15554-15-1

Basic information

• Product Name: Aluminum phthalocyanine hydroxide
• Synonyms: Aluminum,hydroxy[29H,31H-phthalocyaninato(2-)-N29,N30,N31,N32]-, (SP-5-12)-; Aluminum,hydroxy[phthalocyaninato(2-)]- (7CI); 29H,31H-Phthalocyanine, aluminum complex;A 13Y; Aluminum phthalocyanine hydroxide;Hydroxy[phthalocyaninato(2-)]aluminum; Hydroxyaluminum phthalocyanine; SanyoCyanine Blue A 13Y
• CAS NO: 15554-15-1
• Molecular Formula: C₃₂H₁₇AlN₈O
• Molecular Weight: 556.523
• Mol File: 15554-15-1.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Aluminum phthalocyanine hydroxide(CAS DataBase Reference)
• NIST Chemistry Reference: Aluminum phthalocyanine hydroxide(15554-15-1)
• EPA Substance Registry System: Aluminum phthalocyanine hydroxide(15554-15-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 15554-15-1(Hazardous Substances Data)

Usage

Description

Aluminum phthalocyanine hydroxide is a dark blue, crystalline organic compound that belongs to the phthalocyanine family. It is derived from phthalic acid and is known for its unique electronic and optical properties.

Uses

Used in Photodynamic Therapy:
Aluminum phthalocyanine hydroxide is used as a photosensitizer for the treatment of certain types of cancer and other medical conditions. It aids in the selective destruction of cancerous cells when activated by light.
Used in Dye and Pigment Manufacturing:
Aluminum phthalocyanine hydroxide is used as a key component in the production of dyes and pigments, providing vibrant colors and stability to various products.
Used as a Catalyst in Chemical Reactions:
Aluminum phthalocyanine hydroxide serves as an effective catalyst in various chemical reactions, enhancing the efficiency and selectivity of the processes.
Used in Solar Energy Conversion:
Due to its unique electronic and optical properties, aluminum phthalocyanine hydroxide has potential applications in solar energy conversion, contributing to the development of more efficient solar cells.
Used in Electronic Devices:
Aluminum phthalocyanine hydroxide can be utilized in the manufacturing of electronic devices, such as sensors and transistors, due to its electronic properties.
Used in Optical Materials:
Aluminum phthalocyanine hydroxide's optical properties make it suitable for use in the development of optical materials, such as optical filters and waveguides, for various applications in the telecommunications and imaging industries.

Upstream product

• 925-47-3 diethyl thioglycolate 
• 95-92-1 oxalic acid diethyl ester 
• 14282-56-5 diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate disodium salt 
• 14154-42-8 chloroaluminum phthalocyanine 
• 7732-18-5 water 
• 7664-93-9 sulfuric acid 
• 202865-76-7 C₉H₉BrFNO 
• 458-10-6 N-(3-fluoro-4-methylphenyl)acetamide 
• 452-77-7 3-fluoro-4-methyl-phenylamine 
• 143655-70-3 C₁₅H₁₇FN₂O₃ 

Downstream Products

• 1388709-61-2 aluminum phthalocyanine benzoate 
• 1388709-56-5 aluminum phthalocyanine propionate 
• 115949-70-7 aluminum phthalocyanine acetate 
• 51961-93-4 fluoro-aluminium phthalocyanine 

Relevant articles and documents

A substituted EDOT precursor: Diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate

The title compound. C10H12O6S, has been obtained as dark-yellow chunk-shaped crystals, together with the expected thin white needles. The structures of the two phases are identical. Two independent molecules compose the asymmetric unit: one molecule is totally planar, whereas a methyl group of the second molecule points out of the plane. Each molecule participates in several intra- and intermolecular hydrogen bonds and short contacts. The overall structure can be regarded as parallel sheets of molecules. Within a sheet, molecules are connected to one another in an infinite network via numerous short intermolecular contacts. Sheets are connected via hydrogen bonds and short contacts, in particular involving the methyl groups.

Phthalocyanine compound with high thermal stability and high chemical resistance, method for production thereof and ink composition and printing article using the same

The present invention relates to an aluminum phthalocyanine compound substituted with an ethoxy group having excellent heat resistance and chemical resistance, a method for preparing the same, an ink composition and a printed article using the same. To the present invention, an ethoxy aluminum phthalocyanine compound having 1 a structure represented by the following formula, which is a phthalocyanine 650 - 840 nm-substituted phthalocyanine in which an ethoxy group 1050nm is substituted with aluminum in a central metal, is synthesized with high yield. The compound of formula ([I) as claimed in 1] Claim (by machine translation)

Preparation of an EDOT-based polymer: Optoelectronic properties and electrochromic device application

Here we present the synthesis, characterization and electropolymerization of a new EDOT-based monomer; 5,10-dihydrobenzo[f]thieno[3,4-b][1,4]dioxocine (DTD). Electrochemical polymerization of DTD was performed potentiostatically by using dichloromethane (DCM) as solvent and tetrabutylammonium hexafluorophosphate (TBPF6) as supporting electrolyte. Homopolymer [P(DTD)] films and copolymer [P(DTD-co-TPA)] films of DTD prepared by using 4-(2,5-di(thiophen-2-yl)-1H-pyrrole-1-yl)butane-1-amine (TPA) were characterized via CV and UV-vis spectroscopy. Spectroelectrochemical analysis of P(DTD) revealed electronic transitions at 585 nm (π-π transition) with an electronic band gap of 1.69 eV. Electrochromic studies revealed that P(DTD) has competitive properties to EDOT. Furthermore, a dual-type complementary colored polymer electrochromic device based on P(DTD) and P(TPA) was constructed in sandwich configuration. Spectroelectrochemical studies revealed that the oxidized state of the device shows a blue color whereas it is yellow in the reduced state. The maximum contrast (Δ%T) and switching time of the device were measured as 25.5% and 0.5 s for 385 nm and 21% and 1.0 s for 550 nm.