Alachlor solution - analytical standard, 10 ug/ml in ethyl acetate,u=6% , CAS No.15972-60-8

CAS: 15972-60-8 Cat. No.: A109969 Molecular Weight: 269.77 Beilstein Registry Number: 2944476 EC Number: 240-110-8
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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. 10 ug/ml in ethyl acetate,u=6%
Synonyms
alachlor|15972-60-8|Lasagrin|Metachlor|Methachlor|Alanex|Alachlore|Alochlor|Pillarzo|Lasso|2-chloro-N-(2,6-diethylphenyl)-N-(methoxymethyl)acetamide|Chimiclor|Alanox|LAZO|Lasso micro-tech|Alatox 480|2-Chloro-2',6'-diethyl-N-(methoxymethyl)acetanilide|Acet
Storage
Room temperature
Shipped In
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1ml
A109969-1ml
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Why this grade

analytical standard, 10 ug/ml in ethyl acetate,u=6% Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships FedEx DG Service 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 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
alachlor | 15972-60-8 | Lasagrin | Metachlor | Methachlor | Alanex | Alachlore | Alochlor | Pillarzo | Lasso | 2-chloro-N-(2, 6-diethylphenyl)-N-(methoxymethyl)acetamide | Chimiclor | Alanox | LAZO | Lasso micro-tech | Alatox 480 | 2-Chloro-2', 6'-diethyl-N-(methoxymethyl)acetanilide | Acet
Specifications & Purity
analytical standard, 10 ug/ml in ethyl acetate, u=6%
Storage
Room temperature
Shipped In
FedEx DG Service
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Analytical standard
Names and Identifiers
Canonical SmilesCCC1=C(C(=CC=C1)CC)N(COC)C(=O)CCl
IUPAC Name2-chloro-N-(2,6-diethylphenyl)-N-(methoxymethyl)acetamide
InChIKeyXCSGPAVHZFQHGE-UHFFFAOYSA-N
INCHI1S/C14H20ClNO2/c1-4-11-7-6-8-12(5-2)14(11)16(10-18-3)13(17)9-15/h6-8H,4-5,9-10H2,1-3H3
Isomeric SMILES CCC1=C(C(=CC=C1)CC)N(COC)C(=O)CCl
WGK Germany 3
RTECS AE1225000
UN Number 2588
Packing Group I
Molecular Weight 269.77
Beilstein 2944476
Reaxy-Rn 2944476
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2944476&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
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
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 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
Arabidopsis thaliana (307 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Setaria viridis (435 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Phaseolus vulgaris (518 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
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCS20 3-ketoacyl-CoA synthase 19 (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FAE1 3-ketoacyl-CoA synthase 18 (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCS2 3-ketoacyl-CoA synthase 17 (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCS5 3-ketoacyl-CoA synthase 5 (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCS17 Probable 3-ketoacyl-CoA synthase 2 (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCS1 3-ketoacyl-CoA synthase 1 (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Stellaria media (151 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Digitaria ciliaris (285 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Poa annua (183 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Amaranthus blitum subsp. oleraceus (34 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.

1 results found

Lot NumberCertificate TypeDateItem
I1819133Certificate of AnalysisNov 06, 2025 A109969
Chemical and Physical Properties
SolubilityHard to dissolve in water, soluble in ether, acetone, benzene, chloroform, and ethanol.
SensitivityLight sensitive.
Melt Point(°C)40-41°C
Molecular Weight269.770 g/mol
XLogP33.500
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count6
Exact Mass269.118 Da
Monoisotopic Mass269.118 Da
Topological Polar Surface Area29.500 Ų
Heavy Atom Count18
Formal Charge0
Complexity248.000
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. 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. Peng Xu, Rui Wei, Peng Wang, Xiang Li, Chunyan Yang, Tianyao Shen, Tong Zheng, Guangshan Zhang.  (2023)  CuFe2O4/diatomite actuates peroxymonosulfate activation process: Mechanism for active species transformation and pesticide degradation.  WATER RESEARCH,      [PMID:36934540] [10.1016/j.watres.2023.119843]
3. Peng Xu, Xiang Li, Rui Wei, Chunyan Yang, Tianyao Shen, Peng Wang, Guangshan Zhang.  (2023)  High adaptability and stability FeCo2O4/diatomite composite for efficient peroxymonosulfate activation: Performance, water matrix impact, and mechanism.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.142204]
4. Tianyao Shen, Xiaojing Wang, Jiaqin Li, Chunyan Yang, Peng Xu, Hua Chai, Peng Wang, Guangshan Zhang.  (2022)  Construction of 3D ternary layered double hydroxides on nickel foam for enhancing dielectric barrier discharge plasma to degrade DUR: Performance, mechanism and energy efficiency.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.140790]
5. Lifang Fan, Guifang Liang, Caiyun Zhang, Li Fan, Wenjun Yan, Yujing Guo, Shaomin Shuang, Yingpu Bi, Feng Li, Chuan Dong.  (2020)  Visible-light-driven photoelectrochemical sensing platform based on BiOI nanoflowers/TiO2 nanotubes for detection of atrazine in environmental samples.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:33412470] [10.1016/j.jhazmat.2020.124894]
6. Zhang Wenjie, Wang Jun, Wang Jinhua, Zhu Lusheng, Lv Ning, Wang Rui, Ahmad Zulfiqar.  (2019)  New Insights into Dose- and Time-Dependent Response of Five Typical PPCPs on Soil Microbial Respiration.  BULLETIN OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY,  103  (1): (193-198).  [PMID:31218411] [10.1007/s00128-019-02655-5]
7. Fuyou Du, Lingshun Sun, Qiulian Zen, Wei Tan, Zhenfang Cheng, Guihua Ruan, Jianping Li.  (2019)  A highly sensitive and selective “on-off-on” fluorescent sensor based on nitrogen doped graphene quantum dots for the detection of Hg2+ and paraquat.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2019.02.109]
8. 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]
9. 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]
10. Xinyu Luo, Ziyi Liu, Linfan Wang, Liwei Gao, Dingfeng Wang, Ting Zhang, Da Chen.  (2024)  Smartphone-assisted sensing platform based on dual-responsive nitrogen-doped carbon dots for enzyme-free and visual quantitative detection of Cu2+ and glyphosate.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.112166]
11. 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]
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