3-Nitrophthalhydrazide (CAS 3682-15-3): Synthesis, Applications, and Sourcing Guide
For professionals in organic chemistry and chemical manufacturing, understanding key intermediates like 3-Nitrophthalhydrazide (CAS 3682-15-3) is fundamental. This compound serves as a versatile building block, enabling a wide range of chemical syntheses. This article provides a detailed look at its synthesis, primary applications, and essential considerations for purchasing this vital chemical.
What is 3-Nitrophthalhydrazide?
3-Nitrophthalhydrazide, identified by its CAS number 3682-15-3, is an organic compound characterized by a phthalhydrazide heterocyclic structure substituted with a nitro group. Its molecular formula is C8H5N3O4, and it typically appears as a light yellow to brown to dark green powder or crystalline solid. A notable physical property is its high melting point, often recorded as exceeding 300°C, indicative of its thermal stability. This stability makes it a reliable choice for various chemical processes.
Synthesis Pathways for 3-Nitrophthalhydrazide
The preparation of 3-Nitrophthalhydrazide often starts with 3-nitrophthalic acid or its anhydride. A common method involves reacting 3-nitrophthalic acid with hydrazine sulfate in the presence of a base, followed by heating and purification. The synthesis requires careful control of reaction conditions to ensure good yields and purity. For example, procedures often involve evaporation to dryness, heating in a solvent like tetralin, and subsequent purification steps, such as precipitation from aqueous solutions after acidification. Manufacturers employ optimized processes to deliver consistent, high-purity product.
Key Applications in Organic Chemistry
The primary role of 3-Nitrophthalhydrazide is as an intermediate in organic synthesis. Its applications include:
- Precursor for Chemiluminescent Compounds: A significant use is its conversion to 3-aminophthalhydrazide, a vital component in the synthesis of luminol. Luminol is widely recognized for its chemiluminescent properties, used in forensic science and biochemical assays.
- Building Block for Pharmaceuticals: The phthalhydrazide scaffold, with its nitro functionalization, can be a starting point for synthesizing various pharmaceutical intermediates or even active pharmaceutical ingredients (APIs). Its structure can be modified to introduce specific biological activities.
- Synthesis of Dyes and Specialty Chemicals: The inherent chemical structure lends itself to the development of novel dyes, pigments, and other specialty chemicals, offering opportunities for innovation in material science and industrial chemistry.
Sourcing 3-Nitrophthalhydrazide Effectively
When you need to buy 3-Nitrophthalhydrazide, particularly for industrial or research applications, several factors are critical:
- Purity: Ensure the product meets your application's purity requirements, typically ≥97%.
- Supplier Reliability: Partner with reputable manufacturers and suppliers who can guarantee consistent quality and timely delivery.
- Pricing: Obtain quotes for your required quantities, comparing prices from various sources to secure the best value. Manufacturers in China often provide competitive pricing.
- Documentation: Always request the Material Safety Data Sheet (MSDS) and Certificate of Analysis (COA) for product safety and quality verification.
In summary, 3-Nitrophthalhydrazide is a fundamental intermediate with diverse applications. By understanding its synthesis, utility, and the best practices for sourcing, chemical professionals can effectively procure this essential compound to drive their projects forward.
Perspectives & Insights
Silicon Analyst 88
“This compound serves as a versatile building block, enabling a wide range of chemical syntheses.”
Quantum Seeker Pro
“This article provides a detailed look at its synthesis, primary applications, and essential considerations for purchasing this vital chemical.”
Bio Reader 7
“3-Nitrophthalhydrazide, identified by its CAS number 3682-15-3, is an organic compound characterized by a phthalhydrazide heterocyclic structure substituted with a nitro group.”