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1-(2,4-dichlorophenoxy)propan-2-one, also known as 2,4-Dichlorophenoxyacetone (2,4-D), is a synthetic organic compound that belongs to the family of chlorophenoxy herbicides. It is commonly used as a selective herbicide to control broadleaf weeds in various agricultural settings, as well as in residential lawns. 2,4-D works by mimicking the plant hormone auxin, which causes uncontrolled growth and ultimately leads to the death of the targeted plants. While it is effective at controlling weeds, the use of 2,4-D has been the subject of controversy due to its potential health and environmental risks. Exposure to 2,4-D has been associated with a range of health concerns, including skin and eye irritation, respiratory issues, and potential carcinogenic effects. As a result, its use is regulated in many countries and it is important to follow proper safety precautions when handling this chemical.

17199-30-3

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17199-30-3 Usage

Uses

Used in Agricultural Industry:
1-(2,4-dichlorophenoxy)propan-2-one is used as a selective herbicide for controlling broadleaf weeds in various agricultural settings. It is effective in targeting and eliminating unwanted plants without causing significant harm to the desired crops.
Used in Residential Landscaping:
1-(2,4-dichlorophenoxy)propan-2-one is also used in residential lawns to manage and control broadleaf weeds, helping to maintain a clean and well-kept appearance for homeowners.
However, it is important to note that due to the potential health and environmental risks associated with 2,4-D, its use is regulated in many countries, and proper safety precautions must be followed when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 17199-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,9 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17199-30:
(7*1)+(6*7)+(5*1)+(4*9)+(3*9)+(2*3)+(1*0)=123
123 % 10 = 3
So 17199-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2O2/c1-6(12)5-13-9-3-2-7(10)4-8(9)11/h2-4H,5H2,1H3

17199-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4-dichlorophenoxy)propan-2-one

1.2 Other means of identification

Product number -
Other names 2,4-Dichlorphenol-acetolether

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:17199-30-3 SDS

17199-30-3Relevant academic research and scientific papers

Discovery of a potent enoyl-acyl carrier protein reductase (FabI) inhibitor suitable for antistaphylococcal agent

Kim, Yun Gyeong,Seo, Jae Hong,Kwak, Jin Hwan,Shin, Kye Jung

, p. 4481 - 4486 (2015/10/12)

We report the discovery, synthesis, and biological activities of phenoxy-4-pyrone and phenoxy-4-pyridone derivatives as novel inhibitors of enoyl-acyl carrier protein reductase (FabI). Pyridone derivatives showed better activities than pyrone derivatives

Discovery of amino-acetonitrile derivatives, a new class of synthetic anthelmintic compounds

Ducray, Pierre,Gauvry, Noelle,Pautrat, Francois,Goebel, Thomas,Fruechtel, Joerg,Desaules, Yves,Weber, Sandra Schorderet,Bouvier, Jacques,Wagner, Trixie,Froelich, Olivier,Kaminsky, Ronald

, p. 2935 - 2938 (2008/12/22)

A new series of amino-acetonitrile derivatives (AAD) have been discovered that exhibit high anthelmintic activity against parasitic nematode species such as Haemonchus contortus and Trichostrongylus colubriformis. Significantly, these compounds also demonstrate activity against nematode strains resistant to the currently available broad-spectrum anthelmintics. The discovery, synthesis, structure-activity relationship and biological results are presented.

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