Vi är professionella 3,8-dibromo-1,10-phenanthroline cas no:100125-12-0 tillverkare i Kina i över 10 år, med bulk högkvalitativa kemiska produkter i lager.

Structure, properties, spectra, suppliers and links for: phenanthroline, 66-71-7. 1,10-Phenanthroline [ACD/Index Name] [ACD/IUPAC Name].

Pris: 791 kr. e-bok, 2013. Laddas ned direkt. Köp boken Analytical Applications of 1,10-Phenanthroline and Related Compounds av Alfred A. Schilt (ISBN  Acid-grade and ceramic-grade fluorspar -- Determination of iron content -- 1,10-Phenanthroline spectrometric method - ISO 9061:1993. The characteristics of the binding reaction of surfactant-cobalt(III) complex, cis-[Co(phen)(2)(C14H29NH2)]Cl-2 center dot 3H(2)O (phen =1,10-phenanthroline,  Structural diversities and spectroscopic properties of bis and tris(1,10-phenanthroline)copper(II) complexes.

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Mycopathologia  1,10-Phenanthroline monohydrate. Formula: C12H8N2 • H2O. MW: 198.22 g/mol . Storage/Handling: Store desiccated at room temperature under inert gas. Danger! According to the harmonised classification and labelling (CLP00) approved by the European Union, this substance is toxic if swallowed, is very toxic to  The solid forms emerging from an experimental screening programme of 1,10- phenanthroline (o-phen), a heavily used bidentate ligand, and interconversion  The room temperature solubility of 1,10-phenanthroline monohydrate was estimated in 24 different solvents.

Get contact details & address of companies manufacturing and supplying Phenanthroline, 1 10-Phenanthroline across India. 1,10-Phenanthroline sc-255888 Hazard Alert Code Key: EXTREME HIGH MODERATE LOW Section 1 - CHEMICAL PRODUCT AND COMPANY IDENTIFICATION PRODUCT NAME 1,10-Phenanthroline STATEMENT OF HAZARDOUS NATURE CONSIDERED A HAZARDOUS SUBSTANCE ACCORDING TO OSHA 29 CFR 1910.1200.

1,10-Phenanthroline can be used as: A cathode buffer layer to improve the efficiency of organic solar cells. A conventional chelator to study its efficacy in Fenton 

For more information about this application, proceed to downlaod  SPCEs modified with 1,10-phenanthroline-5,6-dione are ideal for detecting NADH evolution in enzymatic dehydrogenase based sensors. Väga 0,11 g hemihydrat 2,9-dimetyl-1,10-phenanthroline (neocuproine) till en torr 100 mL-bägare. Tillsätt 50 mL 0,10 mol/L saltsyra (HCl) och  alpha-toluenesulphonyl fluoride. 1,10-phenanthroline.

1,10-Phenanthroline monohydrate CAS 5144-89-8 GR ACS - Find MSDS or SDS, a COA, data sheets and more information.

View information & documentation regarding 1,10-Phenanthroline monohydrate, including CAS, MSDS & more. 1,10-phenanthroline Regulatory process names 9 Translated names 22 CAS names 1 IUPAC names 8 Other identifiers 3 Print infocard Open Substance Regulatory Obligations 1,10-Phenanthroline is an inhibitor of metallopeptidases, with one of the first observed instances reported in carboxypeptidase A. Inhibition of the enzyme occurs by removal and chelation of the metal ion required for catalytic activity, leaving an inactive apoenzyme. 1,10-Phenanthroline targets mainly zinc metallopeptidases, with a much lower Abstract Ligand‐promoted copper‐catalyzed cascade reactions have become a robust tool for the synthesis of cyclic compounds. Although numerous ligands have been developed, this review focuses on the introduction of commercially available 1,10‐phenanthroline‐promoted copper‐catalyzed cascade reactions in recent years. Synonym: Tris(1,10-phenanthroline)ruthenium(II) chloride hydrate Empirical Formula (Hill Notation): C 36 H 24 Cl 2 N 6 Ru · xH 2 O Molecular Weight: 712.59 (anhydrous basis) Synonym: 1,10-Phenanthroline hydrochloride monohydrate, o-Phenanthroline hydrochloride monohydrate Empirical Formula (Hill Notation): C 12 H 8 N 2 · HCl · H 2 O Molecular Weight: 234.68

Origin: Indien UNSPSC: 12-35-00-00 Aqua-(dicyanamido-κN)(2,9-dimethyl-1,10-phenanthroline-κN,N')(nitrato-κO,O')cobalt(II)-2,9-dimethyl-1,10-phenanthroline-water (2/1/2).
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Figure 2 from FIR Spectra of compounds: (a) Be(ClO4 pic. Ag(1,10-phenanthroline)2](ClO4) | CAS#.

OXIDE 1 1,10-Phenanthroline, 1-oxide N N O [1891-19-6] C 12 H 8 N 2 O (MW 196.21) InChI = 1S/C12H8N2O/c15/h1-8H InChIKey = OFEFUDKSXOZQFL-UHFFFAOYSA-N (functionalization at the 2-position of the Looking for online definition of 1,10-phenanthroline or what 1,10-phenanthroline stands for? 1,10-phenanthroline is listed in the World's largest and most 1,10-Phenanthroline is a classic chelating bidentate ligand for transition metal ions that has played an important role in the development of coordination chemistry. It is an inhibitor of metallopeptidases. 1.1 Product Identifier Product Name 1-10-Phenanthroline Hydrate Other Names CAS No. 5144-89-8 Index No. 613-092-00-8 EC No. 200-629-2 Product Code S6101809 1.2 Relevant identified uses of the substances or mixture and uses advised against Product Use Laboratory chemicals, manufacture of substances, Scientific R&D 1.3 Details of the supplier of Compound 1,10-Phenanthroline monohydratewith free spectra: 2 NMR, 8 FTIR, 4 Raman, 2 UV-Vis, and 2 MS. 1,10-Phenanthroline may decrease effectiveness of Technetium Tc-99m oxidronate as a diagnostic agent.
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The kinetics of the racemization of [Ni(phen)3]2+ were investigated in the presence of 1-alkanesulfonate ions (n-CnH2n+1SO3−; n=8, 10, 12, and 14).

It has a role as an EC 3.4.19.3 (pyroglutamyl-peptidase I) inhibitor and an EC 2.7.1.1 (hexokinase) inhibitor. 1,10-Phenanthroline is soluble in methanol at 500 micrograms per mL, or in water at 3 milligrams per mL. It is also soluble in benzene and acetone. 1,10-Phenanthroline forms a stable complex with Fe (II) ion called ferroin, which is used as an indicator in Fe (II) salt titrations. Ferroin is also used in the determination of other metals, such as nickel, ruthenium, and silver. The molar absorptivity of the Fe (II) complex with 1,10-phenanthroline is 1.10 · 10 4 (a = 0.20) at λ max 512 nm, and that of the complex with 2,2'-bipyridyl is 8.7-10 3 at λ max 522 nm. Solutions of the complexes with phenanthroline and bipyridyl are stable, and the Fe (II) bound in the complex is resistant to oxidation.

1,10-Phenanthroline chloride monohydrate CAS 18851-33-7 GR for analysis and redox indicator [reagent for iron(II)] Reag. Ph Eur - Find MSDS or SDS, a COA, data sheets and more information.

It is inhibited by bacitracin, chelating agents EDTA and 1,10-phenanthroline, and by thiol-blocking reagents such as N-ethylmaleimide, but not phosphoramidon. Particles of magnesium sodium silicate on which are ionically bonded chiral complexes of tris(1,10-phenanthroline)ruthenium, for use in the manufacture of high  1,10-phenanthroline is a phenanthroline. It has a role as an EC 3.4.19.3 (pyroglutamyl-peptidase I) inhibitor and an EC 2.7.1.1 (hexokinase) inhibitor. 1,10-Phenanthroline is soluble in methanol at 500 micrograms per mL, or in water at 3 milligrams per mL. It is also soluble in benzene and acetone. 1,10-Phenanthroline forms a stable complex with Fe (II) ion called ferroin, which is used as an indicator in Fe (II) salt titrations. Ferroin is also used in the determination of other metals, such as nickel, ruthenium, and silver.

1,10-Phenanthroline, anhydrous is used as a chelating agent, used as bidendate nitrogen ligands in Heck type reactions as an alternative to phospine ligands. It is widely used as an indicator for alkyllithium reagents and an inhibitor of metallopeptidase enzymes. Use of 1,10-Phenanthroline o-Phenanthroline (1,10-Phenanthroline), a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells. o-Phenanthroline (1,10-Phenanthroline) forms a red chelate with Fe2+ that absorbs maximally at 510 nm[1]. 2010-01-01 · The title structure, C 12 H 9 N 2 + ·C 4 H 5 O 6 − ·3H 2 O, shows that one of the protons of d-tartaric acid has been transferred to 1,10-phenanthroline.The d-hydrogen tartrate anions are joined together in a head-to-tail fashion via a short hydrogen bond with donor–acceptor distance of 2.4554 (12) Å, unsymmetrical O—H distances of 1.01 (4) Å and 1.45 (4) Å, and a 174 (4)° O—H 1,10-Phenanthroline is a versatile ligand employed in the spectrophotometric determination of metals and photocatalytic reduction of carbon dioxide.