DE69026202T2 - Photographisches Silberhalogenidmaterial - Google Patents

Photographisches Silberhalogenidmaterial

Info

Publication number: DE69026202T2
Authority: DE; Germany
Prior art keywords: group; general formula; hydrogen atom; alkyl; aryl
Prior art date: 1989-11-15
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 - Fee Related

Application number

DE1990626202

Other languages

German (de)

English (en)

Other versions

DE69026202D1 (de

Inventor

Takahiro Ogawa

Shun Takada

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Konica Minolta Inc

Original Assignee

Konica Minolta Inc

Priority date (The priority date 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 date listed.)

1989-11-15

Filing date

1990-11-14

Publication date

1996-11-14

1990-11-14 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1996-05-02 Publication of DE69026202D1 publication Critical patent/DE69026202D1/de

1996-11-14 Application granted granted Critical

1996-11-14 Publication of DE69026202T2 publication Critical patent/DE69026202T2/de

2010-11-15 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims description 99
229910052709 silver Inorganic materials 0.000 title claims description 53
239000004332 silver Substances 0.000 title claims description 53
239000000463 material Substances 0.000 title claims description 45
125000000217 alkyl group Chemical group 0.000 claims description 74
125000003118 aryl group Chemical group 0.000 claims description 47
150000001875 compounds Chemical class 0.000 claims description 33
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 33
125000000753 cycloalkyl group Chemical group 0.000 claims description 29
125000004432 carbon atom Chemical group C* 0.000 claims description 28
125000001424 substituent group Chemical group 0.000 claims description 24
239000003795 chemical substances by application Substances 0.000 claims description 22
125000002947 alkylene group Chemical group 0.000 claims description 19
125000000623 heterocyclic group Chemical group 0.000 claims description 19
125000005843 halogen group Chemical group 0.000 claims description 18
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
125000003545 alkoxy group Chemical group 0.000 claims description 11
125000000732 arylene group Chemical group 0.000 claims description 11
239000003960 organic solvent Substances 0.000 claims description 11
238000009835 boiling Methods 0.000 claims description 10
125000005647 linker group Chemical group 0.000 claims description 10
230000003647 oxidation Effects 0.000 claims description 10
238000007254 oxidation reaction Methods 0.000 claims description 10
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 10
125000004414 alkyl thio group Chemical group 0.000 claims description 9
125000005110 aryl thio group Chemical group 0.000 claims description 9
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 8
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
125000003342 alkenyl group Chemical group 0.000 claims description 7
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 7
125000002252 acyl group Chemical group 0.000 claims description 6
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
238000006243 chemical reaction Methods 0.000 claims description 6
125000000962 organic group Chemical group 0.000 claims description 6
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 5
125000004391 aryl sulfonyl group Chemical group 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
150000002430 hydrocarbons Chemical class 0.000 claims description 5
125000000335 thiazolyl group Chemical group 0.000 claims description 5
125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 4
125000003277 amino group Chemical group 0.000 claims description 4
238000005859 coupling reaction Methods 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 3
150000002148 esters Chemical group 0.000 claims description 3
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
125000005360 alkyl sulfoxide group Chemical group 0.000 claims description 2
230000008878 coupling Effects 0.000 claims description 2
238000010168 coupling process Methods 0.000 claims description 2
150000002576 ketones Chemical class 0.000 claims description 2
150000001408 amides Chemical class 0.000 claims 1
239000010410 layer Substances 0.000 description 70
239000000839 emulsion Substances 0.000 description 45
239000000243 solution Substances 0.000 description 23
239000003381 stabilizer Substances 0.000 description 21
108010010803 Gelatin Proteins 0.000 description 19
229920000159 gelatin Polymers 0.000 description 19
239000008273 gelatin Substances 0.000 description 19
235000019322 gelatine Nutrition 0.000 description 19
235000011852 gelatine desserts Nutrition 0.000 description 19
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
239000007864 aqueous solution Substances 0.000 description 15
239000000975 dye Substances 0.000 description 15
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
230000035945 sensitivity Effects 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 12
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
239000000084 colloidal system Substances 0.000 description 11
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 9
238000004061 bleaching Methods 0.000 description 9
230000001235 sensitizing effect Effects 0.000 description 9
238000012360 testing method Methods 0.000 description 9
238000000576 coating method Methods 0.000 description 8
SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 8
238000003860 storage Methods 0.000 description 8
239000006096 absorbing agent Substances 0.000 description 7
125000004442 acylamino group Chemical group 0.000 description 7
239000011248 coating agent Substances 0.000 description 7
239000006185 dispersion Substances 0.000 description 7
238000000034 method Methods 0.000 description 7
239000003755 preservative agent Substances 0.000 description 7
239000011780 sodium chloride Substances 0.000 description 7
239000002904 solvent Substances 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
125000004104 aryloxy group Chemical group 0.000 description 6
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 6
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 6
238000011161 development Methods 0.000 description 6
239000000203 mixture Substances 0.000 description 6
230000003287 optical effect Effects 0.000 description 6
229910000027 potassium carbonate Inorganic materials 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 6
235000019345 sodium thiosulphate Nutrition 0.000 description 6
125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 6
ZJOJXRSMJNWWRN-UHFFFAOYSA-N 3-amino-6-[2-(4-aminophenyl)ethenyl]benzene-1,2-disulfonic acid Chemical class C1=CC(N)=CC=C1C=CC1=CC=C(N)C(S(O)(=O)=O)=C1S(O)(=O)=O ZJOJXRSMJNWWRN-UHFFFAOYSA-N 0.000 description 5
206010070834 Sensitisation Diseases 0.000 description 5
125000004423 acyloxy group Chemical group 0.000 description 5
229910052801 chlorine Inorganic materials 0.000 description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
125000005842 heteroatom Chemical group 0.000 description 5
239000000049 pigment Substances 0.000 description 5
230000008313 sensitization Effects 0.000 description 5
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
102100033183 Epithelial membrane protein 1 Human genes 0.000 description 4
239000004285 Potassium sulphite Substances 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
229910021607 Silver chloride Inorganic materials 0.000 description 4
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 4
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
108010008594 epithelial membrane protein-1 Proteins 0.000 description 4
230000000670 limiting effect Effects 0.000 description 4
238000002156 mixing Methods 0.000 description 4
125000001624 naphthyl group Chemical group 0.000 description 4
BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 4
235000019252 potassium sulphite Nutrition 0.000 description 4
230000002335 preservative effect Effects 0.000 description 4
238000012545 processing Methods 0.000 description 4
230000009467 reduction Effects 0.000 description 4
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 4
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 4
229910001961 silver nitrate Inorganic materials 0.000 description 4
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
125000004149 thio group Chemical group *S* 0.000 description 4
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
229960000583 acetic acid Drugs 0.000 description 3
239000002253 acid Substances 0.000 description 3
125000004448 alkyl carbonyl group Chemical group 0.000 description 3
125000005422 alkyl sulfonamido group Chemical group 0.000 description 3
239000000908 ammonium hydroxide Substances 0.000 description 3
125000005129 aryl carbonyl group Chemical group 0.000 description 3
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 3
125000005421 aryl sulfonamido group Chemical group 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
125000003438 dodecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
238000001035 drying Methods 0.000 description 3
238000011156 evaluation Methods 0.000 description 3
239000012362 glacial acetic acid Substances 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
229960003330 pentetic acid Drugs 0.000 description 3
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
229920000036 polyvinylpyrrolidone Polymers 0.000 description 3
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 3
230000001681 protective effect Effects 0.000 description 3
239000011241 protective layer Substances 0.000 description 3
230000003068 static effect Effects 0.000 description 3
125000003341 7 membered heterocyclic group Chemical group 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 2
229920001174 Diethylhydroxylamine Polymers 0.000 description 2
102100033176 Epithelial membrane protein 2 Human genes 0.000 description 2
108050009423 Epithelial membrane protein 2 Proteins 0.000 description 2
102100030146 Epithelial membrane protein 3 Human genes 0.000 description 2
101710143764 Epithelial membrane protein 3 Proteins 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
239000004793 Polystyrene Substances 0.000 description 2
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
ZYRABDXZSUJSGF-UHFFFAOYSA-L [O-]C(CN(CCN(CC([O-])=O)CC(O)=O)CC(O)=O)=O.N.O.O.[Fe+2] Chemical compound [O-]C(CN(CCN(CC([O-])=O)CC(O)=O)CC(O)=O)=O.N.O.O.[Fe+2] ZYRABDXZSUJSGF-UHFFFAOYSA-L 0.000 description 2
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
125000004466 alkoxycarbonylamino group Chemical group 0.000 description 2
125000003282 alkyl amino group Chemical group 0.000 description 2
125000003806 alkyl carbonyl amino group Chemical group 0.000 description 2
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
239000002216 antistatic agent Substances 0.000 description 2
125000004658 aryl carbonyl amino group Chemical group 0.000 description 2
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 2
125000005135 aryl sulfinyl group Chemical group 0.000 description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
235000019445 benzyl alcohol Nutrition 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
229910052794 bromium Inorganic materials 0.000 description 2
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
125000000392 cycloalkenyl group Chemical group 0.000 description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 2
238000009826 distribution Methods 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical group 0.000 description 2
150000002605 large molecules Chemical class 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
125000005499 phosphonyl group Chemical group 0.000 description 2
150000003014 phosphoric acid esters Chemical class 0.000 description 2
229920013639 polyalphaolefin Polymers 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 2
JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
230000003595 spectral effect Effects 0.000 description 2
150000003413 spiro compounds Chemical class 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000003107 substituted aryl group Chemical group 0.000 description 2
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
ILFIRBGRMCGNOO-UHFFFAOYSA-N 1,1-bis($l^{1}-oxidanyl)ethene Chemical group [O]C([O])=C ILFIRBGRMCGNOO-UHFFFAOYSA-N 0.000 description 1
RJFCFNWLPJRCLR-UHFFFAOYSA-N 1-prop-2-enylnaphthalene Chemical group C1=CC=C2C(CC=C)=CC=CC2=C1 RJFCFNWLPJRCLR-UHFFFAOYSA-N 0.000 description 1
AFBBKYQYNPNMAT-UHFFFAOYSA-N 1h-1,2,4-triazol-1-ium-3-thiolate Chemical compound SC=1N=CNN=1 AFBBKYQYNPNMAT-UHFFFAOYSA-N 0.000 description 1
BKUSIKGSPSFQAC-RRKCRQDMSA-N 2'-deoxyinosine-5'-diphosphate Chemical compound O1[C@H](CO[P@@](O)(=O)OP(O)(O)=O)[C@@H](O)C[C@@H]1N1C(NC=NC2=O)=C2N=C1 BKUSIKGSPSFQAC-RRKCRQDMSA-N 0.000 description 1
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 1
125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 1
ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 1
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
229940100484 5-chloro-2-methyl-4-isothiazolin-3-one Drugs 0.000 description 1
IDCLTMRSSAXUNY-UHFFFAOYSA-N 5-hydroxylansoprazole Chemical compound CC1=C(OCC(F)(F)F)C=CN=C1CS(=O)C1=NC2=CC(O)=CC=C2N1 IDCLTMRSSAXUNY-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 1
125000005115 alkyl carbamoyl group Chemical group 0.000 description 1
125000005196 alkyl carbonyloxy group Chemical group 0.000 description 1
125000005153 alkyl sulfamoyl group Chemical group 0.000 description 1
125000005278 alkyl sulfonyloxy group Chemical group 0.000 description 1
125000005281 alkyl ureido group Chemical group 0.000 description 1
125000000304 alkynyl group Chemical group 0.000 description 1
IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
125000005116 aryl carbamoyl group Chemical group 0.000 description 1
125000005199 aryl carbonyloxy group Chemical group 0.000 description 1
125000005279 aryl sulfonyloxy group Chemical group 0.000 description 1
UMEAURNTRYCPNR-UHFFFAOYSA-N azane;iron(2+) Chemical compound N.[Fe+2] UMEAURNTRYCPNR-UHFFFAOYSA-N 0.000 description 1
QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
229910001864 baryta Inorganic materials 0.000 description 1
230000006399 behavior Effects 0.000 description 1
150000001555 benzenes Chemical group 0.000 description 1
125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 1
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
JHXKRIRFYBPWGE-UHFFFAOYSA-K bismuth chloride Chemical compound Cl[Bi](Cl)Cl JHXKRIRFYBPWGE-UHFFFAOYSA-K 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
235000012241 calcium silicate Nutrition 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
239000000919 ceramic Substances 0.000 description 1
229910000333 cerium(III) sulfate Inorganic materials 0.000 description 1
230000008859 change Effects 0.000 description 1
PBHVCRIXMXQXPD-UHFFFAOYSA-N chembl2369102 Chemical compound C1=CC(S(=O)(=O)O)=CC=C1C(C1=CC=C(N1)C(C=1C=CC(=CC=1)S(O)(=O)=O)=C1C=CC(=N1)C(C=1C=CC(=CC=1)S(O)(=O)=O)=C1C=CC(N1)=C1C=2C=CC(=CC=2)S(O)(=O)=O)=C2N=C1C=C2 PBHVCRIXMXQXPD-UHFFFAOYSA-N 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
239000003086 colorant Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000007766 curtain coating Methods 0.000 description 1
150000001924 cycloalkanes Chemical group 0.000 description 1
150000001925 cycloalkenes Chemical group 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
125000002704 decyl 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])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000010612 desalination reaction Methods 0.000 description 1
238000000586 desensitisation Methods 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
WMWXXXSCZVGQAR-UHFFFAOYSA-N dialuminum;oxygen(2-);hydrate Chemical class O.[O-2].[O-2].[O-2].[Al+3].[Al+3] WMWXXXSCZVGQAR-UHFFFAOYSA-N 0.000 description 1
DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 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
125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
238000007765 extrusion coating Methods 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011521 glass Substances 0.000 description 1
229920000578 graft copolymer Polymers 0.000 description 1
229940093915 gynecological organic acid Drugs 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 1
125000002883 imidazolyl group Chemical group 0.000 description 1
238000007654 immersion Methods 0.000 description 1
239000011229 interlayer Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
CLJDCQWROXMJAZ-UHFFFAOYSA-N n-[2-(4-amino-n-ethyl-3-methylanilino)ethyl]methanesulfonamide;sulfuric acid Chemical compound OS(O)(=O)=O.CS(=O)(=O)NCCN(CC)C1=CC=C(N)C(C)=C1 CLJDCQWROXMJAZ-UHFFFAOYSA-N 0.000 description 1
125000004957 naphthylene group Chemical group 0.000 description 1
125000002560 nitrile group Chemical group 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
235000010292 orthophenyl phenol Nutrition 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
125000005498 phthalate group Chemical class 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
229920000137 polyphosphoric acid Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
239000001103 potassium chloride Substances 0.000 description 1
235000011164 potassium chloride Nutrition 0.000 description 1
239000010970 precious metal Substances 0.000 description 1
230000008569 process Effects 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical group C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 1
230000005855 radiation Effects 0.000 description 1
238000009877 rendering Methods 0.000 description 1
238000007788 roughening Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229910052711 selenium Inorganic materials 0.000 description 1
239000011669 selenium Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
238000002791 soaking Methods 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000010186 staining Methods 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000758 substrate Substances 0.000 description 1
125000001174 sulfone group Chemical group 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003536 tetrazoles Chemical group 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
150000003852 triazoles Chemical group 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
239000012463 white pigment Substances 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
RZLVQBNCHSJZPX-UHFFFAOYSA-L zinc sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Zn+2].[O-]S([O-])(=O)=O RZLVQBNCHSJZPX-UHFFFAOYSA-L 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
- 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
- G03C7/392—Additives
- G03C7/39208—Organic compounds
- 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
- 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
- G03C7/32—Colour coupling substances
- G03C7/3225—Combination of couplers of different kinds, e.g. yellow and magenta couplers in a same layer or in different layers of the photographic material

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

DE1990626202 1989-11-15 1990-11-14 Photographisches Silberhalogenidmaterial Expired - Fee Related DE69026202T2 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP29809289A JPH03157646A (ja)	1989-11-15	1989-11-15	ハロゲン化銀写真感光材料

Publications (2)

Publication Number	Publication Date
DE69026202D1 DE69026202D1 (de)	1996-05-02
DE69026202T2 true DE69026202T2 (de)	1996-11-14

Family

ID=17855062

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE1990626202 Expired - Fee Related DE69026202T2 (de)	1989-11-15	1990-11-14	Photographisches Silberhalogenidmaterial

Country Status (5)

Country	Link
EP (1)	EP0429240B1 (ja)
JP (1)	JPH03157646A (ja)
AU (1)	AU642442B2 (ja)
CA (1)	CA2030041A1 (ja)
DE (1)	DE69026202T2 (ja)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0628866A1 (en) *	1993-06-04	1994-12-14	Konica Corporation	A silver halide color photographic light-sensitive material
JPH09166853A (ja)	1995-12-15	1997-06-24	Konica Corp	ハロゲン化銀カラー写真感光材料の画像形成方法
FR2786889B1 (fr)	1998-12-03	2001-02-02	Eastman Kodak Co	Procede pour empecher la croissance des micro-organismes dans les dispersions photographiques
US6448281B1 (en)	2000-07-06	2002-09-10	Boehringer Ingelheim (Canada) Ltd.	Viral polymerase inhibitors
EP2335700A1 (en)	2001-07-25	2011-06-22	Boehringer Ingelheim (Canada) Ltd.	Hepatitis C virus polymerase inhibitors with a heterobicylic structure
US20040009440A1 (en)	2002-07-11	2004-01-15	Alice Moon	Coating composition for photographic materials
AR047706A1 (es)	2004-02-20	2006-02-08	Boehringer Ingelheim Int	Inhibidores de polimerasa viral
JP5015154B2 (ja)	2005-08-12	2012-08-29	ベーリンガーインゲルハイムインターナショナルゲゼルシャフトミットベシュレンクテルハフツング	ウイルスポリメラーゼインヒビター
WO2017030892A1 (en)	2015-08-14	2017-02-23	Reaction Biology Corp.	Histone deacetylase inhibitors and methods for use thereof
KR200481239Y1 (ko) *	2016-07-14	2016-09-05	김성구	유해 조수 퇴치 장치

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH07117731B2 (ja) *	1987-03-20	1995-12-18	コニカ株式会社	形成される色素の分光吸収特性が良好なハロゲン化銀写真感光材料
JP2601272B2 (ja) *	1987-04-28	1997-04-16	コニカ株式会社	迅速処理においても感度、カブリの写真性能の劣化がなく、さらにバクテリア、カビ等による腐敗、分解作用が良好に防止されるハロゲン化銀写真感光材料
DE68921015T2 (de) *	1988-02-19	1995-09-14	Fuji Photo Film Co Ltd	Verfahren zur Verarbeitung von farbphotographischem Silberhalogenidmaterial.
JP2665619B2 (ja) *	1989-11-14	1997-10-22	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料

1989
- 1989-11-15 JP JP29809289A patent/JPH03157646A/ja active Pending
1990
- 1990-11-14 AU AU66612/90A patent/AU642442B2/en not_active Ceased
- 1990-11-14 DE DE1990626202 patent/DE69026202T2/de not_active Expired - Fee Related
- 1990-11-14 EP EP90312399A patent/EP0429240B1/en not_active Expired - Lifetime
- 1990-11-15 CA CA 2030041 patent/CA2030041A1/en not_active Abandoned

Also Published As

Publication number	Publication date
CA2030041A1 (en)	1991-05-16
DE69026202D1 (de)	1996-05-02
AU642442B2 (en)	1993-10-21
EP0429240B1 (en)	1996-03-27
AU6661290A (en)	1991-05-23
EP0429240A1 (en)	1991-05-29
JPH03157646A (ja)	1991-07-05

Publication	Publication Date	Title
DE2703145C2 (ja)	1988-07-14
DE3789277T2 (de)	1994-07-07	Lichtempfindliches photographisches Silberhalogenidmaterial, das einen gelben Kuppler enthält.
EP0283324B1 (en)	1993-09-15	Light-sensitive silver halide color photographic material
DE2651363A1 (de)	1977-05-12	Photographischer kuppler und seine verwendung
DE4323512A1 (de)	1994-04-28	Fotografisches Aufzeichnungsmaterial
DE69624530T2 (de)	2003-06-12	Photographische Elemente enthaltend Magentafarbkuppler und Verbindungen, welche das Ausbleichen vermindern
DE69026202T2 (de)	1996-11-14	Photographisches Silberhalogenidmaterial
DE3784150T2 (de)	1993-06-03	Lichtempfindliches photographisches silberhalogenidmaterial.
DE3633364C3 (de)	1995-07-13	Farbfotografisches Aufzeichnungsmaterial mit einem Farbkuppler vom Pyrazoloazol-Typ
DE3739025A1 (de)	1988-05-26	Verfahren zur behandlung bzw. entwicklung eines photographischen silberhalogenid-farbumkehrmaterials
DE69227654T2 (de)	1999-05-20	Farbphotographisches Silberhalogenidmaterial
DE4031644A1 (de)	1991-04-18	Lichtempfindliches photographisches silberhalogenidmaterial
DE69222603T2 (de)	1998-04-23	Photographisches Element mit 2-Äquivalenten-Magentafarbkuppler und Filterfarbstoff
DE3624544C2 (de)	1996-02-01	Farbfotografisches Aufzeichnungsmaterial mit einem Farbkuppler vom Pyrazoloazol-Typ
DE69600209T2 (de)	1998-11-05	Photographische Elemente enthaltend magentafarbbildende Kuppler und Verbindungen die Ausbleichen reduzieren
DE3876148T2 (de)	1993-04-15	Magenta-farbstoff bildender kuppler.
DE69223958T2 (de)	1998-06-04	Farbphotographisches photoempfindliches silberhalogenidmaterial
DE3779717T2 (de)	1992-12-24	Photographisches silberhalogenidmaterial und verfahren zur bildung eines farbbildes darauf.
DE69525598T2 (de)	2002-09-05	Blaugrünkuppler enthaltendes photographisches Material
DE3546137C2 (de)	1996-10-02	Photographisches Silberhalogenid-Aufzeichnungsmaterial
DE3636824A1 (de)	1988-05-05	Farbfotografisches aufzeichnungsmaterial mit einem gelb-dir-kuppler
DE3885539T2 (de)	1994-02-24	Farbphotographisches lichtempfindliches Silberhalogenidmaterial, das eine Epoxy-Verbindung enthält.
DE69205114T2 (de)	1996-03-07	Farbphotographisches Silberhalogenidmaterial.
DE68922547T2 (de)	1995-08-17	Farbphotographisches Silberhalogenidmaterial.
DE19503885A1 (de)	1996-08-08	Farbfotografisches Material

Legal Events

Date	Code	Title	Description
1997-04-24	8364	No opposition during term of opposition
2008-09-11	8339	Ceased/non-payment of the annual fee