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Powder Talc

Fine mineral powder for pharmaceutical processing and industrial formulations

Powder Talc is a finely divided, naturally occurring hydrated magnesium silicate. It has a smooth, unctuous feel and is practically insoluble in water. In pharmaceutical manufacturing, appropriately qualified talc is used as a glidant, lubricant, diluent and anti-adherent, depending on the formulation.

CAS
14807-96-6
Material
Hydrated magnesium silicate
Form
Fine white powder
White talcum powder on a dark surface
Fine talc powder. Product illustration.
Product overview

Understanding the material

Talc is a mineral material rather than a single synthetic chemical of fixed purity. Its source, associated minerals, particle distribution and processing influence suitability. Pharmaceutical enquiries should identify the required grade and include mineral-purity and asbestos-test documentation; an industrial talc description is not sufficient for pharmaceutical qualification.

Identity & properties

Product Identity & Specifications

Chemical identity, physical characteristics and key specifications for Powder Talc.

ParameterDescription / valueBasis / application
Material identityNatural hydrated magnesium silicateSelected and milled mineral
CAS number14807-96-6Talc
Ideal mineral formulaMg₃Si₄O₁₀(OH)₂Natural associated minerals may vary
AppearanceWhite or almost white fine powderGeneral pharmaceutical description
TextureSmooth / unctuousPlate-like mineral particles
Water solubilityPractically insolubleDisperses as particles rather than dissolving
Main pharmaceutical functionsGlidant, lubricant and diluentAdditional anti-adherent use depends on formulation
Particle sizeGrade-specific distributionState the method, micron limits or sieve requirement
Bulk characteristicsBulk / tapped density as requiredRelevant to dispensing and powder processing
Asbestos requirementNo detectable asbestos for pharmaceutical-grade talcReview the method and test documentation
Mineral and chemical purityAssociated minerals, soluble matter and relevant elementsAssess against the intended standard
Microbiological qualityApplication-specific limitsImportant for a material of natural origin

Identity and published standard

USP–NF: Talc

The published definition describes selected, powdered, natural hydrated magnesium silicate. Talc containing detectable asbestos is not pharmaceutical grade. Particle size, mineral purity and the applicable test evidence form part of grade selection.

View published monograph

A published standard describes the material; conformity of the offered grade is confirmed through its current specification and COA.

For further information and current COA/specification, please contact us.

Request current COA & specification
Where it is used

Applications & functional benefits

01

Tablets and capsules

Used in suitable powder formulations to assist flow or lubrication. Grade and quantity must be evaluated together with the other ingredients and manufacturing process.

02

Tablet and pellet coating

Selected talc grades can act as anti-adherents in coating systems. Particle distribution and dispersion quality matter when preparing a uniform coating suspension.

03

Industrial mineral filler

Industrial formulations may select talc for its mineral and physical characteristics. The required fineness, colour and compatibility differ from pharmaceutical purchasing requirements.

Choose the right material

Choosing the appropriate talc grade

Selection pointPharmaceutical requirementIndustrial requirement
Quality basisRelevant pharmacopoeia and qualified supplier documentationEnd-use specification for the formulation
Particle sizeDistribution suited to dosage-form processingFineness and physical performance suited to the application
Mineral purityDocumented identity and applicable asbestos / impurity controlsPurity and composition appropriate to the end use
Microbial qualityLimits matched to the intended pharmaceutical applicationRequirements specified for the particular product
Manufacturing considerations

Formulation & processing

Specify distribution, not only mesh

A mesh number describes a sieve designation; it does not fully characterise the powder. Where performance is sensitive, request the test method and a particle-size distribution or agreed sieve-residue limits.

Assess dispersion and process performance

For a coating or liquid dispersion, assess wetting and suspension uniformity. For a dry blend, assess flow and lubrication in the complete formula rather than inferring performance from appearance alone.

Review the mineral source

Combine the mineral identity, impurity controls and applicable asbestos-test report in supplier qualification. The absence of visible fibres or a white colour is not evidence of pharmaceutical-grade suitability.

Quality review

What to check in the specification

  • Mineral identity and associated minerals: confirm the required talc grade.
  • Asbestos absence: request documented results using the applicable analytical method.
  • Particle-size distribution and bulk density: specify test method and units.
  • Relevant elemental impurities and soluble matter: assess against the applicable specification.
  • Microbial quality: review the requirements and treatment history relevant to pharmaceutical use.

Current product documentation

Request a current COA, complete specification, SDS, particle-size data and applicable asbestos-test documentation. State clearly whether the enquiry is for pharmaceutical or industrial use.

Request documents for Powder Talc
Supply & handling

Packing, storage & handling

Packing and quotation details

Specify the required bag size, moisture protection and quantity for the quotation. The offered grade, manufacturer, packing and sample arrangement will be confirmed. For evaluation, request enough material to check dispersion or powder-flow behaviour in the intended process.

Storage and safe handling

Keep in well-closed containers in a dry, clean area. Minimise airborne dust during weighing, bag opening and transfer; use the extraction and personal-protection measures specified in the SDS. Protect pharmaceutical material from cross-contamination and verify package integrity on receipt.

Product questions

Frequently asked questions

Does talc dissolve in water?

No. Talc is practically insoluble in water. A mixture containing talc is a dispersion or suspension, which requires suitable handling to keep particles distributed.

Can industrial talc replace pharmaceutical talc?

The grades should not be treated as interchangeable. Pharmaceutical use requires the relevant quality specification and supporting qualification evidence.

Is “asbestos-free” wording enough?

Request the applicable analytical method and documentation. A statement alone does not provide the same information as a traceable test report.

Technical information sources

Need more information?

Contact SBS for further product details, current COA, specification, packing and a quotation for your requirement.

Contact SBS for details and documents