Metronidazole Powder
Metronidazole powder is commonly sourced as an antimicrobial API for pharmaceutical manufacturing and related formulation projects. Buyers usually review assay, pharmacopeial alignment, intended dosage form, documentation, and packaging before quotation and supply planning.
- API-oriented metronidazole raw material for pharmaceutical manufacturing
- Commonly reviewed against BP, EP, USP, or agreed specification standards
- Suitable for oral, topical, and other finished dosage form development projects
- Batch documentation support for technical and procurement evaluation
- Sample, packaging, and export coordination for B2B supply projects
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
Metronidazole powder is a synthetic nitroimidazole antimicrobial active ingredient commonly used in pharmaceutical manufacturing.
It is typically supplied as an API-grade powder for further processing, and buyers often review assay, pharmacopeial standard, dosage-form suitability, and documentation readiness before procurement.
It is commonly considered for finished-product development where antimicrobial API quality, batch consistency, and regulatory review are important.
Applications
Pharmaceutical Manufacturing
Commonly reviewed for oral solid dosage forms, oral liquid development, topical products, and other pharmaceutical dosage-form projects depending on the target market and formulation plan.
Contract Manufacturing Projects
Suitable for manufacturers and procurement teams evaluating metronidazole as a bulk API for specification-driven supply and finished-product development.
Veterinary Pharmaceutical Development
May be reviewed for selected veterinary pharmaceutical projects where permitted by local regulation and product-registration requirements. Regulatory assessment is necessary before market-specific positioning.
How to Choose the Right Grade / Form
For pharmaceutical manufacturing projects
Confirm the required standard reference, target dosage form, destination market, and document expectations before selecting the supply specification.
For regulated or registration-driven projects
Review technical documentation, quality requirements, and market-entry pathway early in the sourcing process.
For veterinary pharmaceutical evaluation
Confirm local regulatory acceptability, target species, dosage-form direction, and documentation scope before positioning the material for development.
Technical & Formulation Notes
Technical Notes
Metronidazole is mainly positioned as a pharmaceutical active ingredient rather than a consumer-facing functional ingredient.
For sourcing evaluation, the most important points are usually pharmacopoeial alignment, assay control, impurity profile, powder handling, packaging protection, and document availability.
Procurement review should focus on whether the material matches the intended dosage-form pathway, target market requirements, and technical documentation workflow.
Manufacturing & Process
The product is generally handled as a specification-driven pharmaceutical raw material. Manufacturing-route discussion, batch documentation, and process-related technical questions should be reviewed according to the intended market and project scope.
Compatibility / Formulation Notes
Metronidazole powder should be evaluated in the context of the intended dosage form, target specification standard, and market-specific regulatory pathway.
For development projects, buyers often confirm assay range, powder characteristics, packaging protection, documentation availability, and downstream formulation compatibility early in the sourcing process.
For regulated markets, technical, regulatory, and registration review should be completed before commercial launch or market-positioning decisions.
Extended QC & Test Items
Depending on the intended use, review may include assay, appearance, identification, loss on drying, residue on ignition, related substances, particle characteristics, packing integrity, and other specification-linked control items.
Product specifications
| Test | Specification | Method |
|---|---|---|
| Appearance | White or almost white crystalline powder | Visual |
| Assay | Typically 99.0% or according to agreed specification standard | Per specification |
| Molecular Formula | C6H9N3O3 | Reference |
| Molecular Weight | 171.15 | Reference |
| Standard | BP / EP / USP or agreed specification | Reference |
| Supply Type | Bulk pharmaceutical raw material | Reference |
| Documents | COA, SDS/MSDS, TDS/specification sheet | Available on request |
Storage, Shelf Life & Packaging
Storage
Store in a tightly closed container in a cool, dry place, protected from moisture, heat, and direct light.
Shelf Life
Shelf-life details should be confirmed according to batch, packaging format, and storage conditions during technical or commercial review.
Packaging & Logistics
Sample Packing
Small evaluation quantities can be arranged for specification review, compatibility checks, and procurement assessment.
Bulk Packing
Standard commercial packaging can be discussed according to order volume, handling preference, and destination-market requirements.
Logistics Support
Shipment planning can be coordinated according to lead time, packaging protection, export documents, and agreed Incoterms.
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
Specification-focused support
Suitable for buyers sourcing pharmaceutical raw materials with defined technical-review requirements.
Documentation-first communication
Supports efficient evaluation of assay, standard reference, packaging, and shipment planning.
Flexible supply discussion
Sample support, packaging coordination, and export communication can be discussed according to project stage.
B2B procurement coordination
Supports quotation review, lead-time planning, and commercial communication for bulk supply projects.
FAQ
1) What is metronidazole powder used for in B2B supply?
It is commonly sourced as a pharmaceutical raw material for finished dosage-form development and manufacturing projects.
2) What do buyers usually review before purchasing metronidazole powder?
Most buyers review assay, standard reference, document package, intended dosage form, packaging format, and batch consistency before procurement.
3) Can metronidazole powder be used for veterinary products?
Possible veterinary positioning depends on the target species, dosage form, and local regulatory framework. Regulatory review is essential before project development or market positioning.
4) Are samples available?
Sample availability can usually be discussed based on project stage, specification, and shipping destination.
5) What documents can be provided?
Routine B2B document support generally includes COA, SDS/MSDS, and specification/TDS, with additional support depending on the destination market and project requirements.
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