Description

Brydiofin is a specialized chemical compound with the CAS registry number 142582-81-8. This high-purity intermediate is critical for ensuring the quality and efficacy of advanced pharmaceutical formulations. It is primarily utilized by research institutions and manufacturers in the pharmaceutical and fine chemical industries for the synthesis of active pharmaceutical ingredients (APIs) and other complex organic molecules.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel active pharmaceutical ingredients (APIs) and drug candidates.
• Organic Synthesis: Used as a versatile reagent or intermediate in complex multi-step organic reactions, including coupling and functionalization processes.
• Research & Development: Serves as a critical material in medicinal chemistry and process development laboratories for exploratory synthesis and route scouting.
• Fine Chemical Production: Employed in the manufacture of high-value, low-volume specialty chemicals requiring precise molecular architecture.
• Agrochemical Synthesis: Potential use as an intermediate in the development of advanced crop protection agents and pesticides.
• Material Science: Can be investigated as a monomer or precursor for the development of specialty polymers and advanced materials.

Basic Information

Product Name	Brydiofin
CAS No.	142582-81-8
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-; 2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol; 4,5-Bis(hydroxymethyl)-2,2-dimethyl-1,3-dioxolane; (4R,5R)-(-)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol; (R,R)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol; (4S,5S)-(+)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol; (S,S)-2,2-Dimethyl-1,3-dioxolane-4,5-dimethanol; Solketal derivative
EINECS	Contact for details

Quality Control

Our Brydiofin is manufactured under strict quality management systems to ensure batch-to-batch consistency and reliability. Each lot undergoes rigorous analytical testing, including chromatographic purity analysis and identity confirmation, to meet the stringent requirements of pharmaceutical-grade intermediates. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with every shipment to support your quality assurance and regulatory compliance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption, which may affect product stability and performance. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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