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for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Cinosulfuron (Standard) is the analytical standard of Cinosulfuron. This product is intended for research and analytical applications. Cinosulfuron is a selective herbicide with excellent inhibitory activity against a variety of broadleaf weeds and is widely used in crop fields to protect the growth of crops. Cinosulfuron can effectively manage weed problems by inhibiting specific enzyme activity. Cinosulfuron is used in agriculture to increase crop yield and quality and ensure efficient use of farmland.
| Canonical Smiles | COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC2=NC(=NC(=N2)OC)OC |
|---|---|
| IUPAC Name | 1-(4,6-dimethoxy-1,3,5-triazin-2-yl)-3-[2-(2-methoxyethoxy)phenyl]sulfonylurea |
| InChIKey | WMLPCIHUFDKWJU-UHFFFAOYSA-N |
| INCHI | 1S/C15H19N5O7S/c1-24-8-9-27-10-6-4-5-7-11(10)28(22,23)20-13(21)16-12-17-14(25-2)19-15(18-12)26-3/h4-7H,8-9H2,1-3H3,(H2,16,17,18,19,20,21) |
| Isomeric SMILES | COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC2=NC(=NC(=N2)OC)OC |
| WGK Germany | 2 |
| RTECS | DB2070000 |
| PubChem CID | 92420 |
| Molecular Weight | 413.41 |
| Beilstein | 8162781 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzenesulfonamides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzenesulfonamides |
| Alternative Parents | Benzenesulfonyl compounds Phenoxy compounds Phenol ethers 2-methoxy-1,3,5-triazines Alkyl aryl ethers Sulfonyls Organosulfonic acids and derivatives Heteroaromatic compounds Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Benzenesulfonamide - Benzenesulfonyl group - Phenol ether - Phenoxy compound - Alkoxy-s-triazine - 2-methoxy-1,3,5-triazine - Alkyl aryl ether - 1,3,5-triazine - Triazine - Organic sulfonic acid or derivatives - Heteroaromatic compound - Organosulfonic acid or derivatives - Sulfonyl - Ether - Azacycle - Organoheterocyclic compound - Dialkyl ether - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring. |
| External Descriptors | Sulfonylurea herbicides |
| Flash Point(°C) | 144 °C |
|---|---|
| Melt Point(°C) | 140-145°C |
| 1. 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). [PMID:35953636] [10.1038/s41598-022-17982-7] |
| 2. 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, [PMID:29111703] [10.1021/acs.jafc.7b04022] |
| 3. Lu Qianqian, Xu Xinxin, Qu Aihua, Liu Liqiang, Li Yuzhe, Sun Maozhong, Xu Chuanlai, Kuang Hua. (2024) A multi-colloidal gold immunochromatography assay for rapid and simultaneous detection of 13 herbicides. Nano Research, [PMID:] [10.1007/s12274-024-6858-0] |