Nicarbazin

Base Information

• Chemical Name: Nicarbazin
• CAS No.: 330-95-0
• Deprecated CAS: 8027-87-0
• Molecular Formula: C13H10N4O5^.C6H8N2O
• Molecular Weight: 426.389
• Hs Code.: 38249099
• European Community (EC) Number: 206-359-1
• NSC Number: 7171
• UNII: 11P9NUA12U
• DSSTox Substance ID: DTXSID6034762
• Wikipedia: Nicarbazin
• Wikidata: Q2020694
• NCI Thesaurus Code: C76086
• ChEMBL ID: CHEMBL95855
• Mol file: 330-95-0.mol

Synonyms:Nicarbazin;Nicarbazine

Chemical Property of Nicarbazin

Chemical Property:

• Appearance/Colour: Light yellow crystalline powder
• Vapor Pressure: 4.32E-07mmHg at 25°C
• Melting Point: 265-275oC
• Refractive Index: 1.6000 (estimate)
• Boiling Point: 414.8 °C at 760 mmHg
• Flash Point: 204.7 °C
• PSA: 178.78000
• Density: 1.4663 (rough estimate)
• LogP: 5.13840
• Storage Temp.: 0-6°C
• Solubility.: DMSO: soluble0.5mg/mL
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 426.12878232
• Heavy Atom Count: 31
• Complexity: 582

Purity/Quality:

99%min , ^*data from raw suppliers

Nicarbazin ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Uses -> Animal Feed Additives
• Canonical SMILES: CC1=CC(=NC(=O)N1)C.C1=CC(=CC=C1NC(=O)NC2=CC=C(C=C2)[N+](=O)[O-])[N+](=O)[O-]
• Uses: Nicarbazin, is a coccidiostat, which is an antiprotozoal agent that acts upon Coccidia parasites.It is a contraceptive for resident Canada geese and waterfowl. It is used to study avian reproduction and is used to interfere with the formation of the vitelline (yolk) membrane in bird eggs. It has been used to study how delivery method can effect plasma levels of 4,4′-dinitrocarbanilide (DNC), which is the active anticoccidial component of Nicarbazin.

Technology Process of Nicarbazin

There total 1 articles about Nicarbazin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ Nicarb (330-95-0)

Guidance literature:

EtOH, N,N'-Bis-(4-nitrophenyl)-harnstoff, CH3-C(O)-CH2-C(O)-CH3, Harnstoff, HCl, 2-Hydroxy-4,6-dimethylpyrimidin;

Refernces