JP2012515827A - キレート剤及びそれに関する方法 - Google Patents
キレート剤及びそれに関する方法 Download PDFInfo
- Publication number
- JP2012515827A JP2012515827A JP2011546960A JP2011546960A JP2012515827A JP 2012515827 A JP2012515827 A JP 2012515827A JP 2011546960 A JP2011546960 A JP 2011546960A JP 2011546960 A JP2011546960 A JP 2011546960A JP 2012515827 A JP2012515827 A JP 2012515827A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- salt
- acidic
- chelating agent
- composition
- 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.)
- Pending
Links
- 239000002738 chelating agent Substances 0.000 title claims abstract description 70
- 238000000034 method Methods 0.000 title description 8
- 150000003839 salts Chemical class 0.000 claims abstract description 80
- 230000002378 acidificating effect Effects 0.000 claims abstract description 62
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 25
- 150000001342 alkaline earth metals Chemical class 0.000 claims abstract description 18
- 125000003277 amino group Chemical group 0.000 claims abstract description 7
- VKZRWSNIWNFCIQ-WDSKDSINSA-N (2s)-2-[2-[[(1s)-1,2-dicarboxyethyl]amino]ethylamino]butanedioic acid Chemical group OC(=O)C[C@@H](C(O)=O)NCCN[C@H](C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-WDSKDSINSA-N 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 71
- 239000002253 acid Substances 0.000 claims description 48
- PQHYOGIRXOKOEJ-UHFFFAOYSA-N 2-(1,2-dicarboxyethylamino)butanedioic acid Chemical group OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O PQHYOGIRXOKOEJ-UHFFFAOYSA-N 0.000 claims description 24
- -1 Dicalcium imino disuccinate Chemical compound 0.000 claims description 19
- JYXGIOKAKDAARW-UHFFFAOYSA-N N-(2-hydroxyethyl)iminodiacetic acid Chemical group OCCN(CC(O)=O)CC(O)=O JYXGIOKAKDAARW-UHFFFAOYSA-N 0.000 claims description 19
- 238000004061 bleaching Methods 0.000 claims description 17
- 239000011575 calcium Substances 0.000 claims description 8
- 159000000000 sodium salts Chemical class 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 4
- LDRSIESVOZZZPH-UHFFFAOYSA-N calcium;2-[carboxymethyl(2-hydroxyethyl)amino]acetic acid Chemical compound [Ca].[Ca].OCCN(CC(O)=O)CC(O)=O LDRSIESVOZZZPH-UHFFFAOYSA-N 0.000 claims description 2
- XELRNYQRHVCELV-UHFFFAOYSA-L calcium;magnesium;diacetate Chemical compound [Mg+2].[Ca+2].CC([O-])=O.CC([O-])=O XELRNYQRHVCELV-UHFFFAOYSA-L 0.000 claims 1
- 229940080260 iminodisuccinate Drugs 0.000 claims 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 34
- 150000002978 peroxides Chemical class 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 12
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 11
- 229960003330 pentetic acid Drugs 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- CIEZZGWIJBXOTE-UHFFFAOYSA-N 2-[bis(carboxymethyl)amino]propanoic acid Chemical compound OC(=O)C(C)N(CC(O)=O)CC(O)=O CIEZZGWIJBXOTE-UHFFFAOYSA-N 0.000 description 10
- DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 9
- 229940090960 diethylenetriamine pentamethylene phosphonic acid Drugs 0.000 description 8
- 239000002243 precursor Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 6
- 238000004851 dishwashing Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 description 5
- AURFNYPOUVLIAV-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]-2-hydroxyacetic acid Chemical compound OC(=O)C(O)N(CC(O)=O)CCN(CC(O)=O)CC(O)=O AURFNYPOUVLIAV-UHFFFAOYSA-N 0.000 description 5
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000008367 deionised water Substances 0.000 description 5
- 229910021641 deionized water Inorganic materials 0.000 description 5
- XNCSCQSQSGDGES-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]propyl-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)C(C)CN(CC(O)=O)CC(O)=O XNCSCQSQSGDGES-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical compound NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 229910052723 transition metal Inorganic materials 0.000 description 4
- 150000003624 transition metals Chemical class 0.000 description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
- IAFYJQKMJLWKKI-UHFFFAOYSA-N OC(=O)C(O)C(O)(C(O)=O)NC(O)(C(O)=O)C(O)C(O)=O Chemical compound OC(=O)C(O)C(O)(C(O)=O)NC(O)(C(O)=O)C(O)C(O)=O IAFYJQKMJLWKKI-UHFFFAOYSA-N 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 150000001412 amines Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229960001484 edetic acid Drugs 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ZWVKLVQFUVAASH-ZPUQHVIOSA-N (e)-2-[[(e)-1,2-dicarboxyethenyl]amino]but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)\N\C(C(O)=O)=C\C(O)=O ZWVKLVQFUVAASH-ZPUQHVIOSA-N 0.000 description 2
- ZWVKLVQFUVAASH-CCAGOZQPSA-N (z)-2-[[(z)-1,2-dicarboxyethenyl]amino]but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)/N\C(C(O)=O)=C/C(O)=O ZWVKLVQFUVAASH-CCAGOZQPSA-N 0.000 description 2
- ARHHHLXAKOLHIS-UHFFFAOYSA-N 2-[(1,2-dicarboxy-1-hydroxyethyl)amino]-2-hydroxybutanedioic acid Chemical compound OC(=O)CC(O)(C(O)=O)NC(O)(C(O)=O)CC(O)=O ARHHHLXAKOLHIS-UHFFFAOYSA-N 0.000 description 2
- DMEVAEALQSFSQC-UHFFFAOYSA-N 2-[carboxymethyl(2-hydroxyethyl)amino]acetic acid;magnesium Chemical compound [Mg].[Mg].OCCN(CC(O)=O)CC(O)=O DMEVAEALQSFSQC-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- PDIZYYQQWUOPPK-UHFFFAOYSA-N acetic acid;2-(methylamino)acetic acid Chemical group CC(O)=O.CC(O)=O.CNCC(O)=O PDIZYYQQWUOPPK-UHFFFAOYSA-N 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 239000003139 biocide Substances 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical class OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000010412 laundry washing Methods 0.000 description 2
- 239000002324 mouth wash Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 2
- 150000004965 peroxy acids Chemical class 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- 238000004076 pulp bleaching Methods 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- GYBINGQBXROMRS-UHFFFAOYSA-J tetrasodium;2-(1,2-dicarboxylatoethylamino)butanedioate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CC(C([O-])=O)NC(C([O-])=O)CC([O-])=O GYBINGQBXROMRS-UHFFFAOYSA-J 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 239000000606 toothpaste Substances 0.000 description 2
- DCCWEYXHEXDZQW-BYPYZUCNSA-N (2s)-2-[bis(carboxymethyl)amino]butanedioic acid Chemical compound OC(=O)C[C@@H](C(O)=O)N(CC(O)=O)CC(O)=O DCCWEYXHEXDZQW-BYPYZUCNSA-N 0.000 description 1
- ISPONMNRRGAISO-BUOKYLHBSA-N (e)-but-2-enedioic acid;ethane-1,2-diamine Chemical compound NCCN.OC(=O)\C=C\C(O)=O.OC(=O)\C=C\C(O)=O ISPONMNRRGAISO-BUOKYLHBSA-N 0.000 description 1
- ISPONMNRRGAISO-PAMPIZDHSA-N (z)-but-2-enedioic acid;ethane-1,2-diamine Chemical compound NCCN.OC(=O)\C=C/C(O)=O.OC(=O)\C=C/C(O)=O ISPONMNRRGAISO-PAMPIZDHSA-N 0.000 description 1
- RWISDUHFHDEVCZ-UHFFFAOYSA-N 2,3-dihydroxybutanedioic acid ethane-1,2-diamine Chemical compound NCCN.OC(=O)C(O)C(O)C(O)=O.OC(=O)C(O)C(O)C(O)=O RWISDUHFHDEVCZ-UHFFFAOYSA-N 0.000 description 1
- MCXHMLOPWNBGHH-UHFFFAOYSA-N 2-(1,2-dicarboxyethylamino)butanedioic acid;magnesium Chemical compound [Mg].[Mg].OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O MCXHMLOPWNBGHH-UHFFFAOYSA-N 0.000 description 1
- PFARUPKOWSCVRX-UHFFFAOYSA-N 2-[carboxymethyl(2,3-dihydroxypropyl)amino]acetic acid Chemical compound OCC(O)CN(CC(O)=O)CC(O)=O PFARUPKOWSCVRX-UHFFFAOYSA-N 0.000 description 1
- KWYJDIUEHHCHCZ-UHFFFAOYSA-N 3-[2-[bis(2-carboxyethyl)amino]ethyl-(2-carboxyethyl)amino]propanoic acid Chemical compound OC(=O)CCN(CCC(O)=O)CCN(CCC(O)=O)CCC(O)=O KWYJDIUEHHCHCZ-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- NXQLETUDPAVCIE-WNQIDUERSA-N C(C)OC(C(C(=O)O)OCC)C(=O)O.N[C@@H](CC(=O)O)C(=O)O Chemical compound C(C)OC(C(C(=O)O)OCC)C(=O)O.N[C@@H](CC(=O)O)C(=O)O NXQLETUDPAVCIE-WNQIDUERSA-N 0.000 description 1
- 102000011632 Caseins Human genes 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 229940120146 EDTMP Drugs 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- ZTVCAEHRNBOTLI-UHFFFAOYSA-L Glycine, N-(carboxymethyl)-N-(2-hydroxyethyl)-, disodium salt Chemical compound [Na+].[Na+].OCCN(CC([O-])=O)CC([O-])=O ZTVCAEHRNBOTLI-UHFFFAOYSA-L 0.000 description 1
- 102000011782 Keratins Human genes 0.000 description 1
- 108010076876 Keratins Proteins 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000008043 acidic salts Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000006294 amino alkylene group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- XNOQNFJEPBFKLL-UHFFFAOYSA-N butanedioic acid;1,2-diaminopropan-2-ol Chemical compound CC(N)(O)CN.OC(=O)CCC(O)=O.OC(=O)CCC(O)=O XNOQNFJEPBFKLL-UHFFFAOYSA-N 0.000 description 1
- ZFXVRMSLJDYJCH-UHFFFAOYSA-N calcium magnesium Chemical compound [Mg].[Ca] ZFXVRMSLJDYJCH-UHFFFAOYSA-N 0.000 description 1
- YXQKDXIRGHMLCP-UHFFFAOYSA-N calcium;2-(1,2-dicarboxyethylamino)butanedioic acid Chemical compound [Ca].[Ca].OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O YXQKDXIRGHMLCP-UHFFFAOYSA-N 0.000 description 1
- OGQRLFNIJCDJAO-UHFFFAOYSA-N calcium;2-(1,2-dicarboxyethylamino)butanedioic acid;magnesium Chemical compound [Mg].[Ca].OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O OGQRLFNIJCDJAO-UHFFFAOYSA-N 0.000 description 1
- SVBBYUBJAIUDMM-UHFFFAOYSA-N calcium;2-[carboxymethyl(2-hydroxyethyl)amino]acetic acid;magnesium Chemical compound [Mg].[Ca].OCCN(CC(O)=O)CC(O)=O SVBBYUBJAIUDMM-UHFFFAOYSA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000007891 compressed tablet Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- UVKUROBJJFEEEK-UHFFFAOYSA-J dimagnesium;2-(1,2-dicarboxylatoethylamino)butanedioate Chemical compound [Mg+2].[Mg+2].[O-]C(=O)CC(C([O-])=O)NC(C([O-])=O)CC([O-])=O UVKUROBJJFEEEK-UHFFFAOYSA-J 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 1
- 238000007772 electroless plating Methods 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- ZJZLXRSWXQWJBB-UHFFFAOYSA-N ethane-1,2-diamine;2-hydroxybutanedioic acid Chemical compound NCCN.OC(=O)C(O)CC(O)=O.OC(=O)C(O)CC(O)=O ZJZLXRSWXQWJBB-UHFFFAOYSA-N 0.000 description 1
- IGBSXRIJNMDLFB-UHFFFAOYSA-N ethane-1,2-diamine;pentanedioic acid Chemical compound NCCN.OC(=O)CCCC(O)=O.OC(=O)CCCC(O)=O IGBSXRIJNMDLFB-UHFFFAOYSA-N 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000008202 granule composition Substances 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- DKPHLYCEFBDQKM-UHFFFAOYSA-H hexapotassium;1-phosphonato-n,n-bis(phosphonatomethyl)methanamine Chemical compound [K+].[K+].[K+].[K+].[K+].[K+].[O-]P([O-])(=O)CN(CP([O-])([O-])=O)CP([O-])([O-])=O DKPHLYCEFBDQKM-UHFFFAOYSA-H 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 239000003501 hydroponics Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- NMUOATVLLQEYHI-UHFFFAOYSA-N iminoaspartic acid Chemical compound OC(=O)CC(=N)C(O)=O NMUOATVLLQEYHI-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical group [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 229940051866 mouthwash Drugs 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 239000002455 scale inhibitor Substances 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 159000000008 strontium salts Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229940080258 tetrasodium iminodisuccinate Drugs 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
- 239000007852 tooth bleaching agent Substances 0.000 description 1
- 229940034610 toothpaste Drugs 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
- C11D3/26—Organic compounds containing nitrogen
- C11D3/33—Amino carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
- C07C229/10—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
- C07C229/12—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of acyclic carbon skeletons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3839—Polyphosphonic acids
- C07F9/3873—Polyphosphonic acids containing nitrogen substituent, e.g. N.....H or N-hydrocarbon group which can be substituted by halogen or nitro(so), N.....O, N.....S, N.....C(=X)- (X =O, S), N.....N, N...C(=X)...N (X =O, S)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Detergent Compositions (AREA)
Abstract
Description
20g(0.11モル)の2−ヒドロキシエチルイミノ二酢酸(HEIDA)を、200mlの脱イオン水中に懸濁させた。これに13.05g(0.22モル)のMg(OH)2を加え、混合物を17時間撹拌した。白色の結晶固体が溶液から析出するまで、この溶液を濃縮した。これをろ過によって収集し、オーブンで40℃にて24時間乾燥させて、MgHEIDAの式の化合物を得た。
50gの2−ヒドロキシエチルイミノ二酢酸二ナトリウム塩(28%活性、0.06モル)を取り、50mlの脱イオン水に溶解させた13.9g(0.12モル)のCaCl2と混合した。白色沈殿がすぐに生成し、ろ過により収集した。固体をオーブンで40℃にて24時間乾燥させて、CaHEIDAの式の化合物を得た。
20g(0.08モル)のイミノ二コハク酸(IDS)を200mlの脱イオン水中に懸濁させた。これに9.56g(0.16モル)のMg(OH)2を加え、混合物を17時間撹拌した。白色の結晶固体が溶液から析出するまで、この溶液を濃縮した。これをろ過によって収集し、オーブンで40℃にて24時間乾燥させて、Mg2IDSの式の化合物を得た。
100gのイミノ二コハク酸四ナトリウム(38%活性、0.1モル)を取り、50mlの脱イオン水に溶解させた22.1gの(0.2モル)CaCl2と混合した。白色沈殿がすぐに生成し、ろ過により収集した。固体をオーブンで40℃にて24時間乾燥させて、Ca2IDSの式の化合物を得た。
Claims (10)
- アミン官能基を含む酸性キレート剤の塩であって、前記塩が前記キレート剤がもたらす酸性プロトン1モル当たり少なくとも0.25モルのアルカリ土類金属を含み、前記酸性キレート剤がエチレンジアミン二コハク酸ではない塩。
- 酸性キレート剤がアミノカルボン酸キレート剤である、請求項1に記載の塩。
- 酸性キレート剤がアミノポリカルボン酸である、請求項1又は2に記載の塩。
- 酸性キレート剤がイミドコハク酸及びヒドロキシエチルイミド二酢酸から選択される、請求項1〜3のいずれかに記載の塩。
- 酸性キレート剤がイミノ二コハク酸である、請求項4に記載の塩。
- 酸性キレート剤がヒドロキシエチルイミノ二酢酸である、請求項4に記載の塩。
- キレート剤がもたらす酸性プロトン1モル当たり少なくとも0.4モルのアルカリ土類金属を含む、請求項1〜6のいずれかに記載の塩。
- イミノ二コハク酸二カルシウム(Ca2IDS)、イミノ二コハク酸カルシウムマグネシウム(CaMgIDS)、イミノ二コハク酸二マグネシウム(Mg2IDS)、ヒドロキシエチルイミノ二酢酸二カルシウム(Ca2HEIDA)、ヒドロキシエチルイミノ二酢酸カルシウムマグネシウム(CaMgHEIDA)、及びヒドロキシエチルイミノ二酢酸二マグネシウム(MgHEIDA)、並びにその非化学量論的な等価物から選択される、請求項1〜7のいずれかに記載の塩。
- 請求項1〜8のいずれかに記載の塩を含む組成物。
- 同等量の遊離酸又はナトリウム塩を使用した場合に必要となるよりも少量の過酸素種を含む組成物において同等の漂白効果を得るための、請求項1〜8のいずれかに記載の塩の使用。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0901207.1 | 2009-01-26 | ||
GBGB0901207.1A GB0901207D0 (en) | 2009-01-26 | 2009-01-26 | Chelating agents and methods relating thereto |
PCT/GB2010/050088 WO2010084351A1 (en) | 2009-01-26 | 2010-01-21 | Chelating agents and methods relating thereto |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2012515827A true JP2012515827A (ja) | 2012-07-12 |
Family
ID=40469056
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011546960A Pending JP2012515827A (ja) | 2009-01-26 | 2010-01-21 | キレート剤及びそれに関する方法 |
Country Status (6)
Country | Link |
---|---|
US (1) | US8801962B2 (ja) |
EP (1) | EP2389353B1 (ja) |
JP (1) | JP2012515827A (ja) |
AR (1) | AR077524A1 (ja) |
GB (1) | GB0901207D0 (ja) |
WO (1) | WO2010084351A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101669772B1 (ko) * | 2015-11-19 | 2016-10-27 | 오씨아이 주식회사 | 구리 식각용 조성물 |
WO2017086758A1 (ko) * | 2015-11-19 | 2017-05-26 | 오씨아이 주식회사 | 구리 식각용 조성물 및 과산화수소계 금속 식각용 조성물 |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102009060814A1 (de) * | 2009-12-30 | 2011-07-07 | inprotec AG, 79423 | Verfahren zur Herstellung eines Feststoffs mit hinreichend geringer Hygroskopizität, der Glutaminsäure-N,N-diessigsäure (GLDA) oder ein Derivat davon enthält |
GB201016001D0 (en) * | 2010-09-23 | 2010-11-10 | Innospec Ltd | Composition and method |
TW201607894A (zh) * | 2014-08-22 | 2016-03-01 | 穗曄實業股份有限公司 | 具有臭味淨化功能的水性溶液 |
US11432545B2 (en) | 2017-06-05 | 2022-09-06 | Arxada, LLC | Fast kill disinfectant wiping composition and premoistened wipes made from same |
EP3887033A1 (en) * | 2018-11-28 | 2021-10-06 | Cube Biotech GmbH | Solid-phase chelator material, method for producing thereof and use thereof for the purification of proteins |
CN112745820A (zh) * | 2021-02-01 | 2021-05-04 | 西南石油大学 | 一种硫酸钡溶垢剂 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02292385A (ja) * | 1989-03-06 | 1990-12-03 | Chevron Res Co | 酢酸マグネシウムカルシウム及びキレート化剤を含む除氷組成物 |
WO1997030209A1 (en) * | 1996-02-19 | 1997-08-21 | Kemira Chemicals Oy | Process for bleaching of a high yield pulp |
JPH10508902A (ja) * | 1994-11-11 | 1998-09-02 | ザ アソシエイテッド オクテル カンパニー リミテッド | 金属清浄および除氷組成物 |
JP2000072414A (ja) * | 1998-09-03 | 2000-03-07 | Oriental Chemical Ind | 溶解性の改善された過炭酸ナトリウムの組成物 |
JP2004035549A (ja) * | 2002-04-29 | 2004-02-05 | Bayer Ag | イミノジコハク酸アンモニウム金属塩の製法および該イミノジコハク酸アンモニウム金属塩 |
US20070231276A1 (en) * | 2006-03-31 | 2007-10-04 | Deepak Sharma | Stable dental whitening compositions |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL276367A (ja) | 1961-03-24 | |||
DE2735816C3 (de) * | 1977-08-09 | 1981-08-13 | Basf Ag, 6700 Ludwigshafen | Verfahren zum Entschlichten und Bleichen von Textilgut |
US4155738A (en) * | 1978-03-30 | 1979-05-22 | Allergan Pharmaceuticals, Inc. | Method of stabilizing a peroxide-containing composition |
FR2503746A1 (fr) * | 1981-04-09 | 1982-10-15 | Air Liquide | Composition activante pour le blanchiment au moyen de produits peroxydes |
GR76237B (ja) * | 1981-08-08 | 1984-08-04 | Procter & Gamble | |
DE3268039D1 (en) * | 1981-09-28 | 1986-01-30 | Basf Ag | Granular bleach activator |
JPS60120358A (ja) | 1983-12-05 | 1985-06-27 | Konishiroku Photo Ind Co Ltd | 写真用発色現像剤組成物 |
US4614646A (en) | 1984-12-24 | 1986-09-30 | The Dow Chemical Company | Stabilization of peroxide systems in the presence of alkaline earth metal ions |
GB8726673D0 (en) | 1987-11-13 | 1987-12-16 | Procter & Gamble | Hard-surface cleaning compositions |
JPH01153509A (ja) * | 1987-12-11 | 1989-06-15 | Tokai Denka Kogyo Kk | 高純度過酸化水素の製造方法 |
DE68913727T2 (de) | 1989-05-23 | 1994-09-29 | Procter & Gamble | Chelatierungsmittel enthaltende Reinigungs- und Waschmittelzusammensetzungen. |
ES2113882T3 (es) | 1990-04-24 | 1998-05-16 | Flustat Pty Ltd | Vacuna oral que comprende un antigeno asociado superficialmente con eritrocitos. |
DE4029297A1 (de) | 1990-09-15 | 1992-03-19 | Huels Chemische Werke Ag | Aminodicarbonsaeuren und deren derivate als stabilisatoren fuer die sauerstoffbleiche bei der textilwaesche |
US5362412A (en) | 1991-04-17 | 1994-11-08 | Hampshire Chemical Corp. | Biodegradable bleach stabilizers for detergents |
DE4113003A1 (de) | 1991-04-20 | 1992-10-22 | Huels Chemische Werke Ag | Eiweiss als bioabbaubarer stabilisator fuer die sauerstoffbleiche der textilwaesche |
US5208369A (en) | 1991-05-31 | 1993-05-04 | The Dow Chemical Company | Degradable chelants having sulfonate groups, uses and compositions thereof |
US5332518A (en) * | 1992-04-23 | 1994-07-26 | Kao Corporation | Stable slurry-coated sodium percarbonate, process for producing the same and bleach detergent composition containing the same |
AU665813B2 (en) | 1992-05-11 | 1996-01-18 | Sulzer Medizinaltechnik Ag | Process and apparatus for producing endoprostheses |
DE4319935A1 (de) | 1993-06-16 | 1994-12-22 | Basf Ag | Verwendung von Glycin-N,N-diessigsäure-Derivaten als Komplexbildner für Erdalkali- und Schwermetallionen |
US6160194A (en) * | 1993-09-08 | 2000-12-12 | The Connecticut Agricultural Experiment Station | Soil decontamination using ferric chelates and peroxide |
SE505980C2 (sv) * | 1993-12-23 | 1997-10-27 | Bim Kemi Ab | Sätt att förhindra peroxidnedbrytande enzymer vid blekning med väteperoxid |
EP0862408B1 (en) * | 1995-09-25 | 2003-02-19 | Robert Eric Montgomery | Tooth bleaching compositions |
FI115469B (fi) | 1996-02-19 | 2005-05-13 | Kemira Oyj | Menetelmä kemiallisen selluloosamateriaalin käsittelemiseksi |
BE1011785A3 (fr) * | 1998-03-10 | 2000-01-11 | Solvay | Procede de blanchiment et/ou de delignification de pates a papier chimiques. |
US20080305182A1 (en) * | 2002-11-15 | 2008-12-11 | Ramirez Jose A | Hydrogen peroxide disinfectant containing a cyclic carboxylic acid and/or aromatic alcohol |
WO2005110090A1 (en) * | 2004-05-14 | 2005-11-24 | Virox Technologies Inc. | Hydrogen peroxide-based skin disinfectant |
CA2584421C (en) * | 2004-11-05 | 2013-05-14 | Virox Technologies Inc. | Cleaning and disinfectant compositions |
US20070190172A1 (en) * | 2006-01-13 | 2007-08-16 | Aseptix Technologies B.V. | Enhanced activity biocidal hydrogen peroxide composition |
US7658953B2 (en) * | 2006-01-13 | 2010-02-09 | Aseptix Research B.V. | Enhanced activity biocidal hydrogen peroxide composition |
EP1811080A1 (en) | 2006-01-24 | 2007-07-25 | Solvay SA | Process for the bleaching of mechanical paper pulp |
US20070231277A1 (en) * | 2006-03-31 | 2007-10-04 | Deepak Sharma | Multicomponent whitening compositions and containers |
GB0714575D0 (en) * | 2007-07-26 | 2007-09-05 | Innospec Ltd | Composition |
GB0721587D0 (en) * | 2007-11-02 | 2007-12-12 | Innospec Ltd | Process for bleaching pulp |
GB201016001D0 (en) * | 2010-09-23 | 2010-11-10 | Innospec Ltd | Composition and method |
-
2009
- 2009-01-26 GB GBGB0901207.1A patent/GB0901207D0/en not_active Ceased
-
2010
- 2010-01-21 EP EP10702729.4A patent/EP2389353B1/en not_active Not-in-force
- 2010-01-21 US US13/146,322 patent/US8801962B2/en not_active Expired - Fee Related
- 2010-01-21 WO PCT/GB2010/050088 patent/WO2010084351A1/en active Application Filing
- 2010-01-21 JP JP2011546960A patent/JP2012515827A/ja active Pending
- 2010-01-26 AR ARP100100167A patent/AR077524A1/es not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02292385A (ja) * | 1989-03-06 | 1990-12-03 | Chevron Res Co | 酢酸マグネシウムカルシウム及びキレート化剤を含む除氷組成物 |
JPH10508902A (ja) * | 1994-11-11 | 1998-09-02 | ザ アソシエイテッド オクテル カンパニー リミテッド | 金属清浄および除氷組成物 |
WO1997030209A1 (en) * | 1996-02-19 | 1997-08-21 | Kemira Chemicals Oy | Process for bleaching of a high yield pulp |
JP2000072414A (ja) * | 1998-09-03 | 2000-03-07 | Oriental Chemical Ind | 溶解性の改善された過炭酸ナトリウムの組成物 |
JP2004035549A (ja) * | 2002-04-29 | 2004-02-05 | Bayer Ag | イミノジコハク酸アンモニウム金属塩の製法および該イミノジコハク酸アンモニウム金属塩 |
US20070231276A1 (en) * | 2006-03-31 | 2007-10-04 | Deepak Sharma | Stable dental whitening compositions |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101669772B1 (ko) * | 2015-11-19 | 2016-10-27 | 오씨아이 주식회사 | 구리 식각용 조성물 |
WO2017086758A1 (ko) * | 2015-11-19 | 2017-05-26 | 오씨아이 주식회사 | 구리 식각용 조성물 및 과산화수소계 금속 식각용 조성물 |
CN108291314A (zh) * | 2015-11-19 | 2018-07-17 | Oci有限公司 | 铜蚀刻用组合物及过氧化氢类金属蚀刻用组合物 |
CN108291314B (zh) * | 2015-11-19 | 2020-09-11 | Oci有限公司 | 铜蚀刻用组合物及过氧化氢类金属蚀刻用组合物 |
Also Published As
Publication number | Publication date |
---|---|
GB0901207D0 (en) | 2009-03-11 |
AR077524A1 (es) | 2011-09-07 |
EP2389353A1 (en) | 2011-11-30 |
US8801962B2 (en) | 2014-08-12 |
EP2389353B1 (en) | 2017-03-08 |
US20120068113A1 (en) | 2012-03-22 |
WO2010084351A1 (en) | 2010-07-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8801962B2 (en) | Chelating agents and methods relating thereto | |
JP2749436B2 (ja) | N,n’‐(1‐オキソ‐1,2‐エタンジイル)ビス‐(アスパラギン酸)、その塩、および洗剤組成物における用途 | |
JP5600059B2 (ja) | 組成物 | |
EP0817768B1 (en) | Amino nitrile intermediate for the preparation of alanine diacetic acid | |
CN1065563C (zh) | 用于手洗或其它低水洗涤体系的包括n-酰基己内酰胺的漂白组合物 | |
KR20100061687A (ko) | 글루탐산-n,n-디아세트산의 알칼리금속염, 그의 제조 방법 및 용도 | |
JP2013540860A (ja) | 自動食器洗い用組成物 | |
JP2001342453A (ja) | キレート剤組成物 | |
JPH11349989A (ja) | 洗剤組成物 | |
JP2010534735A (ja) | 1−ヒドロキシエチリデン−1,1−ジホスホン酸とエチレンジアミンジコハク酸又はその塩との付加物、その調製方法、並びにその使用 | |
EP2090646A1 (en) | Surface treatment composition containing phosphonic acid compounds | |
EP0866787B1 (en) | An amino nitrile intermediate for the preparation of 2-hydroxyethyl iminodiacetic acid | |
US6288263B1 (en) | Intermediates for the preparation of N-[2-(carboxymethoxy)ethyl]-N-(carboxymethyl)glycine | |
JP2018507950A (ja) | キレート剤の混合物、及び該混合物の製造方法 | |
JPH08100196A (ja) | 液体漂白剤組成物 | |
ES2881309T3 (es) | Proceso para preparación de mezclas de enantiómeros, y mezclas de enantiómeros | |
EP1004660B1 (en) | An amino nitrile intermediate for the preparation of 2-hydroxyethyl iminodiacetic acid | |
JP4266405B2 (ja) | 酸性アミノ酸誘導体の製造方法 | |
US5488130A (en) | Amino nitrile intermediate for the preparation of 2-hydroxypropyl iminodiacetic acid | |
JPH09132797A (ja) | 黴汚れ洗浄剤組成物 | |
MXPA97007502A (en) | Intermediario de aminonitrilo for the preparation of dianic acid from alan |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20121205 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140320 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20140619 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20140626 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140708 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20150224 |