NicarbazinCAS# 330-95-0 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 330-95-0 | SDF | Download SDF |
PubChem ID | 9507 | Appearance | Powder |
Formula | C19H18N6O6 | M.Wt | 426.4 |
Type of Compound | N/A | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | 1,3-bis(4-nitrophenyl)urea;4,6-dimethyl-1H-pyrimidin-2-one | ||
SMILES | CC1=CC(=NC(=O)N1)C.C1=CC(=CC=C1NC(=O)NC2=CC=C(C=C2)[N+](=O)[O-])[N+](=O)[O-] | ||
Standard InChIKey | UKHWDRMMMYWSFL-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C13H10N4O5.C6H8N2O/c18-13(14-9-1-5-11(6-2-9)16(19)20)15-10-3-7-12(8-4-10)17(21)22;1-4-3-5(2)8-6(9)7-4/h1-8H,(H2,14,15,18);3H,1-2H3,(H,7,8,9) | ||
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
||
About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
||
Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. |
Nicarbazin Dilution Calculator
Nicarbazin Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.3452 mL | 11.7261 mL | 23.4522 mL | 46.9043 mL | 58.6304 mL |
5 mM | 0.469 mL | 2.3452 mL | 4.6904 mL | 9.3809 mL | 11.7261 mL |
10 mM | 0.2345 mL | 1.1726 mL | 2.3452 mL | 4.6904 mL | 5.863 mL |
50 mM | 0.0469 mL | 0.2345 mL | 0.469 mL | 0.9381 mL | 1.1726 mL |
100 mM | 0.0235 mL | 0.1173 mL | 0.2345 mL | 0.469 mL | 0.5863 mL |
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. |
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- 3,4-Secocucurbita-4,24-diene-3,26,29-trioic acid
Catalog No.:BCN1458
CAS No.:329975-47-5
- TTP 22
Catalog No.:BCC2017
CAS No.:329907-28-0
- Viomycin
Catalog No.:BCC3930
CAS No.:32988-50-4
- Tobramycin
Catalog No.:BCC4739
CAS No.:32986-56-4
- 10-Deacetylbaccatin III
Catalog No.:BCN5251
CAS No.:32981-86-5
- Methyl (2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenylpropanoate
Catalog No.:BCN8520
CAS No.:32981-85-4
- Cinaciguat
Catalog No.:BCC1484
CAS No.:329773-35-5
- 2-Acetyl-3-ethylpyrazine
Catalog No.:BCC8512
CAS No.:32974-92-8
- Pinoresinol diacetate
Catalog No.:BCN5250
CAS No.:32971-25-8
- FPR A14
Catalog No.:BCC7498
CAS No.:329691-12-5
- 7-O-Methylaloeresin A
Catalog No.:BCN2849
CAS No.:329361-25-3
- Sanggenol L
Catalog No.:BCN3692
CAS No.:329319-20-2
- Kumatakenin
Catalog No.:BCN5252
CAS No.:3301-49-3
- ent-16beta,17-Dihydroxy-19-kauranoic acid
Catalog No.:BCN1457
CAS No.:3301-61-9
- Cyanidin-3-O-sambubioside chloride
Catalog No.:BCN3150
CAS No.:33012-73-6
- SU6656
Catalog No.:BCC6392
CAS No.:330161-87-0
- TC HSD 21
Catalog No.:BCC6228
CAS No.:330203-01-5
- Boc-β-Ala-OH
Catalog No.:BCC3051
CAS No.:3303-84-2
- Aloe-emodin-8-O-beta-D-glucopyranoside
Catalog No.:BCN1456
CAS No.:33037-46-6
- H-Orn(Z)-OH
Catalog No.:BCC3003
CAS No.:3304-51-6
- Peramivir
Catalog No.:BCC1846
CAS No.:330600-85-6
- TCTU
Catalog No.:BCC2689
CAS No.:330641-16-2
- HCTU
Catalog No.:BCC2818
CAS No.:330645-87-9
- KH 7
Catalog No.:BCC7787
CAS No.:330676-02-3
Degradation of 4,4'-Dinitrocarbanilide in Chicken Breast by Thermal Processing.[Pubmed:29992813]
J Agric Food Chem. 2018 Aug 8;66(31):8391-8397.
Nicarbazin is one of the major anticoccidials used in broiler feeds. The compound 4,4'-dinitrocarbanilide (DNC) is the marker residue of concern left from Nicarbazin in chicken meat. The effect of thermal processing on DNC content accumulated in chicken breast was assessed, and samples were analyzed by liquid chromatography-tandem mass spectrometry. Five conventional cooking methods were evaluated: boiling, grilling, microwaving, frying, and roasting. To ensure DNC in meat, broilers were fed Nicarbazin without withdrawal period. All heating methods surpassed the 70 degrees C end point core temperature in chicken breast. Maximum DNC degradation was reached at 10 min for boiling, at 30 min for grilling, and at 2 min for microwaving, and no further reduction was observed for longer thermal processing time. Boiling was more efficient in reducing DNC (69%). Grilling, microwaving, and frying achieved on average 55% of degradation. The outcomes reported herein may be considered in decision-making regarding further review of maximum residue limits.
Iron-Nicarbazin derived platinum group metal-free electrocatalyst in scalable-size air-breathing cathodes for microbial fuel cells.[Pubmed:29970929]
Electrochim Acta. 2018 Jul 1;277:127-135.
In this work, a platinum group metal-free (PGM-free) catalyst based on iron as transitional metal and Nicarbazin (NCB) as low cost organic precursor was synthesized using Sacrificial Support Method (SSM). The catalyst was then incorporated into a large area air-breathing cathode fabricated by pressing with a large diameter pellet die. The electrochemical tests in abiotic conditions revealed that after a couple of weeks of successful operation, the electrode experienced drop in performances in reason of electrolyte leakage, which was not an issue with the smaller electrodes. A decrease in the hydrophobic properties over time and a consequent cathode flooding was suspected to be the cause. On the other side, in the present work, for the first time, it was demonstrated the proof of principle and provided initial guidance for manufacturing MFC electrodes with large geometric areas. The tests in MFCs showed a maximum power density of 1.85Wm(-2). The MFCs performances due to the addition of Fe-NCB were much higher compared to the iron-free material. A numerical model using Nernst-Monod and Butler-Volmer equations were used to predict the effect of electrolyte solution conductivity and distance anode-cathode on the overall MFC power output. Considering the existing conditions, the higher overall power predicted was 3.6mWat 22.2Sm(-1) and at inter-electrode distance of 1cm.
Blood Glucose Concentrations in Nicarbazin-Fed Broiler Chickens.[Pubmed:29620456]
Avian Dis. 2018 Mar;62(1):114-116.
Four floor pen studies were carried out to evaluate the effects of Nicarbazin (NIC) administration on blood glucose concentrations and the onset of hypoglycemia in broiler chickens. All tests involved continuous NIC feeding at 0, 100, or 125 ppm to 28 days of age. In each study, birds were reared at both standard environmental temperatures and at 3 C below this level. In addition, two studies were conducted in the presence of coccidial infection and two were carried out in noninfected broilers. At 26 days of age in each test, two birds per pen were bled by puncture of the brachial vein, and whole blood glucose concentrations were determined. Results indicated that the administration of NIC to broilers for 26 days had no effect on blood glucose concentrations, although graded levels of NIC tended to increase these values. In addition, no evidence of hypoglycemia was recorded in any of the trials. In a similar fashion, blood glucose was unaffected by environmental temperature and coccidial challenge. These findings support previous work showing that NIC administration does not influence blood glucose levels and indicate that the product is not involved when field diagnoses use reduced blood glucose and hypoglycemia as indicators of production anomalies.