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Guaifenesin IP USP API

Guaifenesin IP USP API

Product Details:

  • Refractive Rate Not applicable (solid)
  • Usage Used in the formulation of cough syrups and cold medications
  • Application Pharmaceutical, expectorant in cough preparations
  • Smell Odorless
  • Molecular Formula C10H14O4
  • EINECS No 202-222-5
  • Ingredients Guaifenesin
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Guaifenesin IP USP API Price And Quantity

  • 100 Kilograms

Guaifenesin IP USP API Product Specifications

  • >= 99%
  • IP/USP
  • C10H14O4
  • 29094900
  • 198.22 g/mol
  • Active Pharmaceutical Ingredient (API)
  • 78-82C
  • Crystalline
  • NO
  • 93-14-1
  • Powder / Crystalline
  • White or almost white crystalline powder
  • Pharmaceutical, expectorant in cough preparations
  • Odorless
  • C10H14O4
  • 202-222-5
  • Not applicable (solid)
  • Used in the formulation of cough syrups and cold medications
  • 1.214 Gram per cubic centimeter(g/cm3)
  • Neutral
  • Slightly bitter
  • Guaifenesin
  • Non-toxic, expectorant, soluble in water
  • 5 years under proper storage
  • Keep container tightly closed in a cool, dry, and well-ventilated place
  • Soluble in water and alcohol
  • Not more than 20 ppm
  • Max 0.5%
  • 9.4
  • Not less than 99.0% and not more than 101.0% of C10H14O4, calculated on the dried basis
  • +2.0 to +4.0
  • Not applicable (decomposes on heating)
  • HDPE containers or fiber drums with double polyethylene liners
  • Complies with ICH guidelines
  • Below 30C
  • Infrared absorption, meets requirements

Guaifenesin IP USP API Trade Information

  • 1000 Kilograms Per Month
  • 7 Days

Product Description



Experience the sizzling demand for our Hot-selling Guaifenesin IP/USP API, the superior choice for pharmaceutical formulations. Crafted with prodigious precision, it boasts a triumphant purity level of 99% and a neutral pH, making it the trusted expectorant in cough preparations worldwide. This high-grade crystalline powder is odorless, slightly bitter, and non-toxic-soluble in both water and alcohol, ensuring easy formulation. Compliance with stringent ICH guidelines and robust packaging secures every batch's exceptional quality. Grab yours now and enhance your product line with this industry-leading API.

Outstanding Features & Versatile Usage

Guaifenesin IP USP API stands out for its neutral pH, non-toxic nature, and remarkable solubility in water and alcohol. Suitable for pharmaceutical manufacturers, this prodigious ingredient is primarily used in the preparation of cough syrups and cold medicines. Its expectorant properties make it ideal for alleviating respiratory discomfort. With consistent identification by infrared absorption, this API ensures reliable results, supporting the development of high-efficacy medications for widespread health concerns.


Robust Packaging and Supply Reliability

Shipped in HDPE containers or fiber drums with double polyethylene liners, Guaifenesin IP USP API arrives securely and safely. We offer flexible supply options to match your production needs, making order completion straightforward and efficient. Our sample policy ensures that potential partners can evaluate quality before committing. Large-scale orders are quickly processed and dispatched, guaranteeing reliability for distributors and manufacturers who require a dependable source for timely fulfillment.


FAQ's of Guaifenesin IP USP API:


Q: How is Guaifenesin IP USP API commonly used in pharmaceutical applications?

A: Guaifenesin IP USP API is primarily used in the formulation of cough syrups and cold medications as an expectorant, helping to ease respiratory symptoms and promote mucus clearance.

Q: What are the key benefits of choosing your Guaifenesin API?

A: Our Guaifenesin IP USP API offers superior purity (99%), meets strict ICH guidelines for heavy metals and residual solvents, and is supplied in secure, robust packaging to ensure quality remains uncompromised during transit and storage.

Q: Where should Guaifenesin API be stored for maintaining its efficacy?

A: Guaifenesin API should be stored in tightly closed containers, kept in a cool, dry, and well-ventilated place at temperatures below 30C to preserve its stability and extend shelf life.

Q: What is your supply ability and how are samples handled?

A: We maintain a strong supply ability and offer a clear sample policy, allowing customers to receive product samples for quality evaluation before finalizing an order. Samples are shipped promptly to enable informed decision-making.

Q: How is the identification and quality of your API ensured?

A: Identification is carried out using infrared absorption, and every batch meets stringent assay, heavy metal, and purity standards as required by IP/USP. Comprehensive quality control ensures each shipment is fully compliant and reliable.

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