JPH08511255A - アルカリ土類金属−及び重金属イオンのための生物学的に分解可能な錯化剤としてのグリシン−n,n−二酢酸−誘導体の使用及びその製法 - Google Patents
アルカリ土類金属−及び重金属イオンのための生物学的に分解可能な錯化剤としてのグリシン−n,n−二酢酸−誘導体の使用及びその製法Info
- Publication number
- JPH08511255A JPH08511255A JP7501306A JP50130695A JPH08511255A JP H08511255 A JPH08511255 A JP H08511255A JP 7501306 A JP7501306 A JP 7501306A JP 50130695 A JP50130695 A JP 50130695A JP H08511255 A JPH08511255 A JP H08511255A
- Authority
- JP
- Japan
- Prior art keywords
- group
- glycine
- diacetic acid
- alkyl
- acid derivative
- 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.)
- Granted
Links
- 229910052757 nitrogen Inorganic materials 0.000 title claims abstract description 77
- 239000008139 complexing agent Substances 0.000 title claims abstract description 32
- 229910001385 heavy metal Inorganic materials 0.000 title claims abstract description 23
- 229910052784 alkaline earth metal Inorganic materials 0.000 title claims abstract description 16
- 150000002500 ions Chemical class 0.000 title claims abstract description 16
- 150000001342 alkaline earth metals Chemical class 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title claims description 17
- 238000002360 preparation method Methods 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 79
- -1 alkali metal salts Chemical class 0.000 claims abstract description 60
- 239000003599 detergent Substances 0.000 claims abstract description 51
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical class OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims abstract description 36
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 16
- 150000003863 ammonium salts Chemical class 0.000 claims abstract description 10
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 claims description 48
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 28
- 238000004140 cleaning Methods 0.000 claims description 28
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 24
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 24
- 238000004061 bleaching Methods 0.000 claims description 23
- 125000000623 heterocyclic group Chemical group 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 17
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- BSRDNMMLQYNQQD-UHFFFAOYSA-N iminodiacetonitrile Chemical compound N#CCNCC#N BSRDNMMLQYNQQD-UHFFFAOYSA-N 0.000 claims description 16
- 239000004471 Glycine Substances 0.000 claims description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 229910052760 oxygen Inorganic materials 0.000 claims description 15
- 239000001301 oxygen Substances 0.000 claims description 15
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 11
- 235000013305 food Nutrition 0.000 claims description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 150000001340 alkali metals Chemical group 0.000 claims description 8
- 235000013361 beverage Nutrition 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 7
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 6
- DFNYGALUNNFWKJ-UHFFFAOYSA-N aminoacetonitrile Chemical class NCC#N DFNYGALUNNFWKJ-UHFFFAOYSA-N 0.000 claims description 5
- 238000004851 dishwashing Methods 0.000 claims description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
- 125000000739 C2-C30 alkenyl group Chemical group 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 229920003023 plastic Polymers 0.000 claims description 4
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 3
- 150000002332 glycine derivatives Chemical class 0.000 claims description 3
- 239000004922 lacquer Substances 0.000 claims description 3
- 125000002560 nitrile group Chemical group 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 claims description 2
- KHUXNRRPPZOJPT-UHFFFAOYSA-N phenoxy radical Chemical group O=C1C=C[CH]C=C1 KHUXNRRPPZOJPT-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 7
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 238000001212 derivatisation Methods 0.000 claims 1
- 230000004720 fertilization Effects 0.000 claims 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 claims 1
- 229910021645 metal ion Inorganic materials 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 238000009987 spinning Methods 0.000 claims 1
- 239000011575 calcium Substances 0.000 abstract description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052791 calcium Inorganic materials 0.000 abstract description 6
- 239000000843 powder Substances 0.000 abstract description 6
- 239000000835 fiber Substances 0.000 abstract description 5
- 239000002324 mouth wash Substances 0.000 abstract description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 36
- 239000000243 solution Substances 0.000 description 30
- 150000003839 salts Chemical class 0.000 description 29
- 239000007864 aqueous solution Substances 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 17
- 238000004448 titration Methods 0.000 description 14
- 239000002253 acid Substances 0.000 description 13
- 238000004519 manufacturing process Methods 0.000 description 13
- 102000008133 Iron-Binding Proteins Human genes 0.000 description 12
- 108010035210 Iron-Binding Proteins Proteins 0.000 description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- 239000000047 product Substances 0.000 description 11
- 239000000725 suspension Substances 0.000 description 11
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- 238000001816 cooling Methods 0.000 description 8
- 229910052748 manganese Inorganic materials 0.000 description 8
- 239000011572 manganese Substances 0.000 description 8
- 238000003860 storage Methods 0.000 description 8
- 239000004753 textile Substances 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 229920001131 Pulp (paper) Polymers 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 5
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- 229910052802 copper Inorganic materials 0.000 description 5
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- 150000002431 hydrogen Chemical group 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 159000000000 sodium salts Chemical class 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 4
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 159000000007 calcium salts Chemical class 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 235000013336 milk Nutrition 0.000 description 4
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- 210000004080 milk Anatomy 0.000 description 4
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- 238000007254 oxidation reaction Methods 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 239000003755 preservative agent Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 230000006641 stabilisation Effects 0.000 description 4
- 238000011105 stabilization Methods 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
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- QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 description 3
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- QXDMQSPYEZFLGF-UHFFFAOYSA-L calcium oxalate Chemical compound [Ca+2].[O-]C(=O)C([O-])=O QXDMQSPYEZFLGF-UHFFFAOYSA-L 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
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- 229910052737 gold Inorganic materials 0.000 description 3
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- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
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- 229960001922 sodium perborate Drugs 0.000 description 3
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- 239000000080 wetting agent Substances 0.000 description 3
- UWYZHKAOTLEWKK-UHFFFAOYSA-N 1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2CNCCC2=C1 UWYZHKAOTLEWKK-UHFFFAOYSA-N 0.000 description 2
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- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 2
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
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- 238000002955 isolation Methods 0.000 description 1
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- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
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- 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
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- 235000010755 mineral Nutrition 0.000 description 1
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- 239000004570 mortar (masonry) Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
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- KRIOVPPHQSLHCZ-UHFFFAOYSA-N phenyl propionaldehyde Natural products CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- LFSXCDWNBUNEEM-UHFFFAOYSA-N phthalazine Chemical compound C1=NN=CC2=CC=CC=C21 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
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- 239000011591 potassium Substances 0.000 description 1
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- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
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- 235000019353 potassium silicate Nutrition 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
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- 150000004671 saturated fatty acids Chemical class 0.000 description 1
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- 239000000176 sodium gluconate Substances 0.000 description 1
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- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
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- 235000010265 sodium sulphite Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
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- 238000001694 spray drying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
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- 238000000954 titration curve Methods 0.000 description 1
- 208000004371 toothache Diseases 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- OHOTVSOGTVKXEL-UHFFFAOYSA-K trisodium;2-[bis(carboxylatomethyl)amino]propanoate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C(C)N(CC([O-])=O)CC([O-])=O OHOTVSOGTVKXEL-UHFFFAOYSA-K 0.000 description 1
- XWNXEWLCHSLQOI-UHFFFAOYSA-K trisodium;triacetate Chemical compound [Na+].[Na+].[Na+].CC([O-])=O.CC([O-])=O.CC([O-])=O XWNXEWLCHSLQOI-UHFFFAOYSA-K 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
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- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
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- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
- C07C227/18—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/26—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing carboxyl groups by reaction with HCN, or a salt thereof, and amines, or from aminonitriles
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- 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
- C07C229/16—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 hydrocarbon radicals substituted by amino or carboxyl groups, e.g. ethylenediamine-tetra-acetic acid, iminodiacetic acids
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- 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
- C07C229/26—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 more than one amino group bound to the carbon skeleton, e.g. lysine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/24—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
- C07C255/25—Aminoacetonitriles
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- 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
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- C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
- C11D17/065—High-density particulate detergent compositions
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- 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
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- C11D3/33—Amino carboxylic acids
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
- D06L4/12—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen combined with specific additives
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/30—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using reducing agents
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1026—Other features in bleaching processes
- D21C9/1042—Use of chelating agents
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- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/305—Additives other than developers
- G03C5/3053—Tensio-active agents or sequestering agents, e.g. water-softening or wetting agents
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- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/38—Fixing; Developing-fixing; Hardening-fixing
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- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/51—Chelating agents
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- 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
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- C11D2111/10—Objects to be cleaned
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- 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
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- C11D2111/10—Objects to be cleaned
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Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.一般式 I: [式中、 Rはヒドロキシ基、ホルミル基、C1−〜C4−アルコキシ基、フェノキシ基又は C1−〜C4−アルコキシカルボニル基5個までを付加的に置換分として有してい てよく、かつ隣接していない5個までの酸素原子で中断されていてよいC1−〜 C30−アルキル又はC2−〜C30−アルケニル基、式:−(CH2)k−O−(A1 O)m−(A2O)n−Y(ここで、A1及びA2は相互に依存せずにC−原子数2 〜4の1,2−アルキレン基を表し、Yは水素、C1−〜C12−アルキル、フェ ニル又はC1−〜C4−アルコキシカルボニルを表し、かつkは数値1、2又は3 で、m及びnはそれぞれ0〜50までの数値を表し、この際m+nからなる合計は少 なくとも4を有する)のアルコキシレート基、又はアルキル基中にC−原子1〜 20個を有するフェニルアルキル基、付加的にベンゼン環縮合していてよい、窒 素、酸素及び硫黄の群からのヘテロ原子3個までを有する5又は6員の不飽和又 は飽和複素環式環を表し、この際Rの意味において挙げたすべてのフェニル 核及び複素環式環は更に付加的に置換分としてC1−〜C4−アルキル基、ヒドロ キシ基、カルボキシル基、スルホ基又はC1−〜C4−アルコキシカルボニル基3 個までを有していてよく、又はRは式: (ここで、AはC1−〜C12−アルキレン橋又は化学結合を表す)の基を表し、 かつ Mは水素、アルカリ金属、アルカリ土類金属、アンモニウム又は置換アンモニウ ムの相応する化学量論量を表す]のグリシン−N,N−二酢酸−誘導体のアルカ リ土類金属−及び重金属イオンのための錯化剤としての金属、プラスチック、ラ ッカー又はガラスの硬い表面用工業清浄工程用、飲料及び食品産業用アルカリ清 浄行程用並びに食器清浄用清浄剤組成物中への使用。 2.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有する金属、プラ スチック、ラッカー又はガラスの硬い表面用工業清浄剤組成物。 3.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有する飲料及び食 品産業用のアルカリ性清浄剤組成物。 4.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有する食器用清浄 剤組成物。 5.粉末状小型及び超小型洗剤組成物及び液体洗剤 組成物中へのアルカリ土類金属−及び重金属イオンの錯化剤としての請求項1記 載のグリシン−N,N−二酢酸誘導体Iの使用。 6.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有する粉末状小型 及び超小型洗剤組成物。 7.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有する液体洗剤組 成物。 8.製紙産業における漂白浴中へのアルカリ土類金属−及び重金属イオンの錯 化剤としての請求項1記載のグリシン−N,N−二酢酸誘導体Iの使用。 9.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有する製紙産業用 漂白浴。 10.写真漂白−及び漂白固定浴中へのアルカリ土類金属−及び重金属イオン の錯化剤としての請求項1記載のグリシン−N,N−二酢酸誘導体Iの使用。 11.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有する写真漂白 −及び漂白固定浴。 12.製糸産業における前処理−及び漂白浴中へのアルカリ土類金属−及び重 金属イオンの錯化剤としての請求項1記載のグリシン−N,N−二酢酸誘導体I の使用。 13.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有する製糸産業 における前処理−及び漂白浴。 14.ガルヴァーニ浴中へのアルカリ土類金属−及 び重金属イオンの錯化剤としての請求項1記載のグリシン−N,N−二酢酸誘導 体Iの使用。 15.請求項1記載のグリシン−N,N−二酢酸誘導体Iを含有するガルヴァ ーニ浴。 16.植物施肥中へのアルカリ土類金属−及び重金属イオンの錯化剤としての グリシン−N,N−二酢酸誘導体Iの使用。 17.一般式 I: [式中、 Rはヒドロキシ基、ホルミル基、C1−〜C4−アルコキシ基、フェノキシ基又は C1−〜C4−アルコキシカルボニル基5個までを付加的に置換分として有してい てよく、かつ隣接していない5個までの酸素原子で中断されていてよいC1−〜 C30−アルキル又はC2−〜C30−アルケニル基、式:−(CH2)k−O−(A 10)m−(A2O)n−Y(ここで、A1及びA2は相互に依存せずにC−原子数 2〜4の1,2−アルキレン基を表し、Yは水素、C1−〜C12−アルキル、フ ェニル又はC1−〜C4−アルコキシカルボニルを表し、かつkは数値1、2又は 3で、m及びnはそれぞれ0〜50までの数値を表し、この際m+nからなる合計は 少なくとも4を有する)のアルコキシレート基、又はアルキル基中にC−原子1 〜20個を有するフェニ ルアルキル基、付加的にベンゼン環縮合していてよい、窒素、酸素及び硫黄の群 からのヘテロ原子3個までを有する5又は6員の不飽和又は飽和複素環式環を表 し、この際Rの意味において挙げたすべてのフェニル核及び複素環式環は更に付 加的に置換分としてC1−〜C4−アルキル基、ヒドロキシ基、カルボキシル基、 スルホ基又はC1−〜C4−アルコキシカルボニル基3個までを有していてよく、 又はRは式: (ここで、AはC1−〜C12−アルキレン橋又は化学結合を表す)の基を表し、 かつ Mは水素、アルカリ金属、アルカリ土類金属、アンモニウム又は置換アンモニウ ムの相応する化学量論量を表す]のグリシン−N,N−二酢酸−誘導体を製造す る方法において、 A)相応する2−置換グリシン又は2−置換グリシンニトリル又は式; の2倍体グリシン、又は式; の2倍体グリシンニトリルをホルムアルデヒド及びシアン化水素と反応させるか 、又は B)イミノ二酢酸又はイミノジアセトニトリルを相応するモノアルデヒド又は式 ;OHC−A−CHOのジアルデヒド及びシアン化水素又はアルカリ金属シアン 化物と反応させ、引き続き存在するニトリル基を加水分解しカルボキシル基にす ることを特徴とする、グリシン−N,N−二酢酸−誘導体の製法。 18.中間体である、2−位で基Rにより置換されたグリシン−N,N−ジア セトニトリル及びグリシンニトリル−N,N−ジアセトニトリル[ここでRはヒ ドロキシ基、ホルミル基、C1−〜C4−アルコキシ基、フェノキシ基又はC1− 〜C4−アルコキシカルボニル基5個までを付加的に置換分として有していてよ く、かつ隣接していない5個までの酸素原子で中断されていてよいC1−〜C30 −アルキル又はC2−〜C30−アルケニル基、式:−(CH2)k−O−(A1O)m −(A2O)n−Y(ここで、A1及びA2は相互に依存せずにC−原子数2〜4 の1,2−アルキレン基を表し、Yは水素、C1−〜C12−アルキル、フェニル 又はC1−〜C4−アルコキシカルボニルを表し、かつkは数値1、2又は3で、m 及びnはそれぞれ0〜50までの数値を表し、この際m+nからなる合計は少なく とも4を有する)のアルコキシレート基、又はアルキル基中にC−原子1〜20 個を有するフェニルアルキ ル基、付加的にベンゼン環縮合していてよい、窒素、酸素及び硫黄の群からのヘ テロ原子3個までを有する5又は6員の不飽和又は飽和複素環式環を表し、この 際Rの意味において挙げたすべてのフェニル核及び複素環式環は更に付加的に置 換分としてC1−〜C4−アルキル基、ヒドロキシ基、カルボキシル基、スルホ基 又はC1−〜C4−アルコキシカルボニル基3個までを有していてよい]及び式; [式中、Xはカルボン酸−又はニトリル官能基を表す]の2倍体のグリシン−N ,N−ジアセトニトリル及び2倍体のグリシンニトリル−N,N−ジアセトニト リル。 19.一般式Ia: [式中、R′はヒドロキシ基、ホルミル基、C1−〜C4−アルコキシ基、フェノ キシ基又はC1−〜C4−アルコキシカルボニル基5個までを付加的に置換分とし て有していてよく、かつ隣接していない5個までの 酸素原子で中断されていてよいC4−〜C30−アルキル又はC2−〜C30−アルケ ニル基、式:−(CH2)k−O−(A1O)m−(A2O)n−Y(ここで、A1及 びA2は相互に依存せずにC−原子数2〜4の1,2−アルキレン基を表し、Y は水素、C1−〜C12−アルキル、フェニル又はC1−〜C4−アルコキシカルボ ニルを表し、かつkは数値1、2又は3で、m及びnはそれぞれ0〜50までの数 値を表し、この際m+nからなる合計は少なくとも4を有する)のアルコキシレー ト基、又はアルキル基中にC−原子1〜20個を有するフェニルアルキル基、付 加的にベンゼン環縮合していてよい、窒素、酸素及び硫黄の群からのヘテロ原子 3個までを有する5又は6員の不飽和又は飽和複素環式環を表し、この際Rの意 味において挙げたすべてのフェニル核及び複素環式環は更に付加的に置換分とし てC1−〜C4−アルキル基、ヒドロキシ基、カルボキシル基、スルホ基又はC1 −〜C4−アルコキシカルボニル基3個までを有していてよく、又はR′は式: (ここで、A′はC1−〜C12−アルキレン橋を表す)の基を表すが、但しR′ に関してC6H13、C10H21 、C14H29及びC16H33の脂肪族基並びにベンジル基は除く、及び Mは水素、アルカリ金属、アルカリ土類金属、アンモニウム又は置換アンモニウ ムの相応する化学量論量を表す]のグリシン−N,N−二酢酸誘導体。
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DE4444347A1 (de) * | 1994-12-14 | 1996-06-20 | Basf Ag | Verwendung von Glycin-N,N-diessigsäure-Derivaten als Komplexbildner für Erdalkali- und Schwermetallionen bei der Förderung und beim Transport von Erdöl und Erdgas |
US5481018A (en) * | 1995-03-31 | 1996-01-02 | The Dow Chemical Company | Amino nitrile intermediate for the preparation of alanine diacetic acid |
DE19518986A1 (de) * | 1995-05-29 | 1996-12-05 | Basf Ag | Verfahren zur Herstellung von Glycin-N,N-diessigsäure-Derivaten durch Umsetzung von Glycinderivaten oder deren Vorstufen mit Formaldehyd und Cyanwasserstoff oder von Iminodiacetonitril oder Imindodiessigsäure mit entsprechenden Aldehyden und Cyanwasserstoff in wäßrig-saurem Medium |
DE19518987A1 (de) * | 1995-05-29 | 1996-12-05 | Basf Ag | Verfahren zur Herstellung von Glycin-N,N-diessigsäure-Derivaten durch Umsetzung von Glycinderivaten oder deren Vorstufen mit Formaldehyd und Alkalimetallcyanid in wäßrig-alkalischem Medium |
DE19543162A1 (de) * | 1995-11-18 | 1997-05-22 | Basf Ag | Feste Textilwaschmittel-Formulierung aus anorganischen Buildern, Glycin-N,N-diessigsäure-Derivaten als organische Cobuilder sowie anionischen und nichtionischen Tensiden |
DE69603506T2 (de) * | 1995-12-11 | 2000-01-13 | Unilever N.V., Rotterdam | Reinigung einer komplettanlage |
EP0783034B1 (en) * | 1995-12-22 | 2010-08-18 | Mitsubishi Rayon Co., Ltd. | Chelating agent and detergent comprising the same |
JP3221831B2 (ja) * | 1996-01-22 | 2001-10-22 | 花王株式会社 | 非イオン性高密度粒状洗剤組成物 |
JP3221830B2 (ja) * | 1996-01-22 | 2001-10-22 | 花王株式会社 | 高密度粒状洗剤組成物 |
JP3810854B2 (ja) * | 1996-01-22 | 2006-08-16 | 花王株式会社 | 高密度粉末洗剤組成物 |
DE19607800A1 (de) * | 1996-03-01 | 1997-09-04 | Henkel Ecolab Gmbh & Co Ohg | Reinigungsmittel für Anlagen der Lebensmittelindustrie, seine Verwendung und Verfahren zum Reinigen dieser Anlagen |
GB2311537A (en) * | 1996-03-29 | 1997-10-01 | Procter & Gamble | Rinse composition for dishwashers |
US6159922A (en) * | 1996-03-29 | 2000-12-12 | The Procter & Gamble Company | Bleaching composition |
GB2311535A (en) * | 1996-03-29 | 1997-10-01 | Procter & Gamble | Detergent compositions |
GB2311542A (en) * | 1996-03-29 | 1997-10-01 | Procter & Gamble | Percarbonate bleach composition |
GB2311541A (en) * | 1996-03-29 | 1997-10-01 | Procter & Gamble | Oxygen-releasing bleach composition |
GB2311538A (en) * | 1996-03-29 | 1997-10-01 | Procter & Gamble | Detergent compositions |
US6172036B1 (en) * | 1996-03-29 | 2001-01-09 | The Procter & Gamble Company | Rinsing compositions containing an amino tricarboxylic acid and an organic polymer |
GB2311536A (en) * | 1996-03-29 | 1997-10-01 | Procter & Gamble | Dishwashing and laundry detergents |
JPH09310091A (ja) * | 1996-05-22 | 1997-12-02 | Kao Corp | 硬質表面用洗浄剤組成物 |
ES2142680T3 (es) * | 1996-06-19 | 2000-04-16 | Unilever Nv | Composicion para el tratamiento de suelos. |
ES2300287T3 (es) * | 1996-06-21 | 2008-06-16 | Reckitt Benckiser N.V. | Detergentes de baja alcalinidad para lavavajillas con contenido en acido metilglicindiacetico (mgda). |
US6162259A (en) * | 1997-03-25 | 2000-12-19 | The Procter & Gamble Company | Machine dishwashing and laundry compositions |
EP0991745A1 (en) * | 1997-06-24 | 2000-04-12 | Unilever N.V. | Additive for a detergent formulation, detergent formulation comprising such an additive and use of said formation for cleaning bottles |
JP3290382B2 (ja) * | 1997-07-18 | 2002-06-10 | 花王株式会社 | 粉末洗剤組成物 |
EP1002046B1 (de) * | 1997-07-30 | 2003-04-16 | Basf Aktiengesellschaft | Feste textilwaschmittel-formulierung enthaltend glycin-n, n-diessigsäure-derivate |
WO1999006513A1 (de) * | 1997-07-30 | 1999-02-11 | Basf Aktiengesellschaft | Feste textilwaschmittel-formulierung auf basis von glycin-n,n-diessigsäure-derivaten mit stark reduziertem anteil an weiteren anionischen tensiden |
US6367030B1 (en) * | 1997-10-09 | 2002-04-02 | Matsushita Electric Industrial Co., Ltd. | Address conversion circuit and address conversion system with redundancy decision circuitry |
US6197736B1 (en) * | 1998-12-22 | 2001-03-06 | The Boeing Company | Alkaline cleaning solution |
US6346217B1 (en) | 1999-06-02 | 2002-02-12 | Water Whole International, Inc. | Composition and method for cleaning drink water tanks |
US6240935B1 (en) * | 2000-03-30 | 2001-06-05 | The Boeing Company | Boelube R dissolving alkaline cleaning solution |
US7003228B2 (en) * | 2001-09-11 | 2006-02-21 | Vitesse Semiconductor Corporation | Method and apparatus for improved high-speed adaptive equalization |
FR2852836B1 (fr) * | 2003-03-25 | 2008-02-15 | Oreal | Utilisation d'acides hydroxycarboxyliques et de leurs sels comme agents complexants dans des compositions reductrices pour la decoloration ou la deformation permanente de fibres keratiniques |
US20050011017A1 (en) * | 2003-03-25 | 2005-01-20 | L'oreal S.A. | Oxidizing composition comprising hydroxycarboxylic acids and salts thereof as complexing agents for dyeing, bleaching or permanently reshaping keratin fibres |
US7303588B2 (en) * | 2003-03-25 | 2007-12-04 | L'oreal S.A. | Composition for dyeing keratinous fibers, comprising at least one polycarboxylic acid or a salt, ready-to-use composition comprising it, implementation process and device |
US20050036970A1 (en) * | 2003-03-25 | 2005-02-17 | L'oreal S.A. | Reducing compositions for bleaching or permanently reshaping keratin fibres comprising polycarboxylic acids and salts thereof as complexing agents |
FR2852838B1 (fr) * | 2003-03-25 | 2008-01-18 | Oreal | Utilisation d'acides polycarboxyliques et leurs sels comme agents complexants dans des compositions oxydantes pour la coloration, la decoloration ou la deformation permanente de fibres keratiniques |
US20050039270A1 (en) * | 2003-03-25 | 2005-02-24 | L'oreal S.A. | Use of polycarboxylic acids and salts thereof as complexing agents in oxidizing compositions for dyeing, bleaching or permanently reshaping keratin fibres |
FR2852832B1 (fr) | 2003-03-25 | 2008-06-27 | Oreal | Composition de coloration pour fibres keratiniques comprenant un acide hydroxycarboxilique ou un sel, composition prete a l'emploi la comprenant, procede de mise en oeuvre et dispositif |
US7038875B2 (en) * | 2003-07-31 | 2006-05-02 | Seagate Technology Llc | Dynamic measurement of head media spacing modulation |
DE102004038991A1 (de) * | 2004-08-10 | 2006-02-23 | Henkel Kgaa | Alkalisierungsmittel-haltiges Mittel zum Aufhellen und/oder Färben von keratinhaltigen Fasern, insbesondere Blondiermittel für menschliche Haare |
TW200619368A (en) * | 2004-10-28 | 2006-06-16 | Nissan Chemical Ind Ltd | Polishing composition for silicon wafer |
DE102005041349A1 (de) * | 2005-08-31 | 2007-03-01 | Basf Ag | Reinigungsformulierungen für die maschinelle Geschirrreinigung enthaltend hydrophil modifizierte Polycarboxylate |
DE102005041347A1 (de) † | 2005-08-31 | 2007-03-01 | Basf Ag | Reinigungsformulierungen für die maschinelle Geschirrreinigung enthaltend hydrophil modifizierte Polycarboxylate |
GB0522658D0 (en) | 2005-11-07 | 2005-12-14 | Reckitt Benckiser Nv | Composition |
US9027647B2 (en) | 2006-08-04 | 2015-05-12 | Halliburton Energy Services, Inc. | Treatment fluids containing a biodegradable chelating agent and methods for use thereof |
US8567503B2 (en) * | 2006-08-04 | 2013-10-29 | Halliburton Energy Services, Inc. | Composition and method relating to the prevention and remediation of surfactant gel damage |
US9120964B2 (en) * | 2006-08-04 | 2015-09-01 | Halliburton Energy Services, Inc. | Treatment fluids containing biodegradable chelating agents and methods for use thereof |
US9127194B2 (en) | 2006-08-04 | 2015-09-08 | Halliburton Energy Services, Inc. | Treatment fluids containing a boron trifluoride complex and methods for use thereof |
US8567504B2 (en) * | 2006-08-04 | 2013-10-29 | Halliburton Energy Services, Inc. | Composition and method relating to the prevention and remediation of surfactant gel damage |
WO2008076055A1 (en) * | 2006-12-19 | 2008-06-26 | Akzo Nobel N.V. | Process of pulping |
MX2010003825A (es) | 2007-10-18 | 2010-04-27 | Ecolab Inc | Composiciones de limpieza solidas, auto-solidificables, comprimidas, y metodos para hacerlas. |
US20100190676A1 (en) * | 2008-07-22 | 2010-07-29 | Ecolab Inc. | Composition for enhanced removal of blood soils |
GB0901207D0 (en) | 2009-01-26 | 2009-03-11 | Innospec Ltd | Chelating agents and methods relating thereto |
MY153903A (en) | 2009-05-20 | 2015-04-15 | Basf Se | Method for producing a spray powder containing one or more glycine-n,n-diacetic acid derivatives and use of the spray powder to produce compression agglomerates |
US20110009299A1 (en) * | 2009-07-10 | 2011-01-13 | Van Zanten Ryan | Emulsion stabilizing agents for drilling and completion fluids |
EP2308834A1 (de) | 2009-10-05 | 2011-04-13 | Basf Se | Verfahren zur Isolierung von Methylglycinnitril-N,N-diacetonitril |
KR20120129946A (ko) | 2010-02-09 | 2012-11-28 | 바스프 에스이 | 세제 조성물 |
EP2534238A1 (en) | 2010-02-09 | 2012-12-19 | Basf Se | Builder composition |
TR201810936T4 (tr) | 2010-04-23 | 2018-08-27 | Industrial Chemicals Group Ltd | Deterjan bileşimi. |
EP2383329A1 (en) | 2010-04-23 | 2011-11-02 | The Procter & Gamble Company | Particle |
ES2579217T3 (es) | 2010-04-23 | 2016-08-08 | The Procter & Gamble Company | Partícula |
US8754026B2 (en) | 2010-09-27 | 2014-06-17 | Basf Se | Process for producing granules comprising one or more complexing agent salts |
EP2621892B1 (de) | 2010-09-27 | 2015-07-29 | Basf Se | Verfahren zur herstellung eines granulates enthaltend eines oder mehrere komplexbildnersalze |
US8802894B2 (en) | 2011-04-04 | 2014-08-12 | Basf Se | Process for the preparation of aqueous solutions of methylglycine-N,N-diacetic acid trialkali metal salts |
CA2833150C (en) | 2011-04-14 | 2020-10-06 | Basf Se | A method of dissolving and/or inhibiting the deposition of scale on a surface of a system |
CN103517894A (zh) * | 2011-05-03 | 2014-01-15 | 巴斯夫欧洲公司 | 制备结晶l-mgda三碱金属盐的方法 |
US8881823B2 (en) | 2011-05-03 | 2014-11-11 | Halliburton Energy Services, Inc. | Environmentally friendly low temperature breaker systems and related methods |
US9227915B2 (en) | 2011-05-03 | 2016-01-05 | Basf Se | Process for the preparation of a crystalline L-MGDA trialkali metal salt |
GB2491619B (en) * | 2011-06-09 | 2014-10-01 | Pq Silicas Bv | Builder granules and process for their preparation |
WO2012171859A1 (en) * | 2011-06-13 | 2012-12-20 | Akzo Nobel Chemicals International B.V. | Improved corrosion resistance when using chelating agents in chromium-containing equipment |
KR20140041805A (ko) | 2011-06-29 | 2014-04-04 | 바스프 에스이 | 농업에서 아미노카르복실레이트의 용도 |
US9403731B2 (en) | 2011-06-29 | 2016-08-02 | Basf Se | Modified aminocarboxylates with improved storage stability and processability |
DE102012102859A1 (de) * | 2012-04-02 | 2013-11-14 | Osram Opto Semiconductors Gmbh | Optoelektronisches Bauelement umfassend eine Konverterträgerschicht, und Verfahren zur Herstellung eines optoelektronischen Bauelements umfassend eine Konverterträgerschicht |
US9334716B2 (en) | 2012-04-12 | 2016-05-10 | Halliburton Energy Services, Inc. | Treatment fluids comprising a hydroxypyridinecarboxylic acid and methods for use thereof |
US8772527B2 (en) | 2012-04-27 | 2014-07-08 | Basf Se | Process for isomerization of cis-2-pentenenitrile to 3-pentenenitriles |
JP6063829B2 (ja) * | 2012-06-28 | 2017-01-18 | ライオン株式会社 | 繊維製品用の液体洗浄剤 |
US9670399B2 (en) | 2013-03-15 | 2017-06-06 | Halliburton Energy Services, Inc. | Methods for acidizing a subterranean formation using a stabilized microemulsion carrier fluid |
US9850512B2 (en) | 2013-03-15 | 2017-12-26 | The Research Foundation For The State University Of New York | Hydrolysis of cellulosic fines in primary clarified sludge of paper mills and the addition of a surfactant to increase the yield |
RU2531914C1 (ru) * | 2013-03-18 | 2014-10-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Российский государственный аграрный университет-МСХА имени К.А. Тимирязева" (ФГБОУ ВПО РГАУ-МСХА имени К.А. Тимирязева) | Способ санитарной обработки доильного оборудования |
MY176177A (en) * | 2013-09-13 | 2020-07-24 | Basf Se | Mixtures of enantiomers, and process for making such mixtures |
MX2016007729A (es) | 2013-12-13 | 2017-08-04 | Basf Se | Microorganismo recombinante para la produccion mejorada de productos quimicos finos. |
SI2902544T1 (sl) * | 2014-01-30 | 2017-09-29 | Archroma France Sas | Vodni sestavek, ki obsega polivalentno kovino, ki tvori komplekse s kabonatnimi ligandi in ligandi karboksilne kisline, ter njegova uporaba |
US9951363B2 (en) | 2014-03-14 | 2018-04-24 | The Research Foundation for the State University of New York College of Environmental Science and Forestry | Enzymatic hydrolysis of old corrugated cardboard (OCC) fines from recycled linerboard mill waste rejects |
MX2017011976A (es) | 2015-03-18 | 2018-02-09 | Basf Se | Microorganismo recombinante para la produccion mejorada de quimicos finos. |
KR20180008545A (ko) * | 2015-05-13 | 2018-01-24 | 바스프 에스이 | 킬레이트제의 혼합물의 제조 방법 |
RU2017146342A (ru) | 2015-06-04 | 2019-07-10 | Басф Се | Рекомбинантный микроорганизм для улучшенного получения химических продуктов тонкого органического синтеза |
CN107690478B (zh) | 2015-06-12 | 2023-02-03 | 巴斯夫欧洲公司 | 用于改善丙氨酸生产的重组微生物 |
CN111630143A (zh) | 2018-01-30 | 2020-09-04 | 伊士曼化工公司 | 包含氨基羧酸类螯合剂的组合物 |
DE102019124958B4 (de) | 2019-09-17 | 2023-03-23 | Zschimmer & Schwarz Mohsdorf GmbH & Co. KG. | Phosphonsäurederivate und Verfahren zu deren Herstellung |
PL3822335T3 (pl) | 2019-11-15 | 2023-03-13 | Basf Se | Kompozycje czyszczące i ich zastosowanie |
US20240300887A1 (en) | 2021-01-15 | 2024-09-12 | Basf Se | Process for manufacturing carboxylic acids |
US20230008538A1 (en) | 2021-06-30 | 2023-01-12 | Ascend Performance Materials Operations Llc | Process for preparing nitrile intermediates for nitrogen-containing chelators |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2500019A (en) * | 1946-10-08 | 1950-03-07 | Frederick C Bersworth | Method of producing polycarboxylic amino acids |
NL6713990A (ja) * | 1966-10-20 | 1968-04-22 | ||
DE1643238C3 (de) * | 1967-08-16 | 1974-09-05 | Basf Ag, 6700 Ludwigshafen | Verfahren zur kontinuierlichen Herstellung von Alkalisalzen der Nitrilotriessigsäure |
FR2051931A5 (ja) * | 1969-07-02 | 1971-04-09 | Pechiney Saint Gobain | |
FR2057682A5 (ja) | 1969-08-26 | 1971-05-21 | Grace W R Ltd | |
US3733355A (en) | 1970-07-28 | 1973-05-15 | Hooker Chemical Corp | Production of nitrilotriacetic acid and the analogs therefor |
US3969257A (en) * | 1971-07-23 | 1976-07-13 | Colgate-Palmolive Company | Washing and bleaching composition containing bleach, activator and a nitrilotricarboxylic acid compound |
US3961932A (en) * | 1974-01-07 | 1976-06-08 | Ciba-Geigy Corporation | Process for coating granular fertilizers with chelated micronutrients |
US4001133A (en) * | 1974-11-04 | 1977-01-04 | Basf Wyandotte Corporation | Method of washing glassware and inhibited cleaning solution and additive composition useful therein |
US4066517A (en) * | 1976-03-11 | 1978-01-03 | Oxy Metal Industries Corporation | Electrodeposition of palladium |
JPS5346915A (en) * | 1976-10-09 | 1978-04-27 | Nitto Chem Ind Co Ltd | Preparation of alkali salt of aminopolyacetic acid |
DE2834629A1 (de) | 1978-08-08 | 1980-02-28 | Standard Elektrik Lorenz Ag | Ablenkjochhalterung |
JPS55160099A (en) * | 1979-05-18 | 1980-12-12 | Kureha Chemical Ind Co Ltd | Detergent composition |
JPS55157695A (en) * | 1979-05-18 | 1980-12-08 | Kureha Chemical Ind Co Ltd | Detergent composition |
US4287080A (en) * | 1979-09-17 | 1981-09-01 | The Procter & Gamble Company | Detergent compositions which contain certain tertiary alcohols |
JPS5851994B2 (ja) * | 1979-12-05 | 1983-11-19 | 呉羽化学工業株式会社 | 無リン洗剤組成物 |
GR77131B (ja) * | 1982-03-10 | 1984-09-07 | Procter & Gamble | |
US4769168A (en) * | 1985-08-05 | 1988-09-06 | Colgate-Palmolive Company | Low phosphate or phosphate free nonaqueous liquid nonionic laundry detergent composition and method of use |
DE3531563A1 (de) * | 1985-09-04 | 1987-03-05 | Benckiser Knapsack Gmbh | Holzstoffbleiche |
US4806263A (en) * | 1986-01-02 | 1989-02-21 | Ppg Industries, Inc. | Fungicidal and algicidal detergent compositions |
DE3706823A1 (de) * | 1986-03-04 | 1987-09-10 | Fuji Photo Film Co Ltd | Verfahren zur ausbildung eines farbbildes |
DE3712329A1 (de) * | 1987-04-11 | 1988-10-20 | Basf Ag | Verfahren zur herstellung von serin-n,n-diessigsaeure und derivaten, ihre verwendung insbesondere als komplexbildner und diese enthaltende wasch- und reinigungsmittel |
DE3829847A1 (de) * | 1988-09-02 | 1990-03-15 | Basf Ag | Wasch- und reinigungsmittel |
DE3838093A1 (de) * | 1988-11-10 | 1990-05-17 | Basf Ag | Verwendung von copolymerisaten als zusatz zu fluessigwaschmitteln |
DE3914980A1 (de) * | 1989-05-06 | 1990-12-06 | Basf Ag | 2-methyl- und 2-hydroxymethyl-serin-n,n-diessigsaeure und ihre derivate |
CA2027518A1 (en) * | 1990-10-03 | 1992-04-04 | Richard L. Tadsen | Process for preparing high density detergent compositions containing particulate ph sensitive surfactant |
US5177243A (en) * | 1991-12-12 | 1993-01-05 | W. R. Grace & Co.-Conn. | N,N'-diacetic acid-N'-cyanomethyl, salts thereof, and their preparation |
EP0553569B1 (en) * | 1991-12-27 | 1996-12-04 | Konica Corporation | Method for processing silver halide color photographic light-sensitive materials |
CZ280524B6 (cs) * | 1992-01-17 | 1996-02-14 | Unilever Nv | Částicové detergenční směsi |
DE4211713A1 (de) * | 1992-04-08 | 1993-10-14 | Basf Ag | Verfahren zur Herstellung von Aminodicarbonsäure-N,N-diessigsäuren |
DE4319935A1 (de) * | 1993-06-16 | 1994-12-22 | Basf Ag | Verwendung von Glycin-N,N-diessigsäure-Derivaten als Komplexbildner für Erdalkali- und Schwermetallionen |
US5481018A (en) * | 1995-03-31 | 1996-01-02 | The Dow Chemical Company | Amino nitrile intermediate for the preparation of alanine diacetic acid |
DE19518986A1 (de) * | 1995-05-29 | 1996-12-05 | Basf Ag | Verfahren zur Herstellung von Glycin-N,N-diessigsäure-Derivaten durch Umsetzung von Glycinderivaten oder deren Vorstufen mit Formaldehyd und Cyanwasserstoff oder von Iminodiacetonitril oder Imindodiessigsäure mit entsprechenden Aldehyden und Cyanwasserstoff in wäßrig-saurem Medium |
-
1993
- 1993-06-16 DE DE4319935A patent/DE4319935A1/de not_active Withdrawn
-
1994
- 1994-06-07 AT AT97101598T patent/ATE257466T1/de active
- 1994-06-07 DE DE59410198T patent/DE59410198D1/de not_active Expired - Lifetime
- 1994-06-07 EP EP97122735A patent/EP0846753B1/de not_active Expired - Lifetime
- 1994-06-07 DE DE59410351T patent/DE59410351D1/de not_active Expired - Lifetime
- 1994-06-07 AT AT97122735T patent/ATE226241T1/de active
- 1994-06-07 WO PCT/EP1994/001838 patent/WO1994029421A1/de active IP Right Grant
- 1994-06-07 US US08/545,768 patent/US5786313A/en not_active Expired - Lifetime
- 1994-06-07 AT AT94920434T patent/ATE196921T1/de active
- 1994-06-07 DK DK94920434T patent/DK0703971T3/da active
- 1994-06-07 DK DK97122735T patent/DK0846753T3/da active
- 1994-06-07 CA CA002162122A patent/CA2162122C/en not_active Expired - Lifetime
- 1994-06-07 EP EP97101598A patent/EP0781762B1/de not_active Expired - Lifetime
- 1994-06-07 EP EP03008611A patent/EP1334961A1/de not_active Withdrawn
- 1994-06-07 ES ES97122735T patent/ES2184955T3/es not_active Expired - Lifetime
- 1994-06-07 ES ES94920434T patent/ES2151551T3/es not_active Expired - Lifetime
- 1994-06-07 EP EP94920434A patent/EP0703971B1/de not_active Expired - Lifetime
- 1994-06-07 ES ES97101598T patent/ES2214562T3/es not_active Expired - Lifetime
- 1994-06-07 DK DK97101598T patent/DK0781762T3/da active
- 1994-06-07 DE DE59409549T patent/DE59409549D1/de not_active Expired - Lifetime
- 1994-06-07 JP JP50130695A patent/JP3615546B2/ja not_active Expired - Lifetime
- 1994-06-07 EP EP99111836A patent/EP0976818A1/de not_active Withdrawn
-
1998
- 1998-05-06 US US09/073,244 patent/US6008176A/en not_active Expired - Lifetime
- 1998-05-06 US US09/073,243 patent/US6005141A/en not_active Expired - Lifetime
-
2004
- 2004-07-12 JP JP2004204856A patent/JP4243225B2/ja not_active Expired - Lifetime
-
2008
- 2008-03-10 JP JP2008059565A patent/JP4741622B2/ja not_active Expired - Lifetime
-
2011
- 2011-02-18 JP JP2011033296A patent/JP2011148802A/ja active Pending
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011148802A (ja) * | 1993-06-16 | 2011-08-04 | Basf Se | アルカリ土類金属−及び重金属イオンのための生物学的に分解可能な錯化剤としてのグリシン−n,n−二酢酸−誘導体の製法 |
US6174852B1 (en) | 1996-01-22 | 2001-01-16 | Kao Corporation | High-density powdered detergent composition |
JPH10175929A (ja) * | 1996-11-29 | 1998-06-30 | Basf Ag | 十分に低い吸湿性を有するグリシン−n,n−ジ酢酸誘導体からの結晶性固体の製造法 |
JPH1135978A (ja) * | 1997-05-19 | 1999-02-09 | Kao Corp | 漂白剤含有洗剤組成物 |
JP2001514164A (ja) * | 1997-08-21 | 2001-09-11 | ビーエーエスエフ アクチェンゲゼルシャフト | 長鎖グリシン−n,n−二酢酸誘導体の製造方法 |
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ATE196921T1 (de) | 2000-10-15 |
EP0781762B1 (de) | 2004-01-07 |
JP2011148802A (ja) | 2011-08-04 |
JP4243225B2 (ja) | 2009-03-25 |
ES2184955T3 (es) | 2003-04-16 |
EP0846753A1 (de) | 1998-06-10 |
DE4319935A1 (de) | 1994-12-22 |
EP0976818A1 (de) | 2000-02-02 |
ATE226241T1 (de) | 2002-11-15 |
ES2214562T3 (es) | 2004-09-16 |
JP4741622B2 (ja) | 2011-08-03 |
EP0846753B1 (de) | 2002-10-16 |
EP0703971A1 (de) | 1996-04-03 |
JP2004323533A (ja) | 2004-11-18 |
EP1334961A1 (de) | 2003-08-13 |
JP2008247902A (ja) | 2008-10-16 |
WO1994029421A1 (de) | 1994-12-22 |
EP0703971B1 (de) | 2000-10-11 |
DK0846753T3 (da) | 2002-11-04 |
ATE257466T1 (de) | 2004-01-15 |
US6005141A (en) | 1999-12-21 |
DE59409549D1 (de) | 2000-11-16 |
EP0781762A1 (de) | 1997-07-02 |
DE59410351D1 (de) | 2004-02-12 |
US5786313A (en) | 1998-07-28 |
CA2162122C (en) | 2005-11-22 |
ES2151551T3 (es) | 2001-01-01 |
DE59410198D1 (de) | 2002-11-21 |
US6008176A (en) | 1999-12-28 |
JP3615546B2 (ja) | 2005-02-02 |
DK0781762T3 (da) | 2004-03-08 |
DK0703971T3 (da) | 2000-11-13 |
CA2162122A1 (en) | 1994-12-22 |
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