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Available Variants1 g
CHA.76489-1g
Price
€71.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.76489-1g | €71.40 |
97%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C4H8O2 |
|---|---|
| CAS Number | 64491-68-5 |
| Molecular Weight | 88.11 |
| UNSPSC Code | 12352005 |
| NACRES | NA.22 |
| PubChem Substance ID | 24868956 |
| MDL number | MFCD00273366 |
| Beilstein/REAXYS Number | 102505 |
| Assay | 97% |
Safety Information Handling visibility
| pictograms |
GHS02
GHS07
  GHS02,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H225,H315,H319,H335 |
| pcodes | P210 - P233 - P240 - P241 - P303 + P361 + P353 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| supp_hazards | EUH019 |
| Storage Class | 3 - Flammable liquids |
| wgk | WGK 3 |
| flash_point_f | 62.6 °F - closed cup |
| flash_point_c | 17 °C - closed cup |
| ppe | Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
(S)-(+)-Glycidyl methyl ether, with a CAS number of 64491-68-5, is a chiral epoxide that has garnered significant attention in the realm of organic synthesis. This compound is a versatile intermediate, utilized in the preparation of various enantiopure molecules, including pharmaceuticals and agrochemicals. The presence of the glycidyl moiety allows for facile ring-opening reactions, which can be exploited to introduce diverse functional groups. Furthermore, the methyl ether substituent provides a site for further modification, enabling the synthesis of complex molecules with high regio- and stereoselectivity. As a result, (S)-(+)-Glycidyl methyl ether has become a valuable building block in asymmetric synthesis, facilitating the creation of biologically active compounds with defined stereochemistry. Its applications continue to expand, driven by the ongoing demand for enantiopure molecules in various fields.
