Aluminum Alloy 8011
Dingang
7606125000
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Pharmaceutical aluminum foil is used in blister lidding, cold-form Alu-Alu laminates, strip packs, tropical blister structures and other high-barrier pharmaceutical packaging. The correct material specification depends on whether the foil functions as a hard blister lid, a soft cold-forming aluminum layer, a sealing web or a component of a multilayer laminate.
The existing supply range includes AA8011, AA8021 and AA8079 with O, H14 and H18 conditions available according to application, thicknesses from 0.015 to 0.08 mm and customized widths typically from 50 to 1600 mm. Exact alloy, temper, gauge and surface requirements should be defined separately for each pharmaceutical packaging structure.
For conventional PTP blister lidding, hard-temper foil such as 8011-H18 is commonly selected together with a print primer or protective coating and a heat-seal lacquer. Cold-form Alu-Alu packaging instead requires a soft, highly formable aluminum layer, commonly 8021-O or suitable 8079-O, laminated with polymer layers such as OPA and PVC.
Pharmaceutical package qualification should consider the complete foil or laminate construction, forming web, lacquer, adhesive, printing system, pinhole limits, seal integrity, traceability and destination-market requirements rather than relying on aluminum alloy designation alone.
Request Pharmaceutical Aluminum Foil Price
| Item | Specification |
|---|---|
| Alloy | 8011 / 8021 / 8079 according to packaging structure and required mechanical properties |
| Temper | O / H14 / H18 according to application; tempers are not interchangeable between PTP lidding and cold forming |
| General Thickness Range | 0.015–0.08 mm according to the existing supply range; final gauge depends on PTP, strip, tropical or cold-form application |
| Width | Customized, typically 50–1600 mm according to the existing supply information and converting requirements |
| Surface | Bright / matte surface configuration according to rolling route, printing, lacquering or lamination requirement |
| Pinhole Requirement | Pinhole inspection method and acceptance limit should be agreed according to foil gauge and pharmaceutical package specification; no universal pinhole-free claim is applied |
| Form | Coil / jumbo roll / slit roll according to converting equipment |
| Processing Compatibility | Printing, protective coating, heat-seal lacquering, lamination, slitting and cold-form converting according to the approved foil specification |
| Typical Pharmaceutical Uses | PTP blister lidding, cold-form Alu-Alu, strip packaging, tropical blister, sachets and high-barrier pharmaceutical laminates |
| Regulatory Documentation | Required material, coating, migration, traceability, quality-system or destination-market documentation should be agreed for the exact supplied structure before production |
| Packing | Moisture-resistant export packing suitable for pharmaceutical foil coils and international transportation |
| Packaging Type | Typical Foil Selection | Key Purchasing Parameters |
|---|---|---|
| PTP Blister Lidding | 8011-H18 or other approved hard pharmaceutical foil; commonly around 20–30 μm depending on package design | Gauge, hardness, primer, printing, HSL coat weight, PVC/PVDC/PP compatibility, seal strength and pinhole limits |
| Cold-Form Alu-Alu | 8021-O or suitable 8079-O; aluminum layer commonly around 45–60 μm within an OPA/Al/PVC laminate | Elongation, forming depth, laminate structure, adhesive bond, cavity geometry, pinholes and delamination resistance |
| Strip Packaging | Soft pharmaceutical foil or foil-containing sealing structure according to the strip-pack design | Foil gauge, seal coating, printability, tear behavior, seal strength and line speed |
| Tropical Blister | High-barrier OPA/Al/HSL or equivalent approved laminate used with a thermoformed blister system | OPA gauge, aluminum gauge, HSL, forming behavior, PVC blister compatibility and sealing performance |
| Pharmaceutical Sachets / Pouches | Aluminum foil as one layer of a multilayer flexible laminate | Complete laminate construction, sealant layer, adhesive, flex durability, printing and barrier requirements |
Discuss Your Pharmaceutical Packaging Structure
AA8011 in a hard temper such as H18 is commonly used as the aluminum substrate for conventional push-through blister lidding. The foil is typically combined with a protective or printable outer layer and a heat-seal lacquer on the sealing side.
A typical lidding structure can be expressed as protective coating or primer / printing ink where required / aluminum foil / heat-seal lacquer. Exact coating chemistry and coat weight depend on the forming web and packaging-line requirements.
Hard-temper foil provides the handling and push-through characteristics expected in conventional blister lidding. O-temper cold-forming foil should not be substituted automatically for H18 lidding material.
PTP aluminum commonly uses gauges around 20, 25 or 30 μm, but final thickness should follow the approved package design, blister-machine requirements, push-through performance and customer specification.
The heat-seal lacquer must match the forming web used by the blister package, such as PVC, PVDC-coated PVC, PP or another approved material. Seal temperature, pressure, dwell time and line speed should be validated using the actual package.
Where pharmaceutical information or branding is printed on the foil, specify the primer, ink system, printing process, curing requirements and protective overcoat where required.
AA8021 in O temper is widely selected as the aluminum layer in cold-form pharmaceutical laminates where high ductility is needed to form blister cavities at room temperature.
A common cold-form laminate is OPA / aluminum / PVC. The polyamide layer supports forming and mechanical performance, the aluminum provides the primary high-barrier layer, and the PVC surface provides compatibility with downstream blister packaging processes.
Cold-form laminates commonly use an aluminum layer around 45–60 μm. Total laminate thickness is substantially greater because the OPA, PVC, adhesive and other functional layers are added separately.
Cold-form performance depends on elongation, foil gauge, rolling direction, laminate construction, forming-tool geometry and cavity depth. The material should be validated using representative production laminate rather than bare foil properties alone.
Deep forming can create high localized strain. Adhesive bond strength and aluminum ductility should be controlled so the laminate forms without unacceptable cracking, layer separation or loss of barrier integrity.
AA8079 is used in selected pharmaceutical and high-barrier foil applications. Depending on temper and converter specification, it can be supplied for hard blister foil or as a soft, formable foil component in specialized laminates.
8079 should not be selected only because a package requires a higher barrier. An intact continuous aluminum layer is itself the principal barrier; alloy selection is more closely related to required mechanical properties, forming behavior, foil gauge, rolling quality and downstream converting.
Hard 8079 foil can be evaluated for blister lidding where its mechanical and converting characteristics meet the approved foil specification.
Soft 8079 foil can also be evaluated for high-elongation laminate applications where the converter requires specific tensile strength, elongation and surface characteristics.
| Selection Factor | PTP Blister Lidding | Cold-Form Alu-Alu |
|---|---|---|
| Function | Lidding web sealed over a formed blister cavity | Forming web itself is cold formed into the drug cavity |
| Typical Foil Condition | Hard temper | Soft O temper |
| Typical Alloy | 8011-H18; other approved hard foil alloys may also be used | 8021-O or suitable 8079-O |
| Typical Aluminum Gauge | Approximately 20–30 μm depending on design | Approximately 45–60 μm aluminum layer depending on laminate design |
| Typical Structure | Primer or OP / ink where required / Al / HSL | OPA / Al / PVC or another validated cold-form laminate |
| Main Mechanical Requirement | Stable lidding, printability and designed push-through behavior | High ductility and fracture-free cavity forming |
| Seal Requirement | HSL must match PVC, PVDC, PP or other approved forming web | Cold-form laminate normally works with a separate lidding web to complete the blister package |
Choose PTP or Cold-Form Pharmaceutical Foil
Tropical blister foil is a high-barrier aluminum-containing laminate used to enhance the protection of conventional thermoformed blister packaging. It is different from cold-form Alu-Alu even though both contain an aluminum barrier layer.
A typical tropical structure can use OPA / aluminum / heat-seal coating. It is formed around an existing thermoformed blister and heat sealed to the compatible blister web, adding another barrier layer without replacing the original formed cavity.
Tropical blister can be considered when a thermoformed blister needs additional moisture, light or gas protection but the manufacturer wants to retain the basic thermoforming process and blister cavity format.
The order specification should state the actual OPA, aluminum and heat-seal layer construction rather than using an ambiguous name. Total laminate thickness, forming behavior and sealing compatibility should be confirmed for the selected blister line.
Strip packaging encloses individual tablets, capsules or other dosage forms between sealing webs without using a preformed blister cavity. Aluminum-containing structures can provide high barrier protection when properly sealed.
Strip foil is normally softer than conventional PTP lidding because the material must conform around the dosage form during sealing. Gauge, lacquer, seal strength and tear characteristics should be matched to the strip-pack equipment and medicine geometry.
The seal must provide package integrity around the dosage form without excessive material distortion. Where seal strength is contract-critical, define the sealing conditions, specimen preparation, test method and acceptance range.
Opening performance should be evaluated with the complete strip construction. Foil thickness, laminate layers and sealant chemistry can all affect consumer opening force.
An intact continuous aluminum layer is opaque and provides an extremely effective barrier against light, moisture vapor and gases. This makes aluminum valuable for medicines that require protection from environmental exposure.
The finished pharmaceutical package is not determined by the aluminum layer alone. Pinholes, forming cracks, flex damage, adhesive failure, heat-seal defects, channel leaks and damage during converting can reduce package integrity.
Moisture-sensitive formulations require a complete packaging system with an appropriately low moisture transmission rate and reliable sealing. Final shelf-life performance should be established using the finished package and drug product.
The metal layer provides a strong gas barrier when intact, but actual package performance still depends on seals, edges, forming integrity and laminate construction.
Aluminum prevents direct light transmission through the intact metal layer and can therefore be used in packaging systems for light-sensitive pharmaceutical products.
A blanket “pinhole-free” claim should not replace a measurable quality specification. Pinhole frequency depends strongly on foil gauge, rolling quality and inspection sensitivity.
For barrier-critical pharmaceutical applications, specify the inspection method, minimum detectable pinhole size, allowable count, inspected area and sampling plan.
Very thin foil is more sensitive to pinhole formation, so pinhole criteria become increasingly important as gauge is reduced.
Cold-forming foil is thicker but must also survive high strain during cavity forming. Forming trials should confirm that unacceptable cracks or barrier defects are not created during production.
PTP blister foil normally requires a heat-seal lacquer on the side that contacts the forming web. Lacquer chemistry must be matched to the actual substrate and sealing conditions.
For conventional PVC blister webs, specify a heat-seal coating validated for the actual PVC formulation and the intended temperature, pressure and dwell time.
Where PVDC-coated PVC is used to increase barrier performance, verify that the lidding lacquer provides the required seal to the coated forming web.
PP and other polymers can require different heat-seal chemistry. Container or forming-film material should therefore be stated explicitly with the inquiry.
Where heat-seal coat weight is critical, specify the nominal value and tolerance together with the sealing substrate and required seal strength.
Pharmaceutical lidding often carries product identification, dosage information, batch coding and branding. The foil surface should therefore be compatible with the selected printing and coating process.
A printable primer can be applied where the converter requires stable ink adhesion. Primer chemistry should be matched to the chosen ink and curing system.
An outer protective lacquer can be used to protect printing where required. Resistance to heat, abrasion and downstream processing should be defined for the actual packaging line.
Where converting capability allows, foil can be specified as bare, primer-coated, lacquered or otherwise prepared for customer printing. The precise supply condition should be agreed before production.
Dingang supplies pharmaceutical aluminum foil for converters and packaging manufacturers requiring controlled alloy, temper, gauge, surface condition and repeatable roll quality.
The final material should be selected against the actual packaging process, including blister lidding, printing, heat-seal lacquering, lamination, cold forming, slitting and rewinding requirements.
For repeat pharmaceutical orders, critical parameters such as alloy, temper, foil gauge, width, roll dimensions, pinhole criteria, coating structure and required batch documentation should be fixed in the agreed purchase specification.
PTP lidding and cold-form blister laminates are widely used for tablets and capsules. Selection depends on moisture sensitivity, light sensitivity, package size, dispensing method and production equipment.
Cold-form or enhanced-barrier structures can be considered for formulations requiring greater protection from water vapor than a conventional thermoformed blister provides.
Aluminum foil can be incorporated into flexible pharmaceutical laminates for powders and granules. The foil is only one layer of the package, so sealant film, adhesive, puncture resistance and compatibility with the contents should also be specified.
Soft foil structures can be used in strip packaging where paired webs seal around individual dosage forms without a separately formed blister cavity.
Confirm the ordered alloy and temper against the agreed material documentation. PTP hard foil and cold-form soft foil should not be interchanged without technical qualification.
Verify foil thickness using the agreed measurement method and tolerance. Gauge consistency affects winding, printing, sealing and forming performance.
Apply the agreed pinhole inspection method and acceptance criteria appropriate to the gauge and intended package.
Check for excessive rolling oil, particles, scratches, corrosion, stains and contamination that could interfere with coating, printing, adhesive bonding or pharmaceutical packaging cleanliness.
For foil that will be coated or laminated, surface condition should support the selected primer, lacquer or adhesive. Production trials are recommended for new chemistry or laminate constructions.
Check roll alignment, winding tension, telescoping, edge damage, core condition and other roll characteristics that can affect high-speed converting.
Before approving a new PTP or cold-form structure, test representative production material on the actual blister equipment using intended line speed, forming geometry, sealing conditions and forming film.
The finished pharmaceutical package should be qualified as a complete container-closure system. The aluminum foil is one component of that system and should be evaluated together with forming film, coating, adhesive, printing, seals and the pharmaceutical product.
The package should provide the level of moisture, oxygen, light and contamination protection required by the drug product throughout the intended shelf life and distribution environment.
Packaging components and coatings should be compatible with the pharmaceutical product and with each other under the intended manufacturing, storage and use conditions.
Blister and strip seals should be validated under representative processing and storage conditions. Heat-seal lacquer selection alone does not establish finished-package integrity.
Where pharmaceutical traceability is required, define the documentation linking supplied coils to production lots, material certificates and applicable inspection records.
Request Pharmaceutical Foil Technical Data
State PTP blister lidding, cold-form Alu-Alu, strip pack, tropical blister, sachet or another pharmaceutical packaging structure.
Provide the approved alloy and temper, such as 8011-H18 for suitable PTP applications or 8021-O / 8079-O for compatible cold-form structures.
State the aluminum layer thickness independently from primer, lacquer, adhesive, OPA, PVC or other laminate layers.
Provide finished width, core ID, maximum roll OD, roll weight, winding direction and any splice restrictions required by the converting equipment.
For PTP foil, state whether the lidding must seal to PVC, PVDC-coated PVC, PP or another forming material.
State protective coating, printable primer, printing ink, heat-seal lacquer and required coat weights where applicable.
Specify the test method, detection limit and allowable pinhole count rather than relying on a general surface-quality description.
For cold-form foil, state tensile, elongation, forming-depth or other agreed mechanical criteria. For PTP, define the required hard-temper and push-through performance where applicable.
Where heat sealing is required, provide temperature, pressure, dwell time, line speed, seal-strength target and forming-web material.
State whether foil will be supplied bare, primer-coated or printed and define ink, colors, artwork, curing and abrasion requirements where relevant.
State material certificates, batch traceability, coating documentation, migration or extractables information, quality-system documentation, inspection reports and destination-market requirements before production.
| Packing | Standard export wooden case with moisture-resistant protection according to foil gauge, coil size and shipment requirements |
| Roll Orientation | Eye-to-wall or eye-to-sky according to coil dimensions, handling method and customer requirements |
| Delivery Reference | Existing commercial reference: approximately 20–35 days; actual lead time depends on alloy, temper, gauge, width, coating, printing, quantity and production schedule |
| 20 ft Container Reference | Approximately 18–22 MT depending on roll dimensions, packing method, payload limits and transport requirements |
| 40 ft Container Reference | Approximately 20–24 MT depending on roll dimensions, packing method, payload limits and transport requirements |
For an accurate quotation, please provide the pharmaceutical packaging type, alloy and temper, aluminum gauge, width, core ID, roll OD or roll weight, forming web, laminate structure where applicable, primer or heat-seal lacquer requirement, printing requirement, pinhole acceptance criteria, forming depth or mechanical requirements, sealing conditions, quantity, required technical and regulatory documents, packing requirement and destination.
Get a Pharmaceutical Aluminum Foil Quote
Pharmaceutical aluminum foil is aluminum foil engineered for use as a lidding, forming, sealing or barrier component in blister packs, strip packs, cold-form laminates and other pharmaceutical packaging systems.
8011 in hard temper is widely used for conventional PTP blister lidding. 8021-O is widely used as a highly formable aluminum layer in cold-form Alu-Alu laminates. 8079 can be used in selected hard blister or soft laminate applications depending on temper and converter requirements.
Hard temper such as H18 is commonly used for conventional push-through blister lidding because the foil must retain stable lidding characteristics while allowing the dosage form to break through the designed lid.
O temper is commonly selected because high ductility is required when the aluminum-containing laminate is cold formed into blister cavities.
Common PTP aluminum gauges include approximately 20, 25 and 30 μm. Final gauge depends on push-through performance, converting equipment and the approved package specification.
The aluminum layer in cold-form laminates is commonly around 45–60 μm, but the finished OPA/Al/PVC laminate has a much greater total thickness.
PTP foil is normally a hard aluminum lidding web sealed over a formed blister. Alu-Alu is a soft, multilayer cold-forming web that is mechanically formed into the drug cavity itself.
A typical structure can include protective coating or printable primer, printing ink where required, aluminum foil and a heat-seal lacquer on the sealing side.
OPA / aluminum foil / PVC is a common cold-form structure. Exact polymer gauges, adhesive system and aluminum thickness depend on the approved package.
Tropical foil is an aluminum-based high-barrier laminate, commonly using an OPA/Al/HSL-type structure, that is added to enhance protection around a conventional thermoformed blister.
No. Cold-form Alu-Alu is the forming web used to create the cavity, while tropical foil is typically an additional high-barrier laminate used with a thermoformed blister structure.
Strip packaging seals dosage forms between paired webs without a preformed blister cavity. Aluminum-containing strip structures are selected according to seal strength, flexibility and required barrier performance.
Pinhole performance should be defined by an agreed inspection method and acceptance limit. Foil gauge strongly affects pinhole probability, so a measurable criterion is more appropriate than a blanket pinhole-free claim.
An intact continuous aluminum layer provides extremely high barrier performance and blocks light, but finished-package protection also depends on pinholes, forming integrity, laminate bonds and seals.
Yes, when the foil uses a heat-seal lacquer validated for the actual PVC forming web and production sealing conditions.
Yes, with an appropriate heat-seal system. The PVDC-coated forming web should be identified before lacquer selection and seal qualification.
Yes. Pharmaceutical lidding can be prepared with a suitable primer or coating for compatible printing processes. Ink, curing and protective-overcoat requirements should be approved before production.
Heat-seal lacquer can be specified where the supplied product and production capability include coating. The forming web, coat weight, sealing conditions and required seal strength should be defined.
Yes. Soft aluminum foil is widely used as a barrier layer in pharmaceutical laminates. Adhesive compatibility, surface cleanliness, wettability and forming requirements should be confirmed.
8021-O is more commonly associated with soft cold-forming applications. Do not substitute it directly for hard PTP lidding unless the complete blister structure has been technically qualified.
No. 8079 can be used in different pharmaceutical foil applications depending on temper and mechanical requirements. The packaging structure, not the alloy number alone, should determine selection.
No. Pharmaceutical packaging qualification includes the manufacturing and quality system, supplied material, coatings, traceability, package design and applicable regulatory requirements. Compliance scope should be confirmed through the relevant documentation.
Required documentation can be discussed for the exact supplied foil or laminate. Buyers should state the destination market and required regulatory, migration, quality or technical documents before production.
Typical qualification can include gauge, width, surface quality, pinholes, mechanical properties, printability, coating adhesion, seal strength, forming performance, laminate bond and package-integrity testing according to the application.
Custom width, core ID, roll OD and roll weight can be discussed within production capability. Provide the converting-machine requirements with the inquiry.
Foil rolls can be protected with moisture-resistant wrapping and suitable export wooden cases or pallets according to roll size, cleanliness and handling requirements.
The existing commercial reference is approximately 20–35 days. Actual lead time depends on alloy, temper, foil gauge, coating, printing, dimensions, quantity and production schedule.
Please provide packaging type, alloy and temper if known, foil thickness, width, core ID, roll dimensions, forming web or laminate structure, primer or heat-seal lacquer requirement, printing requirement, pinhole criteria, mechanical or forming requirements, sealing conditions, quantity, required documentation, packing requirement and destination.
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