Description

Calane (Pharmaceutical Grade) is a high-purity chemical intermediate essential for modern pharmaceutical synthesis. This compound matters because it offers the stringent quality and consistency required for the development and manufacturing of active pharmaceutical ingredients (APIs). It is primarily needed by pharmaceutical companies, research institutions, and CDMOs (Contract Development and Manufacturing Organizations) engaged in the production of complex therapeutic agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for the discovery and optimization of new drug candidates.
• Process Chemistry: Employed in scale-up and optimization studies for commercial drug manufacturing.
• Reference Standard: Serves as a high-purity standard for analytical method development and quality control.

Basic Information

Product Name	Calane (Pharmaceutical Grade)
CAS No.	36676-08-1
Molecular Formula	C15H12O2
Molecular Weight	224.26 g/mol
Synonyms	2-(4-Methoxyphenyl)-1,3-indandione; 2-(p-Methoxyphenyl)-1H-indene-1,3(2H)-dione; 4-Methoxyphenyl-1,3-indandione; Calane; Pharmaceutical Intermediate 36676-08-1
EINECS	Contact for details

Quality Control

Our Calane (Pharmaceutical Grade) is manufactured under strict quality management systems. The product undergoes rigorous analytical testing to ensure it meets the high-purity standards demanded for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with each batch and is available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); ensure containers are kept tightly sealed to prevent absorption of atmospheric moisture.

Specification

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

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