GB610569A - Improvements in or relating to the production of dyes and the sensitisation of photographic emulsions - Google Patents
Improvements in or relating to the production of dyes and the sensitisation of photographic emulsionsInfo
- Publication number
- GB610569A GB610569A GB1001846A GB1001846A GB610569A GB 610569 A GB610569 A GB 610569A GB 1001846 A GB1001846 A GB 1001846A GB 1001846 A GB1001846 A GB 1001846A GB 610569 A GB610569 A GB 610569A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- toluenesulphonate
- ethyl
- dyes
- methylbenzthiazole
- 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
- 239000000975 dye Substances 0.000 title abstract 3
- 206010070834 Sensitisation Diseases 0.000 title 1
- 239000000839 emulsion Substances 0.000 title 1
- VUQUOGPMUUJORT-UHFFFAOYSA-N methyl 4-methylbenzenesulfonate Chemical compound COS(=O)(=O)C1=CC=C(C)C=C1 VUQUOGPMUUJORT-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- JJPSZKIOGBRMHK-UHFFFAOYSA-N 2,6-dimethylquinoline Chemical compound N1=C(C)C=CC2=CC(C)=CC=C21 JJPSZKIOGBRMHK-UHFFFAOYSA-N 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- BBVLSXAFRQLPBD-UHFFFAOYSA-N CC(C=C1)=CC=C1S(OC)(=O)=O.C[S+]1C(C=CC=C2)=C2N=C1 Chemical compound CC(C=C1)=CC=C1S(OC)(=O)=O.C[S+]1C(C=CC=C2)=C2N=C1 BBVLSXAFRQLPBD-UHFFFAOYSA-N 0.000 abstract 1
- SJLJHVITDDTVMW-UHFFFAOYSA-N C[S+]1C2=CC=CC=C2N=C1 Chemical compound C[S+]1C2=CC=CC=C2N=C1 SJLJHVITDDTVMW-UHFFFAOYSA-N 0.000 abstract 1
- 150000001450 anions Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- VRZVPALEJCLXPR-UHFFFAOYSA-N ethyl 4-methylbenzenesulfonate Chemical compound CCOS(=O)(=O)C1=CC=C(C)C=C1 VRZVPALEJCLXPR-UHFFFAOYSA-N 0.000 abstract 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/10—The polymethine chain containing an even number of >CH- groups
- C09B23/105—The polymethine chain containing an even number of >CH- groups two >CH- groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Methine dyes are prepared by condensing, in the presence of a basic condensing agent, a compound of the general formula <FORM:0610569/IV (c)/1> wherein R1 is a hydrocarbon group and R4 alkyl or aralkyl with a compound of the formula <FORM:0610569/IV (c)/2> wherein R5 is H or a hydrocarbon group, R2 is an alkyl hydroxylkyl, aralkyl, or hydroxyaralkyl group, R3 is H or alkyl or aralkyl, D1 is the residue of a 5- or 6-membered heterocyclic ring, which may have fused-on rings, D2 is the residue of a heterocyclic nitrogen ketomethylene ring, X is an anion, and n is 0 or 1. Dyes specified are such that R1 is ethyl and R4 methyl, and derived from p-toluquinaldine methyl-p-toluenesulphonate, 1-methylbenzthiazole methyl- or ethyl-p-toluenesulphonate, 1-methylbenzoxazole methyl-p-toluenesulphonate, 1-methyl-b -naphthathiazole methyl-p-toluenesulphonate, and m -thiazoline methyl-p-toluenesulphonate; both R1 and R4 are ethyl and derived from 1-methylbenzthiazole methyl-p-toluenesulphonate or b -hydroxyethiodide; and R1 is ethyl and R4 benzyl and derived from 1-methylbenzthiazole methodide. Specifications 489,335, 547,060, [Group XX], and 597,446 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1001846A GB610569A (en) | 1946-04-01 | 1946-04-01 | Improvements in or relating to the production of dyes and the sensitisation of photographic emulsions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1001846A GB610569A (en) | 1946-04-01 | 1946-04-01 | Improvements in or relating to the production of dyes and the sensitisation of photographic emulsions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB610569A true GB610569A (en) | 1948-10-18 |
Family
ID=9959917
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1001846A Expired GB610569A (en) | 1946-04-01 | 1946-04-01 | Improvements in or relating to the production of dyes and the sensitisation of photographic emulsions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB610569A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2534112A (en) * | 1948-10-02 | 1950-12-12 | Ilford Ltd | Certain thio derivatives of alpha alkylidene cyanoacetic esters |
US2573555A (en) * | 1948-10-02 | 1951-10-30 | Ilford Ltd | Method for making methine dyestuffs |
US2693472A (en) * | 1950-03-20 | 1954-11-02 | Ilford Ltd | Polymethine compounds |
DE1060073B (en) * | 1954-11-04 | 1959-06-25 | Ici Ltd | Process for the preparation of sensitizing dyes |
-
1946
- 1946-04-01 GB GB1001846A patent/GB610569A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2534112A (en) * | 1948-10-02 | 1950-12-12 | Ilford Ltd | Certain thio derivatives of alpha alkylidene cyanoacetic esters |
US2573555A (en) * | 1948-10-02 | 1951-10-30 | Ilford Ltd | Method for making methine dyestuffs |
US2693472A (en) * | 1950-03-20 | 1954-11-02 | Ilford Ltd | Polymethine compounds |
DE1060073B (en) * | 1954-11-04 | 1959-06-25 | Ici Ltd | Process for the preparation of sensitizing dyes |
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