CAS No. 7481-89-2

Batch: Purity:99.95
Zalcitabine  Chemical Structure
Chemical Structure
Check the Zalcitabine product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name 4-amino-1-[(2R,5S)-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
CAS Number 7481-89-2
Molecular Formula

C9H13N3O3

Molecular Weight (MW) 211.22
SMILES C1CC(OC1CO)N2C=CC(=NC2=O)N
InChIKey WREGKURFCTUGRC-POYBYMJQSA-N

Ordering Information

Biological Activity

Zalcitabine is a pyrimidine nucleoside analog and HIV reverse transcriptase inhibitor (NARTI). As a deoxycytidine derivative lacking a 3'-hydroxyl group, zalcitabine is intracellularly phosphorylated in T cells into its active metabolite, dideoxycytidine triphosphate (ddCTP). Active ddCTP serves as an alternative substrate for viral reverse transcriptase and incorporates into nascent viral DNA, resulting in DNA chain termination and inhibition of retroviral replication. [1]

How to Prepare Stock Solution?

Concentration Volume Mass
🧮 Molarity Calculator

Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
Water 42 mg/mL
DMSO 8 mg/mL (37.87 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Ethanol Insoluble
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).
Note: Technical data last updated: Sep 1, 2026.