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Methiocarb Solution in Methanol - 100μg/mL in methanol,uncertain:3%, high purity , CAS No.2032-65-7

    Grade & Purity:
  • 100μg/mL in methanol,uncertain:3%
In stock
Item Number
BWY359287
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Availability
Price Qty
BWY359287-1.2ml
1.2ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$69.90

Basic Description

Synonyms METHIOCARB | Mercaptodimethur | 2032-65-7 | Mesurol | Metmercapturon | Draza | 3,5-Dimethyl-4-(methylthio)phenyl methylcarbamate | Methiocarbe | Mesurol Phenol | 3,5-Dimethyl-4-(methylthio)phenol methylcarbamate | Bayer 37344 | 3,5-Dimethyl-4-methylthiophenyl N-methylcarbamate
Specifications & Purity 100μg/mL in methanol,uncertain:3%
Storage Temp Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class 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
Description 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

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
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Faah Anandamide amidohydrolase (3907 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Brassica napus (1186 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
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Frankliniella occidentalis (90 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Theba pisana (23 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 (3,5-dimethyl-4-methylsulfanylphenyl) N-methylcarbamate
INCHI 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)
InChIKey YFBPRJGDJKVWAH-UHFFFAOYSA-N
Smiles CC1=CC(=CC(=C1SC)C)OC(=O)NC
Isomeric SMILES CC1=CC(=CC(=C1SC)C)OC(=O)NC
WGK Germany 3
RTECS FC5775000
UN Number 2757
Packing Group I
Molecular Weight 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=

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

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

Chemical and Physical Properties

Molecular Weight 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

Citations of This Product

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,  1664  (462799). 
2. MingYan Wang, JunRao Huang, Meng Wang, DongEn Zhang, Jun Chen.  (2014)  Electrochemical nonenzymatic sensor based on CoO decorated reduced graphene oxide for the simultaneous determination of carbofuran and carbaryl in fruits and vegetables.  FOOD CHEMISTRY,  151  (191). 
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,     
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,  81  (44). 
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,  204  (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,     

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