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Guaifenesin IP USP
Guaifenesin IP USP

Guaifenesin IP USP

MOQ : 100 Kilograms

Guaifenesin IP USP Specification

  • EINECS No
  • 202-222-5
  • Smell
  • Odorless
  • Boiling point
  • 215C
  • Taste
  • Slightly bitter
  • Solubility
  • Soluble in water, slightly soluble in ethanol
  • HS Code
  • 29094900
  • Molecular Formula
  • C10H14O4
  • Ph Level
  • Not less than 4.5, Not more than 7.0
  • Shelf Life
  • 5 years
  • Melting Point
  • 77-78C
  • Molecular Weight
  • 198.22 g/mol
  • Storage
  • Store in a cool, dry place
  • Heavy Metal (%)
  • Not more than 0.001%
  • Loss on Drying
  • Not more than 0.5%
  • Color
  • White
  • Structural Formula
  • C10H14O4
  • Poisonous
  • Non-poisonous
  • Particle Size
  • 90% passes through 60 mesh
  • Medicine Name
  • Guaifenesin IP/USP
  • Chemical Name
  • Guaifenesin
  • CAS No
  • 93-14-1
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • IP/USP
  • Usage
  • Expectorant, used to relieve chest congestion
  • Purity(%)
  • 99% Min.
  • Appearance
  • White or almost white crystalline powder
  • Physical Form
  • Solid
  • Optical Rotation
  • +12 to +14 (c=2, water)
  • Labeling & Packing
  • HDPE drums with double poly liner, as per customer requirement
  • Related Substances (Total Impurities)
  • Not more than 0.1%
  • Residual Solvents
  • Meets current ICH-Q3C
  • Sulfate
  • Not more than 0.02%
  • Chloride
  • Not more than 0.014%
  • Bacterial Endotoxins
  • Less than 0.5 EU/mg
  • Assay
  • 98.0% to 102.0% (on dried basis)
  • Identification
  • IR/UV/Chromatographic methods conform
 

Guaifenesin IP USP Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • Supply Ability
  • 500 Kilograms Per Month
  • Delivery Time
  • 10 Days
 

About Guaifenesin IP USP



Discover the reduced price marvel of Guaifenesin IP/USP, an active pharmaceutical ingredient (API) celebrated for its top-notch purity (99% min.) and magnificent expectorant properties. This new offering meets stringent international standards, including IP/USP grades and ICH-Q3C compliance. Redeem industry-leading performance with guaranteed low impurities-chloride, sulfate, and heavy metals-delivered in robust HDPE drums to preserve integrity. Perfect for manufacturers, exporters, or wholesalers seeking a dependable, odorless, white crystalline powder, Guaifenesin ensures efficacy in relieving chest congestion. Experience pharmaceutical brilliance at an advantageous value.

Comprehensive Application & Usage of Guaifenesin IP/USP

Guaifenesin IP/USP serves as a magnificent expectorant, extensively used in pharmaceutical formulations to relieve chest congestion. Its application surfaces include oral syrups, tablets, and other solid dosage forms where rapid and effective mucolytic action is required. The top-notch compound is utilized by manufacturers and researchers, providing unparalleled support as an active ingredient within medicinal products designed to clear mucus and ease respiratory discomfort.


Sample Policy & Supply Dynamics of Guaifenesin IP/USP

Sample rates for Guaifenesin IP/USP can be easily requested for evaluation or exchange, ensuring confidence in quality before substantial purchases. With a robust domestic market presence and reliable supply ability, the product is quickly dispatched nationwide. As a trusted distributor in India, we adapt to client needs, ensuring timely delivery and satisfaction. The streamlined supply chain guarantees uninterrupted service for all pharmaceutical partners.


FAQ's of Guaifenesin IP USP:


Q: How is Guaifenesin IP/USP typically used in pharmaceutical applications?

A: Guaifenesin IP/USP is commonly used as an expectorant to alleviate chest congestion by thinning mucus, making it easier to cough up. It is formulated into syrups, tablets, and other dosage forms for respiratory relief.

Q: What are the key benefits of choosing this top-notch Guaifenesin IP/USP?

A: This Guaifenesin IP/USP features high purity (minimum 99%), low levels of impurities, and compliance with international standards. Its marvelous quality makes it a reliable choice for manufacturers seeking effective, safe, and consistent results.

Q: When can I expect my Guaifenesin IP/USP sample to be dispatched?

A: Samples are typically dispatched promptly upon order confirmation, ensuring rapid evaluation for your development process. Contact our team for specific timelines based on your location in India.

Q: Where is Guaifenesin IP/USP sourced and supplied from?

A: This product is manufactured and distributed in India, with a strong supply network catering to both domestic and international customers, ensuring timely and secure delivery.

Q: What process ensures the purity and safety of each batch?

A: Each batch of Guaifenesin IP/USP undergoes rigorous quality testing, including IR/UV/chromatographic identification, heavy metal and impurity assessment, and compliance with ICH-Q3C residual solvent requirements.

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