CAS No. 330-95-0

Batch: Purity:98
Nicarbazin Chemical Structure
Chemical Structure
Check the Nicarbazin product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name 1,3-bis(4-nitrophenyl)urea;4,6-dimethyl-1H-pyrimidin-2-one
CAS Number 330-95-0
Molecular Formula

C13H10N4O5.C6H8N2O

Molecular Weight (MW) 426.38
SMILES CC1=CC(=NC(=O)N1)C.C1=CC(=CC=C1NC(=O)NC2=CC=C(C=C2)[N+](=O)[O-])[N+](=O)[O-]
InChIKey UKHWDRMMMYWSFL-UHFFFAOYSA-N

Biological Activity

Nicarbazin is an equimolar complex comprising 4,4'-dinitrocarbanilide and 2-hydroxy-4,6-dimethylpyrimidine that acts as a broad-spectrum anticoccidial and anti-parasitic agent. It exerts antiparasitic effects primarily by disrupting ATP synthesis and energy metabolism in Eimeria species, such as Eimeria tenella. This metabolic impairment inhibits second-generation schizont development, ultimately suppressing parasite replication and controlling coccidial infections in host tissues.

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 9 mg/mL (21.1 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Water Insoluble
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).

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Note: Technical data last updated: Sep 1, 2026.