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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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N118531-25g
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25g |
3
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$137.90
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| Synonyms | Nicosulfuron, PESTANAL(R), analytical standard | 2-(N-((4,6-Dimethoxypyrimidin-2-yl)carbamoyl)sulfamoyl)-N,N-dimethylnicotinamide | 2-[[[[(4,6-Dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-N,N-dimethyl-3-pyridinecarboxamide | AKOS015851875 | Mila |
|---|---|
| Specifications & Purity | ≥95% |
| Shipped In | Normal |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Pyridines and derivatives |
| Subclass | Pyridinesulfonamides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyridinesulfonamides |
| Alternative Parents | Nicotinamides Sulfonylureas Alkyl aryl ethers Pyrimidines and pyrimidine derivatives Tertiary carboxylic acid amides Organosulfonic acids and derivatives Heteroaromatic compounds Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Carboximidic acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Pyridine-2-sulfonamide - Nicotinamide - Pyridinecarboxamide - Pyridine carboxylic acid or derivatives - Alkyl aryl ether - Sulfonylurea - Pyrimidine - Heteroaromatic compound - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Tertiary carboxylic acid amide - Sulfonyl - Organosulfonic acid or derivatives - Carboxamide group - Carboximidic acid derivative - Carboxylic acid derivative - Ether - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as pyridinesulfonamides. These are heterocyclic compounds containing a pyridine ring substituted by one or more sulfonamide groups. |
| External Descriptors | Sulfonylurea herbicides |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Pubchem Sid | 504754698 |
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| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754698 |
| IUPAC Name | 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-N,N-dimethylpyridine-3-carboxamide |
| INCHI | InChI=1S/C15H18N6O6S/c1-21(2)13(22)9-6-5-7-16-12(9)28(24,25)20-15(23)19-14-17-10(26-3)8-11(18-14)27-4/h5-8H,1-4H3,(H2,17,18,19,20,23) |
| InChIKey | RTCOGUMHFFWOJV-UHFFFAOYSA-N |
| Smiles | CN(C)C(=O)C1=C(N=CC=C1)S(=O)(=O)NC(=O)NC2=NC(=CC(=N2)OC)OC |
| Isomeric SMILES | CN(C)C(=O)C1=C(N=CC=C1)S(=O)(=O)NC(=O)NC2=NC(=CC(=N2)OC)OC |
| WGK Germany | 1 |
| RTECS | US4615000 |
| UN Number | 3077 |
| Packing Group | III |
| Molecular Weight | 410.41 |
| Reaxy-Rn | 7233432 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7233432&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | May 08, 2024 | N118531 |
| Solubility | 400mg/kg water (pH buffered, final pH 5.01), 120g/kg (pH7 buffered, final pH 6.85), 39.2g/kg (pH9 buffered, final pH 8.8), solubility in organic solvents (g/kg): acetone 18, acetonitrile 23, chloroform and dimethylformamide 64, dichloromethane 160, ethano |
|---|---|
| Melt Point(°C) | 142°C |
| Molecular Weight | 410.400 g/mol |
| XLogP3 | 0.600 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 6 |
| Exact Mass | 410.101 Da |
| Monoisotopic Mass | 410.101 Da |
| Topological Polar Surface Area | 161.000 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 642.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Qingyun Ma, Qingqing Li, Jie Wang, Rebecca E. Parales, Lin Li, Zhiyong Ruan. (2023) Exposure to three herbicide mixtures influenced maize root-associated microbial community structure, function and the network complexity. ENVIRONMENTAL POLLUTION, 336 (122393). |
| 2. Ruiyu Fu, Tingze Ren, Yanhui Zhang, Xiaoli Guo, Xin Di. (2023) A new sample treatment strategy based on supramolecular solvent for determination of herbicide residues in water samples by Box-Behnken design. MICROCHEMICAL JOURNAL, 187 (108390). |
| 3. Ting Zhao, Xiaochen Liang, Xinjie Guo, Xingjie Yang, Jialiang Guo, Xia Zhou, Xueqin Huang, Wenqian Zhang, Yiqing Wang, Zhaowei Liu, Zhengjin Jiang, Hongke Zhou, Haibo Zhou. (2023) Smartphone-based colorimetric sensor array using gold nanoparticles for rapid distinguishment of multiple pesticides in real samples. FOOD CHEMISTRY, 404 (134768). |
| 4. Jianan Liu, Jinjin Cheng, Chunli Zhou, Liya Ma, Xiaolong Chen, Yong Li, Xing Sun, Xiaolong Yan, Renhua Geng, Qun Wan, Xiangyang Yu. (2023) Uptake kinetics and subcellular distribution of three classes of typical pesticides in rice plants. SCIENCE OF THE TOTAL ENVIRONMENT, 858 (159826). |
| 5. Li Miaomiao, Li Qingqing, Yao Jun, Sunahara Geoffrey, Duran Robert, Zhang Qinghua, Ruan Zhiyong. (2022) Transcriptomic response of Pseudomonas nicosulfuronedens LAM1902 to the sulfonylurea herbicide nicosulfuron. Scientific Reports, 12 (1): (1-13). |
| 6. Xiaoli Guo, Tingze Ren, Jianchun Ji, Yan Yang, Xin Di. (2022) An alternative analytical strategy based on QuEChERS and dissolvable layered double hydroxide dispersive micro-solid phase extraction for trace determination of sulfonylurea herbicides in wolfberry by LC–MS/MS. FOOD CHEMISTRY, 396 (133652). |
| 7. Qingyun Ma, Hao Tan, Jinlong Song, Miaomiao Li, Zhiye Wang, Rebecca E. Parales, Lin Li, Zhiyong Ruan. (2022) Effects of long-term exposure to the herbicide nicosulfuron on the bacterial community structure in a factory field. ENVIRONMENTAL POLLUTION, 307 (119477). |
| 8. Yuan-Yuan Zhang, Shuang Gao, Minh-Tu Hoang, Zi-Wei Wang, Xin Ma, Yue Zhai, Na Li, Li-Xia Zhao, Ying Fu, Fei Ye. (2020) Protective efficacy of phenoxyacetyl oxazolidine derivatives as safeners against nicosulfuron toxicity in maize. PEST MANAGEMENT SCIENCE, 77 (1): (177-183). |
| 9. Liang Ting, Gao Lei, Qin Dongli, Chen Ligang. (2019) Determination of Sulfonylurea Herbicides in Grain Samples by Matrix Solid-Phase Dispersion with Mesoporous Structured Molecularly Imprinted Polymer. Food Analytical Methods, 12 (9): (1938-1948). |
| 10. Shan Zhou, Jinlong Song, Weiwei Dong, Yingchun Mu, Qi Zhang, Ziwen Fan, Yanwei Wang, Delong Kong, Yiqing Zhou, Xu Jiang, Bin Zhao, Gang Han, Zhiyong Ruan. (2017) Nicosulfuron Biodegradation by a Novel Cold-Adapted Strain Oceanisphaera psychrotolerans LAM-WHM-ZC. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 65 (47): (10243–10249). |
| 11. Zhang Hui, Li Mengya, Li Jie, Wang Guangli, Liu Yuan. (2017) Purification and properties of a novel quizalofop-p-ethyl-hydrolyzing esterase involved in quizalofop-p-ethyl degradation by Pseudomonas sp. J-2. Microbial Cell Factories, 16 (1): (1-10). |
| 12. Hui Zhang, Mengya Li, Jie Li, Guangli Wang, Feng Li, Dayong Xu, Yuan Liu, Minghua Xiong. (2017) A key esterase required for the mineralization of quizalofop-p-ethyl by a natural consortium of Rhodococcus sp. JT-3 and Brevundimonas sp. JT-9. JOURNAL OF HAZARDOUS MATERIALS, 327 (1). |
| 13. Xiaoxiao You, Ligang Chen. (2016) Analysis of sulfonylurea herbicides in grain samples using molecularly imprinted polymers on the surface of magnetic carbon nanotubes by extraction coupled with HPLC. Analytical Methods, 8 (5): (1003-1012). |
| 14. Zhengyuan Gao, Chenggang Gu, Xiuli Fan, Lezu Shen, Zhihua Jin, Fang Wang, Xin Jiang. (2024) Biochemical insights into the biodegradation mechanism of typical sulfonylureas herbicides and association with active enzymes and physiological response of fungal microbes: A multi-omics approach. ENVIRONMENT INTERNATIONAL, 190 (108906). |
| 15. Qianhang Zhai, Yue Liu, Lining Zheng, Yufeng Xiao, Yulin Wu, Hao Zhang, Jingyuan Chen. (2025) Elucidation of molecular mechanisms underlying degradation of nicosulfuron and its derivative by Klebsiella jilinsis 2N3 using multiomic analysis. JOURNAL OF HAZARDOUS MATERIALS, 490 (137838). |
| 16. Yufei Dai, Xianli Song, Jing Zhao, Limin Wang, Xiaoru Cui, Li Lu, Jingyu Zhang, Haoyu Zhang, Dahai Zhang, Keqiang Li. (2025) Spatiotemporal distribution and potential ecological risks of current-use pesticides (CUPs) in Laizhou Bay, China. MARINE ENVIRONMENTAL RESEARCH, 206 (107042). |