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CAS 97-84-7

N,N,N',N'-Tetramethyl-1,3-diaminobutane TCI T0524

N,N,N',N'-Tetramethyl-1,3-diaminobutane TCI T0524

Chemical Identity

CAS No.
97-84-7
PubChem
CID 7350·SID 87576451
Formula
C8H20N2
Molecular weight
144.26 g/mol
Purity
>98.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-N,1-N,3-N,3-N-tetramethylbutane-1,3-diamine
SMILES
CC(CCN(C)C)N(C)C
InChIKey
AXFVIWBTKYFOCY-UHFFFAOYSA-N
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N,N,N',N'-Tetramethyl-1,3-diaminobutane is a highly reactive organic compound widely used in laboratory settings as a building block for the synthesis of complex organic molecules. This compound features two amine groups attached to a butane backbone, making it a versatile reagent in various chemical reactions. Its role in the laboratory is critical for researchers aiming to create custom molecules with specific structural properties. Due to its reactivity, it is often employed in amidation, condensation, and nitrogen bond formation reactions.

The compound’s unique molecular structure and reactivity make it a preferred choice for synthetic chemists. Its ability to act as both an electron donor and a binding agent in chemical reactions enhances its utility across multiple applications. The molecule’s stability under controlled conditions allows for consistent performance in laboratory experiments. However, its high reactivity necessitates careful handling to ensure safety and efficiency in chemical processes.

In Indonesian laboratories, N,N,N',N'-Tetramethyl-1,3-diaminobutane is commonly used in organic chemistry research, particularly in pharmaceutical and material science applications. It is a key component in the development of new compounds with potential applications in healthcare and industrial materials. Researchers in universities and research institutions rely on this compound to advance their experimental work and explore novel chemical structures.

  • Organic synthesis is a primary application where this compound serves as a versatile building block for creating complex molecular structures.
  • Pharmaceutical research benefits from its reactivity in synthesizing drug molecules with specific functional groups.
  • Material science applications utilize its ability to form stable nitrogen bonds in polymer and composite development.
  • Chemical reaction optimization relies on its role as a reactive intermediate in amidation and condensation processes.
  • Analytical chemistry experiments use it as a standard reference in testing reactivity and molecular interactions.

Brand TCI
CAS number 97-84-7
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 materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed containers made of materials compatible with organic solvents to prevent contamination and evaporation. Due to its high reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Always wear appropriate personal protective equipment, including gloves and safety goggles, when handling this material. Ensure that it is kept separate from strong oxidizing agents and acids to avoid unintended chemical reactions. Proper storage and handling are essential to maintain its chemical integrity and ensure safe laboratory practices.

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