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Cros Carmellose Sodium

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Cros Carmellose Sodium Specification

Heavy Metal (%)
0.002%

Particle Size
90% passes through 100 mesh

Residue on Ignition
14.0%

Viscosity
1040 mPas (1% solution)

Loss on Drying
10%

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

Assay
97.0% 102.0%

Moisture (%)
10%

Molecular Weight
Approximately 990,000 Da

Place of Origin
India

HS Code
39123100

Ph Level
5.0 7.0 (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.

Exceptional Disintegrant Performance

Cros Carmellose Sodium is specifically designed to improve the disintegration of tablets in pharmaceuticals. Its optimized particle size and high purity enable rapid tablet breakup, facilitating faster drug release and absorption. This performance is crucial in modern formulations to ensure that therapeutic compounds act quickly and efficiently after administration.

Quality and Compliance

Manufactured and exported from India, Cros Carmellose Sodium adheres to stringent pharmaceutical grade requirements. Its purity exceeds 99%, with a controlled moisture level and minimal heavy metal content, ensuring product safety and reliability in pharmaceutical manufacturing. Its compliance with global standards makes it a preferred choice for formulators worldwide.

FAQs of Cros Carmellose Sodium:

Q: How is Cros Carmellose Sodium used in tablet manufacturing?

A: Cros Carmellose Sodium acts as a disintegrant in tablet formulations by promoting rapid breakup of the tablet upon exposure to moisture. It is blended with other ingredients during the granulation or direct compression process to ensure efficient disintegration after oral administration.

Q: What benefits does Cros Carmellose Sodium offer in pharmaceutical applications?

A: As a highly pure disintegrant, Cros Carmellose Sodium accelerates tablet dissolution, resulting in faster drug release and improved bioavailability. Its consistent quality and performance make it essential for achieving reliable therapeutic effects.

Q: When should Cros Carmellose Sodium be incorporated into a formulation?

A: It should be added during the tablet formulation stage, typically in the blending process with active pharmaceutical ingredients and other excipients, to ensure optimal disintegration after ingestion.

Q: Where is Cros Carmellose Sodium sourced from?

A: This product is manufactured and exported from India, and it complies with international pharmaceutical standards for quality and safety.

Q: What is the recommended storage condition for Cros Carmellose Sodium?

A: It should be stored in a tightly closed container, in a cool and dry place, to maintain its quality and prevent moisture absorption or contamination.

Q: What are the quality specifications that Cros Carmellose Sodium meets?

A: Cros Carmellose Sodium features an assay of 97.0% 102.0%, particle size with 90% passing through a 100-mesh sieve, moisture content 10%, residue on ignition 14.0%, and heavy metals 0.002%, ensuring adherence to pharmaceutical standards.

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