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1713-12-8

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1713-12-8 Usage

Description

MCPA-1-BUTYL ESTER, also known as 2-(4-chloro-2-methylphenoxy) propanoic acid butyl ester, is a synthetic compound commonly utilized in the agricultural industry as a selective post-emergent herbicide. It is characterized by its low solubility in water and its environmentally friendly nature, which makes it a preferred choice over its parent compound, MCPA (C369470).

Uses

Used in Agricultural Industry:
MCPA-1-BUTYL ESTER is used as a herbicide for controlling a wide range of broadleaf weeds and grasses in various crops. It is particularly effective in controlling weeds such as docks, groundsel, and charlock. The herbicide is absorbed by the leaves and roots of the plants, disrupting their growth and ultimately leading to their death.
The primary reason for the use of MCPA-1-BUTYL ESTER in the agricultural industry is its selective nature, which allows it to target specific weeds without causing significant harm to the desired crop. This selective action minimizes the impact on non-target plants and helps maintain a healthy and productive agricultural ecosystem.
Additionally, the low solubility of MCPA-1-BUTYL ESTER in water contributes to its environmental friendliness. This property reduces the potential for leaching into groundwater and surface water sources, thereby minimizing the risk of water pollution and protecting aquatic ecosystems.

Check Digit Verification of cas no

The CAS Registry Mumber 1713-12-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1713-12:
(6*1)+(5*7)+(4*1)+(3*3)+(2*1)+(1*2)=58
58 % 10 = 8
So 1713-12-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H17ClO3/c1-3-4-7-16-13(15)9-17-12-6-5-11(14)8-10(12)2/h5-6,8H,3-4,7,9H2,1-2H3

1713-12-8SDS

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 MCPA-butyl

1.2 Other means of identification

Product number -
Other names MCPA,butyl 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:1713-12-8 SDS

1713-12-8Relevant articles and documents

Preparation method of phenoxy carboxylic acid herbicide

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, (2019/01/08)

The invention provides a preparation method of a phenoxy carboxylic acid herbicide, comprising the following steps: S1, carrying out a condensation reaction between a phenolic compound and hydroxycarboxylic ester under the action of a catalyst so as to obtain phenoxycarboxylic ester, wherein the catalyst is one or more of protonic acid, solid acid and a supported catalyst; S2, carrying out 2- and/or 4- selecting chlorination reaction between phenoxycarboxylic ester and a chloridizing agent in the presence of a first catalyst and a second catalyst, so as to obtain chlorinated phenoxycarboxylicester, wherein the first catalyst is selected from Lewis acid, and the second catalyst is selected from a C5-C22 thioether compound, a C5-C22 thiazole compound, a C5-C22 isothiazole compound or a C5-C22 thiophene compound; and S3, carrying out an acidolysis reaction on chlorinated phenoxycarboxylic ester so as to obtain the phenoxy carboxylic acid herbicide. By the method, product quality and thelive environment of production can be improved, and ''three wastes (waste gas, waste water and industrial residue)'' are minimized.

Preparation method of chlorophenoxycarboxylic ester

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Paragraph 0103; 0105; 0109; 0111, (2019/01/08)

The invention provides a preparation method of chlorophenoxycarboxylic ester, wherein the preparation method includes the following steps: S1) carrying out 2-site and/or 4-site selective chlorinationreaction of phenoxycarboxylic ester with a chlorinating agent under the action of a catalyst A and a catalyst B to obtain chlorophenoxycarboxylic ester, wherein the catalyst A is Lewis acid, the catalyst B has the following structural formula of R1'-S-R2', and the phenoxycarboxylic ester has any structure represented by the formulas I-IV; and S2) carrying out transesterification reaction of chlorophenoxycarboxylic ester and alcohol under the action of a catalyst to obtain long-chain chlorophenoxycarboxylic ester, wherein the alcohol has the molecular formula of R2OH, and R2 is C4-20 alkyl or cycloalkyl. The method improves the yield and purity of chlorophenoxycarboxylic ester by redesigning of the process route and fine screening of the catalysts and the chlorinating agent. The content ofthe obtained chlorophenoxycarboxylic ester can reach 98.5% or more and the yield can reach 98.5% or more.

Preparation method of chlorophenoxycarboxylic ester

-

Paragraph 0092; 0094, (2019/01/08)

The invention provides a preparation method of chlorophenoxycarboxylic ester, wherein the preparation method includes the following steps: S1) carrying out 2-site and/or 4-site selective chlorinationreaction of phenoxycarboxylic ester with a chlorinating agent under the action of a catalyst A and a catalyst B to obtain chlorophenoxycarboxylic ester, wherein the catalyst A is Lewis acid, the catalyst B is C5-22 thiazoles, isothiazoles and thiophenes or halogenated derivatives thereof, and the phenoxycarboxylic ester has any structure represented by the formulas I-IV; and S2) carrying out transesterification reaction of chlorophenoxycarboxylic ester and alcohol under the action of a catalyst to obtain long-chain chlorophenoxycarboxylic ester, wherein the alcohol has the molecular formula ofR2OH, and R2 is C4-20 alkyl or cycloalkyl. The method improves the yield and purity of chlorophenoxycarboxylic ester by redesigning of the process route and fine screening of the catalysts and the chlorinating agent. The content of the obtained chlorophenoxycarboxylic ester can reach 98.5% or more and the yield can reach 98.5% or more.

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