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57548-58-0

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57548-58-0 Usage

Description

(o-Methylphenoxy)acetic acid sodium salt, also known as sodium 2-(o-methylphenoxy)acetate, is a chemical compound with the molecular formula C9H9NaO3. It is a sodium salt form of the organic compound (o-Methylphenoxy)acetic acid, characterized by its white solid appearance and solubility in water and polar organic solvents. (o-Methylphenoxy)acetic acid sodium salt is widely recognized for its applications in agriculture, where it serves as a herbicide and plant growth regulator.

Uses

Used in Agricultural Industry:
(o-Methylphenoxy)acetic acid sodium salt is used as a herbicide for controlling the growth of weeds and unwanted plants. Its application helps in reducing the competition for resources between crops and weeds, thereby improving crop yield and quality.
(o-Methylphenoxy)acetic acid sodium salt is also used as a plant growth regulator to stimulate the growth of certain crops. By modulating the growth and development of plants, this compound can enhance crop productivity and contribute to more efficient agricultural practices.
It is crucial to handle (o-Methylphenoxy)acetic acid sodium salt with care and adhere to safety guidelines when utilizing it in agricultural or research settings to ensure the safety of both the environment and the individuals involved in its application.

Check Digit Verification of cas no

The CAS Registry Mumber 57548-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,4 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57548-58:
(7*5)+(6*7)+(5*5)+(4*4)+(3*8)+(2*5)+(1*8)=160
160 % 10 = 0
So 57548-58-0 is a valid CAS Registry Number.

57548-58-0SDS

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 Sodium; o-tolyloxy-acetate

1.2 Other means of identification

Product number -
Other names -

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:57548-58-0 SDS

57548-58-0Relevant articles and documents

Continuous preparation method and preparation system of 2-methyl-4-chlorophenoxyacetic acid

-

Page/Page column 0021; 0024; 0035-0061, (2022/01/10)

The present invention belongs to the technical field of 2-methyl-4-chlorophenoxyacetic acid, specifically relates to a continuous preparation method and preparation system of 2-methyl-4-chlorophenoxyacetic acid. The continuous preparation method of 2-methyl-4-chlorophenoxyacetic acid comprising: the o-cresol and the alkali solution into a salt reaction, to obtain a phenol salt solution; after the chloroacetic acid is added to the phenol salt solution for condensation reaction, the reaction solution is evaporated to obtain o-toluoxyacetate; organic solvent and acid are added to the o-toluoxyacetate, after acidification reaction, the reaction mixture is separated from the intermediate solution; chlorine is introduced into the intermediate solution, and after the chlorination reaction, the product solution is separated After crystal separation and drying of the product solution, 2-methyl-4-chlorophenoxyacetic acid was prepared. By configuring an automated control system through continuous production, human resources can be greatly reduced.

Finding new elicitors that induce resistance in rice to the white-backed planthopper Sogatella furcifera

He, Xingrui,Yu, Zhaonan,Jiang, Shaojie,Zhang, Peizhi,Shang, Zhicai,Lou, Yonggen,Wu, Jun

supporting information, p. 5601 - 5603 (2015/11/17)

Herein we report a new way to identify chemical elicitors that induce resistance in rice to herbivores. Using this method, by quantifying the induction of chemicals for GUS activity in a specific screening system that we established previously, 5 candidate elicitors were selected from the 29 designed and synthesized phenoxyalkanoic acid derivatives. Bioassays confirmed that these candidate elicitors could induce plant defense and then repel feeding of white-backed planthopper Sogatella furcifera.

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