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O,O-dimethyl acetylthiophosphoramidate is a chemical compound that functions as a pesticide and insecticide. It is classified as a phosphoramidate, which means it incorporates a phosphorus atom along with an amide functional group. O,O-dimethyl acetylthiophosphoramidate's acetylthiophosphoramidate group is derived from a combination of acetic acid and thiophosphoric acid, endowing it with both acetyl and thiophosphate characteristics. Due to its high toxicity, it is crucial to handle O,O-dimethyl acetylthiophosphoramidate with extreme care, using appropriate protective equipment and adhering to safety protocols. Moreover, its application as a pesticide or insecticide must comply with local regulations and laws.

42072-27-5

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42072-27-5 Usage

Uses

Used in Pesticide Industry:
O,O-dimethyl acetylthiophosphoramidate is used as an active ingredient in pesticides for its potent insecticidal properties. It is effective against a variety of pests, helping to protect crops and maintain agricultural productivity.
Used in Insecticide Formulations:
In the insecticide industry, O,O-dimethyl acetylthiophosphoramidate is utilized as a key component in various formulations designed to control insect populations. Its inclusion in these products contributes to the management of insect-borne diseases and damage to crops and stored products.

Check Digit Verification of cas no

The CAS Registry Mumber 42072-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,7 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42072-27:
(7*4)+(6*2)+(5*0)+(4*7)+(3*2)+(2*2)+(1*7)=85
85 % 10 = 5
So 42072-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H10NO3PS/c1-4(6)5-9(10,7-2)8-3/h1-3H3,(H,5,6,10)

42072-27-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-dimethoxyphosphinothioylacetamide

1.2 Other means of identification

Product number -
Other names Phosphoramidothioic acid,acetyl-,O,O-dimethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:42072-27-5 SDS

42072-27-5Downstream Products

42072-27-5Relevant academic research and scientific papers

Synthesis and characterization of O,S-dimethylphosphoramidothioate and N-acetyl O,S-dimethylphosphoramidothioate

Ghadimi,Mousavi,Rahnama,Rahimi

scheme or table, p. 347 - 354 (2010/07/03)

O,S-Dimethylphosphoramidothioate (methamidophos) and N-acetyl O,S-dimethylphos- phoramidothioate (acephate) were synthesized by new methods to investigate the structure-activity study of acetyl cholinesterase (AChE) inhibition through the parameters of logP,δ 31P, and IC 50. After their characterization by NMR (31P, 31P{1H}, 13C, and 1H), IR, and mass spectroscopy, logP and δ31P (31P chemical shift in NMR) were used to evaluate lipophilicity and electronical properties. The logP values for methamidophos and acephate were experimentally determined by the GC-shake-flask method, and the ability of the compounds to inhibit human AChE was evaluated by a modified Ellman's assay. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.

Development of an enzyme-linked immunosorbent assay for the detection of the organophosphorus insecticide acephate

Lee, Jae Koo,Ahn, Ki Chang,Stoutamire, Donald W.,Gee, Shirley J.,Hammock, Bruce D.

, p. 3695 - 3703 (2007/10/03)

A competitive indirect enzyme-linked immunosorbent assay (ciELISA) for the organophosphorus insecticide acephate, O,S-dimethyl acetylphosphoramidothioate, was developed using a polyclonal antibody. Five different haptens mimicking the analyte were synthesized and conjugated with the carrier proteins bovine serum albumin (BSA) and keyhole limpet hemocyanin (KLH) by the N-hydroxysuccinimide active ester and diazotization methods. Polyclonal antibodies raised against hapten - KLH conjugates in rabbits and hapten - BSA conjugates as coating antigens were screened and selected for the assay in the homologous and heterologous ELISA systems. The effects of various assay conditions such as detergent, organic solvents, pH, and preincubation of the mixture of the polyclonal antibody and the analyte on the sensitivity were evaluated. The IC50 value for acephate was 25 ng/mL in an optimized heterologous system using hapten-4 - BSA as a coating antigen and a polyclonal antibody no. 8377 against hapten-1 - KLH, showing the detection range of 5-140 ng/mL and the lowest detection limit of 2 ng/mL. The cross-reactivities of the structurally related organophosphorus insecticides, including the major metabolite of the analyte, methamidophos, were less than 1%. Recoveries from the analyte-fortified tap water, mulberry leaves, and lettuce samples in the assay were in the range of 72-121% by simple extraction, concentration, and dilution. These results indicate that the ELISA could be a convenient and supplemental analytical tool for monitoring acephate residues in environmental and agricultural samples.

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