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D Alpha Tocopheryl Acetate Powder

1.English Name:DL-α-tocopheryl acetate
2.Appearance:White powder
3.Specification: >50% 700IU
4.CAS No.:7695-91-2
5.Packing Specification: 12kg/drum, 27 drums/tray
6.Delivery: 3-7working days
7.Certification: cGMP,KOSHER,HALAL,BRC,ORGANIC,ISO9001,ISO22000 etc.
8.Main Market: North America, Europe, Switzerland, South Africa, Southeast Asia, Australia, etc.
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  • Product Description

High-Purity D Alpha Tocopheryl Acetate Powder | USP/EP Compliant | Pharmaceutical-Grade

Shaanxi Hongda Phytochemistry Co., Ltd. is a leading manufacturer of premium vitamin derivatives, specializing in high-purity D Alpha Tocopheryl Acetate Powder. We produce this natural vitamin E form through esterification of D-alpha-tocopherol with acetic acid under controlled conditions. Our 5-step process ensures superior quality:

  • Esterification: Food-grade acetic acid reaction at 60-80°C
  • Crystallization: Ethanol-water solvent purification
  • Filtration: Activated carbon treatment for impurity removal
  • Drying: Low-temperature vacuum drying
  • QC Testing: HPLC purity verification (≥99%)

D Alpha Tocopheryl Acetate Powder

Why Should You Pick Our D Alpha Tocopheryl Acetate Powder?

  • Very High Purity: With at least 99% active ingredient that is USP/EP compliant, it works even in delicate recipes.
  • Better Stability: With new low-temperature chemistry, the product can last up to 24 months longer.
  • Global Compliance: Buildings that have been checked out already meet ISO9001,ISO 14001, FDA, and EU GMP standards.
  • Unique Solutions: The particle size can be changed from 50 to 200 µm, and the amount that is packed can be changed from 25 kg drums to small batches.
  • Experience: 25 years of experience in vitamin and amino acid production and R&D

D Alpha Tocopheryl Acetate Powder

Technical Specifications

Items
Specifications
Results
Method
 
Characters
 
Almost white,yellowish or light brown,small particles.
 
Conform
 
Visual
Acidity
≤1.0ml
0.3ml
USP
 
Assay
≥51.5%
≥700IU
52.8%
718IU
 
USP
*Benzo(a)Pyrene
≤2.0ppb
Conform
GC-MS
*Solvent residue-Toluene
≤890ppm
Conform
USP<467>
 
 
 
*Heavy Metals

Lead

≤1.0ppm
Conform
AAS

Arsenic

≤1.0ppm
Conform
AFS

Cadmium

≤1.0ppm
Conform
AAS

Mercury

≤0.1ppm
Conform
AFS
 
 
 
*Microbiology

Aerobic Plate Count

≤1000cfu/g
Conform
USP<61>

Yeast and Molds

≤100cfu/g
Conform
USP<61>

Escherichia Coli

≤10cfu/g
Conform
USP<62>

Salmonella

Negative/25g
Negative
USP<62>

Staphylococcus Aureus

Negative/10g
Negative
USP<62>
 
Conclusion: Conforms to USP-NF 2023 .
 
 
Remarks:*Analyzed as per ten batches.
 


Production Process of D Alpha Tocopheryl Acetate Powder

1. Raw Material Selection

  • Made from vegetable oils that are not genetically modified (soybean and sunflower)
  • Tested three times for purity (>98% α-tocopherol) and impurities

2. Esterification

  • Under nitrogen protection, reacted with food-grade acetic anhydride at 60–80 °C
  • Real-time pH monitoring makes sure that the whole thing is changed.

3. Purification and crystallization

  • Ethanol-water gradient crystallization with a cooling rate of 0.5°C/min
  • Activated carbon filtration gets rid of any leftover dirt.

4. Drying

  • Two-stage process: vacuum drying (40°C max) + fluidized bed drying
  • Final moisture content <0.5%

5. Quality Control & Packaging

  • HPLC purity verification (≥99%)
  • GC-MS solvent residue testing (<300ppm)
  • Nitrogen-flushed aluminum bags inside fiber drums

Key Advantages

  • cGMP-compliant with full batch documentation
  • Preserves natural RRR-α-tocopherol configuration
  • Customizable particle size (50-200μm available)

 

Key Applications 

1. Nutraceutical Products  

  • - Antioxidant booster in multivitamins  
  • - Stability enhancer for omega-3 formulations  
  • - Core ingredient in anti-aging supplements  

2. Pharmaceutical Preparations

  • - Topical creams for skin repair  
  • - Injectable solutions (low-endotoxin batches available)  
  • - Oral dosage forms with improved bioavailability  

3. Cosmetic Formulations  

  • - Anti-oxidation agent in serums and lotions  
  • - UV protection additive in sun care products  

 

Compliance You Can Rely On

Our D Alpha Tocopheryl Acetate Powder complies with:

  • USP-NF and European Pharmacopoeia monographs.
  • ICH Guidelines for assessing stability (Q1A-Q1E).
  • You can get Halal, Kosher, and REACH certifications.

Every batch comes with a Certificate of Analysis (CoA) that shows stability statistics, residual solvent reports, and microbiological limits that can be traced. 

Quality assurance

Certifications 

- cGMP Manufacturing (facilities that the FDA checks)  
- Certified by ISO 9001:2015 and ISO 14001 
- Halal and Kosher certification is also available  
- Full DMF/CEP Documentation Support

certifications

Different ways to order

  • Minimum order quantity: 10 kg (may be changed for long-term relationships).
  • Time to ship: 2 to 4 weeks (faster shipping is possible).
  • Free Samples: Try out our lab-grade stuff without any risk. 

Packaging

FAQ

Q: How can you check the quality of D Alpha Tocopheryl Acetate Powder?

A: We test with HPLC and GC-MS, and additional labs look over the data.

Q: Can you change the size of the particles to make them dissolve better?

A: Yes! Our micronization process changes particles from 50µm to 200µm.

Q: Do you do stability studies for submissions to the government?

A: Yes, for sure. We offer data packages for both short-term and long-term stability that meet ICH standards.

Q: How do you make sure the quality of your work?

A: We test raw materials three times, and we check the quality of every batch more than 25 times.

 

Need a Quote or Technical Details?

Email our pharmaceutical team at duke@hongdanutra.com for bulk pricing, CoA templates, or formulation support.

Your Trusted Partner in D Alpha Tocopheryl Acetate Powder.

Team

 

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