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94-81-5

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94-81-5 Usage

Chemical Properties

Colorless crystal; melts at 100 °C (212 °F);practically insoluble in water (44 mg/L at25 °C/77 °F); readily dissolves in most organicsolvents.

Uses

Different sources of media describe the Uses of 94-81-5 differently. You can refer to the following data:
1. MCPB is used for research regarding herbicides to control weed in crop field.
2. Herbicide.

Definition

ChEBI: A monocarboxylic acid that is butyric acid substituted by a 2-methyl-4-chlorophenoxy group at position 4.

Hazard

Toxic by ingestion.

Health Hazard

MCPB is structurally similar to 2,4-DB,except one methyl group substituting a Clatom in the ring. Toxic properties and thesymptoms are similar to 2,4-DB. It is mod-erately toxic by ingestion and possibly otherroutes of exposure. Skin contact can causeirritation.LD50 oral (rat): 680 mg/kgLD50 oral (mouse): 800 mg/kg.

Agricultural Uses

Herbicide: A metabolite of MCPA (see above). MCPB is a phenoxy herbicide produced as a sodium salt and an acid. Herbicide registered for use on peas prior to flowering. There are no residential uses of MCBP. Target organisms: post-emergence control of Canadian thistle, buttercup, mustard, purslane, ragweed, common lambsquarters, pigweed, smartweed, sowthistle, morning glory and other broad leaf weeds[83] .

Trade name

2 M-4Kh-M; 2M4KhM; 2 M-4XM; 4MCPB; BEXANE; BEXONE; U46 MCPB; LEGUMEX; PDQ; THITROL; TRIFOLEX; TRITROL; TROTOX

Check Digit Verification of cas no

The CAS Registry Mumber 94-81-5 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 94-81:
(4*9)+(3*4)+(2*8)+(1*1)=65
65 % 10 = 5
So 94-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H13ClO3/c1-3-9(11(13)14)15-10-5-4-8(12)6-7(10)2/h4-6,9H,3H2,1-2H3,(H,13,14)

94-81-5 Well-known Company Product Price

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  • Sigma-Aldrich

  • (36145)  MCPB  PESTANAL®, analytical standard

  • 94-81-5

  • 36145-100MG

  • 360.36CNY

  • Detail

94-81-5SDS

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 2-methyl-4-chlorophenoxybutyric acid

1.2 Other means of identification

Product number -
Other names Thitrol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Herbicide
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:94-81-5 SDS

94-81-5Relevant articles and documents

A method for preparing chloro-benzene oxygen carboxylic acid (by machine translation)

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Paragraph 0083; 0085, (2019/01/08)

The invention provides a method for preparing carboxylic acid chloro-benzene oxygen, comprising the following steps: S1) phenoxy fatty alcohol in the catalyst B A and under the action of the catalyst, and the chlorinating agent to 2 bit and/or 4 bit selective chlorination reaction, to obtain chloro-benzene oxygen fatty alcohol; said catalyst A is Lewis acid; said catalyst B is C5 - 22 of the thioether, thiazole, isothiazole, thiophene or their halogenated derivatives; S2) [...] fatty alcohol and water, under the action of a catalyst, and an oxidizing agent for the selective catalytic oxidation reaction, get chloro-benzene oxygen carboxylic acid. The invention through the re-design of the process route, the catalyst and the chlorinating agent fine screening, effectively reduces the energy consumption, the selectivity of the dichloride to improve at the same time avoiding the losses of the active ingredient, the resulting chloro-benzene oxygen carboxylic acid content can be up to 98.5% or more, the total yield can be up to 99% or more. (by machine translation)

Preparation method of phenoxycarboxylic acid herbicide

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Paragraph 0101; 0104, (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 0102; 0105, (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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