Product Overview

3-(3-(diisopropylamino)-1-phenylpropyl)-4-hydroxybenzyl alcohol is an important pharmaceutical intermediate widely used in the synthesis of antidepressants and antipsychotic drugs. It exhibits high chemical stability and good reactivity, making it suitable for research and development, small-scale preparation, pilot-scale production, and commercialization. Due to its complex structure and multi-step organic reaction pathway, this product requires high purity of raw materials and strict process control. We can provide high-quality, customized supply services to support drug development and industrialization.

Applications

• Antidepressant drug synthesis
• Antipsychotic drug intermediates
• Custom intermediate synthesis
• Drug process route optimization
• Pharmaceutical R&D project support

Quality & Supply Capability

English Name: 2-(3-(diisopropylamino)-1-phenylpropyl)-4-(hydroxymethyl)phenol Properties: This product is an aromatic compound containing amino and hydroxyl groups, exhibiting good thermal and chemical stability. Its core functional groups are diisopropylamino and hydroxymethyl, making it suitable for various organic synthesis reactions. Storage Recommendations: Store in a sealed, light-protected, and dry place, referring to the COA/MSDS for specific details. 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 schemes, packaging specifications, and delivery cycles according to customer needs, with a complete quality documentation system to ensure product compliance with pharmaceutical industry standards. Simultaneously, we have a professional technical support team to assist customers in process development, route optimization, and project transformation, ensuring a smooth transition from R&D to production.

Why Choose Bioncan

Focused on pharmaceutical intermediates, possessing extensive synthesis experience and technological expertise. Full-scale supply capability, covering everything from sample production to commercial-scale mass production. Provides complete quality control documentation to meet GMP and regulatory compliance requirements. Supports customized solutions, adjusting purity, impurity control, and packaging specifications according to customer requirements. Provides comprehensive process optimization and scale-up technical support to help customers achieve efficient commercialization and industrialization.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 200801-70-3, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.