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Guaifenesin IP USP export quality API

Guaifenesin IP USP export quality API

Product Details:

  • Properties White or almost white crystalline powder, odorless or almost odorless, stable under recommended storage conditions
  • Ph Level 5.0 - 7.0 (in 5% aqueous solution)
  • Product Type Active Pharmaceutical Ingredient (API)
  • Melting Point 78C - 82C
  • Grade IP/USP Export Quality
  • Application Pharmaceutical formulation, Expectorant
  • Smell Odorless or almost odorless
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Guaifenesin IP USP export quality API Price And Quantity

  • 100 Kilograms

Guaifenesin IP USP export quality API Product Specifications

  • Not less than 99.0%
  • 202-222-5
  • Crystalline
  • 29420090
  • Slightly bitter
  • 36 months from manufacturing date if properly stored
  • 1.25 Gram per cubic centimeter(g/cm3)
  • C10H14O4
  • Not applicable for solid API
  • C10H14O4
  • 93-14-1
  • Guaifenesin
  • Soluble in water, freely soluble in alcohol
  • Store in a tightly closed container, protected from light and moisture at room temperature
  • Active Pharmaceutical Ingredient (API)
  • White or almost white crystalline powder, odorless or almost odorless, stable under recommended storage conditions
  • 5.0 - 7.0 (in 5% aqueous solution)
  • Non-poisonous
  • Powder
  • 198.22 g/mol
  • Odorless or almost odorless
  • Used in the formulation of cough syrups and expectorants
  • White crystalline powder
  • Pharmaceutical formulation, Expectorant
  • 78C - 82C
  • IP/USP Export Quality
  • As per customer specification or typically 90% passes through 80 mesh
  • Not more than 0.1%
  • Packaged in HDPE drums with double polyethylene bags, 25kg or as per customer requirement
  • Not more than 0.025%
  • Not more than 0.5%
  • Decomposes before boiling
  • Not more than 20 ppm
  • Not more than 0.014%
  • Complies with pharmacopeial standards
  • Total impurities not more than 0.5%

Guaifenesin IP USP export quality API Trade Information

  • 1000 Kilograms Per Month
  • 7 Days

Product Description



Capitalise on the unassailable quality of our Guaifenesin IP/USP export-grade API, designed for top-tier pharmaceutical formulations. Unlock astounding purity-at least 99%-with minimal impurities and microbial limits that comply with pharmacopeial benchmarks. Get reliable performance from this white crystalline, non-poisonous powder, perfectly soluble in water and alcohol, making it ideal for expectorants and cough syrups. Our rigorous manufacturing standards guarantee stability, while customized particle size and robust HDPE drum packaging ensure consistent delivery. Partner with us-distributor, exporter, and manufacturer-for remarkable quality and unyielding confidence in your formulations.

Astounding Features and Applications

This superior-quality Guaifenesin IP USP API is meticulously crafted, conforming to advanced pharmaceutical machinery, ensuring uniform particle size and barely perceptible odor. Area of application includes a broad range of pharmaceutical formulation and expectorant syrups. Other features encompass high purity, exceptional stability, and compliance with global export standards. Capitalise on its proven reliability and unlock the efficiency required for modern, large-scale medication manufacturing.


Packaging, Exchange & Transportation Details

Goods are professionally packed in robust HDPE drums with double polyethylene bags, available typically in 25kg quantities or tailored to customer specifications. We offer seamless exchange and secure goods transport, prioritizing your product's safety during transportation. Sample availability ensures you can evaluate quality prior to bulk orders. Our logistics and delivery timeframes are optimised for on-time shipments, safeguarding product integrity from origin to destination.


FAQ's of Guaifenesin IP USP export quality API:


Q: How is Guaifenesin IP USP API typically used in pharmaceutical formulations?

A: Guaifenesin IP USP API is commonly used as an expectorant in cough syrups and other pharmaceutical formulations, aiding the thinning and removal of mucus from the airways.

Q: What benefits does your export-grade Guaifenesin offer over standard grades?

A: Our export-grade Guaifenesin delivers astounding purity of at least 99%, unassailable microbiological standards, and consistent particle size-all packaged for optimal stability, making it ideal for high-demand international markets.

Q: When can I expect delivery after placing my order for Guaifenesin API?

A: Delivery timelines depend on order volume and destination, but our optimised transport network ensures prompt and efficient shipment, with full support from placement to receipt.

Q: Where is your Guaifenesin IP USP sourced and manufactured?

A: Our Guaifenesin IP USP API is meticulously manufactured in India, adhering to rigorous IP and USP standards suitable for global pharmaceutical markets.

Q: What process is followed to ensure the purity and safety of your API?

A: Each batch undergoes stringent quality checks for impurities, heavy metals, and microbial limits, conforming to pharmacopeial standards and ensuring safety and efficacy.

Q: How should Guaifenesin IP USP API be stored for maximum shelf life?

A: To maintain its 36-month shelf life, Guaifenesin should be stored in a tightly closed container, protected from light and moisture, and kept at room temperature.

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