Date published: 2025-9-5

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Acridines and Acridones

Santa Cruz Biotechnology now offers a broad range of Acridines and Acridine derivatives for use in various applications. Acridines are a group of heterocyclic aromatic compounds characterized by their planar structure and bright fluorescence, making them valuable tools in scientific research, particularly in the fields of chemistry and molecular biology. These compounds are widely utilized as DNA intercalators, where they insert themselves between the base pairs of DNA, thereby serving as important agents in the study of nucleic acid structure and function. This property is extensively exploited in fluorescence microscopy and spectroscopy, allowing researchers to visualize and track genetic material in cells and tissues. Moreover, acridines are crucial for developing novel photochemical and photophysical processes, aiding in the design of light-activated materials and sensors. Their unique electronic properties also make them suitable candidates for use in the creation of organic semiconductors and as components in dye-sensitized solar cells. In non-biological chemistry, acridines serve as catalysts and reagents in synthetic organic transformations, facilitating the construction of complex molecular architectures. These diverse applications highlight the significant role of acridines and their derivatives in advancing fundamental scientific knowledge and technological innovations across various disciplines. View detailed information on our available Acridines and Acridine derivatives by clicking on the product name.

Items 31 to 32 of 32 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Nile blue A

3625-57-8sc-203746
sc-203746A
sc-203746B
sc-203746C
sc-203746D
5 g
25 g
100 g
250 g
1 kg
$35.00
$123.00
$326.00
$653.00
$2448.00
(0)

Nile blue A, an acridine dye, showcases remarkable photostability and a unique affinity for nucleic acids, leading to pronounced fluorescence under specific conditions. Its planar structure allows for effective π-π stacking interactions, enhancing its binding to biological macromolecules. The compound's protonation state can shift with pH changes, influencing its spectral properties and reactivity. Additionally, Nile blue A's ability to form aggregates in solution can alter its optical characteristics, making it a subject of interest in various chemical studies.

9-Chloro-2-methoxyacridine

16492-13-0sc-506882
250 mg
$126.00
(0)

9-Chloro-2-methoxyacridine features a distinctive acridine backbone that contributes to its planar structure, enhancing π-π stacking interactions. The presence of the chlorine atom introduces significant electron-withdrawing effects, which can modulate reactivity in electrophilic aromatic substitution reactions. Additionally, the methoxy group influences solvation dynamics, promoting unique hydrogen bonding patterns that facilitate specific molecular interactions in diverse chemical contexts.