Fomina M. V., Nikiforov A. S., Gromov S. P. Modern approaches to the synthesis and prospects for the use of cyanine dyes containing functional groups in the n-substituents // Russian Chemical Reviews. - 2016. - Vol. 85, no. 7. - P. 684-699. Methods for the synthesis of mono-, tri-, penta- and heptamethine cyanine dyes containing functional groups in N-substituents are considered. Approaches suitable for the preparation of both symmetrical and unsymmetrical cyanine dyes are presented. Examples of the practical use of this type of cyanine dyes as fluorescent labels and probes in biology and medicine, as well as of components of photoactive supramolecular structures, photosensitizers and photo- and electroluminescent materials are given. The bibliography includes 106 references. [ DOI ...

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2-(2,6-Diethylphenyl)-4-methoxy-N-(4-methoxynaphthalen-1-yl)-N-methyl-5,6,7,8-tetrahydroquinolin-5-amine | C32H36N2O2 | CID 25192491 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

4-Methoxy-N-[4-(3-methylbutoxy)phenyl]benzene-1-carbothioamide | C19H23NO2S | CID 71385636 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

3-Sulfopropyl acrylate, potassium salt (SPAK) is a functional acrylic acid monomer useful in the synthesis of new generation of super water absorbent, superporous, polymer hydrogels. SPAK mainly used to improve hydrogel properties; e.g., stabilize wate

TY - GEN. T1 - In situ Preparation of Robust Porous Modified Mixed-mode Sulfopropyl Methacrylate Monolithic Capillary for mHPLC Analysis of Pharmaceutical Compounds. AU - Ghanem, Ashraf. PY - 2009. Y1 - 2009. M3 - Conference contribution. BT - HPLC 2009: 34th International Symposium on High-Performance Liquid Phase Separations and Related Techniques. PB - CASSS - An International Separation Science Society. CY - Online. ER - ...

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Acid dye, any bright-coloured synthetic organic compound whose molecule contains two groups of atoms-one acidic, such as a carboxylic group, and one colour-producing, such as an azo or nitro group. Acid dyes are usually applied in the form of their sodium salts, chiefly on wool but also on silk and, to a limited extent, in combination with a mordant, or fixing agent, on cotton and rayon. These dyestuffs produce bright, usually fast shades in a wide range of colours. ...

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The compound 3, which exists in tautomeric equilibria between enamine (form A) and methylene imine (form B), was prepared by addition of ethoxycarbonylmethyl chloride 2 (1.23g, 0.01 mol) to a solution of 3-(ethoxycarbonylmethylene)-2-oxo quinoxaline, 1 [1] (2.32 g, 0.01 mol) in 60 ml DMF, K2CO3 (1.38g, 0.01mol) and triethylbenzylammonium chloride (0.001 mol).[...]

The commonly used fluorescent dye YOYO-1 (YOYO) has, using bulk techniques, been demonstrated to stain DNA heterogeneously at substoichiometric concentrations. We here, using nanofluidic channels and fluorescence microscopy, investigate the heterogeneous staining on the single DNA molecule level and demonstrate that the dye distribution is continuous. The equilibration of YOYO on DNA is extremely slow but can be accelerated by increasing the ionic strength and/or the temperature. Furthermore, we demonstrate how to use the heterogeneous staining as a tool for detailed and time-efficient studies of how fluorescent dyes affect the physical properties of DNA. We show that the relative increase in extension of DNA with increasing amount of YOYO bound is higher at low ionic strengths and also extrapolate the extension of native DNA. Our study reveals important information on how YOYO affects the physical properties of DNA, but it also has broader applications. First, it reveals how cationic intercalators,

Supplied as five vials (5 µL per vial, 1 mM in DMSO). Each vial sufficient for 100-200 live cell imaging cytotoxicity tests in 96-well format. Incucyte® Cytotox Reagents are highly sensitive cyanine nucleic acid dyes ideally suited to a simple mix-and-read, real-time quantification of cell death. Addition of the Incucy

Supplied as five vials (5 µL per vial, 1 mM in DMSO). Each vial sufficient for 100-200 live cell imaging cytotoxicity tests in 96-well format. Incucyte® Cytotox Reagents are highly sensitive cyanine nucleic acid dyes ideally suited to a simple mix-and-read, real-time quantification of cell death. Addition of the Incucy

Supplied as five vials (5 µL per vial, 1 mM in DMSO). Each vial sufficient for 100-200 live cell imaging cytotoxicity tests in 96-well format. Incucyte® Cytotox Reagents are highly sensitive cyanine nucleic acid dyes ideally suited to a simple mix-and-read, real-time quantification of cell death. Addition of the Incucy

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Reding, Raymond[UCL] Ciccarelli, Olga[UCL] Bourdeaux, Christophe[UCL] Gras, Jeremie[UCL] Evrard, V Buts, Jean-Paul[UCL] Carlier, Marianne[UCL] Clapuyt, Philippe[UCL] Clément de clety, Stéphan[UCL] De Kock, Marc[UCL] Hermans, Dominique[UCL] Janssen, M. Moulin, Didier[UCL] Rahier, Jacques[UCL] Saint-Martin, C Sempoux, Christine[UCL] Van Obbergh, Luc[UCL] Veyckemans, Francis[UCL] Lerut, Jan[UCL] de Ville de Goyet, J Sokal, Etienne[UCL] Otte, Jean-Bernard[UCL] (2004) Acta gastro-enterologica Belgica - Vol. 67, no. 2, p. 176-8 (2004) ...

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Cs2UCl6 crystallizes in the trigonal P-3m1 space group. The structure is three-dimensional. Cs1+ is bonded to twelve equivalent Cl1- atoms to form CsCl12 cuboctahedra that share corners with six equivalent CsCl12 cuboctahedra, corners with three equivalent UCl6 octahedra, faces with eight equivalent CsCl12 cuboctahedra, and faces with three equivalent UCl6 octahedra. The corner-sharing octahedral tilt angles are 21°. There are a spread of Cs-Cl bond distances ranging from 3.83-3.89 Å. U4+ is bonded to six equivalent Cl1- atoms to form UCl6 octahedra that share corners with six equivalent CsCl12 cuboctahedra and faces with six equivalent CsCl12 cuboctahedra. All U-Cl bond lengths are 2.63 Å. Cl1- is bonded in a distorted single-bond geometry to four equivalent Cs1+ and one U4+ atom.

UCL Discovery is UCLs open access repository, showcasing and providing access to UCL research outputs from all UCL disciplines.

UCL Discovery is UCLs open access repository, showcasing and providing access to UCL research outputs from all UCL disciplines.

Dequalinium is a quaternary ammonium cation and bolaamphiphile commonly available as the dichloride salt. The bromide, iodide, acetate, and undecenoate salts are known as well. Dequalinium chloride is the active ingredient of several medications: Dequadin an antiseptic and disinfectant. It is a topical bacteriostat. It is used in wound dressings and mouth infections and may also have antifungal action. It may cause skin ulceration. Fluomizin, vaginal tablets containing 10 mg dequalinium chloride, are used for treating vaginal bacterial conditions (i.e. Bacterial Vaginosis and aerobic vaginitis). The dequalinium dication is symmetrical, containing two quaternary quinolinium units linked by an N-decylene chain. Dequalinium salts may be used to treat malaria. As dequalinium chloride, it can be used in lozenges to cure sore throats however while this is effective in vitro, it is not effective in cases of streptococci infections US Patent 4946849. United States Patents and Trademarks Office ...

Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice ...

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Dequalinium Chloride is a medicine available in a number of countries worldwide. A list of US medications equivalent to Dequalinium Chloride is available on the Drugs.com website.

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A fast and reproducible cell- and 96-well plate-based method for the evaluation of P2X7 receptor activation using YO-PRO-1 fluorescent dye

I dye yarn for a living fabric too but Mx dyes. I use a combination of Lanaset Dharma and some Jacquard. The Jacquard colors I use I always mix and often with Dharma or other Acid dyes. I love them. The colors are true weighed mixes are so close that I cannot see a difference in the colors after dyeing and drying. I cannot duplicate some of the basic colors Jacquard carries because the names are similar the colors are not. Jacquard Pink is a great example. It does not look like anyone elses Magenta or Fuschia. It stands alone. Behaves itself with vinegar (used with yarns with Stellina in them) and Citric Acid. I use the Cherry Silver Golden Ochre Aztec Gold and Sky Blue. I do not interchange the Jacquard colors with any other colors when a formula calls for them. If I dont have them on hand I do not dye that colorway. A really good mix is the Dharma Acid Sun Yellow with the Jacquard Aztec Gold overlaid with some other colors. I am happy with Jacquard Acid Dyes and even though I no longer buy ...

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