27360-85-6 Usage
Description
COPPER PHTHALOCYANINE TETRASULFONIC ACID TETRASODIUM SALT is a dark blue to purple crystalline compound known for its unique chemical properties. It is characterized by its solubility in water, which results in a blue color, and its reactions with various chemicals, such as strong sulfuric acid, hydrochloric acid, nitric acid, sodium hypochlorite, and insurance powder solution, which lead to color changes and precipitation.
Uses
Used in Chemical Industry:
COPPER PHTHALOCYANINE TETRASULFONIC ACID TETRASODIUM SALT is used as a chemical indicator for various applications due to its distinct color changes when reacting with different chemicals. This property makes it useful in detecting the presence of specific substances and monitoring chemical reactions.
Used in Analytical Chemistry:
In the field of analytical chemistry, COPPER PHTHALOCYANINE TETRASULFONIC ACID TETRASODIUM SALT serves as a colorimetric reagent. Its color-changing behavior upon interaction with other chemicals allows for the identification and quantification of various substances in a sample.
Used in Pharmaceutical Industry:
COPPER PHTHALOCYANINE TETRASULFONIC ACID TETRASODIUM SALT may also find applications in the pharmaceutical industry, potentially as a component in the development of new drugs or as a diagnostic tool for detecting specific biological markers.
Used in Environmental Science:
In environmental science, COPPER PHTHALOCYANINE TETRASULFONIC ACID TETRASODIUM SALT could be employed as a tool for detecting and monitoring water quality, given its solubility and reactivity with various chemicals. Its color changes can indicate the presence of pollutants or other substances of concern in aquatic environments.
Used in Research and Development:
COPPER PHTHALOCYANINE TETRASULFONIC ACID TETRASODIUM SALT may be utilized in research and development settings to study the interactions between different chemicals and to develop new methods for chemical analysis and detection. Its unique properties can contribute to the advancement of scientific knowledge and the creation of innovative applications.
Preparation
in C.I. Pigment Blue 15 (C.I. 74160) points out the method (2) use 4-Sulfophthalic acid?preparation phthalocyanine. The sun and alkali resistance is better than the fastness of the products directly Copper phthalocyanine, but for cellulose low affinity.
Flammability and Explosibility
Nonflammable
Check Digit Verification of cas no
The CAS Registry Mumber 27360-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,6 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27360-85:
(7*2)+(6*7)+(5*3)+(4*6)+(3*0)+(2*8)+(1*5)=116
116 % 10 = 6
So 27360-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C32H16N8.4CH4O3S.Cu.4Na/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25;4*1-5(2,3)4;;;;;/h1-16H;4*1H3,(H,2,3,4);;;;;/q-2;;;;;+2;4*+1/p-4/rC32H16CuN8.4CH3NaO3S/c1-2-10-18-17(9-1)25-34-27-19-11-3-4-12-20(19)29-36-31-23-15-7-8-16-24(23)32-37-30-22-14-6-5-13-21(22)28-35-26(18)38(25)33(39(27)29,40(28)30)41(31)32;4*1-6(3,4)5-2/h1-16H;4*1H3
27360-85-6Relevant articles and documents
Aqueous aerobic oxidation of alkyl arenes and alcohols catalyzed by copper(ii) phthalocyanine supported on three-dimensional nitrogen-doped graphene at room temperature
Mahyari, Mojtaba,Laeini, Mohammad Sadegh,Shaabani, Ahmad
supporting information, p. 7855 - 7857 (2014/07/08)
Copper(ii) tetrasulfophthalocyanine supported on three-dimensional nitrogen-doped graphene-based frameworks was synthesized and introduced as a bifunctional catalyst for selective aerobic oxidation of alkyl arenes and alcohols to the corresponding carbonyl compounds. The ease of catalyst separation, high turnover, low catalyst loading and recyclability could potentially render it applicable in industrial setting. This journal is the Partner Organisations 2014.
