Solway Green G - 4403-90-1
Solway Green G
Catalog Number: BT-258132
CAS Number: 4403-90-1
Molecular Formula: C28H20N2Na2O8S2
Molecular Weight: 622.6 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction
Description
Solway Green G is a synthetic dye that belongs to the triphenylmethane class of dyes. It is widely used in various industries, including textile, paper, and food, as a colorant. Solway Green G is also used in scientific research as a biological stain and a fluorescent probe.
Properties
CAS Number
4403-90-1
Product Name
Solway Green G
IUPAC Name
sodium;5-methyl-2-[[4-(4-methyl-2-sulfoanilino)-9,10-dioxoanthracen-1-yl]amino]benzenesulfonic acid
Molecular Formula
C28H20N2Na2O8S2
Molecular Weight
622.6 g/mol
InChI
InChI=1S/C28H22N2O8S2.Na/c1-15-7-9-19(23(13-15)39(33,34)35)29-21-11-12-22(30-20-10-8-16(2)14-24(20)40(36,37)38)26-25(21)27(31)17-5-3-4-6-18(17)28(26)32;/h3-14,29-30H,1-2H3,(H,33,34,35)(H,36,37,38);/q;+1
InChI Key
FPAYXBWMYIMERV-UHFFFAOYSA-L
SMILES
CC1=CC(=C(C=C1)NC2=C3C(=C(C=C2)NC4=C(C=C(C=C4)C)S(=O)(=O)O)C(=O)C5=CC=CC=C5C3=O)S(=O)(=O)O.[Na+]
Solubility
5 to 10 mg/mL at 70° F (NTP, 1992)
Slightly soluble in acetone, alcohol, pyridine. Insoluble in chloroform, toluene.
In 2-methoxyethanol 30 mg/mL, ethanol 2 mg/mL, temperature not specified
In water, 60 mg/mL, temperature not specified
Synonyms
6,6'-(1,4-anthraquinonylenediimino)di-m-toluenesulfonic acid disodium salt
acid green 25
acid leather green ag
alizarin brilliant green
C.I. 61570
D and C green #5
D and C green 5
DC green 5
erio fast green gs
Canonical SMILES
CC1=CC(=C(C=C1)NC2=C3C(=C(C=C2)NC4=C(C=C(C=C4)C)S(=O)(=O)[O-])C(=O)C5=CC=CC=C5C3=O)S(=O)(=O)[O-].[Na+].[Na+]
Method of Synthesis or Extraction
Solway Green G is synthesized by the reaction of malachite green with zinc chloride. The reaction yields a green-colored compound, which is then purified by recrystallization. The efficiency of this method is high, and the yield is around 80%. However, the method involves the use of toxic and hazardous chemicals, such as zinc chloride, which can cause environmental pollution and health hazards. Therefore, alternative methods, such as microwave-assisted synthesis and green chemistry approaches, are being explored to reduce the environmental impact and improve safety.
Chemical Structure and Biological Activity
Solway Green G has a molecular formula of C27H33N2Cl and a molecular weight of 416.03 g/mol. It has a triphenylmethane structure with a quaternary ammonium group and a chloride ion. Solway Green G is a cationic dye, which means it can bind to negatively charged molecules, such as DNA and proteins. It is also a fluorescent dye, which means it can emit light when excited by a specific wavelength of light. Solway Green G has been shown to have antimicrobial, antifungal, and antiparasitic activity. It can inhibit the growth of bacteria, fungi, and protozoa by disrupting their cell membranes and metabolic processes.
Biological Effects
Solway Green G has been shown to have various biological effects on cell function and signal transduction. It can induce apoptosis, which is a programmed cell death, in cancer cells. It can also modulate the activity of ion channels and receptors, which are involved in neuronal signaling and synaptic transmission. Solway Green G has been used as a biological stain to visualize cells and tissues in microscopy. However, Solway Green G can also have potential toxic effects on cells and organisms. It can cause DNA damage, oxidative stress, and inflammation, which can lead to cell death and tissue damage.
Applications
Solway Green G has various applications in scientific research, medical research, environmental research, and industrial research. In medical research, Solway Green G is used as a biological stain and a fluorescent probe to visualize cells and tissues. It is also used in drug development as a screening tool to identify potential drug candidates. Solway Green G has been shown to have anticancer, antifungal, and antiparasitic activity, which makes it a promising candidate for drug development. In environmental research, Solway Green G is used to study the effects of pollutants on ecosystems. It can also be used in pollution management to monitor the levels of pollutants in water and soil. In industrial research, Solway Green G is used as a colorant in various products, such as textiles, paper, and food. It can also be used to improve product quality and efficiency. However, the use of Solway Green G in industrial processes can also have health and safety considerations, such as exposure to toxic and hazardous chemicals.
Future Perspectives and Challenges
The use of Solway Green G in scientific research and industrial applications is expected to increase in the future. However, there are also challenges that need to be addressed, such as the environmental impact and safety concerns. Alternative methods, such as green chemistry approaches and biodegradable dyes, are being explored to reduce the environmental impact and improve safety. The development of new technologies, such as nanotechnology and biotechnology, can also provide new opportunities for the application of Solway Green G in scientific research and industrial processes.
Conclusion
Solway Green G is a synthetic dye that has various applications in scientific research, medical research, environmental research, and industrial research. It has a triphenylmethane structure with a quaternary ammonium group and a chloride ion. Solway Green G has been shown to have antimicrobial, antifungal, and antiparasitic activity, as well as potential toxic effects on cells and organisms. The use of Solway Green G in scientific research and industrial applications is expected to increase in the future, but there are also challenges that need to be addressed, such as the environmental impact and safety concerns. Alternative methods and new technologies can provide new opportunities for the application of Solway Green G in various fields.
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