Epalrestat Bulk Supply for Industrial Use

China Factory Direct
CAS number 82159-09-9
Product name Epalrestat
Stock Stock readily available; annual supply capacity exceeding 1,000 tons.
Grade Pharmaceutical GradeReagent Grade
Packaging 25KG/bag
Sample Test Samples Available (Click to Request Samples)
COA View COA
Price Get Quote
Supply Type Bulk / Contract manufacturing / OEM
Shipping FCL / LCL available
Payment Terms Support FOB \ CIF \ EXW quotations, and accept Letter of Credit (L/C).
Manufacturer Greenrock Chemical(China Factory)
Ordering Procedure & Service Assurance
Inquiry
Inquiry
Submit requirements
Quotation
Quotation
Clear pricing
Spec
Spec Confirmation
Avoid mismatch
Sample
Sample Testing
Verify quality
Order
Order
Secure deal
Delivery
Delivery
On-time
Spec Confirmation
Sample Testing
Contract Protection
QC Inspection
On-time Delivery

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FOB (Free On Board)
CIF (Cost, Insurance, Freight)
EXW (Ex Works)

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Sea Freight

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CAS No:82159-09-9
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Documents We Provide for Epalrestat

COA TDS SDS NMR MOA Certificate of Origin Transport Report TSCA Declaration Production Flow Chart
Pre-sale: Only COA, SDS and NMR are available.
Post-sale: Full documentation is provided.
To request documents, please contact us via email at sales@GRchemical.com.
Bulk Epalrestat Supplier from China

17+ years in chemical exports.Fully compliant, reliable supply.Your B2B partner in bulk chemical procurement.

Industrial Applications of Epalrestat

Industry Application Process
Pharmaceuticals Treatment of diabetic neuropathy Synthesized into epalrestat, then formulated into oral tablets or capsules
Pharmaceuticals As an aldose reductase inhibitor High-purity epalrestat crystals produced via chemical synthesis
Research Used as a research reagent High-purity reference standard supplied for laboratory research
Pharmaceuticals Potential use in treating other metabolic disorders Development and optimization of epalrestat derivatives or combination formulations

Manufacturing Quality Control of Epalrestat

Test Item Common Testing Methods Method Overview
Identification Infrared Spectroscopy (IR) Compare the infrared spectrum of the sample with that of the reference substance under the same conditions to confirm the chemical structure.
High-Performance Liquid Chromatography (HPLC) Compare retention times to verify the chromatographic behavior of the sample and reference substance, used for auxiliary identification.
Content Determination High-Performance Liquid Chromatography (HPLC) Use reversed-phase HPLC with a UV detector (typically around 280 nm) to determine the content of the main component using external or internal standard methods.
Related Substances (Impurities) High-Performance Liquid Chromatography (HPLC) Separate impurities using gradient elution or isocratic elution, detect degradation products or by-products, and calculate the limits of each impurity and total impurities.
Residual Solvents Gas Chromatography (GC) Detect residual organic solvents used in the production process, such as methanol, ethanol, acetone, according to ICH guidelines.
Moisture Karl Fischer Titration Determine the moisture content of the sample using volumetric or coulometric methods, to control the stability of the formulation and the manufacturing process.
Polymorphic Analysis X-ray Powder Diffraction (XRD) Confirm whether the polymorphic form of the active pharmaceutical ingredient meets the requirements, preventing differences in solubility and stability caused by different polymorphs.
Particle Size Distribution Laser Diffraction Method Measure the particle size and distribution of the active pharmaceutical ingredient, which affects dissolution rate and bioavailability.
Dissolution Dissolution Test Method (Paddle Method / Basket Method) Used for dosage forms, simulating the release in vivo, evaluating the drug release performance, commonly using UV or HPLC to detect concentration.
Heavy Metals Sulfide Colorimetry or ICP-MS Check for heavy metal impurities such as lead, cadmium, and mercury to ensure compliance with pharmacopoeia limits.
Loss on Ignition Loss on Ignition Test Method After high-temperature incineration, weigh the residue to assess the content of inorganic impurities.
Solution Clarity and Color Visual Colorimetry or Spectrophotometry Check the clarity and color of the solution to ensure it is within acceptable limits, reflecting the purity status.

Technical Specifications of Epalrestat

Test Item Specification
Appearance Yellow Solid
Purity >=98.5% (by HPLC)
Total Impurities <=1.5%
Single Impurity <=0.5%
Water Content (KF) <=0.5%
Melting Point 132–136°C
Residue on Ignition <=0.1%
Heavy Metals <=20 ppm
Specifications vary by industry. Reach out to our technical experts for a COA tailored specifically to your application. Email:selse@GRchemical.com

Download COA of Epalrestat

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NMR Spectra of Epalrestat

Safety Information of Epalrestat

Pictograms
Signal Word Danger
Safety Data Sheet

Packaging of Epalrestat

We have a diverse range of chemicals in stock. Available in Bagged goods (25 kg.),Big bags (500 kg.), Big bags (1000 kg.).

Industrial Epalrestat Procurement FAQ

1. How do you ensure product quality consistency?
We rely on a mature China-based manufacturing system and implement strict batch control and quality inspection for every shipment. Our production process complies with ISO 9001 standards, and a COA is provided for each batch to ensure consistent and reliable quality.

2. Do you offer competitive pricing for bulk orders?
Yes, as a China-based manufacturer and bulk supplier, we provide tiered pricing based on order volume. We support FOB and CIF quotations, as well as L/C payment terms for large transactions to meet international trade requirements.

3. Can you support large-volume or long-term supply?
We have stable production capacity and a well-established supply chain, enabling continuous bulk supply. We support ton-level and container-level orders, as well as long-term cooperation projects.

4. What is your typical lead time?
For in-stock products, shipment can be arranged within 1–3 days. For bulk packaging or customized orders, lead time depends on the specific quantity and production schedule.

5. What documents do you provide?
We can provide complete documentation upon request, including COA, SDS, TDS, and other compliance certificates, meeting industrial procurement and export requirements.

6. Can you customize product specifications or packaging?
Yes, we support customization of parameters such as purity, impurities, residual solvents, and heavy metals. We also offer various bulk packaging options, including 25kg bags, drums, and IBC tanks, suitable for industrial applications and transportation.

7. What shipping options do you support?
We support both FCL (Full Container Load) and LCL (Less than Container Load) shipments, and can flexibly arrange logistics solutions based on order size to meet bulk chemical export needs.

8. Do you provide technical or application support?
Yes, we provide basic application guidance and technical support based on industry experience to help customers optimize product usage.

9. How do you handle compliance and export regulations?
We are familiar with international trade and export regulations, ensuring all products comply with relevant requirements. We also provide complete documentation to support smooth customs clearance and global delivery.

Industrial
Use
Bulk
Supply
Factory
Direct
ISO 9001
Certified
Samples
Available
Stable
Supply