AR055860A1 - Liquidos ionicos derivados de aniones de peracido - Google Patents
Liquidos ionicos derivados de aniones de peracidoInfo
- Publication number
- AR055860A1 AR055860A1 ARP060100596A ARP060100596A AR055860A1 AR 055860 A1 AR055860 A1 AR 055860A1 AR P060100596 A ARP060100596 A AR P060100596A AR P060100596 A ARP060100596 A AR P060100596A AR 055860 A1 AR055860 A1 AR 055860A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- pyrazinidiozine
- cations
- quaternary ammonium
- entity
- Prior art date
Links
- 239000002608 ionic liquid Substances 0.000 title abstract 2
- 150000001450 anions Chemical class 0.000 title 1
- -1 peracid anion Chemical class 0.000 abstract 8
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000002091 cationic group Chemical group 0.000 abstract 3
- 150000001768 cations Chemical class 0.000 abstract 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 abstract 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 abstract 2
- 150000008040 ionic compounds Chemical class 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 abstract 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 abstract 1
- SBYHFKPVCBCYGV-UHFFFAOYSA-O 1-azoniabicyclo[2.2.2]octane Chemical compound C1CC2CC[NH+]1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-O 0.000 abstract 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 abstract 1
- PORQOHRXAJJKGK-UHFFFAOYSA-N 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone Chemical compound CCCCCCCCN1SC(Cl)=C(Cl)C1=O PORQOHRXAJJKGK-UHFFFAOYSA-N 0.000 abstract 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 abstract 1
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 abstract 1
- WRYCSMQKUKOKBP-UHFFFAOYSA-N Imidazolidine Chemical compound C1CNCN1 WRYCSMQKUKOKBP-UHFFFAOYSA-N 0.000 abstract 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 abstract 1
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 abstract 1
- 239000012190 activator Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 239000004599 antimicrobial Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 239000007844 bleaching agent Substances 0.000 abstract 1
- 150000007942 carboxylates Chemical class 0.000 abstract 1
- 229960004830 cetylpyridinium Drugs 0.000 abstract 1
- NEUSVAOJNUQRTM-UHFFFAOYSA-N cetylpyridinium Chemical compound CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 NEUSVAOJNUQRTM-UHFFFAOYSA-N 0.000 abstract 1
- 229960003260 chlorhexidine Drugs 0.000 abstract 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 abstract 1
- 229960001231 choline Drugs 0.000 abstract 1
- 238000004140 cleaning Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003599 detergent Substances 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- ZRALSGWEFCBTJO-UHFFFAOYSA-O guanidinium Chemical compound NC(N)=[NH2+] ZRALSGWEFCBTJO-UHFFFAOYSA-O 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-O hydron;1,2-oxazole Chemical compound C=1C=[NH+]OC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-O 0.000 abstract 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-O hydron;1,3-oxazole Chemical compound C1=COC=[NH+]1 ZCQWOFVYLHDMMC-UHFFFAOYSA-O 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-O hydron;pyrimidine Chemical compound C1=CN=C[NH+]=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-O 0.000 abstract 1
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 230000008018 melting Effects 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 229940112042 peripherally acting choline derivative muscle relaxants Drugs 0.000 abstract 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 abstract 1
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 abstract 1
- 229920000768 polyamine Polymers 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical class C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 abstract 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 abstract 1
- 150000003248 quinolines Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 229930192474 thiophene Natural products 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/40—Peroxy compounds containing nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3945—Organic per-compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Un compuesto ionico que comprende un cation y un anion de perácido de formula: R1-G-OO(-), en donde, G es un oxígeno que contiene entidades seleccionadas del grupo que comprende -C(O)-, -S(O)-, -S(O)2-, -Se(O)-, -Se(O)2, -OC(O)-, -OS(O)-, -OS(O)2-, - OSe(O)-, -OSe(O)2, -NHC(O)-, -NHS(O)-, -NHS(O)2-, -NHSe(O)-, -NHSe(O)2-, -NR2C(O)-, -NR2S(O)-, -NR2S(O)2-, -NR2Se(O)- o -NR2Se(O)2-; R1 y R2 se seleccionan independientemente del grupo que comprende entidades alquilo, alcarilo, aralquilo y arilo C1- 16 lineales o ramificadas, no sustituidas o sustituidas; donde el compuesto ionico tiene una temperatura de fusion de aproximadamente 100sC o menor o tiene la capacidad de fluir a una temperatura de aproximadamente 100sC o menor. El cation se selecciona del grupo que comprende: a) cationes de amonio cuaternario que corresponden a la formula: N(+)-R1R2R3R4, en donde, R1 es alquilo alquilo C6-24, y R2, R3 y R4 alquilo C1-20 o hidroxilalquilo C1-20; b) cationes de diéster amonio cuaternario (DEQA) de siguiente tipo: R4-m-N+-[(CH2)n-Q-R1]m, en donde, cada sustituyente R se selecciona de hidrogeno; un alquilo o hidroxialquilo C1-6, preferentemente metilo, etil, propilo o hidroxietilo y con más preferencia metil; poli(alcoxi C1-3), preferentemente polietoxi; bencilo o una mezcla de éstos; cada m es 2 o 3; cada n es 1 a aproximadamente 4; cada Y es -O-(O)-C-, -C(O)-O-, -NR-C(O)-, o -C(O)-NR-; con la condicion de que, cuando Y es -O-(O)C- o -NR-C(O)-, la suma de los carbonos en cada R1 más uno es C12-22, preferentemente C14-20, en la que cada R1 es un hidrocarbilo o un grupo hidrocarbilo sustituido; c) cationes de alquileno de amonio cuaternario que corresponden a la formula: R4-m- N+-R1m, en donde, cada m es 2 o 3; cada R es independientemente una entidad alquilo o hidroxialquilo C1-6, R1 es independientemente una entidad alquilo o alcoxi C6-22 lineal o ramificada, saturado o insaturada, pero con no más de una R1 inferior a aproximadamente C12, y luego la otra R1 es por lo menos aproximadamente C16, o una entidad de hidrocarbilo o hidrocarbilo sustituido; d) cationes de diamidas grasas de amonio cuaternario correspondientes a la formula: [R1-C(O)-NR-R2-N(R)2-R3-NR-C(O)-R1]+, en donde, R y R1 son tal como se definen en el cation c) más arriba, R2 y R3 son entidades alquileno C1-6; e) surfactantes cuaternarios C8-22; f) ésteres cationicos; g) 4,5-dicloro-2-n-octilo-3-isotiazolona; h) colina y derivados de colina; i) cationes de alquil oxialquileno; j) amonios cuaternarios alcoxilato (AQA, por sus siglas en inglés); k) pirrolidinona, imidazolio, benzimidazolio, pirazolilo, benzpirazolio, tiazolio, benztiazolio, oxazolio, benzoxazolio, isoxazolio, isotiazolio, imidazolidina, guanidinio, indazolio, quinuclidinio, triazolio, isoquinuclidino, piperidinilo, morfolino, piridazinio, pirazinio, triazinio, azepina, diazepina, piridinio, piperidona, pirimidinio, tiofeno y fosfonio sustituidos y no sustituidos; l) activadores de blanqueador cationicos que tienen una entidad de amonio cuaternario; m) agentes antimicrobianos cationicos, tales como cetilpiridinio, clorohexidina y domifén; n) cationes de cafeína alquilatados; o) alquil poliamino carboxilato; y p) mezclas de éstos. Se aplica como líquido detergente convirtiendo activos convencionales en líquidos ionicos cuando la química acuosa o de compuestos de coordinacion puede ser problemática, con ventajas en las formulaciones y en la capacidad de limpieza.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65472205P | 2005-02-18 | 2005-02-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR055860A1 true AR055860A1 (es) | 2007-09-12 |
Family
ID=36927905
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060100596A AR055860A1 (es) | 2005-02-18 | 2006-02-17 | Liquidos ionicos derivados de aniones de peracido |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7786065B2 (es) |
| EP (1) | EP1856039B1 (es) |
| JP (1) | JP5005550B2 (es) |
| AR (1) | AR055860A1 (es) |
| CA (1) | CA2595298C (es) |
| MX (1) | MX2007010059A (es) |
| WO (1) | WO2006091457A2 (es) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2295398B1 (de) * | 2003-08-27 | 2016-04-13 | proionic GmbH & Co KG | Verfahren zur Herstellung ionischer Flüssigkeiten, ionischer Feststoffe oder Gemische derselben |
| US7737102B2 (en) * | 2004-11-01 | 2010-06-15 | The Procter & Gamble Company | Ionic liquids derived from functionalized anionic surfactants |
| US20060094616A1 (en) * | 2004-11-01 | 2006-05-04 | Hecht Stacie E | Ionic liquids derived from surfactants |
| US20060183654A1 (en) * | 2005-02-14 | 2006-08-17 | Small Robert J | Semiconductor cleaning using ionic liquids |
| US7923424B2 (en) * | 2005-02-14 | 2011-04-12 | Advanced Process Technologies, Llc | Semiconductor cleaning using superacids |
| US8455421B2 (en) * | 2008-09-01 | 2013-06-04 | Expelliere Int Ltd | Compositions and methods for the removal of chewing gum residues from substrates |
| US20130059135A1 (en) * | 2010-08-16 | 2013-03-07 | Lg Chem Ltd | Printing composition and a printing method using the same |
| EP2723845B1 (en) | 2011-06-22 | 2019-04-03 | Colgate-Palmolive Company | Choline salt cleaning compositions |
| WO2012177277A1 (en) | 2011-06-22 | 2012-12-27 | Colgate-Palmolive Company | Liquid salt cleaning compositions |
| US8481474B1 (en) | 2012-05-15 | 2013-07-09 | Ecolab Usa Inc. | Quaternized alkyl imidazoline ionic liquids used for enhanced food soil removal |
| US8716207B2 (en) | 2012-06-05 | 2014-05-06 | Ecolab Usa Inc. | Solidification mechanism incorporating ionic liquids |
| CN104853736B (zh) * | 2012-12-20 | 2018-01-09 | 高露洁-棕榄公司 | 含有离子性液体的口腔护理组合物 |
| JP6126956B2 (ja) * | 2013-09-17 | 2017-05-10 | 花王株式会社 | 衣料用洗浄剤組成物 |
| US9783766B2 (en) | 2015-04-03 | 2017-10-10 | Ecolab Usa Inc. | Enhanced peroxygen stability using anionic surfactant in TAED-containing peroxygen solid |
| US10280386B2 (en) | 2015-04-03 | 2019-05-07 | Ecolab Usa Inc. | Enhanced peroxygen stability in multi-dispense TAED-containing peroxygen solid |
| US9920284B2 (en) | 2015-04-22 | 2018-03-20 | S. C. Johnson & Son, Inc. | Cleaning composition with a polypropdxylated 2-(trialkylammonio)ethanol ionic liquid |
| EP3532586B1 (en) | 2016-10-26 | 2022-05-18 | S.C. Johnson & Son, Inc. | Disinfectant cleaning composition with quaternary ammonium hydroxycarboxylate salt |
| US10815453B2 (en) | 2016-10-26 | 2020-10-27 | S. C. Johnson & Son, Inc. | Disinfectant cleaning composition with quaternary ammonium hydroxycarboxylate salt and quaternary ammonium antimicrobial |
| EP3532584A1 (en) | 2016-10-26 | 2019-09-04 | S.C. Johnson & Son, Inc. | Disinfectant cleaning composition with quaternary amine ionic liquid |
| CN106966939B (zh) * | 2017-05-15 | 2021-04-02 | 北京长江脉医药科技有限责任公司 | 一种四烷基过氧化羧酸铵盐化合物及其制备方法与应用 |
| WO2018234638A1 (en) * | 2017-06-22 | 2018-12-27 | Helsingin Yliopisto | Method of joining polymeric biomaterials |
| US10093868B1 (en) * | 2017-11-15 | 2018-10-09 | Baker Hughes, A Ge Company, Llc | Ionic liquid-based hydrogen sulfide and mercaptan scavengers |
| WO2019113513A1 (en) | 2017-12-08 | 2019-06-13 | Baker Hughes, A Ge Company, Llc | Ionic liquid based well asphaltene inhibitors and methods of using the same |
| WO2019241629A1 (en) | 2018-06-15 | 2019-12-19 | Ecolab Usa Inc. | Enhanced peroxygen stability using fatty acid in bleach activating agent containing peroxygen solid |
| EA202091413A1 (ru) | 2018-07-11 | 2020-09-24 | Бейкер Хьюз Холдингз Ллк | Скважинные ингибиторы асфальтенов на основе ионной жидкости и способы их применения |
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-
2006
- 2006-02-01 US US11/345,569 patent/US7786065B2/en not_active Expired - Fee Related
- 2006-02-16 WO PCT/US2006/005372 patent/WO2006091457A2/en not_active Ceased
- 2006-02-16 CA CA2595298A patent/CA2595298C/en not_active Expired - Fee Related
- 2006-02-16 JP JP2007556265A patent/JP5005550B2/ja not_active Expired - Fee Related
- 2006-02-16 EP EP06735156.9A patent/EP1856039B1/en not_active Not-in-force
- 2006-02-16 MX MX2007010059A patent/MX2007010059A/es active IP Right Grant
- 2006-02-17 AR ARP060100596A patent/AR055860A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US7786065B2 (en) | 2010-08-31 |
| EP1856039B1 (en) | 2014-01-01 |
| EP1856039A2 (en) | 2007-11-21 |
| WO2006091457A3 (en) | 2006-12-21 |
| CA2595298C (en) | 2012-01-10 |
| MX2007010059A (es) | 2007-10-02 |
| JP2008531499A (ja) | 2008-08-14 |
| JP5005550B2 (ja) | 2012-08-22 |
| CA2595298A1 (en) | 2006-08-31 |
| US20060189499A1 (en) | 2006-08-24 |
| WO2006091457A2 (en) | 2006-08-31 |
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