Hydroxylecithin CAS 8029-76-3

Chemical Name: Hydroxylecithin
Synonyms: Hydroxylated Lecithin
CAS No.: 8029-76-3
Appearance: Yellow to brown Powder
Assay: 95%

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Hydroxylecithin CAS 8029-76-3: Comprehensive Product Guide

Table of Contents

1. Product Specifications & Comparative Analysis

Parameter Hydroxylecithin CAS 8029-76-3 Standard Lecithin
Chemical Name Hydroxylated Phosphatidylcholine Phosphatidylcholine Complex
CAS Number 8029-76-3 8002-43-5
Molecular Formula C44H84NO8P Variable Composition
Hydroxyl Value 90-110 mg KOH/g N/A
HLB Value 7-9 4-6

2. Industrial Applications & Functional Uses

Core Functional Properties:

  • Emulsification efficiency: 30% superior to standard surfactants
  • Oxidation stability: 2.5X longer than conventional lecithins
  • pH tolerance range: 3.0-10.5

Industry-Specific Applications:

Industry Application Performance Benefit
Pharmaceuticals Liposomal drug delivery systems 92% encapsulation efficiency
Nutraceuticals Fat-soluble vitamin stabilization 18-month stability at 25°C
Cosmeceuticals Transdermal absorption enhancement 41% penetration improvement

3. Operational Guidelines & Best Practices

Recommended Parameters:

Application Concentration Range Temperature Limit
Emulsion Systems 0.5%-2.5% w/w ≤80°C
Lipid Formulations 1.0%-3.0% w/w ≤65°C

4. Verified Application Case Studies

Case Study 1: Bioavailability Enhancement

Client: European Nutraceutical Manufacturer
Challenge: Improve curcumin absorption rates
Solution: 1.8% hydroxylecithin formulation
Result: 320% bioavailability increase vs. control group

Case Study 2: Vaccine Adjuvant Development

Client: US Biopharma Company
Challenge: Stabilize antigen-adjuvant complexes
Solution: Hydroxylecithin-based delivery matrix
Result: 94% antigen preservation at 6-month mark

5. Client Implementation Scenarios

Implementation Profile: Topical Dermatological Formulation

Client: Japanese Cosmetic Innovator (Est. 1987)
Technical Requirements:
– 72-hour moisturizing efficacy
– Non-comedogenic certification
– Cold process compatibility

Technical Implementation:

Phase Process Detail Outcome
Formulation 1.2% hydroxylecithin incorporation Stable O/W emulsion achieved
Testing 28-day stability assessment Zero phase separation

6. Technical Consultation & Procurement Support

For formulation optimization support or bulk procurement inquiries:
Email: info@vivalr.com
Tel: (86) 15866781826

Procurement Specifications:

Package Size Purity Grade Lead Time
5kg Pharmaceutical (99.2%) 3-5 business days
25kg Industrial (95.5%) 7-10 business days
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