Tylosin Powder
Lifeworth supplies Tylosin Powder in Tylosin Tartrate form for veterinary pharmaceutical and animal health applications, with specification review, documentation support, and bulk sourcing options.
- Veterinary API Grade Material
- Tylosin Tartrate Commercial Form
- COA, MSDS & Technical Documents
- Bulk Supply for Commercial Projects
- Specification Review Support
Tell us your application, target specification, and destination market so we can support grade selection, documentation review, and packaging recommendations.
Quick Specs
Identity
INCI Name
Alias
CAS Number
Molecular Formula
Molecular Weight
Quality
Assay
Grade
Standards
Assay Method
Handling
Appearance
Form
Solubility
Applications
Commercial Terms
MOQ
MOQ depends on packaging and specification.
Lead Time
3–7 working days for standard items; bulk orders by schedule.
Incoterms
EXW / FOB / CIF / DAP / DDP
Sample
Free sample (shipping charged)
Quality & Documents
COA (per batch) • SDS/MSDS • TDS/Spec sheet (on request). Additional statements depend on product and market.
Product Overview
Tylosin Powder is a veterinary pharmaceutical ingredient commonly supplied as Tylosin Tartrate for animal health and veterinary API applications.
Buyers usually evaluate chemical form, assay basis, specification requirements and documentation package before commercial qualification.
It is supplied for veterinary pharmaceutical projects with COA, MSDS and technical documentation support.
Applications
Veterinary Pharmaceutical Manufacturing
Tylosin Powder is commonly evaluated by veterinary pharmaceutical manufacturers as an active pharmaceutical ingredient for animal health product development and production. Buyers typically review chemical form, specification requirements, documentation package and batch consistency before commercial qualification.
Companion Animal Veterinary Products
Tylosin Tartrate may be considered for companion animal veterinary product formulations requiring a qualified pharmaceutical ingredient with consistent specifications. Product selection is usually based on application requirements, regulatory expectations and finished formulation considerations.
Poultry and Livestock Veterinary Products
Tylosin Powder is supplied for veterinary companies developing poultry and livestock-related animal health products. Manufacturers generally evaluate specification compliance, quality documentation and supply capability during ingredient sourcing.
Veterinary API Distribution
Tylosin Tartrate is supplied to veterinary API distributors requiring bulk ingredient availability, specification confirmation and export documentation support for commercial sourcing projects.
How to Choose the Right Grade / Form
Tylosin products may be evaluated based on chemical form, specification requirements, analytical data and intended veterinary pharmaceutical applications. Buyers should select the suitable specification according to formulation requirements and regulatory expectations.
| Criteria | Tylosin Base | Tylosin Tartrate | Buyer Consideration |
|---|---|---|---|
| Chemical Form | Free base form of tylosin with different physical and chemical characteristics. | Salt form commonly supplied for commercial veterinary pharmaceutical applications. | Confirm the required chemical form according to formulation and regulatory needs. |
| Commercial Availability | Less commonly selected for routine commercial sourcing. | Widely recognized commercial form for veterinary API supply. | Confirm supplier capability and available documentation. |
| Specification Review | Evaluation may focus on identity, assay and related quality parameters. | Evaluation typically includes assay, identification, purity profile and batch consistency. | Review complete specification documents before qualification. |
| Project Suitability | Selected for specific technical requirements. | Commonly considered for veterinary pharmaceutical manufacturing projects. | Select based on finished product requirements and market regulations. |
Technical & Formulation Notes
Technical Notes
Tylosin Powder is commercially supplied as Tylosin Tartrate, a salt form commonly selected for veterinary pharmaceutical applications. As a fermentation-derived macrolide antibiotic API, it is typically evaluated based on assay, identification, quality parameters and batch consistency.
Manufacturing & Process
Commercial Tylosin Tartrate production involves fermentation-derived tylosin followed by purification and salt formation processes. Manufacturing controls focus on specification compliance, quality consistency and batch documentation.
Compatibility / Formulation Notes
For Veterinary Pharmaceutical Systems
Tylosin Powder selection should consider the intended dosage form, specification requirements and compatibility with the finished veterinary formulation.
For Powder Blending Systems
Uniform mixing, particle characteristics and batch consistency should be evaluated during formulation development and manufacturing processes.
For Documentation Review
Veterinary pharmaceutical projects may require supporting documents including COA, MSDS, technical specifications and quality records.
Extended QC & Test Items
Quality evaluation may include identification, assay determination, related substances, moisture and other parameters according to applicable specifications and customer requirements.
Product specifications
| Test | Specification | Method |
|---|---|---|
| Appearance | White to slightly yellow powder | Visual |
| Identification | Conforms | According to specification |
| Assay | Meets agreed specification | HPLC |
| Related Substances | According to specification | HPLC |
| Moisture | According to specification | QC Method |
Storage, Shelf Life & Packaging
Storage
Store in a sealed container in a cool, dry place. Protect from moisture and direct light exposure.
Shelf Life
Subject to manufacturer specification and storage conditions.
Packaging & Logistics
Standard Packing: Inner double PE bags + outer fiber drum / carton (or aluminum foil bag).
Sample package:10g / 20g /50g / 100g Net Weight Options: 1 kg / 5 kg / 10 kg / 25 kg (customizable).
Palletizing: Export-grade palletized shipment with stretch film and corner protection.
Shipping Methods: Air freight / Sea freight / Express (DHL/UPS/FedEx).
Lead Time: Typically 3–7 working days (subject to stock and QC release).
Labeling: Product name, batch/lot No., manufacturing date, expiry date, storage conditions.
Supply, Documentation & Customization
Documents & Compliance
COA, SDS/MSDS, and TDS/spec sheet available based on product and market requirements.
Customization & Private Label
Custom packing, private label, and labeling support available depending on product type and order scope.
Commercial Support
Sample, lead time, and incoterm options can be discussed according to destination market and supply plan.
Why Source From Lifeworth
Defined Specification Support
Clear product information and specification review support for veterinary ingredient sourcing.
Documentation Assistance
COA, MSDS and technical documents available for supplier evaluation.
Flexible Supply Support
Sample evaluation and commercial supply coordination according to purchasing requirements.
Export-Oriented Service
Support for international buyers requiring ingredient sourcing and shipment coordination.
FAQ
What is Tylosin Powder supplied by Lifeworth?
Tylosin Powder is supplied as Tylosin Tartrate, a veterinary pharmaceutical ingredient used for animal health product manufacturing and related sourcing projects.
Is Tylosin Powder the same as Tylosin Tartrate?
Tylosin Powder is commonly supplied in Tylosin Tartrate form for commercial veterinary applications. Buyers should confirm the chemical form and specification before purchase.
What documents are available for Tylosin Powder?
Typical supporting documents include COA, MSDS and technical specification documents.
Can I request a Tylosin Powder sample?
Samples may be available for technical evaluation before commercial purchasing.
What should buyers confirm before sourcing Tylosin Powder?
Buyers should confirm chemical form, assay requirements, documentation package, regulatory expectations and intended application before commercial sourcing.
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