N-[(3a,5b)-3-hydroxy-24-oxocholan-24-yl]-(9CI) Glycine CAS 474-74-8: Comprehensive Product Guide
Table of Contents
- 1. Product Specifications & Comparative Analysis
- 2. Detailed Applications & Industrial Usage
- 3. Operational Protocols & Best Practices
- 4. Implementation Case Studies
- 5. Client Success Stories
- 6. Expert Consultation & Procurement Guidance
1. Product Specifications & Comparative Analysis
| Parameter | Specification | Competitor A | Competitor B |
|---|---|---|---|
| CAS Number | 474-74-8 | 474-74-8 | N/A |
| Molecular Formula | C₂₆H₄₁NO₄ | C₂₆H₄₁NO₄ | Similar derivatives |
| Purity Grade | ≥98% (HPLC) | 95-97% | 90-92% |
| Storage Conditions | 2-8°C in dark | Ambient | Refrigerated |
2. Detailed Applications & Industrial Usage
Pharmaceutical Development
This bile acid derivative demonstrates exceptional utility in hepatic therapeutic research, particularly for:
- Cholesterol metabolism modulation
- Nuclear receptor activation studies
- Enterohepatic circulation analysis
Biochemical Research
Essential for advanced studies in:
- Membrane permeability assessments
- Steroid transporter interactions
- Enzyme kinetics characterization
3. Operational Protocols & Best Practices
Recommended Handling Procedures
- Reconstitution: Use anhydrous DMSO at 10 mM concentration
- Storage: Aliquot in amber vials under nitrogen atmosphere
- Experimental Applications:
- Cell culture studies: 50-100 μM concentration range
- In vivo models: 10 mg/kg dosage via IV administration
4. Implementation Case Studies
Case 1: Hepatic Fibrosis Research
Research team at University of California demonstrated 40% reduction in collagen deposition using 75 μM concentration in LX-2 cell lines over 72-hour exposure.
Case 2: Drug Delivery Optimization
PharmaTech Inc. achieved 3.2x bioavailability improvement in oral formulations through molecular conjugation techniques.
5. Client Success Stories
Global Pharma Solutions
Challenge: Needed stable analog for FXR receptor studies
Solution: Custom synthesis with >99% purity
Outcome: Accelerated lead compound identification by 8 months
European Research Consortium
Challenge: Required GMP-grade quantities for clinical trials
Solution: Batch production with full ICH compliance
Outcome: Successful Phase IIa completion with optimal safety profile
6. Expert Consultation & Procurement Guidance
Our technical specialists provide:
- Custom synthesis scale-up services
- Regulatory documentation support
- Application-specific formulation advice
Contact our scientific team:
Email: info@vivalr.com
Phone: (86) 15866781826
Procurement Options
| Package | Quantity | Lead Time |
|---|---|---|
| Research Sample | 100mg-1g | 3-5 business days |
| Bulk Order | 100g-1kg | 2-3 weeks |
| Custom Synthesis | 1kg+ | 4-6 weeks |



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