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10443-70-6

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10443-70-6 Usage

General Description

MCPB-ethyl ester is a synthetic herbicide that is commonly used to control broadleaf weeds in various crops such as cereals, oilseed rape, and grassland. It is a member of the phenoxy herbicide family and works by mimicking the action of the plant hormone auxin, disrupting the growth and development of the target weeds. MCPB-ethyl ester is typically applied as a spray to the foliage of the targeted plants and is absorbed through the leaves, where it translocates to the growing points of the plant, ultimately leading to their death. It is important to use this chemical carefully and according to the specific instructions and guidelines provided by regulatory authorities to minimize its impact on the environment and non-target organisms.

Check Digit Verification of cas no

The CAS Registry Mumber 10443-70-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10443-70:
(7*1)+(6*0)+(5*4)+(4*4)+(3*3)+(2*7)+(1*0)=66
66 % 10 = 6
So 10443-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H17ClO3/c1-3-16-13(15)5-4-8-17-12-7-6-11(14)9-10(12)2/h6-7,9H,3-5,8H2,1-2H3

10443-70-6 Well-known Company Product Price

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  • TCI America

  • (E1149)  Ethyl 4-(4-Chloro-2-methylphenoxy)butyrate  >98.0%(GC)

  • 10443-70-6

  • 100mg

  • 990.00CNY

  • Detail
  • TCI America

  • (E1149)  Ethyl 4-(4-Chloro-2-methylphenoxy)butyrate  >98.0%(GC)

  • 10443-70-6

  • 1g

  • 4,190.00CNY

  • Detail

10443-70-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name MCPB-ethyl

1.2 Other means of identification

Product number -
Other names ethyl 4-(4-chloro-o-tolyloxy)butyrate

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:10443-70-6 SDS

10443-70-6Relevant articles and documents

Preparation method of phenoxycarboxylate herbicide

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Paragraph 0091; 0093, (2019/01/08)

The invention provides a preparation method of a phenoxycarboxylate herbicide, wherein the preparation method includes the steps: S1, carrying out condensation reaction of phenol or o-cresol with chlorocarboxylic ester under the action of alkaline substances to obtain phenoxycarboxylic ester, wherein chlorocarboxylic ester has the general formula of ClR1COOR, R1 is C1-3 alkylene or alkylidene, R is C1-10 alkyl of or C3-10 cycloalkyl; and S2, under the action of a first catalyst and a second catalyst, carrying out selective chlorination of the phenoxycarboxylic ester with a chlorinating agent to obtain the chlorophenoxycarboxylic ester represented by the formula I, R3 is H, Cl or CH3, the first catalyst is selected from Lewis acid, and the second catalyst is selected from C5-22 thioether, thiazole, isothiazole or thiophene compounds; and S3, mixing chlorophenoxycarboxylic ester with an alkaline compound, and carrying out alkaline hydrolysis to obtain the phenoxycarboxylate herbicide. The preparation method can improve the product quality and production operation environment, and has low quantity of three wastes.

Preparation method of phenoxycarboxylic acid herbicide

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Paragraph 0097; 0099, (2019/01/08)

The invention provides a preparation method of a phenoxycarboxylic acid herbicide, wherein the preparation method includes the steps: S1, carrying out reaction of anhydrous phenol with an active metalto form phenoxide, and carrying out condensation reaction of the phenoxide with chlorocarboxylic ester to obtain phenoxycarboxylic ester, wherein the chlorocarboxylic ester has the general formula ofClR1COOR, R1 is C1-3 alkylene or alkylidene, and R is C1-10 alkyl or C3-10 of cycloalkyl; S2, carrying out selective chlorination of the phenoxycarboxylic ester with a chlorinating agent in the presence of a first catalyst and a second catalyst to obtain chlorobenzoxycarboxylic ester, wherein the first catalyst is selected from Lewis acid, and the second catalyst is C5-22 thioether, thiazole, isothiazole or thiophene compounds; and S3, carrying out acidolysis reaction of chlorobenzoxycarboxylic ester to obtain the phenoxycarboxylic acid herbicide represented by the formula I, wherein R3 is H,Cl or CH3. The preparation method can improve the product quality and the operation environment of the production site, and has low quantity of three wastes.

Preparation method of phenoxycarboxylic acid herbicide

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Paragraph 0098; 0100, (2019/01/08)

The invention provides a preparation method of a phenoxycarboxylic acid herbicide, wherein the preparation method includes the steps: S1, carrying out condensation reaction of phenol or o-cresol withchlorocarboxylic ester under the action of an alkaline substance to obtain phenoxycarboxylic ester, wherein the chlorocarboxylic ester has the general formula of ClR1COOR, R1 is C1-3 alkylene or alkylidene, and R is C1-10 alkyl or C3-10 cycloalkyl; S2, carrying out selective chlorination of phenoxycarboxylic ester with a chlorinating agent under the action of a first catalyst and a second catalyst, to obtain chlorobenzoxycarboxylic ester, wherein the first catalyst is selected from Lewis acid, the second catalyst is C5-22 thioether compounds, thiazole compounds, isothiazole compounds or thiophene compounds; and S3, carrying out acidolysis reaction of chlorobenzoxycarboxylic ester, to obtain the phenoxycarboxylic acid herbicide represented by the formula I, wherein R3 is H, Cl or CH3. The preparation method can improve the product quality and the operation environment of a production site, and has low quantity of three wastes.

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