Lincomycin Hydrochloride API CAS 859-18-7 | USP Grade Veterinary Antibiotic Manufacturer China
Key Selling Points
- USP‑grade specification with batch‑specific COA available for every shipment
- Flexible supply: samples, pilot batches and commercial bulk orders
- Full documentation: COA, USP test reports, SDS/MSDS and product specs
- Direct factory supply with full batch traceability & strict QC
- Stable powder quality via controlled fermentation, purification and crystallization
- Moisture‑proof sealed packaging and global export service
- Competitive bulk pricing for pharmaceutical and veterinary formulation manufacturers
What Is Lincomycin Hydrochloride USP Grade?
Lincomycin Hydrochloride Powder (CAS 859‑18‑7) is a lincosamide‑class antibacterial raw material derived from microbial fermentation, manufactured complying with United States Pharmacopeia monograph requirements. This white crystalline powder shows good water solubility and is widely used for human‑pharmaceutical and veterinary finished‑dosage‑form production.
This raw material is only for downstream pharmaceutical and veterinary formulation manufacturing and cannot be used directly without further processing. For pharma and veterinary buyers, core procurement verification covers CAS identity, USP assay range, impurity profile and loss‑on‑drying before bulk order confirmation. HDM BIO supplies consistent batches of Lincomycin Hydrochloride Powder with complete analytical records to support supplier qualification audits.
What Is Lincomycin Hydrochloride USP Grade Used For?
Lincomycin hydrochloride raw material is a lincosamide antibacterial starting material active against gram‑positive bacteria and certain anaerobic pathogens. All finished products manufactured from this raw material must comply with local pharmaceutical and veterinary regulatory standards.
‑ Veterinary Injectable Formulations: Core raw material for injectable solutions targeting gram‑positive bacterial infections in livestock.
‑ Oral Solid & Liquid Veterinary Preparations: For oral powder, soluble powder formulation development for swine, poultry and ruminants.
‑ Pharmaceutical R&D Intermediate: USP‑grade technical material for pharma factories producing human‑use lincomycin finished drugs.
‑ Premix intermediate processing for authorized animal‑health products under permitted regional regulatory frameworks.
How Does Lincomycin Hydrochloride Work?
Lincomycin hydrochloride suppresses bacterial protein synthesis to exert bacteriostatic activity:
- Ribosome Binding: Attaches to bacterial 50S ribosomal subunit.
- Inhibit Peptide Chain Elongation: Blocks peptide bond formation and interrupts bacterial protein assembly.
- Suppress Bacterial Proliferation: Restrains reproduction of susceptible gram‑positive and anaerobic bacteria.
It exhibits limited activity against most gram‑negative bacteria.
Lincomycin Hydrochloride USP Grade Manufacturing & Quality Control
HDM BIO executes full‑process QC workflow for Lincomycin Hydrochloride USP Grade:
‑ Starting Material Inspection: Fermentation culture media and intermediates complete identity & purity checks before production.
‑ Microbial Fermentation: Strictly controlled fermentation parameters for lincomycin biosynthesis.
‑ Multi‑Stage Purification & Salt Formation: Refining, hydrochlorination and purification to meet USP impurity limits.
‑ Crystallization & Vacuum Drying: Regulated crystallization and low‑temperature drying to control particle size and moisture.
‑ Milling & Sieving: Adjustable particle‑size processing for different formulation‑technology requirements.
Lincomycin Hydrochloride USP Grade Quality Control & Analytical Testing
Each production batch completes full USP‑aligned testing before release:
‑ Assay Test: Primary quantitative test to verify 90.0%‑105.0% minimum‑maximum USP specification for each batch.
‑ Identity Confirmation: Matching against certified lincomycin hydrochloride reference standard per USP criteria.
‑ Related Substances Test: Control process‑related impurities according to USP monograph limits.
‑ Loss on Drying: Tight moisture testing to prevent powder degradation during storage.
‑ pH & Physical Character Inspection: Test solution pH and physical appearance for formulation‑process compatibility.
What Finished Formulations Can Be Produced With Lincomycin Hydrochloride USP Grade?
Thanks to its USP‑grade purity and good water‑solubility, this raw material supports multiple production routes:
‑ Injectable Solutions: Sterile‑process injectable lincomycin hydrochloride for veterinary and human‑pharmaceutical use.
‑ Water‑Soluble Powders: Oral soluble powder for livestock antibacterial therapy.
‑ Oral Solid Dosage Intermediates: Raw material for tablet and capsule‑form R&D.
‑ Custom R&D intermediates for pharma and animal‑health manufacturers.
Why Choose HDM BIO as Your Lincomycin Hydrochloride USP Grade Manufacturer in China?
HDM BIO is direct factory for lincosamide‑class pharmaceutical‑veterinary raw materials, distinct from trading intermediaries, bringing tangible procurement advantages:
‑ Direct Factory Supply Advantage: No middle‑man links, stable production capacity and flexible batch arrangements for samples through full‑container bulk orders.
‑ Full Batch Traceability: Complete production log and in‑process QC records retained for each lot, supporting third‑party supplier qualification audits. ‑ Complete Export Documentation: Full set of commercial, packing and customs documents for cross‑border raw‑material import clearance.
‑ Comprehensive Analytical Support: Batch COA, HPLC reports, SDS/MSDS supplied free for buyer internal quality review.
‑ Scalable Bulk Supply: Support lab‑scale samples, pilot‑scale batches and large‑volume commercial bulk orders with fixed lead times.
‑ Customized Packaging Solutions: Light‑shield & moisture‑proof packaging options with customizable OEM labeling.
Lincomycin Hydrochloride USP Grade FAQ
1. What is Lincomycin Hydrochloride USP Grade used for?
Lincomycin Hydrochloride USP Grade is lincosamide antibacterial technical raw material complying with USP monograph, for manufacturing human‑pharmaceutical and veterinary antibacterial finished formulations, not for direct administration.
2. What is the CAS number of Lincomycin Hydrochloride?
Official CAS registry number is 859‑18‑7. All production batches strictly match this CAS identity.
3. What does USP Grade mean for lincomycin hydrochloride?
USP Grade means the product meets all assay, impurity, physical‑property requirements described in United States Pharmacopeia monograph, suitable for pharma‑grade formulation production.
4. What assay range do you supply for Lincomycin Hydrochloride USP Grade?
Assay controlled within USP specification 90.0%‑105.0%, real‑batch data shown on batch COA.
5. What storage conditions are required?
Store in sealed container under cool and dry conditions, avoid excessive heat and humidity.
6. Can I get COA before bulk purchase?
Qualified pharma and veterinary manufacturers can request latest‑batch COA and USP test reports for free evaluation before commercial orders.
7. What packaging options are available?
Lab sample foil bags, small‑batch sealed containers and 25kg moisture‑proof fiber drums; custom OEM labeling supported.
8. Do you support worldwide shipping?
Yes, complete export documents are provided for global buyers of pharmaceutical‑veterinary raw material.
factory
Certificates
Shipping & Packing
Request Lincomycin Hydrochloride USP Grade COA & Bulk Quote
Lincomycin Hydrochloride Powder is kept in stable stock for pharmaceutical factories and veterinary‑health enterprises for bulk procurement and formulation R&D.
Contact HDM BIO to request:
- Current product specification
- Batch-specific COA preview
- HPLC analytical information
- Sample availability and lead time
- Formal bulk quotation
- Custom packaging options
- Export documentation support
Request COA | Get Sample | Get Bulk Quote
Contact:
Whatsapp & Mobile: +86 19991242181
Email: sales@hdmbio.com
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