N-Benzylhydroxylamine Hydrochloride (CAS 29601-98-7) Product Guide
Table of Contents
- 1. Product Specifications & Comparative Analysis
- 2. Key Applications & Industrial Uses
- 3. Operational Case Studies
- 4. Verified Client Implementations
- 5. Request Customized Quotation
1. Product Specifications & Comparative Analysis
| Parameter | N-Benzylhydroxylamine HCl | Alternative Compound A | Alternative Compound B |
|---|---|---|---|
| CAS Number | 29601-98-7 | XXXX-XX-X | XXXX-XX-X |
| Molecular Formula | C7H10ClNO | C6H8ClNO | C8H12ClNO |
| Purity Grade | ≥99% (HPLC) | ≥97% | ≥95% |
| Storage Conditions | 2-8°C (desiccated) | Ambient | Refrigerated |
2. Key Applications & Industrial Uses
Pharmaceutical Synthesis: Critical intermediate for β-lactam antibiotics and antiviral agents with enhanced reaction kinetics compared to hydroxylamine derivatives.
Organic Catalysis: Facilitates stereoselective reactions in asymmetric synthesis with 15-20% higher yield efficiency than conventional amines.
Polymer Chemistry: Cross-linking agent for specialty resins with improved thermal stability (up to 220°C sustained performance).
3. Operational Case Studies
Case 1: Pharmaceutical Intermediate Production
Challenge: Required low-temperature stability (-20°C storage) for GMP manufacturing processes.
Solution: Implemented controlled crystallization protocol achieving 99.2% purity with 6-month stability.
Case 2: High-Performance Polymer Development
Challenge: Needed cross-linker with dual functionality for aerospace-grade composites.
Solution: Custom particle size distribution (10-50μm) enabled uniform matrix reinforcement.
4. Verified Client Implementations
Client A: Top-10 Global Pharma Company
Application: Cephalosporin antibiotic intermediate synthesis
Results: Reduced reaction steps from 5 to 3, achieving 92% overall yield
Client B: Advanced Materials Manufacturer
Application: High-temperature resistant epoxy formulation
Results: Increased glass transition temperature by 38°C versus previous formulation
Client C: Contract Research Organization
Application: Novel kinase inhibitor development
Results: Enabled selective N-O bond formation with 99% enantiomeric excess
5. Request Customized Quotation
Contact our technical specialists for:
- Bulk pricing (100kg+ quantities available)
- GMP-certified production options
- Custom particle size distributions
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