Bis(hexamethylene)triamine TCI B1814

Chemical Identity

CAS No.: 143-23-7
PubChem: CID 8924·SID 87564706
Formula: C12H29N3
Molecular weight: 215.38 g/mol
Purity: >95.0%(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N'-(6-aminohexyl)hexane-1,6-diamine
SMILES: C(CCCNCCCCCCN)CCN
InChIKey: MRNZSTMRDWRNNR-UHFFFAOYSA-N

Rp 557.550,00

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Bis(hexamethylene)triamine (BHTA), also known as TCI B1814, is a versatile chemical compound widely used in laboratory settings for its reactivity and structural versatility. As a building block in organic synthesis, BHTA plays a crucial role in the development of polymers, pharmaceuticals, and industrial chemicals. Its unique molecular structure, consisting of three amine groups connected by hexamethylene chains, allows it to participate in a variety of chemical reactions. This makes it an essential tool for chemists working on complex molecule synthesis and modification.

The high reactivity of BHTA, particularly towards electrophilic compounds, makes it a preferred choice for crosslinking and molecular modification reactions. Its three amine groups enable it to undergo substitution, coupling, and bond formation reactions efficiently. This reactivity, combined with its stability under certain conditions, ensures that BHTA remains a reliable and effective reagent in laboratory applications. Its ability to form stable intermediates and participate in multiple reaction pathways further enhances its utility in synthetic chemistry.

In Indonesian laboratories, BHTA is commonly used in chemical research, especially in organic synthesis, polymer chemistry, and analytical chemistry. It serves as a foundational material for developing new compounds and materials. Its widespread use in academic and industrial research settings highlights its importance in advancing chemical innovation and experimentation in the region.

TCI brochures (PDF)

Polyamines 2025-10-21 · p. 2

Related TCI products

Organic synthesis is a key application where BHTA is used to create complex molecules by facilitating substitution and coupling reactions.
Polymer chemistry benefits from BHTA's ability to act as a crosslinking agent, enhancing the structural integrity of synthetic polymers.
Pharmaceutical research utilizes BHTA for the development of new drug compounds due to its reactivity and structural adaptability.
Industrial chemical production relies on BHTA as a building block for manufacturing various chemical products.
Analytical chemistry uses BHTA in the preparation of reagents and standards for accurate chemical analysis and testing.

Brand	TCI
CAS number	143-23-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from moisture and direct sunlight

BHTA should be stored in a cool, dry environment to maintain its chemical stability. It is advisable to keep it in airtight containers to prevent moisture absorption, which could affect its reactivity. Proper ventilation is essential when handling this compound to minimize exposure to vapors. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Storage away from incompatible materials is recommended to ensure safety in the laboratory. Regular monitoring of storage conditions helps maintain the integrity of the compound for optimal performance in chemical applications.

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