GB873124A - Improvements in or relating to a process for the production of photographic colour images - Google Patents
Improvements in or relating to a process for the production of photographic colour imagesInfo
- Publication number
- GB873124A GB873124A GB2326756A GB2326756A GB873124A GB 873124 A GB873124 A GB 873124A GB 2326756 A GB2326756 A GB 2326756A GB 2326756 A GB2326756 A GB 2326756A GB 873124 A GB873124 A GB 873124A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- sulphofluoride
- methyl ester
- benzene
- sodium
- 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
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 9
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 6
- HQLVFFFDPGVGHG-UHFFFAOYSA-N methyl 3-(4-hexadecoxyphenyl)-3-oxopropanoate Chemical compound CCCCCCCCCCCCCCCCOC1=CC=C(C(=O)CC(=O)OC)C=C1 HQLVFFFDPGVGHG-UHFFFAOYSA-N 0.000 abstract 5
- 239000011734 sodium Substances 0.000 abstract 5
- 229910052708 sodium Inorganic materials 0.000 abstract 5
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 4
- -1 5 - (p-Cetyloxybenzoylacetylamino)-2-methylbenzene sodium Chemical compound 0.000 abstract 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 4
- 150000001412 amines Chemical class 0.000 abstract 4
- JDPRRECMRPCSIF-UHFFFAOYSA-N ethyl 3-oxobutanoate;sodium Chemical compound [Na].CCOC(=O)CC(C)=O JDPRRECMRPCSIF-UHFFFAOYSA-N 0.000 abstract 4
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 abstract 4
- 238000007127 saponification reaction Methods 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 3
- MWOBKFYERIDQSZ-UHFFFAOYSA-N benzene;sodium Chemical compound [Na].C1=CC=CC=C1 MWOBKFYERIDQSZ-UHFFFAOYSA-N 0.000 abstract 3
- 150000004702 methyl esters Chemical class 0.000 abstract 3
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 abstract 3
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 3
- HNTGIJLWHDPAFN-UHFFFAOYSA-N 1-bromohexadecane Chemical compound CCCCCCCCCCCCCCCCBr HNTGIJLWHDPAFN-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- XCFSTXSBTCEGTE-UHFFFAOYSA-N S(=O)(=O)(O)F.NC=1C=CC=CC1Cl Chemical compound S(=O)(=O)(O)F.NC=1C=CC=CC1Cl XCFSTXSBTCEGTE-UHFFFAOYSA-N 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- ZERJZUZPWKKYFM-UHFFFAOYSA-N aniline;sulfurofluoridic acid Chemical compound OS(F)(=O)=O.NC1=CC=CC=C1 ZERJZUZPWKKYFM-UHFFFAOYSA-N 0.000 abstract 2
- UNDANMCANJZUAA-UHFFFAOYSA-N benzene sulfurofluoridic acid Chemical compound S(=O)(=O)(O)F.C1=CC=CC=C1 UNDANMCANJZUAA-UHFFFAOYSA-N 0.000 abstract 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 2
- 238000009835 boiling Methods 0.000 abstract 2
- QIFPRIWEPOQQGY-UHFFFAOYSA-N butyl 4-aminobenzenesulfonate Chemical compound CCCCOS(=O)(=O)C1=CC=C(N)C=C1 QIFPRIWEPOQQGY-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- UIIYATJBZBOGMP-UHFFFAOYSA-N ethyl 3-oxo-3-(4-tetradecoxynaphthalen-1-yl)propanoate Chemical compound C(C)OC(CC(=O)C1=CC=C(C2=CC=CC=C12)OCCCCCCCCCCCCCC)=O UIIYATJBZBOGMP-UHFFFAOYSA-N 0.000 abstract 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N methyl acetate Chemical compound COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 abstract 2
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 abstract 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 2
- 235000003270 potassium fluoride Nutrition 0.000 abstract 2
- 239000011698 potassium fluoride Substances 0.000 abstract 2
- 235000011118 potassium hydroxide Nutrition 0.000 abstract 2
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 abstract 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 abstract 2
- NGOTZSLPEOKQGQ-UHFFFAOYSA-N 1-(4-amino-3-methylphenyl)ethanone Chemical compound CC(=O)C1=CC=C(N)C(C)=C1 NGOTZSLPEOKQGQ-UHFFFAOYSA-N 0.000 abstract 1
- SAPGSAHOBOEJDV-UHFFFAOYSA-N 1-(4-hydroxynaphthalen-1-yl)ethanone Chemical compound C1=CC=C2C(C(=O)C)=CC=C(O)C2=C1 SAPGSAHOBOEJDV-UHFFFAOYSA-N 0.000 abstract 1
- KOFZTCSTGIWCQG-UHFFFAOYSA-N 1-bromotetradecane Chemical compound CCCCCCCCCCCCCCBr KOFZTCSTGIWCQG-UHFFFAOYSA-N 0.000 abstract 1
- PRPWALBNZRTMSL-UHFFFAOYSA-N 1-chloro-2-nitrobenzene;sodium Chemical compound [Na].[O-][N+](=O)C1=CC=CC=C1Cl PRPWALBNZRTMSL-UHFFFAOYSA-N 0.000 abstract 1
- XCVWCSLKKQOBGY-UHFFFAOYSA-N 2-acetyl-4-aminobenzenesulfonic acid Chemical compound CC(=O)C1=CC(N)=CC=C1S(O)(=O)=O XCVWCSLKKQOBGY-UHFFFAOYSA-N 0.000 abstract 1
- YAZSBRQTAHVVGE-UHFFFAOYSA-N 2-aminobenzenesulfonamide Chemical compound NC1=CC=CC=C1S(N)(=O)=O YAZSBRQTAHVVGE-UHFFFAOYSA-N 0.000 abstract 1
- DJNSSSCWWNLRJQ-UHFFFAOYSA-N 3-acetyl-6-(chloroamino)-1-methylcyclohexa-2,4-diene-1-sulfonic acid Chemical compound S(=O)(=O)(O)C1(C(NCl)C=CC(=C1)C(C)=O)C DJNSSSCWWNLRJQ-UHFFFAOYSA-N 0.000 abstract 1
- JPVKCHIPRSQDKL-UHFFFAOYSA-N 3-aminobenzenesulfonamide Chemical compound NC1=CC=CC(S(N)(=O)=O)=C1 JPVKCHIPRSQDKL-UHFFFAOYSA-N 0.000 abstract 1
- HKKAXIDQIGDRTH-UHFFFAOYSA-N 3-oxo-N-phenyl-3-(4-tetradecoxynaphthalen-1-yl)propanamide sulfurofluoridic acid Chemical compound S(=O)(=O)(O)F.C(CCCCCCCCCCCCC)OC1=CC=C(C2=CC=CC=C12)C(=O)CC(=O)NC=1C=CC=CC1 HKKAXIDQIGDRTH-UHFFFAOYSA-N 0.000 abstract 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 abstract 1
- JXRGUPLJCCDGKG-UHFFFAOYSA-N 4-nitrobenzenesulfonyl chloride Chemical compound [O-][N+](=O)C1=CC=C(S(Cl)(=O)=O)C=C1 JXRGUPLJCCDGKG-UHFFFAOYSA-N 0.000 abstract 1
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 abstract 1
- CRNVLELHZSSPLT-UHFFFAOYSA-N 5-[[3-(4-hexadecoxyphenyl)-3-oxopropanoyl]amino]benzene-1,3-dicarboxylic acid Chemical compound C(CCCCCCCCCCCCCCC)OC1=CC=C(C(=O)CC(=O)NC=2C=C(C=C(C(=O)O)C2)C(=O)O)C=C1 CRNVLELHZSSPLT-UHFFFAOYSA-N 0.000 abstract 1
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 abstract 1
- 239000005711 Benzoic acid Substances 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 abstract 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- 125000003172 aldehyde group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical group OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 abstract 1
- 235000010233 benzoic acid Nutrition 0.000 abstract 1
- 230000020176 deacylation Effects 0.000 abstract 1
- 238000005947 deacylation reaction Methods 0.000 abstract 1
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- NTBHQNDXAJXRPU-UHFFFAOYSA-N dimethyl 4-aminobenzene-1,2-dicarboxylate Chemical compound COC(=O)C1=CC=C(N)C=C1C(=O)OC NTBHQNDXAJXRPU-UHFFFAOYSA-N 0.000 abstract 1
- DEKPYXUDJRABNK-UHFFFAOYSA-N dimethyl 5-aminobenzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC(N)=CC(C(=O)OC)=C1 DEKPYXUDJRABNK-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 239000011874 heated mixture Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- FUKUFMFMCZIRNT-UHFFFAOYSA-N hydron;methanol;chloride Chemical compound Cl.OC FUKUFMFMCZIRNT-UHFFFAOYSA-N 0.000 abstract 1
- 229960004963 mesalazine Drugs 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- XENTXTUUBRDTST-UHFFFAOYSA-N methyl 2-(3-aminophenoxy)acetate Chemical compound COC(=O)COC1=CC=CC(N)=C1 XENTXTUUBRDTST-UHFFFAOYSA-N 0.000 abstract 1
- DUYHAOVVOQOXCC-UHFFFAOYSA-N methyl 3-(4-hexadecoxy-3-methoxyphenyl)-3-oxopropanoate Chemical compound CCCCCCCCCCCCCCCCOC1=CC=C(C(=O)CC(=O)OC)C=C1OC DUYHAOVVOQOXCC-UHFFFAOYSA-N 0.000 abstract 1
- GNCWCTBHZCBXGL-UHFFFAOYSA-N methyl 4-hydroxy-3-nitrobenzoate Chemical compound COC(=O)C1=CC=C(O)C([N+]([O-])=O)=C1 GNCWCTBHZCBXGL-UHFFFAOYSA-N 0.000 abstract 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 abstract 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 abstract 1
- 229960002216 methylparaben Drugs 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000012286 potassium permanganate Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- 230000001131 transforming effect Effects 0.000 abstract 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 abstract 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
- G03C7/32—Colour coupling substances
- G03C7/36—Couplers containing compounds with active methylene groups
- G03C7/362—Benzoyl-acetanilide couplers
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE559466D BE559466A (enrdf_load_stackoverflow) | 1956-07-27 | ||
| GB2326756A GB873124A (en) | 1956-07-27 | 1956-07-27 | Improvements in or relating to a process for the production of photographic colour images |
| DEG22628A DE1044614B (de) | 1956-07-27 | 1957-07-26 | Verfahren zum Entwickeln eines farbigen Bildes aus reduzierbaren Silbersalzen nach dem Farbentwicklungsverfahren |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2326756A GB873124A (en) | 1956-07-27 | 1956-07-27 | Improvements in or relating to a process for the production of photographic colour images |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB873124A true GB873124A (en) | 1961-07-19 |
Family
ID=10192899
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2326756A Expired GB873124A (en) | 1956-07-27 | 1956-07-27 | Improvements in or relating to a process for the production of photographic colour images |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE559466A (enrdf_load_stackoverflow) |
| DE (1) | DE1044614B (enrdf_load_stackoverflow) |
| GB (1) | GB873124A (enrdf_load_stackoverflow) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2652329A (en) * | 1952-07-31 | 1953-09-15 | Eastman Kodak Co | Color couplers containing isophthalic acid radicals |
-
0
- BE BE559466D patent/BE559466A/xx unknown
-
1956
- 1956-07-27 GB GB2326756A patent/GB873124A/en not_active Expired
-
1957
- 1957-07-26 DE DEG22628A patent/DE1044614B/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE1044614B (de) | 1958-11-20 |
| BE559466A (enrdf_load_stackoverflow) |
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