Ichthammol API
Suitable for buyers evaluating ichthammol for external-use pharmaceutical and topical formulation projects, with sourcing review typically focused on identity, specification basis, handling characteristics, packaging format, and destination-market compliance requirements.
- Ichthammol external-use pharmaceutical ingredient for regulated B2B sourcing projects
- Suitable for topical-system and external-use formulation review
- Sample, COA, SDS/MSDS, and specification support available
- Bulk packing and export coordination for qualified pharmaceutical supply
Tell us your application, target specification, and destination market so we can support grade selection, documentation review, and packaging recommendations.
Quick Specs
Identity
Alias
CAS Number
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
Ichthammol, also referred to as ammonium bituminosulfonate, is an external-use pharmaceutical ingredient commonly reviewed for topical and dermatology-related formulation projects.
It is usually supplied as a dark brown to black viscous liquid or semi-solid under agreed external-use pharmaceutical specification, and buyers often review identity standard, handling behavior, document scope, packaging format, and destination-market requirements before technical or commercial evaluation.
It is commonly considered for qualified topical pharmaceutical development review, compounding discussion, and export-oriented B2B ingredient supply, with sample support and batch documentation available for sourcing reference.
Applications
Topical Pharmaceutical Development Review
Reviewed for external-use pharmaceutical projects where buyers need ichthammol identity confirmation, specification alignment, and batch-document support for internal evaluation.
Compounding and External-Use Formulation Discussion
Can be considered for ointment, salve, and other topical-system discussions where ingredient identity, handling behavior, and document scope are part of the formulation review process.
Regulated B2B Sourcing
Also discussed for destination-market projects that require defined product identity, technical-document alignment, and export-ready bulk handling for external-use ingredient supply.
How to Choose the Right Grade / Form
For specification review
Confirm whether the project should follow USP, BP, Ph.Eur, or another agreed technical basis before supplier comparison.
For topical-system development
Check not only identity basis, but also handling characteristics, packaging plan, and technical-document fit for the intended system.
For market-specific supply
Confirm the required document pack, labeling format, and compliance expectations before quotation and shipment planning.
Before ordering, confirm
Target application; topical-system direction; specification basis; required test items; destination market; document pack.
Technical & Formulation Notes
Technical Notes
Technical review should focus on product identity, specification basis, handling consistency, packaging integrity, and documentation scope rather than consumer-facing use claims.
Before evaluation, buyers are advised to confirm target market, intended topical dosage form, required test items, and compliance-document needs before quotation or scale-up.
Manufacturing & Process
Commercial supply typically involves controlled external-use pharmaceutical ingredient production with in-process QC and batch release against the agreed specification basis.
Final release is usually linked to agreed items such as appearance, identity basis, packaging integrity, and document consistency.
Compatibility / Formulation Notes
Ichthammol should be evaluated within the intended external-use or topical pharmaceutical project scope rather than as a general wellness or consumer ingredient.
Buyers usually confirm identity standard, handling characteristics, packaging format, and documentation scope during technical and commercial review.
Final suitability should be confirmed according to the actual dosage form, process route, destination market, and internal compliance requirements.
Extended QC & Test Items
- Appearance
- Identity basis / specification alignment
- Viscosity or handling-related control, if required
- Sulfur or characteristic quality items according to agreed specification
- Packaging integrity
- Batch traceability linked to COA
Product specifications
| Test | Specification | Method |
|---|---|---|
| Appearance | Dark brown to black viscous liquid or semi-solid / per spec | Visual |
| Identification | Ichthammol / Ammonium Bituminosulfonate | Per agreed specification |
| Quality basis | Per agreed external-use pharmaceutical specification | Per spec |
| CAS No. | 8029-68-3 | Reference |
| Molecular Formula | Variable / complex mixture; refer to spec | Reference |
| Molecular Weight | Variable / complex mixture; refer to spec | Reference |
| Documents | COA per batch; SDS/MSDS and TDS/specification sheet on request | Reference |
Storage, Shelf Life & Packaging
Storage
Store in a cool, dry place in a tightly closed container away from moisture, direct heat, and strong light.
Packaging integrity and storage compliance should be maintained during warehousing and transportation to preserve handling consistency.
Shelf Life
Shelf life should be confirmed according to the specific batch, agreed specification, and original packaging condition.
Please refer to the COA, product label, or specification sheet for the declared shelf-life period of the supplied lot.
Packaging & Logistics
Sample Packing
Small evaluation packs can be arranged for technical and quality review.
Mid-Size Packing
5 kg or 10 kg packing may be arranged according to project and order planning.
Bulk Packing
Normally 25 kg/drum according to order volume, specification basis, and shipment arrangement.
Customization
Custom packaging, labeling, and shipping-mark discussion can be arranged according to destination-market and external-use formulation requirements.
Logistics & Documents
Packing configuration and document pack should be aligned before shipment to support handling, storage, and destination-market review.
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-led sourcing communication
Support for buyers who need ichthammol sourcing aligned with product identity, technical documentation, and destination-market review.
External-use formulation positioning
The product page and sourcing discussion should stay centered on external-use and topical pharmaceutical needs rather than general consumer-health claims.
Batch documentation support
COA per lot with SDS/MSDS and TDS available for technical, quality, and purchasing review.
Export-ready bulk handling
Packaging, labeling, and shipment coordination can be arranged for international external-use pharmaceutical ingredient sourcing projects.
FAQ
1) What is ichthammol?
Ichthammol is an external-use pharmaceutical ingredient also referred to as ammonium bituminosulfonate or ammonium bituminosulphonate.
2) Is this ingredient intended for external use?
Yes. It is generally discussed for topical or external-use pharmaceutical and compounding-related projects rather than internal-use product concepts.
3) Can it be considered for ointment or salve projects?
Yes. It is commonly reviewed for external-use topical systems such as ointment, salve, and related formulation directions, subject to internal formulation evaluation.
4) What documents are available?
COA per batch / lot is available. SDS/MSDS and TDS/specification sheet can be provided on request.
5) Is sample evaluation available?
Yes. Small sample packing can usually be arranged for qualified technical review and sourcing evaluation.
6) What should buyers confirm before ordering?
Please confirm target market, intended topical dosage form, specification basis, packaging requirement, and document scope before scale-up.
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