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115339-34-9

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115339-34-9 Usage

Description

2-Chloro-4-acetamido-6-amino-s-triazine is a chemical compound derived from the photocatalytic degradation of 2-Chloro-s-triazine herbicides. It is characterized by its unique molecular structure, which includes a triazine ring with a chlorine atom, an acetamido group, and an amino group attached to specific positions on the ring.

Uses

Used in Environmental Applications:
2-Chloro-4-acetamido-6-amino-s-triazine is used as a degradation product for the management and reduction of harmful herbicide residues in the environment. Its formation through photocatalytic processes helps in mitigating the negative impacts of these herbicides on ecosystems and human health.
Used in Agricultural Industry:
In the agricultural industry, 2-Chloro-4-acetamido-6-amino-s-triazine serves as a key intermediate in the development of safer and more environmentally friendly herbicides. By understanding its properties and behavior, researchers can design new herbicides with reduced environmental impact while maintaining their effectiveness in controlling weeds.
Used in Chemical Research:
2-Chloro-4-acetamido-6-amino-s-triazine is also utilized as a research compound in the field of chemistry, particularly in the study of triazine-based compounds and their applications. Its unique structure makes it an interesting subject for exploring new reactions, properties, and potential uses in various chemical processes and industries.

Check Digit Verification of cas no

The CAS Registry Mumber 115339-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,3 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 115339-34:
(8*1)+(7*1)+(6*5)+(5*3)+(4*3)+(3*9)+(2*3)+(1*4)=109
109 % 10 = 9
So 115339-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H6ClN5O/c1-2(12)8-5-10-3(6)9-4(7)11-5/h1H3,(H3,7,8,9,10,11,12)

115339-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-4-acetamido-6-amino-s-triazine

1.2 Other means of identification

Product number -
Other names N-(4-Amino-6-chloro-1,3,5-triazin-2-yl)acetamide

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:115339-34-9 SDS

115339-34-9Downstream Products

115339-34-9Relevant articles and documents

Identification of Fenton's reagent-generated atrazine degradation products by high-performance liquid chromatography and megaflow electrospray ionization tandem mass spectrometry

Arnold,Talaat,Hickey,Harris

, p. 452 - 460 (1995)

High-performance liquid chromatography megaflow electrospray tandem mass spectrometry (HPLC/ES-MS/MS) with an on-line radioisotope detector was used to identify [2,4,6-14C]atrazine degradation products generated by treatment with Fenton's reagent (Fe2+ and H2O2). Fenton's reagent produced dealkylated and/or partially oxidized [2,4,6-14C]atrazine products in preference to dechlorinated products. Seven major products were identified by collision-induced dissociation spectra: 4-acetamido-2-chloro-6-(isopropylamino)-s-triazine, 4-amino-2-chloro-6-(isopropylamino)-s-triazine, 4-acetamido-2-chloro-6-(ethylamino)-s-triazine, 6-amino-2-chloro-4(ethylamino)-s-triazine, 4-acetamido-6-amino-2-chloro-s-triazine, 2-chloro-4,6-diamino-s-triazine and the first report of 4-acetamido-2-hydroxy-6-(isopropylamino)-s-triazine. HPLC/ES-MS/MS provided a rapid method for identifying a wide range of atrazine transformation products in aqueous samples and obviated the need for fraction collection, extraction, and chemical derivatization of the more polar atrazine products. Furthermore, because analyte retention times in HPLC/UV and HPLC/ES-MS/MS were similar, compound identities determined using the latter could be directly assigned to peaks in UV chromatograms.

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