Basic blue 26 - 2580-56-5
Basic blue 26
Catalog Number: BT-308652
CAS Number: 2580-56-5
Molecular Formula: C33H32ClN3
Molecular Weight: 506.1 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction
Description
Basic blue 26 is a synthetic dye that belongs to the class of triarylmethane dyes. It is commonly used in various industries, including textiles, paper, and cosmetics. Basic blue 26 is also used in medical and environmental research due to its unique properties.
Properties
CAS Number
2580-56-5
Product Name
Basic blue 26
IUPAC Name
[4-[bis[4-(dimethylamino)phenyl]methylidene]naphthalen-1-ylidene]-phenylazanium;chloride
Molecular Formula
C33H32ClN3
Molecular Weight
506.1 g/mol
InChI
InChI=1S/C33H31N3.ClH/c1-35(2)27-18-14-24(15-19-27)33(25-16-20-28(21-17-25)36(3)4)31-22-23-32(30-13-9-8-12-29(30)31)34-26-10-6-5-7-11-26;/h5-23H,1-4H3;1H
InChI Key
LLWJPGAKXJBKKA-UHFFFAOYSA-N
SMILES
CN(C)C1=CC=C(C=C1)C(=C2C=CC(=[NH+]C3=CC=CC=C3)C4=CC=CC=C24)C5=CC=C(C=C5)N(C)C.[Cl-]
Synonyms
4-(alpha-(4-anilino-1-naphthyl)-p-dimethylamino)benzylidene-2,5-cyclohexadien-1-ylidenedimethyl ammonium chloride
Basic Blue 26
Victoria blue B
Canonical SMILES
CN(C)C1=CC=C(C=C1)C(=C2C=CC(=[NH+]C3=CC=CC=C3)C4=CC=CC=C24)C5=CC=C(C=C5)N(C)C.[Cl-]
Method of Synthesis or Extraction
Basic blue 26 can be synthesized by various methods, including the condensation of benzaldehyde with dimethyl aniline, the reaction of benzaldehyde with dimethyl aniline hydrochloride, and the reaction of benzaldehyde with dimethyl aniline in the presence of zinc chloride. The efficiency and yield of each method depend on the reaction conditions, such as temperature, pressure, and catalysts. The environmental and safety considerations of basic blue 26 synthesis include the use of hazardous chemicals, such as benzaldehyde and dimethyl aniline, and the generation of toxic waste.
Chemical Structure and Biological Activity
The chemical structure of basic blue 26 consists of a triarylmethane core with three aromatic rings and a quaternary ammonium group. Basic blue 26 has a positive charge, which makes it soluble in water and other polar solvents. The mechanism of action of basic blue 26 involves the binding of the dye to biological targets, such as proteins and nucleic acids, through electrostatic and hydrophobic interactions. Basic blue 26 has been shown to exhibit bioactivity and potency against various microorganisms, including bacteria, fungi, and viruses.
Biological Effects
Basic blue 26 has been found to affect cell function and signal transduction by modulating the activity of enzymes and receptors. Basic blue 26 has also been investigated for its potential therapeutic and toxic effects. In medical research, basic blue 26 has been shown to have antimicrobial, antiviral, and anticancer properties. However, the use of basic blue 26 in medical applications is limited due to its potential toxicity and side effects. In environmental research, basic blue 26 has been found to have adverse effects on ecosystems, such as the inhibition of photosynthesis in algae and the disruption of aquatic food chains. Basic blue 26 has also been used in pollution management to remove dyes from wastewater.
Applications
Basic blue 26 has various applications in different fields. In medical research, basic blue 26 has been used in drug development, clinical trials, and findings. Basic blue 26 has been investigated as a potential treatment for bacterial and viral infections, cancer, and Alzheimer's disease. In environmental research, basic blue 26 has been used to study the effects of dyes on ecosystems and to develop sustainable methods for dye removal from wastewater. In industrial research, basic blue 26 has been used in manufacturing processes to improve product quality and efficiency. However, the use of basic blue 26 in industrial applications is limited due to its potential toxicity and health and safety considerations.
Future Perspectives and Challenges
The current limitations in the use and study of basic blue 26 include its potential toxicity, limited bioavailability, and lack of specificity. Possible solutions and improvements include the development of safer and more effective derivatives of basic blue 26, the optimization of synthesis and extraction methods, and the identification of new biological targets. Future trends and prospects in the application of basic blue 26 in scientific research include the development of novel antimicrobial and anticancer agents, the exploration of its potential as a diagnostic tool, and the investigation of its role in signal transduction pathways.
Conclusion:
Basic blue 26 is a synthetic dye with various applications in different fields, including medical, environmental, and industrial research. The method of synthesis or extraction, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges of basic blue 26 have been discussed in this paper. The use of basic blue 26 in scientific research is promising but requires further investigation to overcome its limitations and challenges.
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