Acephate - analytical standard, ≥99% , CAS No.30560-19-1

CAS: 30560-19-1 Cat. No.: A109744 Molecular Weight: 183.17 Beilstein Registry Number: 1936365 EC Number: 250-241-2

GRADE & PURITY Analytical standard, ≥99%

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

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

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

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

Action Type

INHIBITOR

Purity

≥99%

Names and Identifiers

• Canonical Smiles: CC(=O)NP(=O)(OC)SC
• IUPAC Name: N-[methoxy(methylsulfanyl)phosphoryl]acetamide
• InChIKey: YASYVMFAVPKPKE-UHFFFAOYSA-N
• INCHI: 1S/C4H10NO3PS/c1-4(6)5-9(7,8-2)10-3/h1-3H3,(H,5,6,7)
• 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=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organophosphorus compounds
    • Class Organothiophosphorus compounds

• 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.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

Discover Target: SLCO1B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

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

References

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,      [PMID:37648105] [10.1016/j.fct.2023.114000]

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,      [PMID:] [10.1016/j.fbio.2023.102967]

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,      [PMID:37179059] [10.1016/j.aca.2023.341264]

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,      [PMID:] [10.1016/j.cjac.2021.09.004]

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,      [PMID:34034058] [10.1016/j.foodchem.2021.130106]

6. Linfeng Chen, Xike Tian, Yong Li, Liqiang Lu, Yulun Nie, Yanxin Wang.  (2020)  Broad-spectrum pesticide screening by multiple cholinesterases and thiocholine sensors assembled high-throughput optical array system.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:33254811] [10.1016/j.jhazmat.2020.123830]

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,      [PMID:] [10.1021/acsanm.9b00398]

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).  [PMID:30637510] [10.1007/s00604-019-3231-1]

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).  [PMID:35548014] [10.1039/C8RA04953J]

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,      [PMID:40021329] [10.1016/j.aca.2025.343775]

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,      [PMID:38479145] [10.1016/j.foodchem.2024.138859]

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,      [PMID:] [10.1039/D4EN00966E]

13. Xiutan Peng, Yuqing Xu, Weiye Zhou, Yiting Tao, Haiyan Fu, Siying Che, Yuanbin She.  (2025)  Water-soluble tunable ionic liquid probes for the sensitive detection of glyphosate by fluorescence turn-off-on.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.114692]

14. Junjie Qi, Wenhui Hao, Jingkun Li, Yuqi Wan, Guoyong Jiang, Yukihiro Ozaki, Fuwei Pi.  (2025)  PCN222(Fe)@NU-1000 based MOF-on-MOF dual-signal sensing strategy for sensitive detection of phoxim.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.115260]

15. Liqian Niu, Xian Wang, Xinxin Liu, Xin Liu, Shiyue Niu, Bin Yang, Jia Liu, Shuyun Bi.  (2026)  Construction of the SERS substrate of AgNPs modified with N-Acetyl-L-cysteine and ZnO for sensitive detection of acephate.  JOURNAL OF LUMINESCENCE,      [PMID:] [10.1016/j.jlumin.2026.121796]

16. Xingyue Liu, Liucheng Meng, Wen Deng, Yuzhou Yang, Yanling Lou, Jianfeng Xi, Peng Li, Lei Zhang, Weibing Wu.  (2026)  Photo-induced in-situ synthesized nanocellulose-based SERS substrate integrated with molecularly imprinted polymer for selective detection of pesticide residues.  CARBOHYDRATE POLYMERS,      [PMID:41831976] [10.1016/j.carbpol.2026.125050]

17. Xinyu Luo, Dejin Lin, Jingqi Wang, Yihao Zhang, Xinru Liu, Sineng Gao, Da Chen.  (2026)  Aggregation caused quenching of dual-emission nitrogen-doped carbon dots for visual quantitative and ratiometric detection of pesticide residues.  FOOD CHEMISTRY,      [PMID:] [10.1016/j.foodchem.2026.148780]