Pharmaceutical Factory Supply Veterinary Medicine Drug Ep USP Ivermectin 70288-86-7
Pharmaceutical Factory Supply Veterinary Medicine Drug Ep USP Ivermectin 70288-86-7
Veterinary Medicine,Ivermectin ,70288-86-7
Product Name:Ivermectin API Powder
Product Purity: ≥98.0%
CAS No : 70288-86-7
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Description
Ivermectin Powder API (EP / USP)
High-Purity Antiparasitic API Manufacturer | Bulk Ivermectin Raw Material CAS 70288-86-7 Supplier
Scientific Storage:
Keep container tightly sealed to shield from moisture and air. Store in a cool, dry, and dark pharmaceutical warehouse (refrigeration at 2-8°C is optimal). This maintains maximum potency throughout its 24-month stable shelf life.
Keep container tightly sealed to shield from moisture and air. Store in a cool, dry, and dark pharmaceutical warehouse (refrigeration at 2-8°C is optimal). This maintains maximum potency throughout its 24-month stable shelf life.
Product Technical Overview
Ivermectin (CAS 70288-86-7) manufactured and supplied by Shaanxi Sunrise Pharmaceutical Co., Ltd. is a highly potent, broad-spectrum antiparasitic active pharmaceutical ingredient (API). Chemically, Ivermectin is a macrocyclic lactone derivative produced via controlled semi-synthetic fermentation pathways. It exists as a synergistic macrocyclic mixture containing not less than 90.0% of component H2B1a and not more than 10.0% of component H2B1b.
As an established B2B raw material partner, our high-purity Ivermectin powder conforms strictly to European Pharmacopoeia (EP), United States Pharmacopoeia (USP), and British Pharmacopoeia (BP) compendial criteria. It features exceptional crystal form uniformity and excellent lipophilic solubility in organic solvent vectors like methanol, ethanol, and propylene glycol, making it optimized for complex non-clinical formulation lines.
| CAS Number | 70288-86-7 |
| Chemical Type | Macrocyclic Lactone Disaccharide Mixture (Avermectin family) |
| Molecular Formula | C48H74O14 (Component H2B1a) | C47H72O14 (Component H2B1b) |
| Molecular Weight | 875.10 g/mol (H2B1a) | 861.07 g/mol (H2B1b) |
| Component Ratio | H2B1a ≥ 90.0% | H2B1b ≤ 10.0% (EP / USP Monograph) |
| Assay (Dried Basis) | 95.0% – 102.0% |
| Appearance | White to yellowish-white, crystalline powder (highly hygroscopic) |
| Specific Optical Rotation | -17° to -23° |
| Loss on Drying | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Standard Pack | 1 kg/bag (vacuum-sealed foil); 25 kg/cardboard drum |
Core B2B Sourcing Advantages
Strict Component & Purity Control
Utilizing state-of-the-art preparative chromatography, we ensure our Ivermectin powder maintains an optimized H2B1a ratio (≥90.0%). This strict component control limits degradation analogs and related substances below 1.0%, delivering ultra-consistent bio-potency profiles.
Advanced Solvent & Quality Assurance
Our manufacturing and crystallization processes fully comply with ICH Q3C residual solvent directives. Volatile organic solvents are meticulously stripped out under high-vacuum desiccation, preventing localized analytical deviations during downstream compounding.
Scalable & Reliable Global Supply
With advanced commercial-scale fermentation lines and a fully traceable quality management system, Shaanxi Sunrise easily supports everything from laboratory evaluation batches to multi-ton bulk orders with flexible industrial lead times.
Mechanism of Action & Applications
Ivermectin binds selectively and with high affinity to glutamate-gated chloride ion channels, which occur in invertebrate nerve and muscle cells. This binding leads to an increase in the permeability of the cell membrane to chloride ions with hyperpolarization of the nerve or muscle cell, resulting in paralysis and death of the target parasites. Its specific industrial and research applications include:
Veterinary Formulation R&D: Serves as a vital active raw material for non-clinical antiparasitic development, including veterinary oral drenches, pour-on solutions, and injectable configurations.
Laboratory Reference Analytics: Widely employed as an analytical standard for high-performance liquid chromatography (HPLC) calibration and thin-layer chromatography validation assays.
Chemical Synthesis Studies: Utilized as an essential precursor block for developing high-end avermectin-family modifications and investigating structural structural stability changes.
Technical Support & Frequently Asked Questions
What documentation is provided with our Ivermectin shipment? ▼
Every commercial batch of Ivermectin powder is delivered with an full Certificate of Analysis (COA) containing exact HPLC data, a comprehensive Material Safety Data Sheet (MSDS), and a Technical Data Sheet (TDS) for complete quality transparency.
Are smaller packaging quantities available for laboratory evaluation? ▼
Yes, Shaanxi Sunrise supports pilot studies and research infrastructure by offering customizable down-packaged options, including 100g, 200g, and 500g configurations sealed in reinforced vacuum aluminum foil pouches.
How do you ensure batch-to-batch chemical stability? ▼
Our manufacturing operations strictly regulate temperature, moisture, and micro-particle exposure. Our vacuum freeze-drying parameters create an amorphous crystalline form with optimal stability, shielding the material from thermal and oxidative stressors.
⚠ Safety Warning & B2B Compliance Declaration
Mandatory Regulatory Notice: This product represents a raw active chemical substance intended exclusively for industrial manufacturing, formulation research and development, and authorized laboratory scientific analysis. It is not a finished medicine and is not intended for direct human or clinical veterinary applications. Shaanxi Sunrise Pharmaceutical Co., Ltd. strictly sells to verified corporate entities and licensed research institutions only.