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Cros Carmellose Sodium

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Cros Carmellose Sodium Specification

Place of Origin
India

Moisture (%)
10%

Assay
97.0% 102.0%

Ph Level
5.0 7.0 (1% solution)

Loss on Drying
10%

Residue on Ignition
14.0%

Heavy Metal (%)
0.002%

Storage
Store in tightly closed container, in a cool and dry place

HS Code
39123100

Particle Size
90% passes through 100 mesh

Molecular Weight
Approximately 990,000 Da

Viscosity
1040 mPas (1% solution)

Other Names
Croscarmellose Sodium

Type
Pharmaceutical Excipient

Grade
Pharmaceutical Grade

Usage
Disintegrant in Tablet Formulations

Purity
>99%

Application
Tablet disintegrant, pharmaceuticals

Raw Material
Cellulose

Smell
Odorless or Practically Odorless

Color
White

Form
Powder

Cros Carmellose Sodium Trade Information

Payment Terms
Letter of Credit at Sight (Sight L/C), Telegraphic Transfer (T/T)

Supply Ability
5 Ton Per Month

Delivery Time
3 Week

Sample Available
Yes

Sample Policy
Within a certain price range free samples are available

Packaging Details
Fiber drum ,Plastic, Carboys & Barrels.

Main Export Market(s)
Australia, North America, South America, Eastern Europe, Western Europe, Middle East, Africa, Central America, Asia

About Cros Carmellose Sodium

The goodness, we have gained in the market is due to the Cros Carmellose Sodium that is a cross linked polymer of carboxymethyl cellulose sodium and is wide in demand for its excellent drug dissolution and disintegration characteristics. The offered sodium is a vital source to improve bio availability of formulation. It is processed using top-notch quality basic chemicals under the direction of sourced pharmacists at vendors' end. Furthermore, proposed sodium is also checked on defined quality parameters to ensure its purity and effectiveness. Available in several packaging options to meet exact needs of clients, this Cros Carmellose Sodium can be availed from us at market leading prices.

Features:Deta

Purity
Precise composition
Precise pH value
Longer shelf life

Application:

It is used in oral pharmaceutical formulations as a disintegrant for Capsules, Tablets and Granules.
In tablet formulations, it may be used in both direct-compression and wet granulation processes.
When used in wet granulations, the cros carmellose sodium is best added in both the wet and dry stages of the process (intra- and extra granularly) so that the wicking and swelling ability of the disintegrant is best utilized.

Concentrations of up to 5% w/w of cros carmellose sodium may be used as a tablet disintegrant although normally 2% w/w is used in tablets prepared by direct compression and 3% w/w in tablets prepared by a wet-granulation process.