Butachlor solution - analytical standard, 100μg/ml in Petroleum ether , CAS No.23184-66-9

CAS: 23184-66-9 Cat. No.: B306013 Molecular Weight: 311.85 Beilstein Registry Number: 2873811 EC Number: 245-477-8
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GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. 100μg/ml in Petroleum ether
Synonyms
Butachlor, analytical standard | HY-B2042 | NCGC00254842-01 | N-n-butoxymethyl-N-(2,6-diethylphenyl)chloroacetamide | Amichlor | 94NU90OO5K | Butachlor [ANSI:BSI:ISO] | NSC221683 | NSC-221683 | BUTACHLOR | CAS-23184-66-9 | HKPHPIREJKHECO-UHFFFAOYSA- | NCG
Storage
Store at 2-8°C
Shipped In
Wet ice
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1ml
B306013-1ml
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Why this grade

analytical standard, 100μg/ml in Petroleum ether Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 14 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
Butachlor, analytical standard | HY-B2042 | NCGC00254842-01 | N-n-butoxymethyl-N-(2, 6-diethylphenyl)chloroacetamide | Amichlor | 94NU90OO5K | Butachlor [ANSI:BSI:ISO] | NSC221683 | NSC-221683 | BUTACHLOR | CAS-23184-66-9 | HKPHPIREJKHECO-UHFFFAOYSA- | NCG
Specifications & Purity
analytical standard, 100μg/ml in Petroleum ether
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Analytical standard
Names and Identifiers
Pubchem Sid24863591
Canonical SmilesCCCCOCN(C1=C(C=CC=C1CC)CC)C(=O)CCl
IUPAC NameN-(butoxymethyl)-2-chloro-N-(2,6-diethylphenyl)acetamide
InChIKeyHKPHPIREJKHECO-UHFFFAOYSA-N
INCHI1S/C17H26ClNO2/c1-4-7-11-21-13-19(16(20)12-18)17-14(5-2)9-8-10-15(17)6-3/h8-10H,4-7,11-13H2,1-3H3
Isomeric SMILES CCCCOCN(C1=C(C=CC=C1CC)CC)C(=O)CCl
WGK Germany 3
RTECS AE1200000
Molecular Weight 311.85
Beilstein 2873811
Reaxy-Rn 2873811
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2873811&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassAnilides
Intermediate Tree Nodes Not available
Direct ParentAnilides
Alternative Parents Tertiary carboxylic acid amides  Chloroacetamides  Organopnictogen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl chlorides  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Anilide - 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Echinochloa crus-galli (3685 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus niger (16508 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryza sativa (2923 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
unidentified (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pontederia vaginalis (622 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sagittaria pygmaea (155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Echinochloa oryzicola (1513 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Schoenoplectiella juncoides (1014 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cyperus serotinus (164 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

2 results found

Lot NumberCertificate TypeDateItem
J2127465Certificate of AnalysisAug 13, 2024 B306013
J2127460Certificate of AnalysisAug 13, 2024 B306013
Chemical and Physical Properties
Flash Point(°C)100°C
Molecular Weight311.800 g/mol
XLogP34.500
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count9
Exact Mass311.165 Da
Monoisotopic Mass311.165 Da
Topological Polar Surface Area29.500 Ų
Heavy Atom Count21
Formal Charge0
Complexity287.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Linwei Zhang, Xiaoyang Yin, Hongfei Yang, Hao Wen, Shiyun Han, Xiaoming Pan, Huaming Li, Dapeng Peng.  (2023)  A Sensitive and Specific Monoclonal Antibody Based Enzyme-Linked Immunosorbent Assay for the Rapid Detection of Pretilachlor in Grains and the Environment.  Foods,  13  (1): (12).  [PMID:38201043] [10.3390/foods13010012]
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,      [PMID:] [10.1016/j.microc.2023.109497]
3. Yi Wu, Liyuan Zhang, Dongjie Zhang, Runzhong Yu.  (2023)  A surface molecularly imprinted microfluidic paper based device with smartphone assisted colorimetric detection for butachlor in mung bean.  FOOD CHEMISTRY,      [PMID:37816277] [10.1016/j.foodchem.2023.137659]
4. 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]
5. Shuheng Hu, Xin Jin, Xueyan Chen, Bin Lv, Wenhao Xi, Yan Lan, Wei Han, Zimu Xu, Cheng Cheng.  (2023)  Butachlor (BTR) degradation by dielectric barrier discharge plasma in soil: Affecting factors, degradation route, and toxicity assessment.  CHEMOSPHERE,      [PMID:37423413] [10.1016/j.chemosphere.2023.139414]
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).  [PMID:37305969] [10.1039/D3AY00298E]
7. Jing Yu, Hui Zhu, Heli Wang, Brian Shutes, Tingting Niu.  (2023)  Effect of butachlor on Microcystis aeruginosa: Cellular and molecular mechanisms of toxicity.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:36827725] [10.1016/j.jhazmat.2023.131042]
8. 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).  [PMID:36321527] [10.1002/jssc.202200725]
9. 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).  [PMID:38672952] [10.3390/foods13081280]
10. 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,      [PMID:38286351] [10.1016/j.ab.2024.115476]
11. Ma Rong, Yu Shuangshuang, Li Yafang, Lin Yan, Ma Xiaodong.  (2024)  Enhancing the efficiency of polypyrrole-dodecylbenzene sulfonic acid in-tube solid-phase microextraction coating for analysis of nitrogen-containing pesticides in water environments.  Frontiers in Environmental Science,      [PMID:] [10.3389/fenvs.2024.1350170]
12. Bu Ziyun, Si Qiankang, Lu Xiaolin, Wang Pei, Wu Dezhen, Mei Yingying.  (2025)  Monolithic capillary electrochromatographic system based on gold nanoparticles and chitosan chiral molecularly imprinted polymers for enantioseparation of metolachlor and separation of structural analogs.  MICROCHIMICA ACTA,  192  (5): (1-14).  [PMID:40205242] [10.1007/s00604-025-07142-9]
13. Li Huaqiang, Wu Feifei, Ding Yuxian, Long Guozhou, Yin Lei.  (2025)  High-throughput quantification of butachlor by DART-MS/MS coupled with micro-solid-phase extraction and dual fragmentation to enhance selectivity and sensitivity.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,      [PMID:40576763] [10.1007/s00216-025-05975-0]
14. Yong-mei Zhang, Ping-ping Fan, Ling-zhi Zhang, Wei Yu, Song Xia, Fa-li Liu, Xue-de Li.  (2026)  Occurrence, ecological risk, and human health assessment of herbicide residues in Chaohu Lake, China.  Journal of Environmental Chemical Engineering,  14  (2): (121850).  [PMID:] [10.1016/j.jece.2026.121850]
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