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Methyl Lucidenate N CAS NO 1276655-49-2


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CAS No.:1276655-49-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Methyl Lucidenate N CAS NO 1276655-49-2 is a high-purity, specialized triterpenoid derivative, valued for its role as a key reference standard and active pharmaceutical ingredient (API) intermediate. This compound is critical for ensuring analytical accuracy and consistency in research and development. It is primarily utilized by the pharmaceutical, nutraceutical, and advanced research sectors for applications in quality control, bioactivity studies, and the synthesis of novel therapeutic agents.

Application

  • Pharmaceutical Reference Standard: Used for the identification, assay, and purity testing of related ganoderic acid derivatives in QC/QA laboratories.
  • Bioactivity Research: Serves as a key intermediate or standard in pharmacological studies targeting inflammation, oncology, and metabolic disorders.
  • Nutraceutical Development: Employed in the formulation and standardization of high-end mushroom extract supplements, particularly those derived from *Ganoderma lucidum* (Reishi).
  • Analytical Method Development: Essential for developing and validating HPLC, LC-MS, and other chromatographic methods for triterpenoid analysis.
  • Synthetic Chemistry: Acts as a sophisticated building block or precursor for the semi-synthesis of novel triterpenoid analogs with enhanced properties.

Basic Information

Product Name Methyl Lucidenate N
CAS No. 1276655-49-2
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Methyl Lucidenate N; Methyl lucidenate N; Lucidenic acid N methyl ester; Ganoderic acid derivative; Reishi triterpenoid methyl ester; (3β,7β,12β)-3,7,12-Trihydroxy-4,4,14-trimethyl-11,15-dioxochol-8-en-24-oic acid methyl ester (tentative); 1276655-49-2
EINECS Contact for details

Quality Control

Our Methyl Lucidenate N is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods (IR, MS, NMR). We provide a detailed Certificate of Analysis (COA) with every shipment, ensuring traceability and compliance with research and pharmaceutical-grade standards. Specifications can be tailored to meet specific project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and light-sensitive; therefore, containers must be kept sealed in a desiccated environment and handled under appropriate conditions to maintain stability and purity.

Specification

Item Specification
Appearance White to off-white powder
Identification (HPLC) Conforms to reference standard
Identification (IR) Conforms to structure
Purity (HPLC) ≥95.0%
Loss on Drying ≤2.0%
Residue on Ignition ≤0.5%

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

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

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

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