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1-(2,4-dichlorophenoxy)propan-2-ol, commonly known as 2,4-Dichlorophenoxyethanol, is a chemical compound that functions as a herbicide and plant growth regulator. It is a derivative of the herbicide 2,4-D, which operates by interfering with the growth processes of plants, leading to the death of unwanted vegetation. 1-(2,4-dichlorophenoxy)propan-2-ol is recognized for its selective action on broadleaf plants, making it a common choice in agricultural and landscaping applications.

5330-18-7

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5330-18-7 Usage

Uses

Used in Agricultural Industry:
1-(2,4-dichlorophenoxy)propan-2-ol is used as a herbicidal agent for controlling the growth of broadleaf plants and weeds in various agricultural settings. Its selective action allows for the effective management of unwanted vegetation without harming the desired crops.
Used in Landscaping Industry:
In landscaping, 1-(2,4-dichlorophenoxy)propan-2-ol is utilized as a plant growth regulator to maintain the aesthetic appeal of gardens and green spaces. It helps in controlling the growth of broadleaf weeds, ensuring a well-kept appearance.
However, due to its potential as an environmental pollutant and its association with negative health effects in humans and animals, it is crucial to handle and dispose of 1-(2,4-dichlorophenoxy)propan-2-ol with care and in accordance with established regulations. This practice minimizes its impact on the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 5330-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5330-18:
(6*5)+(5*3)+(4*3)+(3*0)+(2*1)+(1*8)=67
67 % 10 = 7
So 5330-18-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10Cl2O2/c1-6(12)5-13-9-3-2-7(10)4-8(9)11/h2-4,6,12H,5H2,1H3

5330-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names EINECS 226-223-5

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:5330-18-7 SDS

5330-18-7Relevant academic research and scientific papers

Synthesis of piperazino and morpholino derivatives of aryloxypropane with potential analgesic and possible antimigraine activities

Ismaiel, Abdulkhader M.,Gad, Laila M.,Ghareib, Salah A.,Bamanie, Faida H.,Moustafa, Mohamed A.

experimental part, p. 381 - 387 (2012/06/05)

Modeling studies demonstrate that aryl piperazines (I), aryloxyalkylamines (II), phenylalkykamines (III) and indolylalkylamines (VI) may interact at 5-HT receptors in a similar manner. Examination of these structures (I-VI) reveals that all possess an aromatic moiety and terminal amine binding sites (Glennon et al., J Med Chem 32(8):1921-1926, 1989). In the present investigation a new series of aryloxyalkylamines (4, 5, 8, and 9) was designed and synthesized, in which the aromatic moiety is a phenyl group substituted at the 2,3-, 2,4-, 2,5-, or 2,6-positions by halogens and the terminal amine is N-methylpiperazine, or morpholine. In addition, the alkyl side chain is ethyl, or substituted ethyl at the α- or β-carbon by a methyl group. The length of the alkyl chain that separates the terminal amine from the ether oxygen atom of the aryloxy group is of major importance, and two-carbon chain appears optimal. The structures of the new compounds were assessed by microanalyses, IR, and NMR. The analgesic activity of selected compounds was performed on experimental animals and proved to be in the range of 85-100% relative to aspirin. Springer Science+Business Media, LLC 2011.

1-(benzylpiperidino)propan-2-ol derivatives, their preparation, their use as antimicrobial agents and the products in which they are present

-

, (2008/06/13)

The invention relates to compounds of the formula: STR1 in which: Ar represents a phenyl group substituted by R2, R3 and R4, or a naphth-1-yl or naphth-2-yl group, unsubstituted or substituted by 1 or 2 halogen atoms; X represents an oxygen atom or a sulfur atom; R1 represents H or a halogen atom; R2 represents a halogen atom, a trifluoromethyl group, a phenyl group which is unsubstituted by 1 or 3 halogen atoms, a benzyl group which is unsubstituted or substituted by 1 to 3 halogen atoms, a phenoxy group which is unsubstituted or substituted by 1 to 3 halogen atoms, or a C1 -C4 alkyl group; R3 and R4 represents H, a halogen atom or a C1 -C4 alkyl group; and the benzyl group substitutes the piperidino radical in the 2-, 3- or 4-position, and their salts with mineral or organic acids. It also relates to a process for the preparation of said compounds and their use as antimicrobial agents, as antiseptic, disinfectant, preservative in different kinds of products (pharmaceutical compositions, cosmetics, agri-foodstuffs). It also relates to said products containing the compounds of formula (I).

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