Description

Oxiranecarboxaldehyde, 3-Hexyl-, (2R,3R)-Rel- (9Ci) is a chiral epoxide derivative, specifically a 3-hexyl-substituted glycidol aldehyde, which serves as a valuable chiral building block and synthetic intermediate. Its defined stereochemistry at the 2 and 3 positions makes it crucial for the enantioselective synthesis of complex molecules where optical purity is paramount. This compound is primarily sought by research and development chemists in the pharmaceutical and fine chemical industries for applications in asymmetric synthesis and the development of active pharmaceutical ingredients (APIs).

Application

• Chiral Intermediate in Pharmaceutical Synthesis: Used as a key starting material or intermediate for the enantioselective construction of drug candidates and active pharmaceutical ingredients (APIs).
• Asymmetric Catalysis Research: Serves as a substrate or ligand precursor in the development and testing of novel asymmetric catalysts.
• Fine Chemical and Agrochemical Production: Employed in the synthesis of enantiomerically pure fine chemicals and advanced agrochemical intermediates.
• Material Science Monomers: Potential use as a specialty monomer for creating polymers with specific chiral or functional properties.
• Academic and Industrial R&D: A critical reagent for methodological studies in organic synthesis and stereochemistry at universities and corporate R&D centers.

Basic Information

Product Name	Oxiranecarboxaldehyde, 3-Hexyl-, (2R,3R)-Rel- (9Ci)
CAS No.	562817-82-7
Molecular Formula	C10H18O2
Molecular Weight	170.25 g/mol
Synonyms	(2R,3R)-3-Hexyloxiranecarboxaldehyde; rel-(2R,3R)-3-Hexylglycidol aldehyde; (2R,3R)-3-Hexylglycidaldehyde; 3-Hexyl-2,3-epoxypropanal; (2R,3R)-3-Hexyl-2-oxiranecarboxaldehyde; Glycidol aldehyde, 3-hexyl-, (2R,3R)-rel-
EINECS	Contact for details

Quality Control

Every batch of Oxiranecarboxaldehyde, 3-Hexyl-, (2R,3R)-Rel- (9Ci) is produced and analyzed under strict quality management protocols to ensure identity, purity, and enantiomeric excess meet the high standards required for advanced synthetic applications. Our products undergo rigorous quality testing, including chiral HPLC and NMR analysis, to ensure compliance with industry standards. Certificates of Analysis (COA) detailing specific batch results for purity, enantiomeric excess, and impurity profiles are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). This compound may be sensitive to moisture and oxidation; consider storage under an inert atmosphere for long-term preservation. Keep away from heat, sparks, and open flames.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (GC/HPLC)	≥ 95.0%
Enantiomeric Excess (Chiral HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%

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