Product Overview

(3-(1H-pyrazol-1-yl)phenyl)methylamine hydrochloride is an important pharmaceutical intermediate widely used in the synthesis of antitumor, anti-inflammatory, and central nervous system drugs, applicable to all stages from early drug development to commercial production. This product possesses well-defined structural characteristics and stable chemical properties, serving as a key starting material or core structural unit. It supports customers in process development and optimization at the pilot, pilot, and scale-up stages, meeting the needs of various synthetic routes, and is an indispensable high-value compound in the pharmaceutical and chemical industry.

Applications

• Antitumor drug synthesis
• Central nervous system drug development
• Construction of anti-inflammatory compounds
• Modification of drug molecular skeletons
• Custom synthesis of pharmaceutical intermediates

Quality & Supply Capability

English Name: (3-(1H-pyrazol-1-yl)phenyl)methanamine hydrochloride Properties: White to off-white crystalline powder containing amino and pyrazole ring structures, exhibiting good chemical stability and reactivity, suitable for various organic synthesis routes. Storage Recommendations: Store in a sealed, light-protected, and dry place, subject to the specific COA/MSDS. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches. Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging. Documentation Support: COA, MSDS, HPLC, NMR, etc. We provide a full-process service from laboratory sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly adjust purity standards, impurity control requirements, packaging specifications, and delivery cycles according to customer needs, while providing a complete quality documentation system to ensure that products meet international pharmaceutical industry standards. We also provide technical support from early R&D to process scale-up, helping customers achieve efficient, stable, and compliant process transformation and project advancement.

Why Choose Bioncan

Focused on pharmaceutical intermediates, possessing extensive synthesis experience and technological expertise. Full-scale supply capabilities, covering all stages from laboratory to commercial production. Provides complete quality control documentation to ensure product compliance and traceability. Supports customized needs, adjusting purity, impurity control, and packaging specifications according to customer requirements. Provides supporting process optimization and scale-up technologies to help customers improve R&D efficiency and production conversion rates.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 1245649-13-1, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.