2,4-Diamino-6-isopropoxy-1,3,5-triazine TCI D2225

Name: TCI D2225 24860-40-0 2,4-Diamino-6-isopropoxy-1,3,5-triazine
Brand: TCI
SKU: TCI2510D222522333
Price: 2686950.0 IDR
Availability: InStock

Rp 2.686.950,00

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Berat 1g

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Description

TCI D2225 2,4-Diamino-6-isopropoxy-1,3,5-triazine is a heterocyclic building block based on a symmetric triazine ring that carries two amino groups together with one isopropoxy group. The 1,3,5-triazine ring is a scaffold highly valued in the laboratory because it is planar, nitrogen-rich, and able to arrange three substituents in a symmetric three-directional pattern. Diamino derivatives such as this product supply two hydrogen-bonding sites and two nucleophilic groups at the same time, so they frequently serve as starting materials for constructing supramolecular molecules, porous networks, resins, and intermediates for agrochemical and pharmaceutical research.

The property that makes this compound a preferred choice is its molecular recognition pattern. The two amino groups flanking a single ring nitrogen form a donor–acceptor–donor motif similar to melamine, a feature that allows multiple directional hydrogen bonds to form with a complementary partner. The isopropoxy group adds a different dimension: this branched chain improves solubility in organic solvents compared with derivatives lacking an alkoxy substituent, while also providing steric hindrance that organizes molecular orientation in the solid state. The triazine ring itself is thermally stable and comparatively robust, which supports its use across a range of synthetic conditions.

In Indonesian laboratories, this building block is typically handled in university and institutional research groups working on organic synthesis, materials chemistry, and supramolecular assembly, as well as in R&D units exploring agrochemical and pharmaceutical intermediates. It is generally weighed out in small portions for exploratory reaction screening, then scaled up once a route is established. Because it is supplied as a defined catalogue item, it is also convenient for teaching laboratories and method-development work where a reproducible triazine scaffold is required.

Laboratory Applications

Supramolecular assembly studies: the melamine-like donor–acceptor–donor motif forms multiple directional hydrogen bonds with complementary partners, making it a dependable component for designed host–guest and self-assembled systems.
Porous network and framework synthesis: the planar, nitrogen-rich triazine core with three symmetrically arranged substituent positions provides the geometric regularity needed to build extended, ordered porous architectures.
Resin and polymer precursor chemistry: the two nucleophilic amino groups offer reactive attachment points for condensation and crosslinking, allowing the triazine unit to be incorporated directly into polymer backbones.
Agrochemical intermediate research: substituted 1,3,5-triazines are a well-established class in agrochemical discovery, and this diamino alkoxy derivative serves as a convenient starting point for analogue preparation.
Pharmaceutical intermediate preparation: the thermally stable heterocyclic scaffold tolerates a range of synthetic conditions, so it can be elaborated at the amino groups during medicinal chemistry route development and screening.

Specifications

Brand: TCI (Tokyo Chemical Industry)
CAS number: 24860-40-0
Chemical name: 2,4-Diamino-6-isopropoxy-1,3,5-triazine
Category: Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes: available in standard TCI catalogue research pack sizes; please confirm the currently listed size when ordering
Storage: keep in a tightly closed original container, in a cool, dry, and well-ventilated place away from light and moisture

Handling and Storage

Store the material in its original tightly closed container in a cool, dry, well-ventilated area, protected from moisture, direct sunlight, and sources of heat or ignition. Amber glass or the manufacturer's supplied container is suitable; avoid transferring to containers that cannot be sealed properly. Handle inside a fume hood using standard personal protective equipment, including safety glasses, nitrile gloves, and a laboratory coat, and avoid generating or inhaling dust when weighing out powder. Use clean, dry spatulas to prevent contamination and close the container promptly after use. Keep away from strong oxidizing agents and incompatible reagents, label all secondary containers clearly, and consult the manufacturer's Safety Data Sheet before first use and before disposal of residues or contaminated waste.