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CAS 105-04-4

N,N,N'-Triethylethylenediamine TCI T0743

N,N,N'-Triethylethylenediamine TCI T0743

Chemical Identity

CAS No.
105-04-4
PubChem
CID 66040·SID 87576594
Formula
C8H20N2
Molecular weight
144.26 g/mol
Purity
>98.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N,N',N'-triethylethane-1,2-diamine
SMILES
CCNCCN(CC)CC
InChIKey
HDCAZTXEZQWTIJ-UHFFFAOYSA-N
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N,N,N'-Triethylethylenediamine (TEEDA), with CAS number 105-04-4, is a versatile chemical compound widely used in laboratory settings for its reactivity and utility in organic synthesis. As a building block in chemistry, it plays a crucial role in the development of complex organic molecules. Its structure, derived from ethylenediamine with ethyl groups attached to each nitrogen atom, enhances its ability to participate in various chemical reactions. This compound is particularly valued for its capacity to react with functional groups such as aldehydes, ketones, and carboxylic acids, making it a key reagent in synthetic pathways.

TEEDA is preferred due to its high reactivity, stability under controlled conditions, and availability in the market. These properties make it a reliable choice for researchers and chemists seeking to synthesize heterocyclic compounds, linkers, and intermediates. Its ability to form stable bonds with different functional groups allows it to be used in substitution, coupling, and molecular modification reactions. Additionally, its predictable behavior in laboratory conditions ensures consistent results, which is essential for scientific research.

In Indonesian laboratories, TEEDA is commonly used in chemical research, industrial chemical production, and pharmaceutical development. It is a staple in academic and research institutions, where it supports the creation of new compounds and the advancement of organic chemistry. Its widespread use across various sectors highlights its importance as a fundamental reagent in the chemical industry.

  • Organic synthesis is a primary application where TEEDA is used to create complex molecules by reacting with functional groups such as aldehydes and ketones.
  • Pharmaceutical development benefits from TEEDA's ability to participate in reactions that form essential intermediates in drug synthesis.
  • Intermediate compound production relies on TEEDA's reactivity to facilitate the formation of key building blocks in chemical manufacturing.
  • Linker molecule creation utilizes TEEDA's capacity to connect different functional groups in molecular structures.
  • Research and development in chemical laboratories frequently employ TEEDA for its consistent performance in synthetic reactions and its role in exploring new chemical pathways.

Brand TCI
CAS number 105-04-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight and incompatible substances

TEEDA should be stored in a cool, dry location, away from direct sunlight and incompatible materials such as strong oxidizing agents. It is recommended to use sealed containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent contamination and maintain its chemical integrity. In laboratory settings, proper ventilation is essential when handling TEEDA to minimize exposure to vapors. Always wear appropriate personal protective equipment, including gloves, goggles, and a lab coat, to ensure safety during handling. Due to its reactivity, TEEDA should be handled with care and stored in a manner that prevents accidental spills or exposure to incompatible substances.

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