2-[(4-Methylpentan-2-yl)amino]-5-(phenylamino)cyclohexa-2,5-diene-1,4-dione TCI P3373

Chemical Identity

CAS No.: 2754428-18-5
Purity: >95.0%(HPLC)(qN

Rp 2.889.600,00

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Berat 10mg 100mg

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TCI P3373, 2-[(4-Methylpentan-2-yl)amino]-5-(phenylamino)cyclohexa-2,5-diene-1,4-dione, is a bioactive compound built on a 1,4-benzoquinone scaffold that carries two amino substituents: a branched alkylamino group and a phenylamino group. It belongs to the research biochemicals category, and scientists use it to study the biological activity of small molecules in experimental systems. The product is for research use only. It is not intended for diagnosis, therapy, or human consumption.

The aminoquinone scaffold is a well-known redox-active motif. Quinones can accept and donate electrons, and they can interact with nucleophilic groups on proteins. Because of this, quinone derivatives are often studied in research on enzyme modulation, oxidative stress, and cellular signaling pathways. In this molecule, the branched alkyl substituent and the phenyl substituent together affect its lipophilicity and how it interacts with biological targets. The 10mg and 100mg pack sizes let researchers begin with preliminary assays and then move on to broader studies without buying more material than they need.

In Indonesia, bioactive compounds like this one are relevant to pharmacology, cell biology, and medicinal chemistry laboratories that carry out compound screening or mechanism-of-action studies. University research groups, government research institutes, and industrial R&D teams can use it to explore structure-activity relationships among quinone derivatives, or as a reference compound in experiments on redox-related biological processes. Having it available through a local laboratory supplier makes it easier to plan exploratory work.

Small-molecule bioactivity screening: the compound's aminoquinone scaffold makes it a suitable candidate for exploratory screens that look at how redox-active small molecules affect biological systems.
Enzyme modulation research: quinones can interact with nucleophilic groups on proteins, so this compound fits studies of how quinone derivatives influence enzyme function.
Oxidative stress studies: because quinones accept and donate electrons, this compound can help researchers examine redox processes and oxidative stress responses in experimental cell models.
Cellular signaling pathway research: quinone derivatives are commonly studied for their effects on signaling, which makes this compound useful for mechanism-focused work in cell biology laboratories.
Structure-activity relationship studies in medicinal chemistry: its combination of branched alkylamino and phenylamino substituents lets researchers compare how lipophilicity and substitution pattern affect target interaction.

Brand	TCI (product code P3373)
CAS number	2754428-18-5
Molecular formula	—
Purity	—
Category	Life Science > Biochemicals and Reagents > Bioactive Compounds
Pack sizes	10mg and 100mg
Physical form	refer to the manufacturer's product documentation
Storage	follow the conditions on the product label and the TCI Safety Data Sheet

Store this compound according to the conditions on the product label and in the manufacturer's Safety Data Sheet. Keep it in its original tightly closed container, in a cool, dry place away from direct light and incompatible materials. Quinone compounds are redox-active, so limit unnecessary exposure to air and moisture. Handle the material in a well-ventilated area or a fume hood, and wear suitable personal protective equipment such as gloves, safety glasses, and a lab coat. Avoid inhaling dust and avoid contact with skin and eyes. Dispose of waste in line with institutional and local chemical waste regulations. This product is for research use only.

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