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1,10-Phenanthroline-5-carboxaldehyde is a chemical compound with the molecular formula C13H9NO, belonging to the phenanthroline family of heterocyclic organic compounds. It is recognized for its chelating properties and its capacity to form stable complexes with metal ions, which makes it a valuable asset in various scientific and industrial applications.

91804-75-0

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91804-75-0 Usage

Uses

Used in Coordination Chemistry:
1,10-Phenanthroline-5-carboxaldehyde is used as a chelating agent for forming stable complexes with metal ions, which is instrumental in coordination chemistry for studying the properties and behaviors of metal complexes.
Used in Analytical Chemistry:
In analytical chemistry, 1,10-Phenanthroline-5-carboxaldehyde is utilized as a reagent, particularly for the detection and quantification of metal ions through the formation of colored complexes that can be measured spectroscopically.
Used in Biochemical Research:
1,10-Phenanthroline-5-carboxaldehyde is employed as a reagent in biochemical research to study the interactions of metal ions with biomolecules, which is crucial for understanding various biological processes and mechanisms.
Used in Industrial Processes:
1,10-Phenanthroline-5-carboxaldehyde is also used in industrial processes where its ability to chelate metal ions is leveraged for applications such as catalysis and the production of metal-containing materials.
Used in the Development of Luminescent Materials:
1,10-Phenanthroline-5-carboxaldehyde is studied for its potential use in the development of luminescent materials, which could have applications in optoelectronics and sensing technologies.
Used as an Antiviral Agent:
1,10-Phenanthroline-5-carboxaldehyde has been investigated for its potential as an antiviral agent, highlighting its possible role in the medical and pharmaceutical fields for the treatment or prevention of viral infections.

Check Digit Verification of cas no

The CAS Registry Mumber 91804-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,0 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91804-75:
(7*9)+(6*1)+(5*8)+(4*0)+(3*4)+(2*7)+(1*5)=140
140 % 10 = 0
So 91804-75-0 is a valid CAS Registry Number.

91804-75-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,10-Phenanthroline-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-Formyl-1.10-phenanthrolin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91804-75-0 SDS

91804-75-0Downstream Products

91804-75-0Relevant academic research and scientific papers

Fluorescent probe ruthenium complex, synthesis method and application thereof

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Paragraph 0047; 0048, (2019/01/15)

The invention discloses a fluorescent probe ruthenium complex, a synthesis method and the application thereof. The complex is obtained by coordination of 5-formyl-1,10-o-phenanthroline as a ligand andruthenium ions. A strong electron-withdrawing formyl is introduced to the 5th site of o-phenanthroline, which coordinates with the metallic ruthenium to obtain a hexa-coordinate ruthenium complex serving as a fluorescent probe for detecting cysteine and homocysteine, wherein the probe shows high sensitivity and high selectivity recognition on the cysteine and the homocysteine. In the presence ofother interfering substances, the fluorescence intensity is not changed significantly, and the probe shows strong interference capability. The probe has fast response and wide pH application range, does not require an organic solvent, and is a ruthenium complex fluorescent probe for detecting cysteine and homocysteine in a 100% aqueous phase.

Organic complex mercury ion probe and preparation method and application thereof

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Paragraph 0040; 0041, (2017/12/28)

The invention discloses an organic complex mercury ion probe and a preparation method and application thereof. The preparation method comprises the steps of enabling rhodamine B to react with hydrazine hydrate to obtain pink solid rhodamine B hydrazide, and enabling 5-methyl phenanthroline to react with selenium dioxide to obtain 5-formyl phenanthroline; enabling a reaction product obtained by reacting the rhodamine B hydrazide and the 5-formyl phenanthroline to react with Ir2(ppy)4Cl2, and then reacting with NH4PF6, thus finally obtain the organic complex mercury ion probe. The preparation method of the probe is simple, and has the advantages of stable light emission, convenient and efficient operation and suitability for qualitatively, quantitatively and quickly detecting mercury ions in a solution, soil, biological cells and the like, and can be widely applied to the fields such as environment detection and biological cell imaging.

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