307554-62-7

Basic information

• Product Name: 9 10-ANTHRACENEDIYL-BIS(METHYLENE)
• Synonyms: 9 10-ANTHRACENEDIYL-BIS(METHYLENE);biochemika90%(hpce);9,10-Anthracenedipropanoicacid, a10,a9-dicarboxy-;2,2'-(Anthracene-9,10-diylbis(methylene)
• CAS NO: 307554-62-7
• Molecular Formula: C₂₂H₁₈O₈
• Molecular Weight: 410.38
• Mol File: 307554-62-7.mol

Chemical Properties

• Melting Point: >300 °C
• Boiling Point: 745.4±60.0 °C(Predicted)
• Appearance: /
• Density: 1.527±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: DMSO: soluble
• PKA: 2.90±0.30(Predicted)
• BRN: 3503804
• CAS DataBase Reference: 9 10-ANTHRACENEDIYL-BIS(METHYLENE)(CAS DataBase Reference)
• NIST Chemistry Reference: 9 10-ANTHRACENEDIYL-BIS(METHYLENE)(307554-62-7)
• EPA Substance Registry System: 9 10-ANTHRACENEDIYL-BIS(METHYLENE)(307554-62-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• RIDADR: UN 3077 9 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 307554-62-7(Hazardous Substances Data)

Usage

Uses

Used in Chemical Assay:
9,10-Anthracene diyl-bis(methylene) is used as a reagent for the assay of oxygen (O2). It offers better characteristics than 9,10-anthracenediyl-bis-dipropionic acid, making it a preferred choice for this application. Its ability to effectively measure oxygen levels is crucial in various chemical and environmental analyses.

Upstream product

• 781-43-1 9,10-dimethylanthracene 
• 120-12-7 anthracene 
• 10387-13-0 9,1-bis(chloromethyl)anthracene 
• 34373-96-1 9,10-dibromomethylanthracene 
• 307554-61-6 9,10-bis<<2,2-di(ethoxycarbonyl)>ethyl>anthracene 

Downstream Products

• 71367-28-7 3,3'-(anthracene-9,10-diyl)dipropionic acid 

Relevant articles and documents

New reagents for determination of the quantum efficiency of singlet oxygen generation in aqueous media

Water-soluble anthracene derivatives containing carboxy, dihydroxyphosphinyl, or pyridinium fragments bound via methylene groups to 9- and 10-carbon atoms were prepared, and their spectra, solubility, and reactivity toward singlet oxygen were studied. Using sodium α,α1-(anthracene-9,10-diyl)bis(methylmalonate) as acceptor, it is possible to determine the quantum efficiency of singlet oxygen generation in aqueous solutions and in microheterogeneous media in the presence of biomacromolecules.

Synthetic β-Cyclodextrin Dimers for Squaraine Binding: Effect of Host Architecture on Photophysical Properties, Aggregate Formation and Chemical Reactivity

Reported herein is the synthesis and application of three novel β-cyclodextrin dimer hosts for the complexation of near infrared (NIR) squaraine dyes in aqueous solution. A series of eight different N-substituted N-methyl anilino squaraine dyes with variable terminal groups are investigated, with an optimal n-hexyl-substituted squaraine guest demonstrating binding constants orders of magnitude higher than the other squaraine–host combinations and comparable to literature-reported systems. Moreover, hydrophobic complexation of the squaraine dyes with the β-cyclodextrin dimer hosts causes drastic changes in the squaraine's photophysical properties, propensity for aggregation and susceptibility to hydrolytic decay.

Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N′-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems

We report herein the synthesis of a new hydrophilic and non-ionic anthracene derivative, the N,N′-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide. The evaluation of this compound as chemical trap of singlet molecular oxygen by using labeling experiments and HPLC-MS analysis showed that it could be efficiently used in biological investigations.