Methiocarb - analytical standard , CAS No.2032-65-7

CAS: 2032-65-7 Cat. No.: M114161 Formula: C₁₁H₁₅NO₂S Peso molecolare: 225.31 Beilstein Registry Number: 1881431 Numero EC: 217-991-2

GRADE & PURITY Analytical standard

Synonyms

Carbamic acid, methyl-, 3,5-dimethyl-4-(methylthio)phenyl ester | Caswell No. 578B | DTXSID3032626 | 4-(Methylthio)-3,5-xylyl methylcarbamate | SD 9228 | Carbamic acid, methyl-, 4-(methylthio)-3,5-xylyl ester | Draza | Methiocarb [ISO] | EPA Pesticide Che

Storage

Store at 2-8°C

Shipped In

Wet ice

Panoramica

Methiocarb, a carbamate pesticide, is used as an insecticide, acaricide, bird repellent, and molluscicide. Methiocarb stimulates cholinergic by inhibiting reversibly acetylcholinesterase activity, making methiocarb a potent neurotoxin.

Specifications

Sinonimi

Carbamic acid, methyl-, 3,5-dimethyl-4-(methylthio)phenyl ester | Caswell No. 578B | DTXSID3032626 | 4-(Methylthio)-3,5-xylyl methylcarbamate | SD 9228 | Carbamic acid, methyl-, 4-(methylthio)-3,5-xylyl ester | Draza | Methiocarb [ISO] | EPA Pesticide Che

Specifiche e purezza

analytical standard

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Standard analitico

Nomi e identificatori

• Sorrisi canonici: CC1=CC(=CC(=C1SC)C)OC(=O)NC
• IUPAC Name: (3,5-dimethyl-4-methylsulfanylphenyl) N-methylcarbamate
• InChIKey: YFBPRJGDJKVWAH-UHFFFAOYSA-N
• INCHI: 1S/C11H15NO2S/c1-7-5-9(14-11(13)12-3)6-8(2)10(7)15-4/h5-6H,1-4H3,(H,12,13)
• Isomeri SMILES: CC1=CC(=CC(=C1SC)C)OC(=O)NC
• WGK Germania: 3
• RTECS: FC5775000
• Numero UN: 2757
• Gruppo di imballaggio: I
• Peso molecolare: 225.31
• Beilstein: 1881431
• Reaxy-Rn: 1881431
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1881431&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Phenoxy compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Phenoxy compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenoxy compounds
• Alternative Parents: m-Xylenes Thiophenol ethers Alkylarylthioethers Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Carboximidic acids and derivatives Organopnictogen compounds Organooxygen compounds Imines Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxy compound - Aryl thioether - Thiophenol ether - M-xylene - Xylene - Alkylarylthioether - Carboximidic acid derivative - Thioether - Sulfenyl compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Imine - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phenoxy compounds. These are aromatic compounds contaning a phenoxy group.
• External Descriptors: Carbamate insecticides

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

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RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

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Faah Anandamide amidohydrolase (3907 Activities)

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Brassica napus (1186 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)

Discover Target: Nr1i2

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Frankliniella occidentalis (90 Activities)

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Theba pisana (23 Activities)

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Insoluble in water, soluble in most organic solvents.
• Peso molecolare: 225.310 g/mol
• XLogP3: 2.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 225.082 Da
• Monoisotopic Mass: 225.082 Da
• Topological Polar Surface Area: 63.600 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 211.000
• 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

Riferimenti

1. Hongying Guo, An Chen, Jinghui Zhou, Yijun Li, Xiwen He, Langxing Chen, Yukui Zhang.  (2022)  Efficient Extraction and Determination of Carbamate Pesticides in Vegetables Based on a Covalent Organic Frameworks with Acylamide Sites.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:35016080] [10.1016/j.chroma.2021.462799]

2. MingYan Wang, JunRao Huang, Meng Wang, DongEn Zhang, Jun Chen.  (2013)  Electrochemical nonenzymatic sensor based on CoO decorated reduced graphene oxide for the simultaneous determination of carbofuran and carbaryl in fruits and vegetables.  FOOD CHEMISTRY,      [PMID:24423520] [10.1016/j.foodchem.2013.11.046]

3. Kai Wu, Yunyou Zhou, Tao Li, Junyong Sun, Xiaoqing Xing, Qian Song.  (2012)  Cadmium Tellurium Quantum Dots in Sol-Gel-Derived Silica Spheres Coated with Calix[6]Arene as an Optical Probe for Dalapon.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2012.703740]

4. Xue-Ping Ding, Dong-Bao Tang, Tao Li, Su-Fan Wang, Yun-You Zhou.  (2011)  A novel spectrofluorometric method for the determination of methiocarb using an amphiphilic p-sulfonatocalix[4]arene.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:21737343] [10.1016/j.saa.2011.05.038]

5. Cong Tian, Ning Zhu, Lu Qiao, Man He, Beibei Chen, Zhekuan Wu, Bin Hu.  (2024)  Magnetic covalent organic framework for magnetic solid-phase extraction of carbamate pesticide residues.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.111065]

6. Xinyue Li, Yue Wang, Cheng Chen, Chao Tian, Xiaoli Yu, Jinglei Liu, Qin Li, Shuling Wang.  (2025)  Sustainable biochar derived from waste lotus seedpod for efficient adsorption of residual carbamate pesticides.  Heliyon,      [PMID:] [10.1016/j.heliyon.2025.e42741]

Domande frequenti

How should this product be stored?

Store at 2–8 °C. Refrigerated storage is required to maintain the specified shelf life.

What does analytical standard mean?

analytical standard is a defined analytical purity tier suitable for quantitative analytical methods. It specifies a minimum assay percentage, controlled limits on common impurities (water, heavy metals, residue on ignition), and lot-to-lot consistency. analytical standard is one of several purity tiers — choose based on the sensitivity and regulatory requirements of your method.

How is this product shipped?

This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 2032-65-7, the molecular formula is C11H15NO2S, and the molecular weight is 225.31 g/mol. InChIKey YFBPRJGDJKVWAH-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.