Budzikiewicz, Herbert et al. published their research in Zeitschrift fuer Naturforschung in 1970 |CAS: 4569-86-2

The Article related to metzner photosynthesis, photosynthesis metzner, janus green photosynthesis, chlorophylls role: cat (catalyst use), uses (uses), photolysis catalysts, photosynthesis, biological and other aspects.Quality Control of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

Budzikiewicz, Herbert; Eckau, H.; Inhoffen, Hans H. published an article in 1970, the title of the article was Photosynthesis in green plants III. Investigation of the chemical processes in Metzner’s model for photosynthesis.Quality Control of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride And the article contains the following content:

Thin-layer chromatog. investigations of the Metzner photosynthesis system show that no diethylsafranine is formed by reaction of Ag with janus green (I). Volume and pH measurements with and without I and chlorophyll a show that Cl formed by photolysis of AgCl, reacts with H2O to give HCl and O and also with I to give decomposition products. The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Quality Control of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

The Article related to metzner photosynthesis, photosynthesis metzner, janus green photosynthesis, chlorophylls role: cat (catalyst use), uses (uses), photolysis catalysts, photosynthesis, biological and other aspects.Quality Control of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Brenner, Sydney et al. published their research in Biochimica et Biophysica Acta in 1953 |CAS: 4569-86-2

The Article related to lymphocytes, mitochondria, stains and staining, animal tissue and other aspects.Category: chlorides-buliding-blocks

Brenner, Sydney published an article in 1953, the title of the article was Supravital staining of mitochondria with phenosafranine dyes.Category: chlorides-buliding-blocks And the article contains the following content:

The more basic a phenosafranine (I) dye, the lower is the concentration of dye necessary for the supravital staining of mitochondria, as determined by studies on the supravital staining of human lymphocyte mitochondria with various sym. and unsym. I dyes. The dyes studied were in the order of increasing basicity of the terminal atoms (as determined by spectral measurements) and staining ability, I, dimethyl-I, diethyl-I, tetramethyl-I, diethyldimethyl-I, tetraethyl-I, and Janus green B. The results are discussed in relation to theories of supravital staining. The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Category: chlorides-buliding-blocks

The Article related to lymphocytes, mitochondria, stains and staining, animal tissue and other aspects.Category: chlorides-buliding-blocks

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Sorokin, Helen P. et al. published their research in American Journal of Botany in 1956 |CAS: 4569-86-2

3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas:4569-86-2) belongs to chlorides. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst. Reference of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

Sorokin, Helen P. published an article in 1956, the title of the article was Living cells of pea seedlings. I. Survey of vacuolar precipitates, mitochondria, and spherosomes.Reference of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride And the article contains the following content:

cf. C.A. 50, 9533b. The topmost portion of the 3rd internode in etiolated 7-day-old pea stems contained a definitely outlined region where Janus Green B (I) was reduced to diethylsafranin. Some cells in this region, particularly those adjacent to the starch sheath, formed stable, copious, brilliant blue-green precipitates of A-type vacuoles. Combined staining with I and neutral red separated red precipitates from blue mitochondria. The latter were recognized by the reversible coloration and decolorization of I under aerobic and anaerobic conditions, resp. They became dark red when incubated with neotetrazolium chloride. The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Reference of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas:4569-86-2) belongs to chlorides. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst. Reference of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Honda, Aki et al. published their patent in 2012 |CAS: 4569-86-2

The Article related to allergen environment determination proteinase coloring dye substrate colorimetry, Biochemical Methods: Biological and other aspects.Reference of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

On January 25, 2012, Honda, Aki; Suzuki, Koji published a patent.Reference of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride The title of the patent was Method for determining allergen in environment, and simple allergen quantitation kit. And the patent contained the following:

An allergen determination method is provided, which enables to conveniently measuring the quantity of a biol. allergen (e.g., acari, pollen) in environment without using an anti-allergen antibody. The method comprises using as a substrate for a proteinase which the allergen possesses a substrate capable of bringing a visible color change as a result of an enzymic reaction, bringing a solution containing this substrate into contact with a measurement object material collected using an adhesive sheet, measuring the proteinase activity in the measurement object material using the color change in the substrate solution as an index, and thereby, determining the biol. allergen. The proteinase substrate used in this method is a coloring compound (e.g, Boc-Val-Leu-Lys-3RAX, Boc-amino acid-3RAX) in which an amino acid or an oligopeptide is bound to at least one amino group of a coloring dye possessing at least one amino group (e.g., cresyl violet, safranine O, methylene violet 3RAX). The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Reference of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

The Article related to allergen environment determination proteinase coloring dye substrate colorimetry, Biochemical Methods: Biological and other aspects.Reference of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Iwasaki, Aki et al. published their patent in 2006 |CAS: 4569-86-2

The Article related to allergen environment determination proteinase coloring dye substrate colorimetry, Biochemical Methods: Biological and other aspects.Quality Control of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

On December 21, 2006, Iwasaki, Aki; Suzuki, Koji published a patent.Quality Control of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride The title of the patent was Method for determining allergen in environment, and simple allergen quantitation kit. And the patent contained the following:

An allergen determination method is provided, which enables to conveniently measuring the quantity of a biol. allergen (e.g., acari, pollen) in environment without using an anti-allergen antibody. The method comprises using as a substrate for a proteinase which the allergen possesses a substrate capable of bringing a visible color change as a result of an enzymic reaction, bringing a solution containing this substrate into contact with a measurement object material collected using an adhesive sheet, measuring the proteinase activity in the measurement object material using the color change in the substrate solution as an index, and thereby, determining the biol. allergen. The proteinase substrate used in this method is a coloring compound (e.g, Boc-Val-Leu-Lys-3RAX, Boc-amino acid-3RAX) in which an amino acid or an oligopeptide is bound to at least one amino group of a coloring dye possessing at least one amino group (e.g., cresyl violet, safranine O, methylene violet 3RAX). The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Quality Control of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

The Article related to allergen environment determination proteinase coloring dye substrate colorimetry, Biochemical Methods: Biological and other aspects.Quality Control of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Cook, Ronald M. et al. published their patent in 2001 |CAS: 4569-86-2

The Article related to fret black hole quencher probe nucleic acid fluorophore, Biochemical Methods: Synthesis and other aspects.SDS of cas: 4569-86-2

On November 15, 2001, Cook, Ronald M.; Lyttle, Matt; Dick, Daren published a patent.SDS of cas: 4569-86-2 The title of the patent was Synthesis and methods for dark quencher probes for donor-acceptor energy transfer. And the patent contained the following:

The invention concerns a family of quenchers of excited state energy that are substantially non-fluorescent, termed “”Black Hole Quenchers”” (BHQs). The quenchers of the invention remedy many of the deficiencies of currently utilized dark quenchers, probes assembled using these quenchers and methods using such quenchers and probes. Further, the dark quenchers are functionalized to allow their rapid attachment to probe that can be engineered to have a desired light absorption profile. The provision of this class of dark quenchers represents a substantial improvement in the design of probes incorporating dark quenchers and methods using such probes. Also provided are methods of using the BHQs, synthesis of such probes incorporating the BHQs and methods of using the probes. The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).SDS of cas: 4569-86-2

The Article related to fret black hole quencher probe nucleic acid fluorophore, Biochemical Methods: Synthesis and other aspects.SDS of cas: 4569-86-2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Ward, Brian W. et al. published their patent in 2005 |CAS: 4569-86-2

The Article related to tracer reagent reaction product analysis, Biochemical Genetics: Methods and other aspects.Recommanded Product: 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

On July 7, 2005, Ward, Brian W.; Ornitz, David M.; Deines, Michael G.; Bittick, Thomas F. published a patent.Recommanded Product: 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride The title of the patent was Tracer reagents that enhance reaction-product analysis. And the patent contained the following:

A composition suitable for formulation of an enzymic reaction mixture, the composition comprising a reaction component essential for an ex-vivo non-polymerase enzymic reaction in which a substrate is catalyzed by an enzyme in a reaction mixture to form a product, and a tracer compatible with the enzyme, the composition being substantially free of the substrate. The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Recommanded Product: 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

The Article related to tracer reagent reaction product analysis, Biochemical Genetics: Methods and other aspects.Recommanded Product: 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Read, David M. et al. published their patent in 2001 |CAS: 4569-86-2

The Article related to dye indicator hydrogen peroxide sterilization medical, Pharmaceuticals: Other and other aspects.Electric Literature of 4569-86-2

On June 7, 2001, Read, David M. published a patent.Electric Literature of 4569-86-2 The title of the patent was Dye indicators for hydrogen peroxide sterilization of medical instruments. And the patent contained the following:

The present invention provides a hydrogen peroxide indicator (for sterilization of medical instruments) that includes a substrate on which is disposed an indicator composition that includes at least one of a select group of colorants. As a result of contact with hydrogen peroxide, the colorants change color, and even become colorless, thereby providing an indication of the presence of hydrogen peroxide. Thus, indicator compositions were prepared by mixing shellac binder solution containing 60% shellac in iso-PrOH , dispersing resin Rhoplex I 545 with a dye, e.g., Malachite green oxalate. After sterilization with H2O2, the dyes showed good contrast between the initial color and the color after exposure to H2O2. The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Electric Literature of 4569-86-2

The Article related to dye indicator hydrogen peroxide sterilization medical, Pharmaceuticals: Other and other aspects.Electric Literature of 4569-86-2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Mills, Andrew et al. published their patent in 2010 |CAS: 4569-86-2

The Article related to uv sensor, Inorganic Analytical Chemistry: Apparatus and other aspects.Application of 4569-86-2

On January 28, 2010, Mills, Andrew; Grosshans, Pauline; McFarlane, Michael published a patent.Application of 4569-86-2 The title of the patent was UV sensor. And the patent contained the following:

The present invention relates to the provision of UV sensitive compositions and sensors comprising the compositions The sensors can find use in a wide range of applications including as dosimeters for indicating the amount of exposure to UV light of a person or an article. The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Application of 4569-86-2

The Article related to uv sensor, Inorganic Analytical Chemistry: Apparatus and other aspects.Application of 4569-86-2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Hasan, Tayyaba et al. published their patent in 2013 |CAS: 4569-86-2

The Article related to lactamase targeted photosensitizer pesticide pest control, Agrochemical Bioregulators: Invertebrate and other aspects.Recommanded Product: 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

On December 27, 2013, Hasan, Tayyaba; Sallum, Ulysses W.; Slatko, Barton; Foster, Jeremy published a patent.Recommanded Product: 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride The title of the patent was β-Lactamase targeted photosensitizers for use as pesticide and in pest detection. And the patent contained the following:

A pesticidal composition is described comprising a pesticidally effective amount of one or more photosensitizers that are linked by one or more moieties cleavable by a β-lactamase expressed by a pest wherein said linked moieties are present in an amount sufficient to quench photoactivation of said photosensitizers and wherein said one or more photosenitizers are capable of generating a phototoxic species upon dequenching and light-activation. The pesticidal composition above, wherein the one or more moieties cleavable by the β-lactamase comprise: a cephalosporin, a penicillin, a penem, a carbapenem, a monocyclic mobactem, or a fragment thereof; and the pests include crop pests, household pests, parasites, industrial pests, and fouling organisms. The experimental process involved the reaction of 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride(cas: 4569-86-2).Recommanded Product: 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

The Article related to lactamase targeted photosensitizer pesticide pest control, Agrochemical Bioregulators: Invertebrate and other aspects.Recommanded Product: 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics