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analytical standard, ≥99% Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Dicamba is a chlorinate methoxy benzoic acid herbicide that increases plant growth rates such that the plant grows faster than it can replenish its nutrient supply
Dicamba (3,6-dichloro-2-methoxybenzoic acid) is an organochlorine compound with plant growth auxin characteristics. Dicamba is used as a herbicide.
| Pubchem Sid | 504750627 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504750627 |
| Sonrisas canónicas | COC1=C(C=CC(=C1C(=O)O)Cl)Cl |
| IUPAC Name | 3,6-dichloro-2-methoxybenzoic acid |
| InChIKey | IWEDIXLBFLAXBO-UHFFFAOYSA-N |
| INCHI | 1S/C8H6Cl2O3/c1-13-7-5(10)3-2-4(9)6(7)8(11)12/h2-3H,1H3,(H,11,12) |
| Isómeros SMILES | COC1=C(C=CC(=C1C(=O)O)Cl)Cl |
| WGK Alemania | 2 |
| RTECS | DG7525000 |
| Número ONU | 3077 |
| Grupo de embalaje | III |
| Peso molecular | 221.04 |
| Beilstein | 2453039 |
| Reaxy-Rn | 2453039 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2453039&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Methoxybenzoic acids and derivatives |
| Direct Parent | O-methoxybenzoic acids and derivatives |
| Alternative Parents | Dichlorobenzoic acids 2-halobenzoic acids 3-halobenzoic acids Halobenzoic acids 1-carboxy-2-haloaromatic compounds Phenoxy compounds Anisoles Benzoyl derivatives Dichlorobenzenes Methoxybenzenes Alkyl aryl ethers Aryl chlorides Vinylogous halides Monocarboxylic acids and derivatives Organochlorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | 2,5-dichlorobenzoic acid - O-methoxybenzoic acid or derivatives - 2-halobenzoic acid or derivatives - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Halobenzoic acid - 3-halobenzoic acid - 2-halobenzoic acid - Benzoic acid - Phenoxy compound - 1,4-dichlorobenzene - Benzoyl - Anisole - Phenol ether - 1-carboxy-2-haloaromatic compound - Methoxybenzene - Alkyl aryl ether - Halobenzene - Chlorobenzene - Aryl halide - Aryl chloride - Vinylogous halide - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Ether - Organohalogen compound - Organochloride - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as o-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 2 of the benzene ring is replaced by a methoxy group. |
| External Descriptors | Benzoic acid herbicides |
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| Punto de ebullición (°C) | ~326.1 °C |
|---|---|
| Punto de fusión (°C) | 112-116°C |
| Peso molecular | 221.030 g/mol |
| XLogP3 | 2.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 219.969 Da |
| Monoisotopic Mass | 219.969 Da |
| Topological Polar Surface Area | 46.500 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 198.000 |
| 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. Wei Song, Caixia Fu, Yuning Fang, Zhuoyue Wang, Ji Li, Xiaolei Zhang, Kalpana Bhatt, Lu Liu, Ningjie Wang, Fang Liu, Shunni Zhu. (2022) Single and combined toxicity assessment of primary or UV-aged microplastics and adsorbed organic pollutants on microalga Chlorella pyrenoidosa. ENVIRONMENTAL POLLUTION, [PMID:36566677] [10.1016/j.envpol.2022.120925] |
| 2. Zhuoyue Wang, Ji Li, Wei Song, Rui Ma, Jingxin Yang, Xiaolei Zhang, Fan Huang, Wenyi Dong. (2022) Rapid degradation of atrazine by a novel advanced oxidation process of bisulfite/chlorine dioxide: Efficiency, mechanism, pathway. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2022.136558] |
| 3. Qi Wu, Wei Wu, Xue Zhan, Xiudan Hou. (2020) Three-dimensional chitosan/graphene oxide aerogel for high-efficiency solid-phase extraction of acidic herbicides in vegetables. NEW JOURNAL OF CHEMISTRY, 44 (25): (10654-10661). [PMID:] [10.1039/D0NJ01960G] |
| 4. Guanglong Ding, Jingyue Tang, Wenbing Zhang, Yanran Li, Junfan Niu, Weichen Wang, Hong Huo, Jianqiang Li, Yongsong Cao. (2020) Synthesized dimers increased herbicidal activity with lowered volatility. CROP PROTECTION, [PMID:] [10.1016/j.cropro.2020.105111] |
| 5. Xiaoli Guo, Yanting Li, Bo Zhang, Lingling Yang, Xin Di, Xin Di. (2019) Development of dispersive solid phase extraction based on dissolvable Fe3O4-layered double hydroxide for high-performance liquid chromatographic determination of phenoxy acid herbicides in water samples. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2019.104443] |
| 6. Yaqing Chang, Zhe Zhang, Jinhui Hao, Wenshu Yang, Jilin Tang. (2016) A simple label free colorimetric method for glyphosate detection based on the inhibition of peroxidase-like activity of Cu(Ⅱ). SENSORS AND ACTUATORS B-CHEMICAL, [PMID:] [10.1016/j.snb.2016.01.048] |
| 7. Tengteng Shao, Huaqing Liu, Aiyun Guo, Dongle Cheng, Xinhan Chen, Shugang Hu, Jian Zhang. (2024) Dicamba herbicide alters microbial community, metabolite composition, and nitrogen-cycling function in the wheat rhizosphere. Rhizosphere, [PMID:] [10.1016/j.rhisph.2024.100998] |
| 8. Jiaxiao Niu, Yanhui Zhang, Hongbo Li, Xiaoqin Hai, Qingxin Lu, Ruiyu Fu, Tingze Ren, Xiaoli Guo, Xin Di. (2024) Switchable deep eutectic solvent as green and efficient media for liquid-phase microextraction of phenoxyacetic acid herbicides in water and food matrices. FOOD CHEMISTRY, [PMID:38237292] [10.1016/j.foodchem.2024.138433] |
| 9. Xiudan Hou, Hui Yu, Shihai Yan, Junxia Xiao, Min Sun, Wei Wu. (2020) Cationic polyelectrolyte/graphene oxide as an efficient sorbent for the extraction and analysis of trace acidic herbicides in vegetables. JOURNAL OF CHROMATOGRAPHY A, [PMID:31973930] [10.1016/j.chroma.2020.460884] |
| 10. Jingyu Zhang, Huihui Hu, Jian Wang, Keqiang Lu, Yunyun Zhou, Lingzhi Zhao, Juanjuan Peng. (2024) Gold nanoclusters-based fluorescence sensor array for herbicides qualitative and quantitative analysis. ANALYTICA CHIMICA ACTA, [PMID:38462337] [10.1016/j.aca.2024.342380] |
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