Phenazine-2,3-diamine TCI D4492

Chemical Identity

Other names: DAP · 2,3-Diaminophenazine · 2,3-Phenazinediamine
CAS No.: 655-86-7
PubChem: CID 410099·SID 468591268
Formula: C12H10N4
Molecular weight: 210.24 g/mol
Purity: >97.0%(HPLC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: phenazine-2,3-diamine
SMILES: C1=CC=C2C(=C1)N=C3C=C(C(=CC3=N2)N)N
InChIKey: VZPGINJWPPHRLS-UHFFFAOYSA-N
MDL: MDL00160693

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Phenazine-2,3-diamine (TCI D4492) is a chemical compound widely used in organic synthesis reactions within laboratory settings. This heterocyclic compound features two nitrogen atoms in its aromatic ring structure, contributing to its high reactivity under various chemical conditions. Its unique molecular configuration makes it a versatile building block for the synthesis of complex molecules. In the laboratory, it serves as a key reagent in the development of new compounds, particularly in the fields of pharmaceuticals, dyes, and industrial chemicals. Its role is essential in the creation of functionalized derivatives and other specialized chemical structures.

The chemical properties of Phenazine-2,3-diamine make it a preferred choice for synthetic chemists. It exhibits good solubility in solvents such as ethylamine and dimethyl sulfoxide, facilitating easy mixing and reaction processes. Its reactivity towards acids, bases, and organic solvents allows for a wide range of chemical transformations. This makes it suitable for substitution, reduction, and coupling reactions. The stability of the compound under controlled conditions ensures reliable results in laboratory experiments, while its reactivity enables the synthesis of diverse chemical products.

In Indonesian laboratories, Phenazine-2,3-diamine is commonly used by researchers in chemistry, pharmacy, and materials science. It plays a vital role in the synthesis of heterocyclic compounds, which are essential in drug development and advanced material research. Its availability and chemical versatility make it a valuable resource for both academic and industrial applications in the region.

Advantages (TCI brochure)

Shows strong fluorescence (550 - 580 nm).
Changes the absorbance and fluorescence intensity by interacting with metal ion species.

TCI brochures (PDF)

Fluorescent Dye for Highly Sensitive Chemosensor DAP 2025-03-31 · p. 1

Related TCI products

Organic synthesis is a primary application where Phenazine-2,3-diamine is used to create complex molecules due to its reactivity and structural versatility.
Pharmaceutical research benefits from this compound as it serves as a precursor for the development of new drugs and therapeutic agents.
Dye and pigment synthesis relies on its ability to participate in various chemical reactions that produce colored compounds with specific properties.
Materials science applications utilize its chemical properties to develop advanced materials with unique functional characteristics.
Industrial chemical production employs this compound for the synthesis of specialized chemical intermediates required in manufacturing processes.

From the TCI brochure

Can be used as a fluorescent sensor to recognize specific metal ions and anion species.
Can be used as a building block for fluorescent dyes with phenazine skeleton.

Brand	TCI
CAS number	655-86-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid, typically in powder or crystalline form
Storage	Store in a cool, dry place away from light and moisture

Data from the TCI brochure

Fluorescence emission	550 - 580 nm

Source: TCI brochure FF116 (2025-03-31)

Phenazine-2,3-diamine should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize direct contact with skin or inhalation. Avoid contact with strong acids, bases, or organic solvents, as these can cause unwanted chemical reactions. Always use appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Proper storage and handling practices ensure the safety of laboratory personnel and the integrity of the compound during use.

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