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AgrochemicalsButachlor Impurity 2

SKU: SAB-15-B

Original price was: ₹60,000.00.Current price is: ₹50,000.00.

Name:2,6-Diethylaniline

CAT. NO.:SAB-15-B

CAS NO.:579-66-8

  • Description
  • Datasheet
  • Additional information

Description

Butachlor Impurity 2

Chemical Name 2,6-Diethylaniline
Catalog Number SAB-15-B
Parent AI Butachlor
Synonyms 2,6-Diethyl-benzenamine; 2,6-Diethyl-aniline; 2,6-Diethylbenzenamine; 2,6-Diethylphenylamine
CAS Number 579-66-8
Molecular Formula C₁₀H₁₅N
Molecular Weight 149.23
Appearance Light Brown Oil
Melting Point NA
Shipping & Storage Information

 

Storage 4°C, Inert atmosphere

Shipping: Free Shipping at Room Temperature in INDIA,  may vary elsewhere,  Stability: rReferDatasheet

Solubility Chloroform (Slightly), Methanol (Slightly)
Stability Air Sensitive
Category Agrochemical Impurity Standard/Metabolites
Description &Applications 2,6-Diethylaniline, also known as N,N-diethylaniline, is an organic compound with the molecular formula C8H15N. It is a colorless liquid with a strong odor and is used in a variety of applications, including as a chemical intermediate, as a solvent, and as a fuel additive. It is also used in the synthesis of a range of compounds, including pharmaceuticals, dyes, and fragrances
References De Datta, S.K. et al.: Weed Res., 11, 41 (1971); Nadagoudar, B.S. et al.: Ind. J. Weed Sci., 13, 129 (1981); Yu, Y. et al.: Tur. Xueb., 39, 575 (2002)

2,6-Diethyl aniline, also known as N,N-diethyl-2,6-xylidine, is a fascinating and versatile organic compound that finds its applications in various fields, including pharmaceuticals, agrochemicals, and materials science. Its unique structure and properties make it a valuable building block in the synthesis of diverse compounds, allowing for the creation of novel substances with a wide range of functionalities.

Chemical Structure: The chemical structure of 2,6-diethyl aniline consists of a central aniline core (a benzene ring with an amino group) that is substituted at positions 2 and 6 with ethyl groups. This substitution pattern imparts distinct chemical and physical properties to the compound, setting it apart from other anilines and related aromatic compounds.

Synthesis: The synthesis of 2,6-diethyl aniline involves the reaction of aniline with diethylamine, resulting in the introduction of the ethyl groups at the desired positions. This synthetic method offers control over the regioselectivity, allowing chemists to target specific isomers.

Properties: The unique molecular structure of 2,6-diethyl aniline gives rise to interesting properties:

  1. Aromatic Nature: The benzene ring in the molecule imparts aromatic characteristics, making it susceptible to electrophilic aromatic substitution reactions.
  2. Basicity: The amino group in the aniline portion of the molecule makes it weakly basic, allowing it to participate in acid-base reactions.
  3. Solubility: The presence of ethyl groups enhances the compound’s solubility in organic solvents, enabling its application in various reaction conditions.

Applications: The versatility of 2,6-diethyl aniline arises from its ability to serve as a precursor for various compounds with diverse applications:

  1. Pharmaceuticals: It can be used as a building block in the synthesis of pharmaceutical intermediates, contributing to the development of new drugs and therapeutic agents.
  2. Agrochemicals: The compound’s structural features make it suitable for the production of agrochemicals, including herbicides, pesticides, and fungicides.
  3. Materials Science: 2,6-Diethyl aniline is employed in the creation of conducting polymers and dyes, contributing to the development of advanced materials with unique electronic and optical properties.
  4. Dyes and Pigments: Its chemical reactivity allows for the generation of various colored compounds, making it useful in the production of dyes and pigments for textiles, inks, and coatings.

Additional information

Pack Size

50mg

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