JPH0477305B2 - - Google Patents
Info
- Publication number
- JPH0477305B2 JPH0477305B2 JP10152383A JP10152383A JPH0477305B2 JP H0477305 B2 JPH0477305 B2 JP H0477305B2 JP 10152383 A JP10152383 A JP 10152383A JP 10152383 A JP10152383 A JP 10152383A JP H0477305 B2 JPH0477305 B2 JP H0477305B2
- Authority
- JP
- Japan
- Prior art keywords
- isothiazolone
- group
- colloidal silver
- methyl
- aqueous
- 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.)
- Expired
Links
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 31
- 150000001875 compounds Chemical class 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims description 2
- 125000005116 aryl carbamoyl group Chemical group 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000000084 colloidal system Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 13
- -1 silver halide Chemical class 0.000 description 12
- 230000001681 protective effect Effects 0.000 description 9
- 241000894006 Bacteria Species 0.000 description 8
- 230000002335 preservative effect Effects 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 239000003755 preservative agent Substances 0.000 description 7
- 229910052709 silver Inorganic materials 0.000 description 7
- 239000004332 silver Substances 0.000 description 7
- 108010010803 Gelatin Proteins 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 239000008273 gelatin Substances 0.000 description 6
- 229920000159 gelatin Polymers 0.000 description 6
- 235000019322 gelatine Nutrition 0.000 description 6
- 235000011852 gelatine desserts Nutrition 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 244000005700 microbiome Species 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000035945 sensitivity Effects 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 239000003429 antifungal agent Substances 0.000 description 3
- 229940121375 antifungal agent Drugs 0.000 description 3
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 230000001954 sterilising effect Effects 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- HKJBTCVEERVODK-UHFFFAOYSA-N 2-[(2-chlorophenyl)methyl]-1,2-thiazol-3-one Chemical compound ClC1=CC=CC=C1CN1C(=O)C=CS1 HKJBTCVEERVODK-UHFFFAOYSA-N 0.000 description 2
- NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 description 2
- SPOCKFADQXUWGS-UHFFFAOYSA-N 3-oxo-n-propyl-1,2-thiazole-2-carboxamide Chemical compound CCCNC(=O)N1SC=CC1=O SPOCKFADQXUWGS-UHFFFAOYSA-N 0.000 description 2
- 244000215068 Acacia senegal Species 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- 102000009027 Albumins Human genes 0.000 description 2
- 108010088751 Albumins Proteins 0.000 description 2
- 229920000084 Gum arabic Polymers 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 229930193140 Neomycin Natural products 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000005844 Thymol Substances 0.000 description 2
- 239000000205 acacia gum Substances 0.000 description 2
- 235000010489 acacia gum Nutrition 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 2
- 229940101006 anhydrous sodium sulfite Drugs 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 230000000843 anti-fungal effect Effects 0.000 description 2
- 229940088710 antibiotic agent Drugs 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003125 aqueous solvent Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 229960000318 kanamycin Drugs 0.000 description 2
- 229930027917 kanamycin Natural products 0.000 description 2
- SBUJHOSQTJFQJX-NOAMYHISSA-N kanamycin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SBUJHOSQTJFQJX-NOAMYHISSA-N 0.000 description 2
- 229930182823 kanamycin A Natural products 0.000 description 2
- 150000002731 mercury compounds Chemical class 0.000 description 2
- 229920005615 natural polymer Polymers 0.000 description 2
- 229960004927 neomycin Drugs 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 229960000790 thymol Drugs 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- 229920003170 water-soluble synthetic polymer Polymers 0.000 description 2
- GVEYRUKUJCHJSR-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C(C)=C1 GVEYRUKUJCHJSR-UHFFFAOYSA-N 0.000 description 1
- DHPRQBPJLMKORJ-XRNKAMNCSA-N (4s,4as,5as,6s,12ar)-7-chloro-4-(dimethylamino)-1,6,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide Chemical compound C1=CC(Cl)=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]4(O)C(=O)C3=C(O)C2=C1O DHPRQBPJLMKORJ-XRNKAMNCSA-N 0.000 description 1
- JCIIKRHCWVHVFF-UHFFFAOYSA-N 1,2,4-thiadiazol-5-amine;hydrochloride Chemical compound Cl.NC1=NC=NS1 JCIIKRHCWVHVFF-UHFFFAOYSA-N 0.000 description 1
- RULKYXXCCZZKDZ-UHFFFAOYSA-N 2,3,4,5-tetrachlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C(Cl)=C1Cl RULKYXXCCZZKDZ-UHFFFAOYSA-N 0.000 description 1
- HSQFVBWFPBKHEB-UHFFFAOYSA-N 2,3,4-trichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1Cl HSQFVBWFPBKHEB-UHFFFAOYSA-N 0.000 description 1
- RWZBSRKRYSOIAS-UHFFFAOYSA-N 2,4-dimethyl-1,2-thiazol-3-one Chemical compound CC1=CSN(C)C1=O RWZBSRKRYSOIAS-UHFFFAOYSA-N 0.000 description 1
- BDOOJCJSTQZQDM-UHFFFAOYSA-N 2-(1-phenylethyl)-1,2-thiazol-3-one Chemical compound S1C=CC(=O)N1C(C)C1=CC=CC=C1 BDOOJCJSTQZQDM-UHFFFAOYSA-N 0.000 description 1
- WDZJNLOCKSPDFK-UHFFFAOYSA-N 2-(2,4,4-trimethylpentan-2-yl)-1,2-thiazol-3-one Chemical compound CC(C)(C)CC(C)(C)N1SC=CC1=O WDZJNLOCKSPDFK-UHFFFAOYSA-N 0.000 description 1
- VDYGJABWVCDOMW-UHFFFAOYSA-N 2-(2-ethoxyhexyl)-1,2-thiazol-3-one Chemical compound CCCCC(OCC)CN1SC=CC1=O VDYGJABWVCDOMW-UHFFFAOYSA-N 0.000 description 1
- HSFILUIYMMOOFQ-UHFFFAOYSA-N 2-(2-phenylethyl)-1,2-thiazol-3-one Chemical compound O=C1C=CSN1CCC1=CC=CC=C1 HSFILUIYMMOOFQ-UHFFFAOYSA-N 0.000 description 1
- KBBVCHDMBBVVCS-UHFFFAOYSA-N 2-(3,4-dichlorophenyl)-1,2-thiazol-3-one Chemical compound C1=C(Cl)C(Cl)=CC=C1N1C(=O)C=CS1 KBBVCHDMBBVVCS-UHFFFAOYSA-N 0.000 description 1
- ZDWLTASUXFDUOP-UHFFFAOYSA-N 2-(3,4-dichlorophenyl)-4-methyl-1,2-thiazol-3-one Chemical compound O=C1C(C)=CSN1C1=CC=C(Cl)C(Cl)=C1 ZDWLTASUXFDUOP-UHFFFAOYSA-N 0.000 description 1
- NFSXZGMSASBOHO-UHFFFAOYSA-N 2-(4-nitrophenyl)-1,2-thiazol-3-one Chemical compound C1=CC([N+](=O)[O-])=CC=C1N1C(=O)C=CS1 NFSXZGMSASBOHO-UHFFFAOYSA-N 0.000 description 1
- OPMCKYBELMAPEN-UHFFFAOYSA-N 2-(hydroxymethyl)-1,2-thiazol-3-one Chemical compound OCN1SC=CC1=O OPMCKYBELMAPEN-UHFFFAOYSA-N 0.000 description 1
- JGWRIEPVQMQWHX-UHFFFAOYSA-N 2-[(2,4-dichlorophenyl)methyl]-1,2-thiazol-3-one Chemical compound ClC1=CC(Cl)=CC=C1CN1C(=O)C=CS1 JGWRIEPVQMQWHX-UHFFFAOYSA-N 0.000 description 1
- YQMPKMMIBGGAJX-UHFFFAOYSA-N 2-[(3,4-dichlorophenyl)methyl]-1,2-thiazol-3-one Chemical compound C1=C(Cl)C(Cl)=CC=C1CN1C(=O)C=CS1 YQMPKMMIBGGAJX-UHFFFAOYSA-N 0.000 description 1
- PQIJDRCKMJCOFO-UHFFFAOYSA-N 2-[(4-chlorophenyl)methyl]-1,2-thiazol-3-one Chemical compound C1=CC(Cl)=CC=C1CN1C(=O)C=CS1 PQIJDRCKMJCOFO-UHFFFAOYSA-N 0.000 description 1
- ZJJDXJDCYJWVAY-UHFFFAOYSA-N 2-[(4-methoxyphenyl)methyl]-1,2-thiazol-3-one Chemical compound C1=CC(OC)=CC=C1CN1C(=O)C=CS1 ZJJDXJDCYJWVAY-UHFFFAOYSA-N 0.000 description 1
- VZZAUYDBJJHFFD-UHFFFAOYSA-N 2-[(4-methylphenyl)methyl]-1,2-thiazol-3-one Chemical compound C1=CC(C)=CC=C1CN1C(=O)C=CS1 VZZAUYDBJJHFFD-UHFFFAOYSA-N 0.000 description 1
- FOSBHMCQJMDNIE-UHFFFAOYSA-N 2-[2-(diethylamino)ethyl]-1,2-thiazol-3-one Chemical compound CCN(CC)CCN1SC=CC1=O FOSBHMCQJMDNIE-UHFFFAOYSA-N 0.000 description 1
- BAPMGYBFLAMFTH-UHFFFAOYSA-N 2-benzyl-1,2-thiazol-3-one;2-chloroacetic acid Chemical compound OC(=O)CCl.O=C1C=CSN1CC1=CC=CC=C1 BAPMGYBFLAMFTH-UHFFFAOYSA-N 0.000 description 1
- JXDBZXGTFLLJPZ-UHFFFAOYSA-N 2-benzyl-1,2-thiazol-3-one;hydrochloride Chemical compound Cl.O=C1C=CSN1CC1=CC=CC=C1 JXDBZXGTFLLJPZ-UHFFFAOYSA-N 0.000 description 1
- JWPUURGEVMUUAB-UHFFFAOYSA-N 2-benzyl-4,5-dichloro-1,2-thiazol-3-one Chemical compound O=C1C(Cl)=C(Cl)SN1CC1=CC=CC=C1 JWPUURGEVMUUAB-UHFFFAOYSA-N 0.000 description 1
- BXQOWUSZAWCFIL-UHFFFAOYSA-N 2-benzyl-5-chloro-1,2-thiazol-3-one Chemical compound S1C(Cl)=CC(=O)N1CC1=CC=CC=C1 BXQOWUSZAWCFIL-UHFFFAOYSA-N 0.000 description 1
- CDMGNVWZXRKJNS-UHFFFAOYSA-N 2-benzylphenol Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1 CDMGNVWZXRKJNS-UHFFFAOYSA-N 0.000 description 1
- TYBHZVUFOINFDV-UHFFFAOYSA-N 2-bromo-6-[(3-bromo-5-chloro-2-hydroxyphenyl)methyl]-4-chlorophenol Chemical compound OC1=C(Br)C=C(Cl)C=C1CC1=CC(Cl)=CC(Br)=C1O TYBHZVUFOINFDV-UHFFFAOYSA-N 0.000 description 1
- CRTPTZMJMAGFEQ-UHFFFAOYSA-N 2-butyl-1,2-thiazol-3-one Chemical compound CCCCN1SC=CC1=O CRTPTZMJMAGFEQ-UHFFFAOYSA-N 0.000 description 1
- ATGFZSOBDDZEEX-UHFFFAOYSA-N 2-chloro-3-hydroxypropanamide Chemical compound NC(=O)C(Cl)CO ATGFZSOBDDZEEX-UHFFFAOYSA-N 0.000 description 1
- QSKPIOLLBIHNAC-UHFFFAOYSA-N 2-chloro-acetaldehyde Chemical compound ClCC=O QSKPIOLLBIHNAC-UHFFFAOYSA-N 0.000 description 1
- FBKMKGRPLVLSKT-UHFFFAOYSA-N 2-chloroacetic acid;2-ethyl-1,2-thiazol-3-one Chemical compound OC(=O)CCl.CCN1SC=CC1=O FBKMKGRPLVLSKT-UHFFFAOYSA-N 0.000 description 1
- DZHDHUNDWJEBHD-UHFFFAOYSA-N 2-chloroacetic acid;2-propyl-1,2-thiazol-3-one Chemical compound OC(=O)CCl.CCCN1SC=CC1=O DZHDHUNDWJEBHD-UHFFFAOYSA-N 0.000 description 1
- UGMFIVLELIRKDJ-UHFFFAOYSA-N 2-chloroacetic acid;4,5-dichloro-2-methyl-1,2-thiazol-3-one Chemical compound OC(=O)CCl.CN1SC(Cl)=C(Cl)C1=O UGMFIVLELIRKDJ-UHFFFAOYSA-N 0.000 description 1
- HHPJKICDWHTLAV-UHFFFAOYSA-N 2-cyclohexyl-1,2-thiazol-3-one Chemical compound O=C1C=CSN1C1CCCCC1 HHPJKICDWHTLAV-UHFFFAOYSA-N 0.000 description 1
- CRBWEAMRKIUGDJ-UHFFFAOYSA-N 2-decyl-1,2-thiazol-3-one Chemical compound CCCCCCCCCCN1SC=CC1=O CRBWEAMRKIUGDJ-UHFFFAOYSA-N 0.000 description 1
- XNZFZRQEAZMSIS-UHFFFAOYSA-N 2-dodecyl-1,2-thiazol-3-one Chemical compound CCCCCCCCCCCCN1SC=CC1=O XNZFZRQEAZMSIS-UHFFFAOYSA-N 0.000 description 1
- DGMOJBDBTHWNLQ-UHFFFAOYSA-N 2-ethyl-1,2-thiazol-3-one;hydrochloride Chemical compound Cl.CCN1SC=CC1=O DGMOJBDBTHWNLQ-UHFFFAOYSA-N 0.000 description 1
- SJXPQSRCFCPWQQ-UHFFFAOYSA-N 2-methyl-1,2-thiazol-2-ium-3-ol;chloride Chemical compound Cl.CN1SC=CC1=O SJXPQSRCFCPWQQ-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- MIHXBHVZQQCTJN-UHFFFAOYSA-N 2-nonyl-1,2-thiazol-3-one Chemical compound CCCCCCCCCN1SC=CC1=O MIHXBHVZQQCTJN-UHFFFAOYSA-N 0.000 description 1
- LYISSSDBZDHABC-UHFFFAOYSA-N 2-phenylmethoxy-1,2-thiazol-3-one Chemical compound O=C1C=CSN1OCC1=CC=CC=C1 LYISSSDBZDHABC-UHFFFAOYSA-N 0.000 description 1
- PXCPEUSDGQTUFR-UHFFFAOYSA-N 2-propyl-1,2-thiazol-3-one Chemical compound CCCN1SC=CC1=O PXCPEUSDGQTUFR-UHFFFAOYSA-N 0.000 description 1
- RDOHZSIGJDHYAK-UHFFFAOYSA-N 2-propyl-1,2-thiazol-3-one;hydrochloride Chemical compound Cl.CCCN1SC=CC1=O RDOHZSIGJDHYAK-UHFFFAOYSA-N 0.000 description 1
- ODQNPFWWAYSDOI-UHFFFAOYSA-N 2-tert-butyl-1,2-thiazol-3-one Chemical compound CC(C)(C)N1SC=CC1=O ODQNPFWWAYSDOI-UHFFFAOYSA-N 0.000 description 1
- KXMGZPAPNMJPEM-UHFFFAOYSA-N 2-tetradecyl-1,2-thiazol-3-one Chemical compound CCCCCCCCCCCCCCN1SC=CC1=O KXMGZPAPNMJPEM-UHFFFAOYSA-N 0.000 description 1
- AHOMZCSSNNRYQR-UHFFFAOYSA-N 3-oxo-n-(2,4,4-trimethylpentan-2-yl)-1,2-thiazole-2-carboxamide Chemical compound CC(C)(C)CC(C)(C)NC(=O)N1SC=CC1=O AHOMZCSSNNRYQR-UHFFFAOYSA-N 0.000 description 1
- CVZDIUZSWUDGOP-UHFFFAOYSA-N 4,5-dichloro-2-methyl-1,2-thiazol-3-one Chemical compound CN1SC(Cl)=C(Cl)C1=O CVZDIUZSWUDGOP-UHFFFAOYSA-N 0.000 description 1
- RGEWBAOMRJHBFF-UHFFFAOYSA-N 4-bromo-2-(2,4,4-trimethylpentan-2-yl)-1,2-thiazol-3-one Chemical compound CC(C)(C)CC(C)(C)N1SC=C(Br)C1=O RGEWBAOMRJHBFF-UHFFFAOYSA-N 0.000 description 1
- PRIJDALNOVDQCY-UHFFFAOYSA-N 4-bromo-2-methyl-1,2-thiazol-3-one Chemical compound CN1SC=C(Br)C1=O PRIJDALNOVDQCY-UHFFFAOYSA-N 0.000 description 1
- XVHUCXHOUDYBOE-UHFFFAOYSA-N 4-bromo-5-chloro-2-methyl-1,2-thiazol-3-one Chemical compound CN1SC(Cl)=C(Br)C1=O XVHUCXHOUDYBOE-UHFFFAOYSA-N 0.000 description 1
- DZTBMORSQXCVFC-UHFFFAOYSA-N 4-bromo-n,5-dimethyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CNC(=O)N1SC(C)=C(Br)C1=O DZTBMORSQXCVFC-UHFFFAOYSA-N 0.000 description 1
- VMEMFXKGJHGWOF-UHFFFAOYSA-N 4-bromo-n-(3-chlorophenyl)-5-methyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound O=C1C(Br)=C(C)SN1C(=O)NC1=CC=CC(Cl)=C1 VMEMFXKGJHGWOF-UHFFFAOYSA-N 0.000 description 1
- DHNFRLYEKYPHRT-UHFFFAOYSA-N 4-bromo-n-methyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CNC(=O)N1SC=C(Br)C1=O DHNFRLYEKYPHRT-UHFFFAOYSA-N 0.000 description 1
- CNJYTSGDZSDJIO-UHFFFAOYSA-N 4-chloro-2-(2,4,4-trimethylpentan-2-yl)-1,2-thiazol-3-one Chemical compound CC(C)(C)CC(C)(C)N1SC=C(Cl)C1=O CNJYTSGDZSDJIO-UHFFFAOYSA-N 0.000 description 1
- CLSNLNBXJUIEFP-UHFFFAOYSA-N 4-chloro-2-(2-phenylethyl)-1,2-thiazol-3-one Chemical compound O=C1C(Cl)=CSN1CCC1=CC=CC=C1 CLSNLNBXJUIEFP-UHFFFAOYSA-N 0.000 description 1
- CFKMVGJGLGKFKI-UHFFFAOYSA-N 4-chloro-m-cresol Chemical compound CC1=CC(O)=CC=C1Cl CFKMVGJGLGKFKI-UHFFFAOYSA-N 0.000 description 1
- ZKQFIKZAIBLJKG-UHFFFAOYSA-N 4-cyano-5-methylsulfanyl-3-oxo-n-phenyl-1,2-thiazole-2-carboxamide Chemical compound O=C1C(C#N)=C(SC)SN1C(=O)NC1=CC=CC=C1 ZKQFIKZAIBLJKG-UHFFFAOYSA-N 0.000 description 1
- XEONYUQRPSZQEQ-UHFFFAOYSA-N 4-cyano-n-methyl-5-methylsulfanyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CNC(=O)N1SC(SC)=C(C#N)C1=O XEONYUQRPSZQEQ-UHFFFAOYSA-N 0.000 description 1
- XCBZZWIBCAJCRB-UHFFFAOYSA-N 4-cyano-n-methyl-5-methylsulfinyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CNC(=O)N1SC(S(C)=O)=C(C#N)C1=O XCBZZWIBCAJCRB-UHFFFAOYSA-N 0.000 description 1
- WFJIVOKAWHGMBH-UHFFFAOYSA-N 4-hexylbenzene-1,3-diol Chemical compound CCCCCCC1=CC=C(O)C=C1O WFJIVOKAWHGMBH-UHFFFAOYSA-N 0.000 description 1
- QGVYXKVTIVOQMD-UHFFFAOYSA-N 5-(bromomethyl)-n-(2-chlorophenyl)-3-oxo-1,2-thiazole-2-carboxamide Chemical compound ClC1=CC=CC=C1NC(=O)N1C(=O)C=C(CBr)S1 QGVYXKVTIVOQMD-UHFFFAOYSA-N 0.000 description 1
- RGVYUPIYFIVQDS-UHFFFAOYSA-N 5-chloro-2-methyl-1,2-thiazol-3-one;hydron;chloride Chemical compound Cl.CN1SC(Cl)=CC1=O RGVYUPIYFIVQDS-UHFFFAOYSA-N 0.000 description 1
- PTMXFIUOGSODQW-UHFFFAOYSA-N 5-chloro-2-octyl-1,2-thiazol-3-one Chemical compound CCCCCCCCN1SC(Cl)=CC1=O PTMXFIUOGSODQW-UHFFFAOYSA-N 0.000 description 1
- VGUWNJNTWIWNMW-UHFFFAOYSA-N 5-chloro-n-ethyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CCNC(=O)N1SC(Cl)=CC1=O VGUWNJNTWIWNMW-UHFFFAOYSA-N 0.000 description 1
- KOMDQYIUYIJDDB-UHFFFAOYSA-N 5-methyl-3-oxo-n-phenyl-1,2-thiazole-2-carboxamide Chemical compound S1C(C)=CC(=O)N1C(=O)NC1=CC=CC=C1 KOMDQYIUYIJDDB-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 125000004442 acylamino group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 239000012615 aggregate Substances 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 1
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 125000005129 aryl carbonyl group Chemical group 0.000 description 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
- 125000005135 aryl sulfinyl group Chemical group 0.000 description 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 description 1
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 description 1
- 125000005110 aryl thio group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- XNSQZBOCSSMHSZ-UHFFFAOYSA-K azane;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate;iron(3+) Chemical compound [NH4+].[Fe+3].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O XNSQZBOCSSMHSZ-UHFFFAOYSA-K 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- KDPAWGWELVVRCH-UHFFFAOYSA-M bromoacetate Chemical compound [O-]C(=O)CBr KDPAWGWELVVRCH-UHFFFAOYSA-M 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-M chloroacetate Chemical compound [O-]C(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-M 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000000586 desensitisation Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- KYQODXQIAJFKPH-UHFFFAOYSA-N diazanium;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [NH4+].[NH4+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O KYQODXQIAJFKPH-UHFFFAOYSA-N 0.000 description 1
- 229960003887 dichlorophen Drugs 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- GUFHJFUHANRFRH-UHFFFAOYSA-N ethyl 2-[(3-oxo-1,2-thiazole-2-carbonyl)amino]acetate Chemical compound CCOC(=O)CNC(=O)N1SC=CC1=O GUFHJFUHANRFRH-UHFFFAOYSA-N 0.000 description 1
- BZBRYBISKLKJCA-UHFFFAOYSA-N ethyl 4-(3-oxo-1,2-thiazol-2-yl)benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1N1C(=O)C=CS1 BZBRYBISKLKJCA-UHFFFAOYSA-N 0.000 description 1
- CHHJLHHGJRFBFL-UHFFFAOYSA-N ethyl N-(carbamothioylamino)-N-(carbamoylamino)carbamate Chemical compound CCOC(=O)N(NC(N)=O)NC(N)=S CHHJLHHGJRFBFL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000005165 hydroxybenzoic acids Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- YHQQLGSJVCQKPR-UHFFFAOYSA-N n'-benzyl-n'-(nitromethyl)ethane-1,2-diamine Chemical compound NCCN(C[N+]([O-])=O)CC1=CC=CC=C1 YHQQLGSJVCQKPR-UHFFFAOYSA-N 0.000 description 1
- JDBGUOYETQDGBL-UHFFFAOYSA-N n,5-dimethyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CNC(=O)N1SC(C)=CC1=O JDBGUOYETQDGBL-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- SETSHPKWWPIJQT-UHFFFAOYSA-N n-(2-chlorophenyl)-5-methyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound S1C(C)=CC(=O)N1C(=O)NC1=CC=CC=C1Cl SETSHPKWWPIJQT-UHFFFAOYSA-N 0.000 description 1
- WGYAVEROXSCCDD-UHFFFAOYSA-N n-(2-methoxyphenyl)-3-oxo-1,2-thiazole-2-carboxamide Chemical compound COC1=CC=CC=C1NC(=O)N1C(=O)C=CS1 WGYAVEROXSCCDD-UHFFFAOYSA-N 0.000 description 1
- PKQAXRYBQYEDCD-UHFFFAOYSA-N n-(3-chlorophenyl)-3-oxo-1,2-thiazole-2-carboxamide Chemical compound ClC1=CC=CC(NC(=O)N2C(C=CS2)=O)=C1 PKQAXRYBQYEDCD-UHFFFAOYSA-N 0.000 description 1
- ZLJITXLJFQVLKX-UHFFFAOYSA-N n-(3-chlorophenyl)-4-cyano-5-methylsulfanyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound O=C1C(C#N)=C(SC)SN1C(=O)NC1=CC=CC(Cl)=C1 ZLJITXLJFQVLKX-UHFFFAOYSA-N 0.000 description 1
- VPGPOJYDQBKTOH-UHFFFAOYSA-N n-(3-chlorophenyl)-5-methyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound S1C(C)=CC(=O)N1C(=O)NC1=CC=CC(Cl)=C1 VPGPOJYDQBKTOH-UHFFFAOYSA-N 0.000 description 1
- JIHBJVYDJRUMEP-UHFFFAOYSA-N n-(3-nitrophenyl)-3-oxo-1,2-thiazole-2-carboxamide Chemical compound [O-][N+](=O)C1=CC=CC(NC(=O)N2C(C=CS2)=O)=C1 JIHBJVYDJRUMEP-UHFFFAOYSA-N 0.000 description 1
- HMJKGINKCNRDPP-UHFFFAOYSA-N n-(4-methoxyphenyl)-3-oxo-1,2-thiazole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1NC(=O)N1C(=O)C=CS1 HMJKGINKCNRDPP-UHFFFAOYSA-N 0.000 description 1
- HQPSBTFNKVNNSM-UHFFFAOYSA-N n-butyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CCCCNC(=O)N1SC=CC1=O HQPSBTFNKVNNSM-UHFFFAOYSA-N 0.000 description 1
- NKMSQSZVYLBQRG-UHFFFAOYSA-N n-dodecyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CCCCCCCCCCCCNC(=O)N1SC=CC1=O NKMSQSZVYLBQRG-UHFFFAOYSA-N 0.000 description 1
- QDSRDMJXSQGYGM-UHFFFAOYSA-N n-ethyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CCNC(=O)N1SC=CC1=O QDSRDMJXSQGYGM-UHFFFAOYSA-N 0.000 description 1
- PCKGHRKNRYYUJY-UHFFFAOYSA-N n-ethyl-5-methyl-3-oxo-1,2-thiazole-2-carbothioamide Chemical compound CCNC(=S)N1SC(C)=CC1=O PCKGHRKNRYYUJY-UHFFFAOYSA-N 0.000 description 1
- XPOIDNGCJWQQCT-UHFFFAOYSA-N n-ethyl-5-methyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CCNC(=O)N1SC(C)=CC1=O XPOIDNGCJWQQCT-UHFFFAOYSA-N 0.000 description 1
- FYXNYYCUQPPCNJ-UHFFFAOYSA-N n-methyl-3-oxo-1,2-thiazole-2-carbothioamide Chemical compound CNC(=S)N1SC=CC1=O FYXNYYCUQPPCNJ-UHFFFAOYSA-N 0.000 description 1
- ARBGYZLXHACKCD-UHFFFAOYSA-N n-methyl-3-oxo-1,2-thiazole-2-carboxamide Chemical compound CNC(=O)N1SC=CC1=O ARBGYZLXHACKCD-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 238000009896 oxidative bleaching Methods 0.000 description 1
- 229940070805 p-chloro-m-cresol Drugs 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- OOCYPIXCHKROMD-UHFFFAOYSA-M phenyl(propanoyloxy)mercury Chemical compound CCC(=O)O[Hg]C1=CC=CC=C1 OOCYPIXCHKROMD-UHFFFAOYSA-M 0.000 description 1
- 229940096826 phenylmercuric acetate Drugs 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 238000000275 quality assurance Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- HERBOKBJKVUALN-UHFFFAOYSA-K trisodium;2-[bis(carboxylatomethyl)amino]acetate;hydrate Chemical compound O.[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O HERBOKBJKVUALN-UHFFFAOYSA-K 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/37—Antiseptic agents
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10152383A JPS59226343A (ja) | 1983-06-07 | 1983-06-07 | 写真用コロイド銀水性組成物の防腐方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10152383A JPS59226343A (ja) | 1983-06-07 | 1983-06-07 | 写真用コロイド銀水性組成物の防腐方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59226343A JPS59226343A (ja) | 1984-12-19 |
| JPH0477305B2 true JPH0477305B2 (enrdf_load_stackoverflow) | 1992-12-08 |
Family
ID=14302849
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10152383A Granted JPS59226343A (ja) | 1983-06-07 | 1983-06-07 | 写真用コロイド銀水性組成物の防腐方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59226343A (enrdf_load_stackoverflow) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59226344A (ja) * | 1983-06-06 | 1984-12-19 | Konishiroku Photo Ind Co Ltd | 写真用水性組成物の防腐方法 |
| US5008150A (en) * | 1987-10-02 | 1991-04-16 | Mitsubishi Paper Mills Limited | Photographic support with an undercoating layer on a resin coated base sheet |
| JP2613415B2 (ja) * | 1988-02-20 | 1997-05-28 | コニカ株式会社 | 画像形成方法 |
| JP2676218B2 (ja) * | 1988-04-01 | 1997-11-12 | コニカ株式会社 | 写真用安定化液 |
| JP3400570B2 (ja) | 1994-10-12 | 2003-04-28 | 富士写真フイルム株式会社 | 記録材料製造装置の殺菌方法 |
-
1983
- 1983-06-07 JP JP10152383A patent/JPS59226343A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59226343A (ja) | 1984-12-19 |
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