MX2015003831A - Una premezcla estable estabilizante de enzima. - Google Patents
Una premezcla estable estabilizante de enzima.Info
- Publication number
- MX2015003831A MX2015003831A MX2015003831A MX2015003831A MX2015003831A MX 2015003831 A MX2015003831 A MX 2015003831A MX 2015003831 A MX2015003831 A MX 2015003831A MX 2015003831 A MX2015003831 A MX 2015003831A MX 2015003831 A MX2015003831 A MX 2015003831A
- Authority
- MX
- Mexico
- Prior art keywords
- premix
- enzyme
- enzyme stabilizer
- organic solvent
- weight
- Prior art date
Links
- 102000004190 Enzymes Human genes 0.000 title claims abstract description 92
- 108090000790 Enzymes Proteins 0.000 title claims abstract description 92
- 239000003381 stabilizer Substances 0.000 title claims abstract description 54
- HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical compound OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 claims abstract description 54
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000003960 organic solvent Substances 0.000 claims abstract description 34
- 239000000203 mixture Substances 0.000 claims description 103
- 239000003599 detergent Substances 0.000 claims description 55
- 239000007788 liquid Substances 0.000 claims description 50
- 238000000034 method Methods 0.000 claims description 18
- 230000000087 stabilizing effect Effects 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 12
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 108091005804 Peptidases Proteins 0.000 claims description 9
- 230000003381 solubilizing effect Effects 0.000 claims description 9
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 8
- 239000004094 surface-active agent Substances 0.000 claims description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 6
- 102000035195 Peptidases Human genes 0.000 claims description 5
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 3
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 claims description 2
- 229940088598 enzyme Drugs 0.000 description 76
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- -1 for example Substances 0.000 description 12
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- YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 3
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- LBUNNMJLXWQQBY-UHFFFAOYSA-N 4-fluorophenylboronic acid Chemical compound OB(O)C1=CC=C(F)C=C1 LBUNNMJLXWQQBY-UHFFFAOYSA-N 0.000 description 2
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- 238000010348 incorporation Methods 0.000 description 2
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- HUMMCEUVDBVXTQ-UHFFFAOYSA-N naphthalen-1-ylboronic acid Chemical group C1=CC=C2C(B(O)O)=CC=CC2=C1 HUMMCEUVDBVXTQ-UHFFFAOYSA-N 0.000 description 2
- KPTRDYONBVUWPD-UHFFFAOYSA-N naphthalen-2-ylboronic acid Chemical compound C1=CC=CC2=CC(B(O)O)=CC=C21 KPTRDYONBVUWPD-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
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- 150000003839 salts Chemical group 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- BWQWUTMZEBYWTC-UHFFFAOYSA-N (1,3,5-trimethylcyclohexa-2,4-dien-1-yl)boronic acid Chemical compound CC1=CC(C)=CC(C)(B(O)O)C1 BWQWUTMZEBYWTC-UHFFFAOYSA-N 0.000 description 1
- NNWSHWNAHZWMDK-UHFFFAOYSA-N (1-borono-4-phenylcyclohexa-2,4-dien-1-yl)boronic acid Chemical compound C1=CC(B(O)O)(B(O)O)CC=C1C1=CC=CC=C1 NNWSHWNAHZWMDK-UHFFFAOYSA-N 0.000 description 1
- QNEGDGPAXKYZHZ-UHFFFAOYSA-N (2,4-dichlorophenyl)boronic acid Chemical compound OB(O)C1=CC=C(Cl)C=C1Cl QNEGDGPAXKYZHZ-UHFFFAOYSA-N 0.000 description 1
- UMOPBIVXPOETPG-UHFFFAOYSA-N (2-acetamidophenyl)boronic acid Chemical compound CC(=O)NC1=CC=CC=C1B(O)O UMOPBIVXPOETPG-UHFFFAOYSA-N 0.000 description 1
- PLVCYMZAEQRYHJ-UHFFFAOYSA-N (2-bromophenyl)boronic acid Chemical compound OB(O)C1=CC=CC=C1Br PLVCYMZAEQRYHJ-UHFFFAOYSA-N 0.000 description 1
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- VXWBQOJISHAKKM-UHFFFAOYSA-N (4-formylphenyl)boronic acid Chemical group OB(O)C1=CC=C(C=O)C=C1 VXWBQOJISHAKKM-UHFFFAOYSA-N 0.000 description 1
- BIWQNIMLAISTBV-UHFFFAOYSA-N (4-methylphenyl)boronic acid Chemical compound CC1=CC=C(B(O)O)C=C1 BIWQNIMLAISTBV-UHFFFAOYSA-N 0.000 description 1
- IVUHTLFKBDDICS-UHFFFAOYSA-N (4-methylsulfanylphenyl)boronic acid Chemical compound CSC1=CC=C(B(O)O)C=C1 IVUHTLFKBDDICS-UHFFFAOYSA-N 0.000 description 1
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- UCNGPRDZLFWXRL-UHFFFAOYSA-N 2-(4-methylphenyl)ethylboronic acid Chemical compound CC1=CC=C(CCB(O)O)C=C1 UCNGPRDZLFWXRL-UHFFFAOYSA-N 0.000 description 1
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- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 1
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- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- JMZFEHDNIAQMNB-UHFFFAOYSA-N m-aminophenylboronic acid Chemical compound NC1=CC=CC(B(O)O)=C1 JMZFEHDNIAQMNB-UHFFFAOYSA-N 0.000 description 1
- 229940035034 maltodextrin Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000302 molecular modelling Methods 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- GKFRVXOKPXCXAK-UHFFFAOYSA-N octylboronic acid Chemical compound CCCCCCCCB(O)O GKFRVXOKPXCXAK-UHFFFAOYSA-N 0.000 description 1
- 238000011022 operating instruction Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000001139 pH measurement Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001308 poly(aminoacid) Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000013042 solid detergent Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- FZEWPLIHPXGNTB-UHFFFAOYSA-N thianthren-1-ylboronic acid Chemical compound S1C2=CC=CC=C2SC2=C1C=CC=C2B(O)O FZEWPLIHPXGNTB-UHFFFAOYSA-N 0.000 description 1
- GCSOJZMPHLRBMJ-UHFFFAOYSA-N thianthren-2-ylboronic acid Chemical compound C1=CC=C2SC3=CC(B(O)O)=CC=C3SC2=C1 GCSOJZMPHLRBMJ-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- ARYHTUPFQTUBBG-UHFFFAOYSA-N thiophen-2-ylboronic acid Chemical compound OB(O)C1=CC=CS1 ARYHTUPFQTUBBG-UHFFFAOYSA-N 0.000 description 1
- QNMBSXGYAQZCTN-UHFFFAOYSA-N thiophen-3-ylboronic acid Chemical compound OB(O)C=1C=CSC=1 QNMBSXGYAQZCTN-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 108010083879 xyloglucan endo(1-4)-beta-D-glucanase Proteins 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- 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
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38663—Stabilised liquid enzyme compositions
-
- 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
- C11D3/16—Organic compounds
- C11D3/166—Organic compounds containing borium
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Enzymes And Modification Thereof (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12187080.2A EP2716644B1 (en) | 2012-10-03 | 2012-10-03 | A stable enzyme stabilizer premix |
| PCT/US2013/063058 WO2014055641A1 (en) | 2012-10-03 | 2013-10-02 | A stable enzyme stabilizer premix |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2015003831A true MX2015003831A (es) | 2015-07-17 |
Family
ID=46963611
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2015003831A MX2015003831A (es) | 2012-10-03 | 2013-10-02 | Una premezcla estable estabilizante de enzima. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20140094398A1 (OSRAM) |
| EP (1) | EP2716644B1 (OSRAM) |
| JP (1) | JP2015532324A (OSRAM) |
| CN (1) | CN104703993A (OSRAM) |
| BR (1) | BR112015007492A2 (OSRAM) |
| CA (1) | CA2886649A1 (OSRAM) |
| IN (1) | IN2015DN02668A (OSRAM) |
| MX (1) | MX2015003831A (OSRAM) |
| RU (1) | RU2015112343A (OSRAM) |
| WO (1) | WO2014055641A1 (OSRAM) |
| ZA (1) | ZA201501905B (OSRAM) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014162001A1 (en) * | 2013-04-05 | 2014-10-09 | Novozymes A/S | Enzyme solubility in liquid detergent and use of detergent composition |
| US20150344817A1 (en) * | 2014-05-30 | 2015-12-03 | The Procter & Gamble Company | Water cluster-dominant boronic acid alkali surfactant compositions and their use |
| MX2019006425A (es) * | 2016-12-01 | 2019-08-14 | Basf Se | Estabilizacion de enzimas en composiciones. |
| CN107043762A (zh) * | 2017-04-21 | 2017-08-15 | 江苏福隆生物技术有限公司 | 一种提高辣根过氧化物酶保存稳定性的保存稳定剂及其保存方法 |
| CN109837270B (zh) * | 2018-06-19 | 2022-09-09 | 深圳市安帝宝科技有限公司 | 一种使肌醇脱氢酶、酮胺氧化酶和鞘磷脂酶在液体中长期稳定的方法 |
| EP3865561B1 (en) * | 2020-02-11 | 2024-02-14 | The Procter & Gamble Company | Process for making a liquid consumer product that includes enzymes |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3761420A (en) * | 1970-06-08 | 1973-09-25 | Staley Mfg Co A E | Stabilized liquid enzyme stain remover |
| US3929678A (en) | 1974-08-01 | 1975-12-30 | Procter & Gamble | Detergent composition having enhanced particulate soil removal performance |
| US5159060A (en) | 1988-05-27 | 1992-10-27 | Mayo Foundation For Medical Education And Research | Cytotoxic boronic acid peptide analogs |
| US4963655A (en) | 1988-05-27 | 1990-10-16 | Mayo Foundation For Medical Education And Research | Boron analogs of amino acid/peptide protease inhibitors |
| CZ230593A3 (en) | 1991-04-30 | 1994-04-13 | Procter & Gamble | Liquid detergents with arylboric acid |
| US5442100A (en) | 1992-08-14 | 1995-08-15 | The Procter & Gamble Company | β-aminoalkyl and β-N-peptidylaminoalkyl boronic acids |
| US5354491A (en) | 1992-08-14 | 1994-10-11 | The Procter & Gamble Company | Liquid detergent compositions containing protease and certain β-aminoalkylboronic acids and esters |
| EP0583536B1 (en) | 1992-08-14 | 1997-03-05 | The Procter & Gamble Company | Liquid detergents containing an alpha-amino boronic acid |
| CA2165155C (en) | 1993-06-14 | 1999-06-29 | Hal Ambuter | Concentrated nil-phosphate liquid automatic dishwashing detergent compositions containing enzyme |
| CN1127014A (zh) * | 1993-07-09 | 1996-07-17 | 诺沃挪第克公司 | 作为酶稳定剂的一烃基硼酸或二烃基硼酸衍生物 |
| US5431842A (en) * | 1993-11-05 | 1995-07-11 | The Procter & Gamble Company | Liquid detergents with ortho-substituted phenylboronic acids for inhibition of proteolytic enzyme |
| US5834415A (en) | 1994-04-26 | 1998-11-10 | Novo Nordisk A/S | Naphthalene boronic acids |
| AR000649A1 (es) | 1995-01-09 | 1997-07-10 | Novo Nordisk As | Composiciones líquidas de enzimas procedimientos para preparar una composición detergente y una composición detergente |
| AU731577B2 (en) * | 1997-03-07 | 2001-04-05 | Procter & Gamble Company, The | Bleach compositions containing metal bleach catalyst, and bleach activators and/or organic percarboxylic acids |
| MXPA02008192A (es) | 2000-02-23 | 2002-11-29 | Procter & Gamble | Composiciones detergentes liquidas para lavanderia que tienen beneficios de remocion de arcilla incrementados. |
| CN101048487B (zh) * | 2004-10-28 | 2010-05-05 | 诺维信公司 | 贮存稳定性改善的洗衣条 |
| WO2007025549A1 (en) | 2005-09-02 | 2007-03-08 | Novozymes A/S | Stabilization of concentrated liquid enzyme additives |
| EP2049640A2 (en) | 2006-08-08 | 2009-04-22 | The Procter and Gamble Company | Clear and/or translucent fabric enhancers comprising nano-sized particles |
| EP2139979B1 (en) * | 2007-03-27 | 2015-02-25 | Novozymes A/S | Stable enzyme solutions and method of manufacturing |
| US7951964B2 (en) * | 2008-04-22 | 2011-05-31 | Unimatec Co., Ltd. | Fluorine-containing boronic acid ester compound and method for producing the same |
| JP5431842B2 (ja) * | 2008-10-21 | 2014-03-05 | セイコーインスツル株式会社 | バッテリ状態監視回路及びバッテリ装置 |
| DE102009000879A1 (de) | 2009-02-16 | 2010-08-19 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
| DE102009045064A1 (de) * | 2009-09-28 | 2011-03-31 | Henkel Ag & Co. Kgaa | Stabilisierte enzymatische Zusammensetzung |
-
2012
- 2012-10-03 EP EP12187080.2A patent/EP2716644B1/en not_active Revoked
-
2013
- 2013-09-24 US US14/034,712 patent/US20140094398A1/en not_active Abandoned
- 2013-10-02 MX MX2015003831A patent/MX2015003831A/es unknown
- 2013-10-02 CN CN201380051908.9A patent/CN104703993A/zh active Pending
- 2013-10-02 IN IN2668DEN2015 patent/IN2015DN02668A/en unknown
- 2013-10-02 JP JP2015534825A patent/JP2015532324A/ja active Pending
- 2013-10-02 CA CA2886649A patent/CA2886649A1/en not_active Abandoned
- 2013-10-02 WO PCT/US2013/063058 patent/WO2014055641A1/en not_active Ceased
- 2013-10-02 RU RU2015112343A patent/RU2015112343A/ru unknown
- 2013-10-02 BR BR112015007492A patent/BR112015007492A2/pt not_active IP Right Cessation
-
2015
- 2015-03-19 ZA ZA2015/01905A patent/ZA201501905B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2716644A1 (en) | 2014-04-09 |
| US20140094398A1 (en) | 2014-04-03 |
| CN104703993A (zh) | 2015-06-10 |
| IN2015DN02668A (OSRAM) | 2015-09-04 |
| WO2014055641A1 (en) | 2014-04-10 |
| BR112015007492A2 (pt) | 2017-07-04 |
| CA2886649A1 (en) | 2014-04-10 |
| JP2015532324A (ja) | 2015-11-09 |
| ZA201501905B (en) | 2017-01-25 |
| RU2015112343A (ru) | 2016-11-27 |
| EP2716644B1 (en) | 2017-04-05 |
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