PRODUCTS / CELLULOSE / PH 101
MICROCRYSTALLINE CELLULOSE

PH 101

Pharmaceutical Grade High Compactibility Direct Compression

High-purity microcrystalline cellulose designed for pharmaceutical formulations where compactibility, binding performance and tablet mechanical strength are essential.

Microcrystalline Cellulose PH 101
PRODUCT PH 101
01 PHARMACEUTICAL GRADE
02 EXCELLENT COMPACTIBILITY
03 EFFECTIVE BINDING
04 DIRECT COMPRESSION
01 / PRODUCT OVERVIEW

Precision cellulose
for stronger formulations.

PH
101

Microcrystalline Cellulose PH 101 is a high-purity pharmaceutical-grade excipient derived from purified cellulose.

It is widely used in solid oral dosage formulations as a multifunctional diluent and binder, particularly where good compactibility and tablet mechanical strength are required.

PH 101 is characterized by a relatively fine particle-size distribution and excellent compactibility. Its particle structure provides a high surface area for interparticle contact during compression, supporting effective particle bonding and the formation of strong, coherent tablets.

PH 101 is particularly suitable for direct-compression formulations and can also be used in other tablet manufacturing processes depending on the overall formulation design.

02 / KEY CHARACTERISTICS

Engineered for
performance.

01

Fine Particle
Distribution

Relatively fine particles provide substantial surface area and particle-to-particle contact.

02

Excellent
Compactibility

Supports strong interparticle bonding during compression and tablet formation.

03

Effective
Binding

Contributes to tablet strength, structural integrity and resistance to mechanical stress.

04

Stable
Performance

White, odorless and chemically stable powder suitable for solid oral dosage formulations.

03 / FUNCTIONAL PROPERTIES

One excipient.
Multiple functions.

01
COMPACTIBILITY

Excellent Compactibility

PH 101 exhibits excellent compactibility under compression. The relatively fine particles provide substantial contact between particles, facilitating the formation of strong interparticle bonds.

02
BINDING

Effective Binding Function

Microcrystalline Cellulose PH 101 provides effective binding functionality and can contribute significantly to tablet strength and integrity.

03
DILUENT / FILLER

Formulation Flexibility

PH 101 can be used as a pharmaceutical diluent or filler to provide bulk and improve the physical structure of solid dosage formulations.

04
COMPRESSION

Reliable Compression Performance

The relatively fine particle size and favorable deformation characteristics support efficient compaction during tablet compression.

04 / PHARMACEUTICAL APPLICATIONS

Built for
solid dosage forms.

PH 101 can be incorporated into a variety of pharmaceutical formulations where compactibility, binding and mechanical integrity are important.

01 Immediate-Release Tablets
02 Direct-Compression Tablets
03 Conventional Compressed Tablets
04 Chewable Tablets
05 Capsule Formulations
06 Solid Oral Dosage Forms
05 / DIRECT COMPRESSION

Strong bonds.
Reliable tablets.

PH 101 is particularly suitable for direct-compression applications where good compactibility and binding performance are required.

During compression, the particles form strong interparticle bonds, helping produce tablets with good mechanical integrity.

FORMULATION NOTE

The suitability of PH 101 for a specific formulation depends on the API characteristics, excipient combination, compression force, tooling and manufacturing process.

06 / PARTICLE SIZE

Surface area
matters.

The relatively fine particle-size distribution of PH 101 contributes to its high surface area and favorable particle-to-particle contact during compression.

+ Strong particle bonding
+ Effective compaction
+ Good mechanical strength
+ Consistent tablet formation
07 / TABLET PERFORMANCE

Designed around
tablet integrity.

01 TABLET
HARDNESS
02 MECHANICAL
INTEGRITY
03 MECHANICAL
STRESS RESISTANCE
04 CONSISTENT
FORMATION

Final tablet hardness, friability, disintegration and dissolution are formulation-dependent properties and should be established through appropriate development and testing.

08 / FORMULATION CONSIDERATIONS

When PH 101
makes sense.

01

High compactibility

02

Effective binding

03

Strong tablet structure

04

Fine-particle MCC characteristics

05

Reliable compression behavior

06

Good mechanical integrity

09 / QUALITY & REGULATORY

Quality built
into every specification.

For pharmaceutical applications, Microcrystalline Cellulose PH 101 should comply with the applicable pharmaceutical specification and relevant pharmacopoeial or customer requirements.

Identification
Cellulose Content / Assay
Loss on Drying
Residue on Ignition
pH
Water-Soluble Substances
Ether-Soluble Substances
Elemental Impurities
Microbial Quality
Particle-Size Distribution
Bulk Density
Customer-Specific Requirements
The final product specification should be established according to the applicable pharmacopoeial requirements and the manufacturer's approved technical specification.
10 / STORAGE & HANDLING

Protect the
material integrity.

Store in tightly closed packaging in a clean, dry and well-ventilated environment.

Clean environment Dry conditions Controlled handling Protected from contamination Protected from direct sunlight

Specific storage conditions, shelf life and packaging requirements should be defined according to the approved product specification and technical documentation.