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Acephate - analytical standard，99%, high purity , CAS No.30560-19-1
Basic Description
Synonyms
Acetamidophos | NCGC00254778-01 | KBio1_001560 | o,S-Dimethyl acetylamidothiophosphate | UNII-3Y417O444D | AKOS006227880 | Chevron RE 12,420 | MFCD00055361 | O,S-Dimethyl acetylphosphoramidothioate | O,S-dimethyl acetylphosphoroamidothioate | Phosphoramid
Specifications & Purity
analytical standard, ≥99%
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.
Grade
analytical standard
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organophosphorus compounds
Class
Organothiophosphorus compounds
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Organothiophosphorus compounds
Alternative Parents
Sulfenyl compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic acyclic compounds
Substituents
Sulfenyl compound - Organothiophosphorus compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as organothiophosphorus compounds. These are organic derivatives of thiophosphonic acid, thiophosphoric acid, dithiophosphoric acid, or phosphorotrithioic acid, or derivatives thereof. Thiophosphonic acid, dithiophosphoric acid, thiophosphoric acid, and phosphorotrithioic acid are thiophosphorus compounds with the formula OP(O)(=S), OP(S)(=S)O, OP(O)(=S)O, and OP(=S)(S)S, respectively.
External Descriptors
Phosphoramido 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)
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
N-[methoxy(methylsulfanyl)phosphoryl]acetamide
INCHI
InChI=1S/C4H10NO3PS/c1-4(6)5-9(7,8-2)10-3/h1-3H3,(H,5,6,7)
InChIKey
YASYVMFAVPKPKE-UHFFFAOYSA-N
Smiles
CC(=O)NP(=O)(OC)SC
Isomeric SMILES
CC(=O)NP(=O)(OC)SC
WGK Germany
2
UN Number
3018
Packing Group
I
Molecular Weight
183.17
Beilstein
1936365
Reaxy-Rn
1936365
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1936365&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Flash Point(°F)
2 °C
Flash Point(°C)
2°C
Molecular Weight
183.170 g/mol
XLogP3
-0.800
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
3
Exact Mass
183.012 Da
Monoisotopic Mass
183.012 Da
Topological Polar Surface Area
80.700 Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
172.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
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.
Yuanhao Zhou, Jiawen Ai, Lingli Cai, Yiyong Yan, BingZhi Wang, Hongzhen Ma, Quan Yu, Jianhua Zhou, Xinming Huo.
(2023)
Deep learning enabled miniature mass spectrometer for rapid qualitative and quantitative analysis of pesticides on vegetable surfaces. FOOD AND CHEMICAL TOXICOLOGY,
180
(114000).
2.
Wenhui Hao, Gengli Huang, Guoyong Jiang, Sa-adu Abiola Dauda, Fuwei Pi.
(2023)
Direct phoxim sensing based on fluorescent metal-organic framework of Nu-1000 induced FRET. Food Bioscience,
55
(102967).
3.
Shizhuang Weng, Le Tang, Mengqing Qiu, Jinghong Wang, Yehang Wu, Rui Zhu, Cong Wang, Pan Li, Wen Sha, Dong Liang.
(2023)
Surface-enhanced Raman spectroscopy charged probes under inverted superhydrophobic platform for detection of agricultural chemicals residues in rice combined with lightweight deep learning network. ANALYTICA CHIMICA ACTA,
1262
(341264).
4.
Guo-Ying CHEN, Hao ZHANG, Cong-Peng ZHAO, Chun-Yan ZHANG, Yuan WANG, Hua CHEN, Feng-Qing YANG.
(2021)
On-line immobilized acetylcholinesterase microreactor based on capillary electrophoresis for the determination of organophosphorus pesticide residues. CHINESE JOURNAL OF ANALYTICAL CHEMISTRY,
49
(11).
5.
Shaofeng Yuan, Changjian Li, Hang Yu, Yunfei Xie, Yahui Guo, Weirong Yao.
(2021)
Selective uptake determines the variation in degradation of organophosphorus pesticides by Lactobacillus plantarum. FOOD CHEMISTRY,
360
(130106).
6.
Linfeng Chen, Xike Tian, Yong Li, Liqiang Lu, Yulun Nie, Yanxin Wang.
(2021)
Broad-spectrum pesticide screening by multiple cholinesterases and thiocholine sensors assembled high-throughput optical array system. JOURNAL OF HAZARDOUS MATERIALS,
402
(123830).
7.
Fan Gao, Lanlan Yang, Jianguo Tang, Zhonglin Du, Yao Wang, Zhongyi Hu, Dongni Han, Linjun Huang, Laurence A. Belfiore.
(2019)
Fin-like CdSeS Nanoplatelets for Pesticide Sensing. ACS Applied Nano Materials,
2
(6):
(3459–3466).
8.
Sun Huaijing, Mei Qingsong, Shikha Swati, Liu Jinliang, Zhang Jing, Zhang Yong.
(2019)
White-light emissive upconversion nanoparticles for visual and colorimetric determination of the pesticide thiram. MICROCHIMICA ACTA,
186
(2):
(1-9).
9.
Fenglian Qi, Yunhe Lan, Zihui Meng, Chunxiao Yan, Shuguang Li, Min Xue, Yifei Wang, Lili Qiu, Xuan He, Xueyong Liu.
(2018)
Acetylcholinesterase-functionalized two-dimensional photonic crystals for the detection of organophosphates. RSC Advances,
8
(51):
(29385-29391).
10.
Zhangchi Xiao, Yong Li, Yulun Nie, Liqiang Lu, Chao Yang.
(2025)
A Cu2+-triggered turn-on fluorescence non-enzymatic probe based on covalent organic framework for the detection of methyl parathion. ANALYTICA CHIMICA ACTA,
1346
(343775).
11.
Siying Che, Yiwan Zhuge, Xinxiang Shao, Xiutan Peng, Haiyan Fu, Yuanbin She.
(2024)
A fluorescence ionic probe utilizing Cu2+ assisted competition for detecting glyphosate abused in green tea. FOOD CHEMISTRY,
447
(138859).
12.
Shoaib Khan, Aoxue Wang, Jiayin Liu, Iltaf Khan, Samreen Sadiq, Aftab Khan, Waleed Yaseen, Saeed Zaman, Abdul Mueed, Yuanyang Miao.
(2024)
Designing MOF-based green nanomaterials for enhanced pathogen resistance and pesticide degradation in tomato plants. Environmental Science-Nano,
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12 Citations
I1817124