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Acetochlor - analytical standard, high purity , CAS No.34256-82-1

In stock
Item Number
A110044
Grouped product items
SKU Size
Availability
Price Qty
A110044-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$65.90
A110044-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$207.90
A110044-500mg
500mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$735.90
A110044-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,275.90
A110044-5g
5g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$3,496.90

Basic Description

Synonyms NCGC00090754-06 | HSDB 6550 | NCGC00090754-01 | NCGC00090754-02 | NCGC00090754-07 | 8L08WMO94K | HMS3029L16 | CHEBI:2394 | Q419732 | SR-01000846094-2 | DTXCID303848 | KBioGR_001265 | Nevirex | Azetochlor | SMR000777859 | Spectrum2_001915 | o-Acetotoluidid
Specifications & Purity analytical standard
Shipped In Normal
Grade analytical standard

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Anilides
Intermediate Tree Nodes Not available
Direct Parent Anilides
Alternative Parents Toluenes  Tertiary carboxylic acid amides  Chloroacetamides  Organopnictogen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl chlorides  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Anilide - Toluene - Tertiary carboxylic acid amide - Chloroacetamide - Carboxamide group - Carboxylic acid derivative - Alkyl chloride - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alkyl halide - Aromatic homomonocyclic compound
Description 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

Associated Targets(Human)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Zea mays (820 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 2-chloro-N-(ethoxymethyl)-N-(2-ethyl-6-methylphenyl)acetamide
INCHI InChI=1S/C14H20ClNO2/c1-4-12-8-6-7-11(3)14(12)16(10-18-5-2)13(17)9-15/h6-8H,4-5,9-10H2,1-3H3
InChIKey VTNQPKFIQCLBDU-UHFFFAOYSA-N
Smiles CCC1=CC=CC(=C1N(COCC)C(=O)CCl)C
Isomeric SMILES CCC1=CC=CC(=C1N(COCC)C(=O)CCl)C
WGK Germany 2
RTECS AB5457000
UN Number 3082
Packing Group III
Molecular Weight 269.77
Beilstein 2859702
Reaxy-Rn 2859702
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2859702&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot Number Certificate Type Date Item
E2515057 Certificate of Analysis May 26, 2025 A110044
A2203078 Certificate of Analysis Oct 19, 2023 A110044
A2203059 Certificate of Analysis Oct 19, 2023 A110044
A2503129 Certificate of Analysis Jan 06, 2022 A110044
D2402011 Certificate of Analysis Jan 06, 2022 A110044
E2322622 Certificate of Analysis Jan 06, 2022 A110044
A2203083 Certificate of Analysis Jan 06, 2022 A110044
K2301042 Certificate of Analysis Nov 24, 2021 A110044

Chemical and Physical Properties

Molecular Weight 269.770 g/mol
XLogP3 3.200
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 6
Exact Mass 269.118 Da
Monoisotopic Mass 269.118 Da
Topological Polar Surface Area 29.500 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 260.000
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

Citations of This Product

1. Xin Wang, Shoulin Li, Cheng Zhang, Wenping Xu, Mengqi Wu, Jiagao Cheng, Zhong Li, Liming Tao, Yang Zhang.  (2024)  Stereoselective toxicity of acetochlor chiral isomers on the nervous system of zebrafish larvae.  JOURNAL OF HAZARDOUS MATERIALS,  464  (133016). 
2. Liling Wang, Yanbin Wang, Yuchuan Qin, Yifeng Zhou.  (2023)  Room-temperature synthesis of ionic liquid@covalent organic frameworks for the solid phase extraction and analysis of six herbicides from water samples.  MICROCHEMICAL JOURNAL,  195  (109497). 
3. 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). 
4. Xin Wang, Li Geng, Mengqi Wu, Wenping Xu, Jiagao Cheng, Zhong Li, Liming Tao, Yang Zhang.  (2023)  Molecular mechanisms of cardiotoxicity induced by acetamide and its chiral isomers.  SCIENCE OF THE TOTAL ENVIRONMENT,  900  (166349). 
5. Xin Wang, Fan Chen, Jian Lu, Mengqi Wu, Jiagao Cheng, Wenping Xu, Zhong Li, Yang Zhang.  (2023)  Developmental and cardiovascular toxicities of acetochlor and its chiral isomers in zebrafish embryos through oxidative stress.  SCIENCE OF THE TOTAL ENVIRONMENT,  896  (165296). 
6. Xiong Chen, Yingxue Li, Juying Li, Li Cao, Cheng Yao.  (2023)  An upconverted nanoparticle–porphyrin metal–organic framework platform for near-infrared detection of nitenpyram.  Analytical Methods,  15  (24): (2946-2954). 
7. Xinyue Zheng, Xujian Duan, Di Lu, Qiuhong Jiang, Yajun Liu, Hongyu Xue, Jiansong You, Lei Yin, Meiyun Shi.  (2022)  Cellular toxicity and pharmacokinetic study of butachlor by ultra-performance liquid chromatography-tandem mass spectrometry based on tandem mass spectrometry cubed technique.  JOURNAL OF SEPARATION SCIENCE,  46  (1): (2200725). 
8. Xiaojing Li, Ruichen Bai, Yichen Bai, Xu Shi, Yuhong Yang, Shiwen Xu.  (2022)  ROS-mediated PPAR/RXR inhibition contributes to acetochlor-induced apoptosis and autophagy in Ctenopharyngodon idella hepatic cells.  FISH & SHELLFISH IMMUNOLOGY,  128  (684). 
9. Xia Zhao, Xu Shi, Qingqing Liu, Xiaojing Li.  (2022)  Tea polyphenols alleviates acetochlor-induced apoptosis and necroptosis via ROS/MAPK/NF-κB signaling in Ctenopharyngodon idellus kidney cells.  AQUATIC TOXICOLOGY,  246  (106153). 
10. Mengna Huang, Yanping Fan, Xiang Yuan, Lin Wei.  (2022)  Color-coded detection of malathion based on enzyme inhibition with dark-field optical microscopy.  SENSORS AND ACTUATORS B-CHEMICAL,  353  (131135). 
11. Ke Wang, Xiaoyan Sun, Bibo Long, Fayong Li, Chong Yang, Junjia Chen, Chunping Ma, Dong Xie, Yen Wei.  (2021)  Green Production of Biodegradable Mulch Films for Effective Weed Control.  ACS Omega,  (47): (32327–32333). 
12. Jie Chen, Jinfeng Ling, Bo Sun, Jian Wang, Baoxue Zhou, Xiaohong Guan, Yuankui Sun.  (2021)  Trace organic contaminants abatement by permanganate/bisulfite pretreatment coupled with conventional water treatment processes: Lab- and pilot-scale tests.  JOURNAL OF HAZARDOUS MATERIALS,  401  (123380). 
13. Xutian Zheng, Chaolun Liu, Jiye Hu.  (2020)  Residues and Dietary Risk Assessments of 2,4-D Isooctyl Ester, Metribuzin, Acetochlor, and 2-Ethyl-6-methylaniline in Corn or Soybean Fields.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  68  (15): (4315–4324). 
14. Xu Jinmeng, Zhang Yan, Wu Kaiqing, Zhang Lina, Ge Shenguang, Yu Jinghua.  (2017)  A molecularly imprinted polypyrrole for ultrasensitive voltammetric determination of glyphosate.  MICROCHIMICA ACTA,  184  (7): (1959-1967). 
15. Yifei Sun, Yan Tang, Zetao Chen, Miaoxiu Ge, Wei Xiong, Luhong Wen.  (2024)  A Facile Determination of Herbicide Residues and Its Application in On-Site Analysis.  Foods,  13  (8): (1280). 
16. Siying Che, Yiwan Zhuge, Xinxiang Shao, Xiutan Peng, Haiyan Fu, Yuanbin She.  (2024)  A fluorescence ionic probe utilizing Cu2+ assisted competition for detecting glyphosate abused in green tea.  FOOD CHEMISTRY,  447  (138859). 
17. Yue Zhang, Lulu Hou, Tiantian Guo, Hongmin Lu, Xin Zhang, Mingwei Xing.  (2025)  An in-depth analysis of the effects of excessive acetochlor exposure on chicken liver health.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,  208  (106280). 
18. Zhipeng Li, Ruochun Zhang, Jun Huang, Dandan Yu, Zhanjun Cheng, Guanyi Chen, Peizhe Sun.  (2025)  Carbon residue from co-pyrolysis of cartons and plastics: Characteristics, environmental behaviors and applications.  JOURNAL OF ENVIRONMENTAL MANAGEMENT,  375  (124296). 
19. Chunyan Zheng, Jie Yang, Yunting Wang, Waqas Ahmed, Amir Khan, Jiannan Li, Jiechang Weng, Sajid Mehmood, Weidong Li.  (2024)  Comprehensive Assessment of Herbicide Toxicity on Navicula sp. Algae: Effects on Growth, Chlorophyll Content, Antioxidant System, and Lipid Metabolism.  Marine Drugs,  22  (9): (387). 
20. Hu Chen-Yan, Ji Sheng-Jie, Dong Zheng-Yu, Wu Yi-Hui, Dong Zi-Yi, Hu Li-Li, Yang Xin-Yu, Liu Hao.  (2024)  Degradation of acetochlor via the UV/persulfate process: Mechanisms, kinetics, and pathways.  Water Reuse,  14  (3): (384-395). 
21. Di Lu, Xinyue Zheng, Hongyu Xue, Jiansong You, Lei Yin, Meiyun Shi.  (2024)  Determination of acetochlor by UPLC-MS3 in cells and its application to a cellular pharmacokinetic study.  ANALYTICAL BIOCHEMISTRY,  688  (115476). 
22. Chen-Yan Hu, Li-Li Hu, Zheng-Yu Dong, Xin-Yu Yang, Hao Liu, Jia-Nan Chen, Ling-Mei Gao.  (2024)  Enhanced degradation of emerging contaminants by Far-UVC photolysis of peracetic acid: Synergistic effect and mechanisms.  WATER RESEARCH,  260  (121943). 
23. Xin Wang, Bo Peng, Cheng Zhang, Mengqi Wu, Wenping Xu, Jiagao Cheng, Liming Tao, Zhong Li, Yang Zhang.  (2024)  Hepatic effects of acetochlor chiral isomers in zebrafish and L02 cells.  SCIENCE OF THE TOTAL ENVIRONMENT,  913  (169781). 
24. Chen-Yan Hu, Li-Li Hu, Tian-Yang Zhang, Xin-Yu Yang, Hao Liu, Jia-Nan Chen, Ling-Mei Gao, Zheng-Yu Dong.  (2025)  Rapid oxidation of emerging contaminants by far-UVC/chlorine system: Energy efficiency and synergistic mechanism.  Journal of Water Process Engineering,  70  (106958). 

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