4-Aminobenzohydrazide TCI A1211

Chemical Identity

CAS No.: 5351-17-7
PubChem: CID 21450·SID 87562684
Formula: C7H9N3O
Molecular weight: 151.17 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ChEBI·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-aminobenzohydrazide
SMILES: C1=CC(=CC=C1C(=O)NN)N
InChIKey: WPBZMCGPFHZRHJ-UHFFFAOYSA-N

Rp 2.306.850,00

~~Rp 1.628.550,00~~ Rp 2.306.850,00

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4-Aminobenzohydrazide is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. It serves as a key building block in organic chemistry, particularly in the development of heterocyclic compounds and hydrazide-based structures. Its versatility makes it an essential reagent in many synthetic pathways, supporting both academic and industrial research. This compound is particularly valuable for its ability to participate in various chemical reactions, enabling the creation of a wide range of functional derivatives.

The compound's high reactivity and capacity to form hydrazide bonds are the primary reasons it is favored in chemical synthesis. These properties allow it to react with functional groups such as carboxylic acids, aldehydes, and ketones, making it a versatile tool in molecular modification. Its stability under controlled laboratory conditions further enhances its reliability in experimental settings. This combination of reactivity and stability ensures that it remains a preferred choice for researchers working on complex chemical structures.

In Indonesian laboratories, 4-Aminobenzohydrazide is commonly used in organic chemistry research, especially in pharmaceutical and bioactive compound synthesis. It is frequently employed by researchers and students for experiments requiring high reactivity and chemical stability. Its role in the development of new drugs and bioactive molecules underscores its importance in both academic and applied research environments.

TCI brochures (PDF)

Covalent Organic Framework (COF) Linkers 2026-05-18 · p. 4

Related TCI products

Synthesis of heterocyclic compounds for drug development due to its ability to form stable hydrazide bonds.
Molecular modification reactions where high reactivity and functional group compatibility are required.
Creation of bioactive molecules through its interaction with carboxylic acid derivatives.
Organic chemistry research in Indonesian laboratories focusing on complex molecule synthesis.
Development of pharmaceutical intermediates using its versatile chemical reactivity.

Brand	TCI
CAS number	5351-17-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and direct sunlight

4-Aminobenzohydrazide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which could affect its reactivity. The compound should be stored away from direct sunlight and heat sources to avoid degradation. In laboratory settings, it is important to handle the material with appropriate personal protective equipment, such as gloves and safety goggles. Proper ventilation should be maintained when working with this compound to ensure safe handling and minimize potential exposure risks.

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