DE279756C - - Google Patents
Info
- Publication number
- DE279756C DE279756C DENDAT279756D DE279756DA DE279756C DE 279756 C DE279756 C DE 279756C DE NDAT279756 D DENDAT279756 D DE NDAT279756D DE 279756D A DE279756D A DE 279756DA DE 279756 C DE279756 C DE 279756C
- Authority
- DE
- Germany
- Prior art keywords
- parts
- developer
- water
- methylaminophenol
- developing
- 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.)
- Active
Links
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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/30—Developers
- G03C5/3021—Developers with oxydisable hydroxyl or amine groups linked to an aromatic ring
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
KAISERLICHESIMPERIAL
PATENTAMT.PATENT OFFICE.
PATENTSCHRIFTPATENT LETTERING
— JVe 279756-KLASSE 576. GRUPPE - JVE 279756- CLASS 576. GROUP
Photographischer Entwickler. Patentiert im Deutschen Reiche vom 5. August 1913 ab.Photographic developer. Patented in the German Empire on August 5, 1913.
Die Verwendung von N - monoalkyliertenThe use of N - monoalkylated
4-Aminophenolen zum Entwickeln des latenten photographischen Bildes ist bekannt und das 4-Methylaminophenol und das 4-Oxyphenylglycin sind wertvolle Entwicklersubstanzen.4-aminophenols for developing the latent photographic image are known and that 4-methylaminophenol and 4-oxyphenylglycine are valuable developer substances.
Nach den bisherigen Kenntnissen war das Entwicklervermögen auf das 4-Aminophenol selbst und seine Monoalkylderivate beschränkt, denn dem 4 - Dimethylaminophenol kommt diese Eigenschaft nicht zu.According to previous knowledge, the developer capacity was due to the 4-aminophenol itself and its monoalkyl derivatives are limited because the 4 - dimethylaminophenol comes this property does not apply.
Es wurde nun überraschenderweise gefunden, daß im 4-Oxyphenil-alkyl-glycin von der Konstitution :It has now surprisingly been found that in 4-oxyphenil-alkyl-glycine the constitution :
AIlCyI-N-CH2-COOHAIlCyI-N-CH 2 -COOH
OHOH
Dialkylderivate des 4-Aminophenols vorliegen, die sich vorzüglich als Entwickler ' eignen. Ihre entwickelnde Kraft ist sehr groß und sie arbeiten äußerst klar. In bezug auf Entwicklungsgeschwindigkeit stehen sie in der Mitte zwischen 4-Methylaminophenol und 4-Oxyphenylglycin. Vor diesen und sonstigen Entwicklern haben sie den besonderen Vorzug außerordentlicher Löslichkeit in Alkalicarbonaten, so daß man ganz konzentrierte, von Ätzalkalien freie Lösungen herstellen kann, die zum Gebrauch nur mit viel Wasser verdünnt zu werden brauchen.Dialkyl derivatives of 4-aminophenol are present, which are particularly suitable as developers. Their developing power is very great and they work extremely clearly. With regard to the speed of development, they are in the Middle between 4-methylaminophenol and 4-oxyphenylglycine. Before these and others Developers they have the particular advantage of extraordinary solubility in alkali carbonates, so that you can produce very concentrated solutions free of caustic alkalis, which can only be diluted with plenty of water for use need to become.
Das bisher nicht beschriebene 4-Oxyphenylmethylglycin kann durch Einwirkung von Chloressigsäure auf 4-Methylaminophenol erhalten werden. Es bildet farblose Nadeln, die sich nach vorhergehendem Erweichen bei 1140 unter Kohlendioxydentwicklung zu zersetzen beginnen. Es löst sich leicht in heißem Wasser, in Alkohol, warmem Eisessig, wenig in siedendem Benzol, sehr schwer in Chloroform und ist unlöslich in Äther, Aceton, Ligroin, Petröläther.4-Oxyphenylmethylglycine, not previously described, can be obtained by the action of chloroacetic acid on 4-methylaminophenol. It forms colorless needles begin to decompose under evolution of carbon dioxide according to the previous softening at 114 0th It dissolves easily in hot water, in alcohol, warm glacial acetic acid, little in boiling benzene, very poorly in chloroform, and is insoluble in ether, acetone, ligroin, and petroleum ether.
Zur Herstellung einer konzentrierten Entwicklerlösung löst man beispielsweise 1 Teil 4-Oxyphenylmethylglycin in 12 Teilen Wasser unter Zusatz von 5 Teilen kristallisiertem Natriumsulfit und 5 Teilen Kaliumcarbonat. Diese Lösung wird zum Gebrauch mit 10 bis 30 Teilen Wasser verdünnt.To prepare a concentrated developer solution, for example, 1 part is dissolved 4-oxyphenylmethylglycine in 12 parts of water with the addition of 5 parts of crystallized sodium sulfite and 5 parts of potassium carbonate. These Solution is diluted with 10 to 30 parts of water for use.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB191318095T | 1913-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE279756C true DE279756C (en) |
Family
ID=34359763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT279756D Active DE279756C (en) | 1913-08-08 |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE279756C (en) |
GB (1) | GB191318095A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2624759A (en) * | 1950-11-01 | 1953-01-06 | Frederick C Bersworth | Substituted poly aralkyl alkylene poly amino poly acetic acids and salts |
US2624760A (en) * | 1950-11-01 | 1953-01-06 | Frederick C Bersworth | Hydroxy-aromatic alkylene di-imino di-acetic acids and salts |
US2624757A (en) * | 1950-11-01 | 1953-01-06 | Frederick C Bersworth | Substituted aralkyl alkylene diamino di acetic acids and salts |
US2624758A (en) * | 1950-11-01 | 1953-01-06 | Frederick C Bersworth | Substituted mono aralkyl alkylene polyamino polyacetic acids |
US2624756A (en) * | 1950-11-01 | 1953-01-06 | Frederick C Bersworth | Metal ion chelating compounds consisting of mono phenyl poly alkylene polyamino polycarboxylic acids and salts |
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0
- DE DENDAT279756D patent/DE279756C/de active Active
-
1913
- 1913-08-08 GB GB191318095D patent/GB191318095A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB191318095A (en) | 1914-03-12 |
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