Biphenyl-4-carboxylic Hydrazide TCI B4350

Chemical Identity

CAS No.: 18622-23-6
PubChem: CID 72718·SID 253662214
Formula: C13H12N2O
Molecular weight: 212.25 g/mol
Purity: >97.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-phenylbenzohydrazide
SMILES: C1=CC=C(C=C1)C2=CC=C(C=C2)C(=O)NN
InChIKey: QEUAQXSDDNDOTG-UHFFFAOYSA-N

Rp 1.696.800,00

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Biphenyl-4-carboxylic Hydrazide is a chemical compound widely used in laboratory settings as a building block for various organic synthesis reactions. It plays a crucial role in the development of complex organic molecules, particularly in reactions involving substitution, reduction, or hydrazide-based transformations. This compound is valued for its structural versatility and functional group reactivity, making it a key reagent in synthetic chemistry. Its unique molecular structure allows it to participate in multiple reaction pathways, contributing to the design of compounds with specific chemical or biological properties.

The compound's stability and controlled reactivity under specific reaction conditions make it a preferred choice for researchers. Its molecular framework combines aromatic rings with a hydrazide group, enabling it to interact with a variety of functional groups. This versatility is particularly beneficial in the synthesis of bioactive compounds or specialized materials. Additionally, its predictable behavior in different chemical environments allows for consistent results in laboratory experiments, enhancing the reliability of synthetic processes.

In Indonesian laboratories, Biphenyl-4-carboxylic Hydrazide is commonly used in organic chemistry research, especially in pharmaceutical and material science applications. It is frequently employed in academic and industrial settings to develop new compounds and understand reaction mechanisms. Its role in both fundamental and applied research makes it an essential component in the chemical toolkit of Indonesian scientists.

Related TCI products

Organic synthesis for the creation of complex molecules with specific functional groups and biological activity.
Pharmaceutical research to develop new drugs and bioactive compounds through hydrazide-based reactions.
Material science applications in the synthesis of polymers and specialty chemicals with tailored properties.
Analytical chemistry for the preparation of standards and reagents used in qualitative and quantitative analysis.
Educational purposes in teaching advanced organic chemistry concepts and reaction mechanisms to students.

Brand	TCI
CAS number	18622-23-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid powder
Storage	Store in a cool, dry place away from direct sunlight

Biphenyl-4-carboxylic Hydrazide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. Due to its hydrazide functionality, it may react with strong oxidizing agents, so storage away from such substances is essential. The compound should be handled in a well-ventilated area to minimize exposure to vapors. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Regular inspection of storage conditions ensures the compound remains safe and effective for use in laboratory applications.

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