Description

Oxirane, 2-Methyl-3-(Phenylmethoxy)Methyl-, trans- is a specialized epoxide derivative, a high-value chiral building block in advanced organic synthesis. Its precise stereochemistry and functional group arrangement make it a critical intermediate for constructing complex molecular architectures with high enantiomeric purity. This compound is essential for research and development chemists in the pharmaceutical and fine chemical industries, particularly for the synthesis of active pharmaceutical ingredients (APIs), agrochemicals, and novel materials.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the asymmetric synthesis of complex drug molecules and active pharmaceutical ingredients (APIs).
• Agrochemical Synthesis: Used in the research and production of advanced pesticides and herbicides where specific stereochemistry is required for bioactivity.
• Fine Chemical Production: Serves as a versatile building block for creating specialty chemicals, flavors, fragrances, and advanced polymers.
• Academic & Industrial R&D: A valuable reagent in methodological development for stereoselective ring-opening reactions and catalysis studies.
• Material Science: Potential precursor for epoxy resins and other polymeric materials with tailored properties.

Basic Information

Product Name	Oxirane, 2-Methyl-3-(Phenylmethoxy)Methyl-, trans-
CAS No.	80374-37-4
Molecular Formula	C12H16O2
Molecular Weight	192.25 g/mol
Synonyms	trans-2-Methyl-3-(benzyloxymethyl)oxirane; (2R,3S)-2-Methyl-3-(phenylmethoxy)methyl-oxirane; (2S,3R)-2-Methyl-3-(benzyloxymethyl)oxirane; Benzyl (2,3-epoxybutyl) ether (trans-); Glycidyl benzyl ether derivative; trans-2-Methyl-3-(benzyloxy)methyloxirane; 1-Benzyloxy-2,3-epoxybutane (trans-); (2R,3S)-rel-2-Methyl-3-[(phenylmethoxy)methyl]oxirane
EINECS	Contact for details

Quality Control

Our production of Oxirane, 2-Methyl-3-(Phenylmethoxy)Methyl-, trans- adheres to stringent quality protocols to ensure batch-to-batch consistency and high enantiomeric purity. Each lot is characterized using advanced analytical techniques including chiral HPLC, GC, NMR, and optical rotation measurement. Certificates of Analysis (COA) detailing purity, enantiomeric excess, and identity are provided with every shipment. We support cGMP-compliant manufacturing for pharmaceutical applications 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). Keep away from heat, sparks, open flames, and strong oxidizing agents. For long-term storage under an inert atmosphere (e.g., nitrogen or argon), please contact our technical team for specific recommendations.

Specification

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

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