE3442145A1 (de) * | 1984-11-17 | 1986-05-22 | Weber, Nikolaus, Dr., 4400 Münster | Verfahren zur herstellung komplexer etherglycerolipide unter verwendung von pflanzlichen zellkulturen |
| US4919833A (en) * | 1987-05-21 | 1990-04-24 | Ciba-Geigy Corporation | Functional fluids |
| JPH01249650A (ja) * | 1988-03-30 | 1989-10-04 | Toshiba Corp | 射出成形用バインダー組成物 |
| EP0450527A3 (en) * | 1990-03-30 | 1991-10-30 | Kao Corporation | N-tris(hydroxymethyl)methylfatty acid amides and cosmetic compositions containing same |
| US5236612A (en) * | 1991-12-31 | 1993-08-17 | Lever Brothers Company, Division Of Conopco, Inc. | Detergent compositions comprising alkyl glycerate cosurfactants |
| JP3699115B2 (ja) * | 1993-09-20 | 2005-09-28 | ウォーターズ コーポレーション | キラール界面活性剤及びそれらのキラール分離における使用方法 |
| DE4420625C1 (de) * | 1994-06-14 | 1995-11-02 | Beiersdorf Ag | Wirkstoffkombination mit einem Gehalt an Glycerylalkylethern und kosmetische und dermatologische Zubereitungen, solche Wirkstoffkombinationen enthaltend |
| JP3413016B2 (ja) * | 1996-06-05 | 2003-06-03 | 積水化学工業株式会社 | 水分散系離型剤 |
| DE19632482A1 (de) * | 1996-08-12 | 1998-02-19 | Basf Ag | Tenside |
| US6019990A (en) * | 1997-11-21 | 2000-02-01 | Natural Nutrition Ltd. As | Conjugated linoleic acid delivery system in cosmetic preparations |
| AU740588B2 (en) * | 1997-11-24 | 2001-11-08 | Scripps Research Institute, The | Inhibitors of gap junction communication |
| JPH11209279A (ja) * | 1998-01-05 | 1999-08-03 | Natural Ltd As | 体重減少および肥満処置の方法 |
| JPH11209775A (ja) * | 1998-01-22 | 1999-08-03 | Idemitsu Kosan Co Ltd | 工作機械油組成物 |
| EP1084098A4 (en) * | 1998-06-09 | 2004-12-22 | Univ Connecticut | INHIBITORS OF THE ANANDAMIDE TRANSPORTER AS ANALGETIC AGENT |
| EP1107979B1 (en) * | 1998-08-31 | 2006-07-05 | Gryphon Therapeutics, Inc. | Lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides |
| US6251931B1 (en) * | 1998-11-24 | 2001-06-26 | The Scripps Research Institute | Inhibitors of gap junction communication |
| FR2790975B1 (fr) * | 1999-03-16 | 2001-06-01 | Capsulis | Milieux sous forme de dispersions complexes, leur procede de preparation et leurs utilisations |
| JP2001234197A (ja) * | 2000-02-24 | 2001-08-28 | Kawaken Fine Chem Co Ltd | 液体洗浄剤組成物 |
| JP2001302600A (ja) * | 2000-04-18 | 2001-10-31 | Kawaken Fine Chem Co Ltd | 脂肪酸アルカノールアミド化合物の製造法 |
| EP1287039A1 (en) * | 2000-04-28 | 2003-03-05 | University College Dublin | Amphiphilic macrocyclic derivatives and their analogues |
| JP2002180086A (ja) * | 2000-12-08 | 2002-06-26 | Kawaken Fine Chem Co Ltd | 増粘剤およびそれを含む高粘度液体洗浄剤組成物 |
| EP1667656A4 (en) * | 2003-09-01 | 2011-12-28 | Mayne Pharma Int Pty Ltd | COMPOSITIONS AND METHODS OF DISTRIBUTING BIOLOGICALLY ACTIVE AGENTS |
-
2002
- 2002-09-05 AU AU2002951216A patent/AU2002951216A0/en not_active Abandoned
-
2003
- 2003-09-04 CN CNA200810188953XA patent/CN101538200A/zh active Pending
- 2003-09-04 CA CA002497322A patent/CA2497322A1/en not_active Abandoned
- 2003-09-04 KR KR1020057003886A patent/KR100948890B1/ko not_active Expired - Fee Related
- 2003-09-04 CN CNA038244373A patent/CN1694865A/zh active Pending
- 2003-09-04 JP JP2004533054A patent/JP2005538151A/ja not_active Ceased
- 2003-09-04 EP EP03793472A patent/EP1534669A4/en not_active Withdrawn
- 2003-09-04 AU AU2003257254A patent/AU2003257254B2/en not_active Ceased
- 2003-09-04 WO PCT/AU2003/001139 patent/WO2004022530A1/en not_active Ceased
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2005
- 2005-03-03 NO NO20051142A patent/NO20051142L/no not_active Application Discontinuation
- 2005-03-04 US US11/071,113 patent/US20050249665A1/en not_active Abandoned
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2010
- 2010-03-24 JP JP2010067498A patent/JP2010209072A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| CN101538200A (zh) | 2009-09-23 |
| US20050249665A1 (en) | 2005-11-10 |
| JP2005538151A (ja) | 2005-12-15 |
| EP1534669A4 (en) | 2007-03-14 |
| EP1534669A1 (en) | 2005-06-01 |
| CN1694865A (zh) | 2005-11-09 |
| AU2003257254A1 (en) | 2004-03-29 |
| WO2004022530A1 (en) | 2004-03-18 |
| KR20050088990A (ko) | 2005-09-07 |
| JP2010209072A (ja) | 2010-09-24 |
| NO20051142L (no) | 2005-04-14 |
| KR100948890B1 (ko) | 2010-03-24 |
| AU2003257254B2 (en) | 2009-02-19 |
| AU2002951216A0 (en) | 2002-09-19 |
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| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |