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Elemolic Acid CAS NO 28282-54-4


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CAS No.:28282-54-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Elemolic Acid CAS NO 28282-54-4 is a naturally occurring pentacyclic triterpenoid acid, valued for its unique chemical structure and biological activity profile. This compound serves as a crucial intermediate and active ingredient in advanced research and development, particularly in the pharmaceutical and nutraceutical sectors. It is essential for manufacturers and R&D laboratories focused on developing novel therapeutics, functional ingredients, and high-purity reference standards.

Application

  • Pharmaceutical Intermediate: Serves as a key starting material or precursor in the synthesis of novel drug candidates, especially those targeting inflammation and metabolic disorders.
  • Nutraceutical & Dietary Supplement Formulation: Incorporated into supplements for its potential bioactive properties, contributing to product efficacy and differentiation.
  • Biomedical & Life Science Research: Used as a reference standard and active compound in pharmacological studies, cytotoxicity assays, and mechanism-of-action research.
  • Cosmeceutical Active Ingredient: Employed in high-end skincare formulations for its potential anti-inflammatory and skin-conditioning benefits.
  • Chemical Synthesis & Process Development: Acts as a sophisticated chiral building block for the synthesis of complex natural product analogs and derivatives.
  • Analytical Standard: Provides a high-purity benchmark for quality control and method development in analytical laboratories using HPLC, LC-MS, or NMR.

Basic Information

Product Name Elemolic Acid
CAS No. 28282-54-4
Molecular Formula C30H48O3
Molecular Weight 456.71 g/mol
Synonyms Elemolic Acid; 3-Oxo-24-norolean-12-en-28-oic Acid; 3-Oxo-24-norolean-12-en-28-oic acid, (4α)-; 24-Norolean-12-ene-3,28-dione; 3-Oxo-24-norolean-12-en-28-oic acid; Norolean-12-ene-3,28-dione derivative
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Quality Control

Our Elemolic Acid is produced and tested under a stringent quality management system to ensure batch-to-batch consistency and high purity. We provide comprehensive analytical documentation, including a Certificate of Analysis (COA) detailing purity, identity, and impurity profiles via validated methods such as HPLC and NMR. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring traceability and reliability for critical applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to minimize exposure to atmospheric moisture.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥ 95.0%
Loss on Drying ≤ 2.0%
Residue on Ignition ≤ 0.5%
Heavy Metals ≤ 20 ppm

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

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Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.