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Pirimiphos-methyl solution - analytical standard,10μg/ml,u=3% in acetone, high purity , CAS No.29232-93-7
Basic Description
Synonyms
Primiphos-methyl | NCGC00163924-02 | NCGC00254624-01 | O-(2-(DIETHYLAMINO)-6-METHYL-4-PYRIMIDINYL) O,O-DIMETHYL PHOSPHOROTHIOATE | Pirimifosmethyl | Pyridimine phosphate | 4-dimethoxyphosphinothioyloxy-N,N-diethyl-6-methyl-2-pyrimidinamine | DTXCID004266
Specifications & Purity
analytical standard, 10μg/ml,u=3% in acetone
Storage Temp
Store at 2-8°C,Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
analytical standard
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
Organic thiophosphoric acids and derivatives
Subclass
Thiophosphoric acid esters
Intermediate Tree Nodes
Aryl thiophosphates
Direct Parent
Pyrimidinyl phosphorothioates
Alternative Parents
Thiophosphate triesters Dialkylarylamines Aminopyrimidines and derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidinyl phosphorothioate - Dialkylarylamine - Thiophosphate triester - Aminopyrimidine - Pyrimidine - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidinyl phosphorothioates. These are organic compounds containing the thiophosphoric acid functional group or a derivative thereof, with the general structure ROP(OR')(OR'')=S, where R= pyrimidine, R' = organyl group , and R\" = any atom.
External Descriptors
Organophosphorus 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.
Associated Targets(Human)
Associated Targets(non-human)
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
4-dimethoxyphosphinothioyloxy-N,N-diethyl-6-methylpyrimidin-2-amine
INCHI
InChI=1S/C11H20N3O3PS/c1-6-14(7-2)11-12-9(3)8-10(13-11)17-18(19,15-4)16-5/h8H,6-7H2,1-5H3
InChIKey
QHOQHJPRIBSPCY-UHFFFAOYSA-N
Smiles
CCN(CC)C1=NC(=CC(=N1)OP(=S)(OC)OC)C
Isomeric SMILES
CCN(CC)C1=NC(=CC(=N1)OP(=S)(OC)OC)C
WGK Germany
3
RTECS
TF1410000
UN Number
3082
Packing Group
III
Molecular Weight
305.33
Beilstein
755726
Reaxy-Rn
755726
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=755726&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Light sensitive.
Melt Point(°C)
15°C
Molecular Weight
305.340 g/mol
XLogP3
4.200
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
7
Rotatable Bond Count
7
Exact Mass
305.096 Da
Monoisotopic Mass
305.096 Da
Topological Polar Surface Area
88.800 Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
310.000
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.
Xinyue Zhang, Zhi Li, Yang Wang, Shuaihua Zhang, Xiaohuan Zang, Chun Wang, Zhi Wang.
(2023)
Preparation of black phosphorus nanosheets/ zeolitic imidazolate framework nanocomposite for high-performance solid-phase microextraction of organophosphorus pesticides. JOURNAL OF CHROMATOGRAPHY A,
1708
(464339).
2.
Kai Zhang, Liangzi Wang, Jingitao liu, Shiyu Zhao, Longfei Ding, Binhua Zhou, Bo Zhao.
(2022)
A Highly Sensitive Electrochemical Methamidophos Immobilized AChE Biosensor for Organophosphorus Pesticides Detection. International Journal of Electrochemical Science,
17
(220443).
3.
Guozheng Zhao, Binhua Zhou, Xiuwen Wang, Jian Shen, Bo Zhao.
(2021)
Detection of organophosphorus pesticides by nanogold/mercaptomethamidophos multi-residue electrochemical biosensor. FOOD CHEMISTRY,
354
(129511).
4.
Kangmiao Guo, Xiaokun Wu, Fan Zhang, Ying Cao, Zenglei Tan, Shuwen Xiao, Lijie Wu.
(2024)
Deep Eutectic Solvents-Based Ultrasonic-Assisted Dispersive Liquid–Liquid Microextraction for the Determination of Organophosphorus Pesticides in Honeysuckle Dew Samples. MOLECULES,
29
(14):
(3423).
5.
Dan Zhao, Gang Yu, Miaoxiu Ge, Mingdai Han, Haibing Meng, Wei Xiong, Luhong Wen.
(2024)
Post-modified linker functionalization of metal organic frameworks for high-efficiency adsorption and quantification of trace organophosphorus pesticides in environmental water. SEPARATION AND PURIFICATION TECHNOLOGY,
346
(127470).
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5 Citations
J1526075