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2,4-Di(tert-amyl)phenoxyacetic acid, commonly known as 2,4-D, is a synthetic auxin herbicide that mimics the action of the natural plant hormone auxin. It is used to control broadleaf weeds in various crops such as corn, wheat, and soybeans by causing uncontrolled growth in the target weeds, leading to their death. However, its potential health and environmental impacts have led to controversy and classification as a possible human carcinogen, with links to reproductive problems and developmental abnormalities in animals.

13402-96-5

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13402-96-5 Usage

Uses

Used in Agricultural Industry:
2,4-D is used as a herbicide for controlling broadleaf weeds in various crops such as corn, wheat, and soybeans. It is effective in mimicking the action of the natural plant hormone auxin, causing uncontrolled growth in the target weeds, which ultimately leads to their death.

Check Digit Verification of cas no

The CAS Registry Mumber 13402-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,0 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13402-96:
(7*1)+(6*3)+(5*4)+(4*0)+(3*2)+(2*9)+(1*6)=75
75 % 10 = 5
So 13402-96-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H28O3/c1-7-17(3,4)13-9-10-15(21-12-16(19)20)14(11-13)18(5,6)8-2/h9-11H,7-8,12H2,1-6H3,(H,19,20)/p-1

13402-96-5 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (A18546)  2,4-Di(tert-pentyl)phenoxyacetic acid, 98%   

  • 13402-96-5

  • 25g

  • 515.0CNY

  • Detail
  • Alfa Aesar

  • (A18546)  2,4-Di(tert-pentyl)phenoxyacetic acid, 98%   

  • 13402-96-5

  • 100g

  • 1641.0CNY

  • Detail
  • Alfa Aesar

  • (A18546)  2,4-Di(tert-pentyl)phenoxyacetic acid, 98%   

  • 13402-96-5

  • 500g

  • 7330.0CNY

  • Detail

13402-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Di(tert-amyl)phenoxyacetic acid

1.2 Other means of identification

Product number -
Other names 2-[2,4-bis(2-methylbutan-2-yl)phenoxy]acetic acid

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:13402-96-5 SDS

13402-96-5Upstream product

13402-96-5Relevant academic research and scientific papers

Process for producing aromatic amide compounds

-

, (2008/06/13)

There is disclosed a process for producing an aromatic amide compound of the general formula (4), including the steps of subjecting an o-nitrophenol compound of the general formula (1) to catalytic reduction in acetone or an aromatic hydrocarbon solvent under the presence of a nickel catalyst to give an o-aminophenol compound of the general formula (2); and (b) subjecting the o-aminophenol compound of the general formula (2) to condensation with an acid chloride compound having a sulfur content of 0.5% or less, based on the weight of the acid chloride compound, of the general formula (3) in acetone or an aromatic hydrocarbon solvent under an atmosphere of an inert gas having an oxygen concentration of 1% or less. The acid chloride compound having a sulfur content of 0.5% or less, based on the weight of the acid chloride compound, of the general formula (3) may be obtained by allowing a carboxylic acid compound of the general formula (5) to react with thionyl chloride and by concentrating the reaction mixture. Also disclosed is another process for producing an aromatic amide compound of the general formula (4), including the step of subjecting an o-aminophenol hydrochloride salt of the general formula (6) to condensation with an acid chloride compound having a sulfur content of 0.8% or less, based on the weight of the acid chloride compound, of the general formula (3) in an inert solvent.

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