Description

Oxiranemethanol,Alpha,3-Bis(1-Methylethyl)-,[2Alpha(R*),3Bta]-(9Ci) is a specialized chiral epoxide derivative, valued for its role as a versatile building block in advanced organic synthesis. Its significance lies in its ability to introduce functional complexity and stereochemical control into target molecules, which is critical for developing high-value fine chemicals and active pharmaceutical ingredients (APIs). This compound is essential for research chemists and process development scientists in the pharmaceutical, agrochemical, and specialty chemical industries seeking to create novel compounds with specific three-dimensional architectures.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the synthesis of complex drug molecules, particularly those requiring specific stereochemistry for biological activity.
• Agrochemical Synthesis: Used in the production of advanced pesticides and herbicides where the stereochemistry of the active ingredient is crucial for efficacy.
• Ligand and Catalyst Development: Serves as a precursor for creating chiral ligands and organocatalysts used in asymmetric synthesis.
• Fine Chemical Production: Employed in the manufacture of specialty chemicals, flavors, and fragrances that require enantiomerically pure components.
• Polymer Modification: Can be used to introduce reactive epoxide and hydroxyl functional groups into polymer chains for cross-linking or property enhancement.
• Academic and Industrial R&D: A valuable reagent for methodological development in organic chemistry and process optimization studies.

Basic Information

Product Name	Oxiranemethanol,Alpha,3-Bis(1-Methylethyl)-,[2Alpha(R*),3Bta]-(9Ci)
CAS No.	134111-22-1
Molecular Formula	C10H20O2
Molecular Weight	172.26 g/mol
Synonyms	2,3-Epoxy-2,3-dihydroxy-4,5-dimethylhexane (stereoisomer); alpha,3-Bis(1-methylethyl)oxiranemethanol; (2R*,3S*)-2,3-Epoxy-4,5-dimethyl-2,3-hexanediol; 2,3-Epoxy-4,5-dimethylhexane-2,3-diol; A chiral glycidol derivative; 2,3-Epoxy-2,3-dihydroxy-4,5-dimethylhexane; (2R,3S)-2,3-Epoxy-4,5-dimethylhexane-2,3-diol (relative configuration)
EINECS	Contact for details

Quality Control

Our production of this chiral building block adheres to strict quality protocols to ensure batch-to-batch consistency and high enantiomeric/excess purity. Quality is verified through advanced analytical techniques including Chiral HPLC, GC, and NMR spectroscopy. A comprehensive Certificate of Analysis (COA) detailing identity, purity, chiral purity, and impurity profile is provided with each shipment to support your quality assurance and regulatory documentation needs.

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 away from heat, sparks, and open flame. Due to the reactive epoxide moiety and potential light sensitivity, prolonged exposure to elevated temperatures or direct light should be avoided to maintain product integrity.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (GC/HPLC)	≥ 97.0%
Chiral Purity (Chiral HPLC)	≥ 98.0% e.e.
Water Content (KF)	≤ 0.5%
Specific Rotation	Contact for details

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