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Uniprofen CAS NO 51234-28-7


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CAS No.:51234-28-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Uniprofen CAS NO 51234-28-7 is a high-purity pharmaceutical intermediate and active ingredient, recognized for its critical role in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs). Its importance lies in providing a reliable and consistent building block for manufacturers requiring stringent quality control in their production processes. This compound is essential for pharmaceutical companies, research institutions, and fine chemical suppliers targeting the development and production of analgesic and anti-inflammatory medications.

Application

  • Pharmaceutical Intermediate: Primary use as a key precursor in the synthesis of ibuprofen and related propionic acid derivative NSAIDs.
  • Active Pharmaceutical Ingredient (API) Manufacturing: Serves as a critical raw material in the production of finished dosage forms.
  • Research & Development: Used in medicinal chemistry for developing new anti-inflammatory compounds and studying structure-activity relationships.
  • Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.
  • Fine Chemical Synthesis: Utilized in custom synthesis and contract manufacturing for specialized chemical entities.

Basic Information

Item Details
Product Name Uniprofen
CAS No. 51234-28-7
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms 2-(4-Isobutylphenyl)propionic Acid; Ibuprofen Intermediate; p-Isobutylhydratropic Acid; (±)-2-(p-Isobutylphenyl)propionic Acid; 4-Isobutyl-α-methylphenylacetic Acid; UNIPROFEN; IBU Intermediate
EINECS Contact for details

Quality Control

Our Uniprofen is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) documenting identity, purity, and impurity profiles are available upon request, supporting compliance with cGMP and relevant pharmacopeial guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep away from heat, sparks, and open flame.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Assay (HPLC) ≥ 98.5%
Related Substances (HPLC) Total impurities ≤ 1.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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