Description

(+)-tert-Butyl glycidyl ether (CAS: 130232-97-2) is a high-purity chiral epoxide compound with the molecular formula C₇H₁₄O₂. This optically active glycidyl ether is widely used as a versatile building block in organic synthesis, particularly in asymmetric reactions and polymer chemistry. The tert-butyl group provides steric hindrance, making it valuable for controlled polymerization and chiral derivatization. Our product is rigorously tested to ensure ≥98% purity (by GC) and optimal enantiomeric excess for research and industrial applications. Supplied in sealed amber glass bottles under inert atmosphere to maintain stability, this compound is ideal for pharmaceutical intermediates, specialty polymers, and advanced material science applications.

Key Specifications:
– CAS Number: 130232-97-2
– Molecular Weight: 130.18 g/mol<br- Boiling Point: ~150°C
– Density: 0.92 g/mL at 25°C
– Optical Rotation: +15° to +18° (c=1, CHCl₃)
– Storage: 2-8°C under nitrogen

Properties

• CAS Number: 130232-97-2
• Complexity: 93.6
• IUPAC Name: (2S)-2-(tert-butoxymethyl)oxirane
• InChI: InChI=1S/C7H14O2/c1-7(2,3)9-5-6-4-8-6/h6H,4-5H2,1-3H3/t6-/m0/s1
• InChI Key: SFJRUJUEMVAZLM-LURJTMIESA-N
• Exact Mass: 130.099379685
• Molecular Formula: C7H14O2
• Molecular Weight: 130.18
• SMILES: CC(C)(C)OC[C@@H]1CO1
• Topological: 21.8
• Monoisotopic Mass: 130.099379685
• Synonyms: 130232-97-2, S-(+)-tert-butyl glycidyl ether, (+)-tert-Butyl glycidyl ether, tert-Butyl glycidyl ether, (+)-, (2S)-2-(tert-butoxymethyl)oxirane, tert-Butyl glycidyl ether, (S)-, UNII-G28UV61J7C, G28UV61J7C, Oxirane, 2-[(1,1-dimethylethoxy)methyl]-, (2S)-, (2S)-2-[(2-methylpropan-2-yl)oxymethyl]oxirane, Oxirane, ((1,1-dimethylethoxy)methyl)-, (+)-, Oxirane, ((1,1-dimethylethoxy)methyl)-, (2S)-, Oxirane, 2-((1,1-dimethylethoxy)methyl)-, (2S)-, (2S)-2-[(tert-butoxy)methyl]oxirane, (S)-(+)-Tert-butyl glycidyl ether, Oxirane, [(1,1-dimethylethoxy)methyl]-, (2S)-, (2S)-2-[(1,1-dimethylethoxy)methyl]Oxirane, (S)-2-t-butoxymethyl-oxiran, SCHEMBL401560, (s)-tert-butyl glycidyl ether, s-(+)-t-Butyl glycidyl ether, SFJRUJUEMVAZLM-LURJTMIESA-N, (S)-2-(tert-butoxymethyl)oxirane, DTXSID601267350, BBL103605, MFCD09750970, STL557415, AKOS006345544, FT40746, AS-15943, CS-0444476, EN300-784646, Oxirane,2-[(1,1-dimethylethoxy)methyl]-,(2S)-, Q27278641

This chiral glycidyl ether serves as a key intermediate in asymmetric synthesis of bioactive compounds and resolution agents. In polymer science, it modifies epoxy resins to enhance thermal stability while introducing chirality for specialty coatings. The tert-butyl group’s steric effects make it valuable for controlled ring-opening polymerizations. Researchers also employ it as a chiral auxiliary in catalytic systems and as a precursor for advanced electrolyte materials.

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