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MCC SANAQ® 200

CAS Number
9004-34-6
EC Number
232-674-9
Chemical Name
Cellulose, Microcrystalline, Cellulose Microcrystalline

Microcrystalline Cellulose is purified, partially depolymerized cellulose prepared by treating alpha cellulose, obtained as a pulp from fibrous plant material, with mineral acids

Properties

Physical Form
  • Powder
  • Solid
Pharma and Nutraceuticals Functions
  • Anti-Caking Agent
  • Binder
  • Bulking Agent
  • Diluent
  • Filler
  • Stabilizer
  • Texturizing Agent
  • Thickener

Product families

Applications

Healthcare & Pharma — Drug Delivery & Care Solutions
  • Oral

Product Families

Pharmaceuticals & Nutraceuticals — Excipients
  • Binders & Disintegrants
  • Carriers & Bulking Agents
  • Emulsifiers & Stabilizers
  • Fillers & Diluents
  • Formulation & Processing Aids
  • Other Excipients

Other characteristics

Brand
MCC SANAQ
Synonyms

Crystalline cellulose, Micro Fibril Cellulose, Pyrocellulose

Functions

Anti-Caking Agent, Binder, Bulking Agent, Diluent, Filler, Stabilizer, Texturizing Agent, Thickener, Viscosity Modifier

Dosage Form
  • Capsules, Tablets
  • Capsules
  • Tablets
Certifications & Compliance

European Pharmacopeia (Ph. Eur.), National Formulary (NF), United States Pharmacopeia (USP)

Odor
odourless
Grade
Pharma Grade
Markets
Healthcare & Pharma
Appearance
White to almost white, fine or granular powder
Technology
Pharmaceuticals & Nutraceuticals
HIGHLIGHTS

MCC SANAQ® is pure microcrystalline cellulose, which chemical and physical identities meet the international standards (Pharm Eur., USP/NF, JP, Kosher).; MCC SANAQ® has excellent compressibility. The outstanding plasticity enables to produce tablets with high temper and ultimate strength. At the same time the tablets have very short disintegration times. Its good flowing properties guarantee high production rates. High microbial purity, color stability and excellent absorption properties of MCC SANAQ® lead to success in all tableting processes.; MCC SANAQ® is a nonreactive substance with homogenous particle size. This makes it ideal as filter Material in separation technology to guarantee results of high quality.

Chemical Inventories
EINECS (EU)
Manufacturing Technology
  • Direct Compression
  • Wet Granulation
Certifications and Compliance
  • European Pharmacopeia (Ph. Eur.)
  • National Formulary (NF)
  • United States Pharmacopeia (USP)

Technical data

Table 1 of 3

8 rows
CharacteristicValueUnitMethod
Residue on Ignition1.8 - 2.2—USP-NF
Bulk Density0.29 - 0.36g/cm3USP-NF
Loss on Dryingmax. 70%USP-NF/Ph. Eur.
pH Value5.0 - 7.5—USP-NF
Conductivity75μ SUSP-NF
Sulphate Ash /Residue on Ignition0.1%USP-NF/Ph. Eur.
Water Soluble Substances0.25%USP-NF/Ph. Eur.
Ether Soluble Substances0.05%USP-NF/Ph. Eur.

Table 2 of 3

4 rows
CharacteristicValueUnitMethod
Total Aerobic Countmax. 1000CFU/gUSP-NF / Ph. Eur.
Moulds and Yeastsmax. 100CFU/gUSP-NF / Ph. Eur.
E. Coli, Pseudomonas AeruginosaNegative in 10 g sample—USP-NF / Ph. Eur.
St. Aureus, Salmonella SpeciesNegative in 10 g sample—USP-NF / Ph. Eur.

Table 3 of 3

1 row
CharacteristicValueUnitMethod
Particle Size120 - 170μmMalvem Method

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