IpfencarbazoneCAS# 212201-70-2 |
2D Structure
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Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
Cas No. | 212201-70-2 | SDF | Download SDF |
PubChem ID | 15457339 | Appearance | Powder |
Formula | C18H14Cl2F2N4O2 | M.Wt | 427.23 |
Type of Compound | N/A | Storage | Desiccate at -20°C |
Solubility | DMSO : 130 mg/mL (304.29 mM; Need ultrasonic) H2O : < 0.1 mg/mL (insoluble) | ||
Chemical Name | 1-(2,4-dichlorophenyl)-N-(2,4-difluorophenyl)-5-oxo-N-propan-2-yl-1,2,4-triazole-4-carboxamide | ||
SMILES | CC(C)N(C1=C(C=C(C=C1)F)F)C(=O)N2C=NN(C2=O)C3=C(C=C(C=C3)Cl)Cl | ||
Standard InChIKey | DHYXNIKICPUXJI-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C18H14Cl2F2N4O2/c1-10(2)25(16-6-4-12(21)8-14(16)22)17(27)24-9-23-26(18(24)28)15-5-3-11(19)7-13(15)20/h3-10H,1-2H3 | ||
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. |
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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. |
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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. |
Description | Ipfencarbazone is a substance being developed for the control of weeds such as watergrass in rice; herbicide agent. |
Ipfencarbazone Dilution Calculator
Ipfencarbazone Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.3407 mL | 11.7033 mL | 23.4066 mL | 46.8132 mL | 58.5165 mL |
5 mM | 0.4681 mL | 2.3407 mL | 4.6813 mL | 9.3626 mL | 11.7033 mL |
10 mM | 0.2341 mL | 1.1703 mL | 2.3407 mL | 4.6813 mL | 5.8516 mL |
50 mM | 0.0468 mL | 0.2341 mL | 0.4681 mL | 0.9363 mL | 1.1703 mL |
100 mM | 0.0234 mL | 0.117 mL | 0.2341 mL | 0.4681 mL | 0.5852 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. |
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Ipfencarbazone is a substance being developed for the control of weeds such as watergrass in rice; herbicide agent.
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[Development of Determination Method of Ipfencarbazone in Agricultural Products, Livestock Products and Seafood by LC-MS/MS].[Pubmed:26537650]
Shokuhin Eiseigaku Zasshi. 2015;56(5):205-10.
A method for the determination of Ipfencarbazone in agricultural products, livestock products and seafood by LC-MS/MS was developed. Agricultural samples were extracted with acetone. An aliquot of crude extract was partitioned with n-hexane and sat. sodium chloride solution. Clean-up was performed using GC/PSA and C18 cartridges. In the case of livestock products and seafood, samples were extracted with a mixture of acetone and n-hexane, and the organic layer was collected. After acetonitrile-hexane partitioning, the extract was cleaned up using PAS and C18 cartridges. The gradient LC separation was performed on a C18 column with acetonitrile-water containing acetic acid as a mobile phase, and MS with positive ion electrospray ionization was used for detection. The average recoveries (n=5) of Ipfencarbazone from 16 kinds of agricultural products, livestock products and seafood spiked at the MRLs or at the uniform limits (0.01 ppm) were 73-101%, and the relative standard deviations were 1.3-5.1%. The limit of quantitation of the developed method was 0.01 mg/kg for Ipfencarbazone.