≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Metolachlor is a commonly used chloroacetamide preemergent pesticide, which can be used for weed control management in a variety of food crops. It can undergo degradation in soil via microbial transformation reactions and hydrolytic reactions.
| Sonrisas canónicas | CCC1=CC=CC(=C1N(C(C)COC)C(=O)CCl)C |
|---|---|
| IUPAC Name | 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide |
| InChIKey | WVQBLGZPHOPPFO-UHFFFAOYSA-N |
| INCHI | 1S/C15H22ClNO2/c1-5-13-8-6-7-11(2)15(13)17(14(18)9-16)12(3)10-19-4/h6-8,12H,5,9-10H2,1-4H3 |
| Isómeros SMILES | CCC1=CC=CC(=C1N(C(C)COC)C(=O)CCl)C |
| WGK Alemania | 2 |
| RTECS | AN3430000 |
| Peso molecular | 283.79 |
| Beilstein | 8396147 |
| Reaxy-Rn | 2743537 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2743537&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 | Anilides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Anilides |
| Alternative Parents | Toluenes Tertiary carboxylic acid amides Chloroacetamides Dialkyl ethers Organopnictogen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl chlorides |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Anilide - Toluene - Chloroacetamide - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Dialkyl ether - Ether - Alkyl chloride - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alkyl halide - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution. |
| External Descriptors | Anilide herbicides |
| Sensibilidad | Light sensitive；Air sensitive ；Heat sensitive |
|---|---|
| Índice de refracción | 1.526-1.529 |
| Punto de inflamación (°C) | 190 °C |
| Punto de ebullición (°C) | 100°C |
| Punto de fusión (°C) | -62.1 °C |
| Peso molecular | 283.790 g/mol |
| XLogP3 | 3.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Exact Mass | 283.134 Da |
| Monoisotopic Mass | 283.134 Da |
| Topological Polar Surface Area | 29.500 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 285.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Zepeng Li, Yuxiang Wu, Zijing Li, Binger Yu, Xinyi Mao, Guoqing Shi. (2023) A lateral flow immunoassay method for the rapid detection of acetochlor and alachlor in vegetable oil by sensitivity enhancement by using dimethyl-β-cyclodextrin. Analytical Methods, 15 (38): (5087-5094). [PMID:37747357] [10.1039/D3AY01379K] |
| 2. Dahu Ding, Shengjiong Yang, Xiaoyong Qian, Liwei Chen, Tianming Cai. (2019) Nitrogen-doping positively whilst sulfur-doping negatively affect the catalytic activity of biochar for the degradation of organic contaminant. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2019.118348] |
| 3. Chao Liu, Liwei Chen, Dahu Ding, Tianming Cai. (2019) From rice straw to magnetically recoverable nitrogen doped biochar: Efficient activation of peroxymonosulfate for the degradation of metolachlor. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2019.05.014] |
| 4. Chao Liu, Liwei Chen, Dahu Ding, Tianming Cai. (2019) Sulfate radical induced catalytic degradation of metolachlor: Efficiency and mechanism. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2019.03.001] |
| 5. Zhijuan Tang, Shaosong Shi, Ruixia Niu, Yulu Zhou, Zhao Wang, Rongrong Fu, Rui Mou, Suming Chen, Pingtao Ding, Guoyong Xu. (2024) Alleviating protein-condensation-associated damage at the endoplasmic reticulum enhances plant disease tolerance. Cell Host & Microbe, [PMID:39111320] [10.1016/j.chom.2024.07.013] |
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