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Cellulose-Based Superdisintegrant · CAS 74811-65-7

Croscarmellose Sodium

[C8H11NaO8]n (cross-linked) Molar mass Polymer (cross-linked carboxymethylcellulose sodium)

The cross-linked cellulose-ether superdisintegrant supplied by Chelora Chemicals — the standard rapid-swelling disintegrant behind fast-dissolving tablet and capsule formulation — exported from Indonesia in bags with full batch documentation on every shipment.

Identification Sheet REP.
Common nameCroscarmellose Sodium
CAS number74811-65-7
CompositionCross-linked carboxymethylcellulose sodium
FormWhite to greyish-white, fibrous or granular powder
AppearanceWhite to greyish-white, free-flowing powder
Common synonymsCroscarmellose Sodium, Cross-linked Sodium CMC, Ac-Di-Sol (brand)
Sodium Content6.5 – 9.5%pharmacopoeial limit
Moisture Content≤10%typical pharmacopoeial limit
Water Absorption≥23 g/gswelling capacity, grade-dependent
pH (1% aqueous dispersion)5.0 – 7.0typical range
AppearanceWhite to greyish-white powderfibrous or granular, free-flowing
Purity OfferedUSP/EP/JP compliantpharmaceutical grade
01 / PRODUCT DOSSIER

What Croscarmellose Sodium is, and why buyers source it

A working overview of the material's chemistry, its role as a rapid-swelling superdisintegrant, and the grade Chelora Chemicals keeps in regular supply.

Croscarmellose Sodium is carboxymethylcellulose sodium that has been chemically cross-linked, converting the normally water-soluble polymer into a water-insoluble but highly water-swellable network. That cross-linked, fibrous structure is what gives it its signature superdisintegrant behaviour: it does not dissolve away but instead swells rapidly and dramatically on contact with water, physically breaking apart the surrounding tablet matrix.

It is a white to greyish-white, fibrous or granular, free-flowing powder, insoluble in water but capable of absorbing many times its own weight in water with rapid swelling. It is chemically and physically stable under normal pharmaceutical storage conditions, though it should be kept dry since its performance depends on being able to absorb water rapidly on demand rather than during storage.

Where it fits in the formulation chain

Croscarmellose Sodium's primary use is as a superdisintegrant in tablet and capsule formulation, added at low levels (typically 0.5–5% w/w) either intragranularly, extragranularly, or both, to promote fast and complete tablet disintegration and drug release. It is widely used in both direct-compression and wet-granulation tablets, and is one of the most commonly specified disintegrants in fast-dissolving and immediate-release formulations.

Grade we supply

Chelora Chemicals offers Croscarmellose Sodium compliant with USP/EP/JP monographs, suitable for direct-compression and wet-granulation tablet and capsule disintegrant applications, supplied with a batch-wise certificate of analysis.

02 / MANUFACTURING ROUTE

How Croscarmellose Sodium is made

An overview of the production route for orientation purposes. Our manufacturing partners' own process parameters and in-process controls are proprietary and are not disclosed beyond what is needed to interpret the certificate of analysis.

Croscarmellose Sodium is manufactured by first preparing carboxymethylcellulose sodium from alkali-treated cellulose reacted with sodium chloroacetate, and then chemically cross-linking selected chains of that polymer, typically under controlled acidic conditions, to render the normally soluble carboxymethylcellulose insoluble while retaining its strong water-absorbing character. The cross-linked product is then purified, dried and milled to the required particle-size grade.

Why controlled cross-linking is the defining step

Cross-linking is what converts an ordinary water-soluble cellulose ether into an insoluble, rapidly swelling superdisintegrant, and controlling the degree of cross-linking precisely is what gives croscarmellose sodium its characteristic fast, high-capacity water uptake, which is why this step, rather than the base carboxymethylcellulose synthesis, defines the finished excipient's performance.

03 / APPLICATIONS

Industries and processes that use it

Croscarmellose Sodium is consumed almost entirely in tablet and capsule disintegrant applications, where its rapid, high-capacity swelling is the main draw. The fields below account for most of the demand we see through our export desk.

Field 01

Tablet Superdisintegrant

Added intragranularly, extragranularly, or both, at low levels to promote fast, complete tablet disintegration and drug release on contact with gastrointestinal fluid.

Field 02

Fast-Dissolving & Orally Disintegrating Tablets

A commonly specified disintegrant in fast-dissolving and orally disintegrating tablet (ODT) formulations, where very rapid disintegration is a key performance requirement.

Field 03

Hard Capsule Disintegration

Used in hard-capsule formulations to promote rapid breakup of the powder or granule fill once the capsule shell dissolves.

Field 04

Wet-Granulation Formulations

Used intragranularly in wet-granulation tablet formulations to maintain fast disintegration despite the densifying effect of granulation.

04 / REACTION CHEMISTRY

How the molecule is typically carried forward

The insoluble, cross-linked fibrous network governs almost all of this material's functional behaviour as a disintegrant. The mechanisms below account for most of how Croscarmellose Sodium performs its disintegration role.

Cross-Linking (Upstream)

Carboxymethylcellulose sodium chains are chemically cross-linked to form the insoluble, water-swellable network that defines croscarmellose sodium.

Rapid Water Wicking (Capillary Action)

On contact with aqueous fluid, the fibrous particle structure wicks water into the tablet matrix rapidly by capillary action, the first step in disintegration.

Swelling (Volume Expansion)

The cross-linked network absorbs many times its own weight in water and swells dramatically in volume without dissolving, generating the mechanical force that breaks the tablet apart.

Tablet Matrix Rupture

The swelling force exceeds the binding strength holding the tablet together, rupturing the compact and releasing the active ingredient for dissolution.

05 / RELATED BUILDING BLOCKS

Croscarmellose Sodium against other amines we supply

Buyers sourcing Croscarmellose Sodium for tablet or capsule disintegrant applications often need a related tableting excipient. A quick reference to what else is on our regular supply list.

ProductCAS NumberCategoryNotes
Croscarmellose Sodium74811-65-7Cellulose-based superdisintegrantThe product on this page — the standard rapid-swelling tablet disintegrant.
Sodium Starch Glycolate9063-38-1Starch-based superdisintegrantThe related starch-based superdisintegrant often compared in formulation development — see its product page.
Microcrystalline Cellulose9004-34-6Purified crystalline celluloseThe standard diluent commonly formulated alongside croscarmellose sodium — see its product page.
Povidone (PVP K30)9003-39-8Synthetic vinyl polymer binderA related tablet-formulation excipient commonly used alongside croscarmellose sodium — see its product page.

Exact physical constants and purity specifications are confirmed per batch on the certificate of analysis — treat the notes above as a sourcing guide, not a specification sheet, for products other than Croscarmellose Sodium.

06 / HAZARD & HANDLING

Safety classification at a glance

Based on GHS classification as commonly listed for this substance. This is a summary for orientation only — always work from the current safety data sheet supplied with your specific batch.

Not Classified

Not classified as hazardous under GHS; a long-established, widely used pharmaceutical excipient.

Dust Precaution

Fine powder may cause transient mechanical irritation to eyes or respiratory tract; handle with standard dust control.

Low Acute Hazard

No significant acute toxicity hazard under normal pharmaceutical handling.

Swelling Note

Absorbs water rapidly; avoid unintended contact with moisture during handling and storage to preserve performance.

PPE Standard

Standard dust mask and gloves are sufficient for routine handling in a pharmaceutical manufacturing environment.

Storage Precaution

Keep dry and sealed; premature moisture exposure can impair swelling performance when used in a formulation.

Hygiene Precaution

Follow standard pharmaceutical good manufacturing practice (GMP) for handling and cross-contamination control.

Signal word

Not Classified — no GHS hazard pictogram applies to this excipient.

This material is not classified as hazardous under GHS and presents no significant acute toxicity hazard under normal pharmaceutical handling, though fine powder may cause transient mechanical irritation to eyes or the respiratory tract and should be handled with standard dust control. Because its function depends on absorbing water rapidly on demand, unintended moisture exposure during storage should be avoided to preserve its disintegrant performance. Full handling and storage guidance is in the MSDS issued with every shipment, and standard pharmaceutical GMP practice should be followed.

07 / STORAGE & SHELF LIFE

Keeping it on spec between delivery and use

General storage guidance for this grade. Site-specific storage rules, segregation requirements and re-test intervals should follow your own EHS procedures and the MSDS issued with your batch.

Storage ConditionCool, dry, tightly sealed
ContainerMoisture-barrier bags
Typical Shelf Life36 – 60 months, sealed
Keep Away FromMoisture, humid storage conditions
Beyond Shelf LifeRe-check swelling capacity & moisture before use

Store in a cool, dry area in tightly sealed, moisture-barrier packaging, away from humid storage conditions, since premature water exposure can impair the material's swelling performance when later used in a formulation. Prompt resealing of opened containers is essential. If a batch is held past its retest date, re-check water-absorption capacity and moisture content before use.

08 / PACKING & EXPORT

How it ships from Indonesia

Standard packing and export terms for this product. Confirm exact figures against your order — they vary slightly by destination and quantity.

Standard Packing25 kg moisture-barrier bags
Bulk PackingNot typically supplied in bulk
Min. OrderFrom 250 kg
Lead Time2 – 4 weeks
Export TermsFOB · CFR · CIF
09 / QUALITY & DOCUMENTATION

What travels with every batch

Specification is agreed before the purchase order, not discovered on arrival. Every shipment of Croscarmellose Sodium leaves with a documented, checkable paper trail.

Doc 01

Certificate of Analysis

Batch-wise assay (by titration/GC), colour and relevant physical constants, issued against the agreed specification so your QC team can check it, not just file it.

Doc 02

Safety Data Sheet

GHS-format SDS in English covering hazard classification, handling, storage, first-aid and spill response for the exact grade of Croscarmellose Sodium shipped.

Doc 03

Technical Data Sheet

Reference physical and chemical properties, recommended storage and typical applications, for internal circulation to your process or R&D teams.

Doc 04

Certificate of Origin

Confirms Indonesian origin for customs clearance and any preferential-duty claim at your destination port.

Doc 05

Dangerous Goods Declaration

UN packing group, classification and shipper's declaration prepared ahead of loading so documentation never holds up customs.

Doc 06

Third-Party Inspection

Independent pre-shipment inspection and re-sampling can be arranged on request, at your cost, for buyers who require it as a matter of policy.

10 / FAQ

Frequently asked questions

What buyers most often ask our sales desk about this grade.

01What is Croscarmellose Sodium used for?+
As a superdisintegrant in tablet and capsule formulation, promoting fast, complete disintegration and drug release, including in fast-dissolving and orally disintegrating tablet (ODT) formulations.
02What is the CAS number of Croscarmellose Sodium?+
Croscarmellose Sodium is referenced under CAS number 74811-65-7, as a cross-linked cellulose derivative rather than a single discrete molecular formula.
03How is Croscarmellose Sodium made?+
By chemically cross-linking carboxymethylcellulose sodium under controlled acidic conditions, converting the normally soluble polymer into an insoluble, rapidly swelling network.
04What grade does Chelora Chemicals supply?+
We supply Croscarmellose Sodium compliant with USP/EP/JP monographs, suitable for direct-compression and wet-granulation disintegrant applications, supplied with a certificate of analysis.
05How does Croscarmellose Sodium work as a disintegrant?+
Its cross-linked fibrous structure wicks water into the tablet rapidly by capillary action and then swells dramatically in volume without dissolving, generating a mechanical force that ruptures the tablet matrix and releases the drug for dissolution.
06Is Croscarmellose Sodium hazardous?+
No, it is not classified as hazardous under GHS and presents no significant acute toxicity hazard under normal pharmaceutical handling, though standard dust control and dry storage are recommended per the MSDS.
07What packing options are available?+
Standard packing is 25 kg moisture-barrier bags; this material is not typically supplied in bulk given its moisture sensitivity.
08How long does delivery take?+
Typical lead time is two to four weeks plus transit, depending on quantity. A firm date is confirmed in the written quotation.
09Can I get a sample before placing a bulk order?+
Yes, small sample quantities of Croscarmellose Sodium can generally be arranged for formulation trials — contact our desk with your application for a sample quote.
10Do you supply Sodium Starch Glycolate as well?+
Yes, we also supply Sodium Starch Glycolate, the related starch-based superdisintegrant, along with Microcrystalline Cellulose and Povidone.
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