Relieve allergy symptoms effectively with our Medicine Grade Levocetirizine HCL, a high-purity solution designed for reliable treatment outcomes. This white crystalline powder delivers consistent performance, ensuring your formulations meet the strictest standards for safety and efficacy.
- 99% assay guarantees optimal potency, supporting precise dosing in pharmaceutical applications
- Solid form with non-volatile properties ensures stable storage and easy integration into production processes
- Backed by comprehensive quality control from source to delivery, providing peace of mind for your supply chain
描述
For industrial manufacturing and laboratory research purposes only.
Product Specifications
| Parameter | Value |
|---|---|
| CAS Number | 130018-77-8 |
| Grade Standard | Medicine Grade |
| Type | Chemicals |
| State | Solid |
| Volatility | Not Volatile |
| Color | White Crystalline Powder |
| Assay | More Than 99% |
| Transport Package | Cardboard Drums or Cartons |
| Specification | gram, kilogram |
| Origin | China |
| HS Code | 2934999099 |
| Production Capacity | 100kg/Month |
Addressing Purity and Consistency Challenges with Levocetirizine HCL (CAS 130018-77-8)
Industrial researchers and manufacturers often face critical obstacles like unpredictable purity levels causing reaction inconsistencies, batch-to-batch variations undermining experimental reproducibility, and supply chain disruptions delaying production timelines. Over our 10+ years in chemical supply, we’ve witnessed how these issues directly impact R&D efficiency and manufacturing yields—especially for specialized compounds requiring precise specifications.
A Stable and Reliable Levocetirizine HCL Supply Solution
Our Levocetirizine HCL addresses these core challenges through rigorous manufacturing control and standardized processes. As a 99% assay medicine grade solid chemical, it delivers the consistency needed for reliable industrial research and production. With a monthly capacity of 100kg, we ensure stable supply to support both small-scale laboratory trials and medium-volume manufacturing requirements across 50+ countries.
Typical Industrial Applications
Levocetirizine HCL serves as a key intermediate in pharmaceutical R&D, chemical synthesis studies, and analytical reference standard development. Its high purity and defined physical properties make it valuable for method validation, process optimization, and quality control testing in industrial laboratories. This white crystalline powder is particularly suited for applications requiring precise chemical composition and low impurity profiles.
Why Key Specifications Matter
The 99% assay level ensures minimal impurity interference, critical for accurate research results and consistent manufacturing outputs. Its solid state and non-volatile nature provide stable handling characteristics, reducing process variability during synthesis or formulation. The white crystalline powder form enables precise dosing and uniform mixing—essential factors in scaling from laboratory protocols to industrial production. These specifications collectively contribute to reliable performance across various research and manufacturing workflows.
Benefits of Quality-Assured Levocetirizine HCL
Using our compliant Levocetirizine HCL minimizes the risks associated with substandard materials, such as failed experiments, production delays, and non-compliant outputs. Unlike lower-grade alternatives, our product meets stringent medicine grade standards, supporting regulatory compliance in pharmaceutical development processes. The consistent quality reduces material waste and rework, ultimately delivering better cost efficiency over the product lifecycle.
Our Quality Assurance Commitment
Every batch undergoes comprehensive testing to verify purity and specifications. We implement strict quality control measures throughout production, from raw material selection to final packaging. Each shipment includes a detailed Certificate of Analysis documenting key parameters, ensuring full traceability. Our technical support team provides expert guidance on product handling and application, backed by years of industry experience.
Certificate of Analysis & Documentation
Each order includes a batch-specific Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS). For research and quality control purposes, detailed testing data can be requested using your order reference number. Comprehensive documentation supports regulatory compliance and quality management systems in industrial and laboratory settings.
Storage & Handling
- Store in a cool, dry, well-ventilated area, sealed and away from direct sunlight.
- Keep away from incompatible materials, food and feed sources.
- Handle with appropriate personal protective equipment (gloves, goggles, lab coat).
- Follow good industrial hygiene practices. Avoid inhalation and skin contact.
- Refer to MSDS for detailed storage and safety instructions.
Order Process
Initiate your purchase by submitting an inquiry with your required quantity and specifications. We can provide samples for evaluation prior to full order placement. Once specifications are confirmed, we process your order and arrange secure delivery in cardboard drums or cartons. Each shipment includes all necessary documentation for industrial and laboratory use.
Frequently Asked Questions
Q: What is the shelf life of Levocetirizine HCL when properly stored?
A: When stored according to recommended conditions in sealed packaging, the product maintains stability for 24 months from the manufacturing date.
Q: Is this product suitable for direct pharmaceutical production?
A: This material is supplied for industrial and laboratory research use only. Additional processing and testing would be required for pharmaceutical manufacturing applications.
Q: What documentation is provided with each shipment?
A: Every order includes a Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS) specific to the batch shipped.
Q: Can packaging be customized for specific requirements?
A: Standard packaging is in cardboard drums or cartons. Custom packaging options may be available for large volume orders—please inquire with our sales team.
Q: How is the 99% assay value determined?
A: Purity is verified using high-performance liquid chromatography (HPLC) analysis, with results documented in the batch-specific COA.







