Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of (r)-(+)-glycidol丨cas 57044-25-4 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.
Specifications of (R)-(+)-Glycidol丨57044-25-4
|
Property |
Value |
|
Appearance |
Colorless to light yellow clear liquid |
|
Chromatographic Purity (by GC) |
97% min |
|
Water (by K.F.) |
0.5% max |
|
Specific Optical Rotation [α] 20/D |
+13° to +18° |
|
Identification (GC) |
The retention time of the major peak in the chromatogram of the sample solution corresponds to that in the chromatogram of the standard solution, as obtained in the purity. |
Transport Information of (R)-(+)-Glycidol丨57044-25-4
|
Parameter |
Specification |
|
UN Number |
2810 |
|
Class |
|
|
Packing Group |
|
|
H.S. Code |
2910900090101 |
|
Stability & Reactivity |
Polymerization may occur under the influences of heat, light |
|
Storage |
Keep container tightly closed. Store in a freezer. |
|
Condition to Avoid |
Heat. Electrical spark Open flame Exposure to moisture. Exposure to light. |
|
Package |
Manufacturing Information of (R)-(+)-Glycidol丨57044-25-4
|
Parameter |
Specification |
|
Capacity |
|
|
Frequency |
|
|
Main Export Countries |
|
|
Capacity/Batch |
500kg/batch |
|
Experience |
Production since 2000 |
|
Facilities |
Introduction
(R)-(+)-Glycidol丨57044-25-4 is an enantiomerically pure form of glycidol, an organic compound with a glycidyl functional group. It is a chiral compound with a hydroxymethyl group (-CH2OH) attached to a three-membered epoxide ring. This molecule plays an important role in various chemical and industrial applications, especially in the synthesis of fine chemicals and pharmaceuticals.
Synthesis:
(R)-(+)-Glycidol丨57044-25-4 can be synthesized via various methods, including:
1.Chiral resolution of racemic glycidol: The racemic mixture of glycidol (which contains both (R) and (S) enantiomers) can be resolved using chiral reagents or catalysts to isolate the (R)-(+)-enantiomer.
2.Direct synthesis from chiral starting materials: The (R)-(+)-form can be directly synthesized from chiral precursors, often through asymmetric reactions, involving the use of chiral reagents or catalysts to ensure the formation of the desired enantiomer.
Applications of (R)-(+)-Glycidol丨57044-25-4
1.Pharmaceutical Industry:
oChiral intermediates: (R)-(+)-Glycidol serves as a key intermediate in the synthesis of various pharmaceuticals. Its chiral nature is crucial in the creation of enantiomerically pure drugs, which is essential for pharmacological efficacy and safety.
oSynthesis of glycidyl derivatives: It is used as a precursor for the synthesis of glycidyl esters and other glycidyl derivatives, which are employed in the production of drug formulations, such as topical creams and ointments.
oSynthesis of active pharmaceutical ingredients (APIs): The (R)-(+)-glycidol moiety can be incorporated into the molecular structure of various APIs to enhance the bioactivity and selectivity of pharmaceutical compounds.
2.Synthesis of Biodegradable Polymers:
o(R)-(+)-Glycidol丨57044-25-4 is used in the synthesis of biodegradable polyesters and other biopolymers. These polymers find applications in biomedical devices, drug delivery systems, and tissue engineering. The chiral center in (R)-(+)-glycidol is essential for the control of polymer properties and their degradation rates.
3.Chiral Building Block in Organic Synthesis:
oAs a chiral building block, (R)-(+)-glycidol is used in the synthesis of other chiral compounds. It is employed in the production of various chirally pure molecules for use in fine chemicals, agrochemicals, and other specialty chemicals.
4.Flavor and Fragrance Industry:
o(R)-(+)-Glycidol can be used in the synthesis of certain flavor compounds and fragrances, where chirality plays a crucial role in the characteristic aroma or taste. The specific enantiomeric form may impart desired sensory properties.
5.Surface Coatings:
oThe glycidyl group in (R)-(+)-glycidol is reactive and can be utilized in the production of epoxy resins. These resins are used in the formulation of surface coatings, adhesives, and encapsulating materials. The chiral nature of the compound may be important in tailoring the properties of these resins for specialized applications.
6.Polymerization Reactions:
o(R)-(+)-Glycidol丨57044-25-4 can be used in ring-opening polymerization reactions to form specific types of polymers or copolymers, such as those with epoxide groups, which are useful in the creation of new materials with desirable mechanical or chemical properties.
Mechanism of Action
The (R)-(+)-Glycidol丨57044-25-4 molecule contains an epoxide ring that is highly reactive due to the strain in the three-membered ring. This reactivity makes it a valuable intermediate for a variety of chemical reactions, including nucleophilic substitutions. The hydroxymethyl group attached to the epoxide ring can undergo various transformations, depending on the reaction conditions and reagents involved. The chirality of the molecule, specifically in the (R)-(+)-configuration, is critical for its selectivity in asymmetric synthesis and for achieving the desired properties in pharmaceuticals and other chemicals.
Conclusion
(R)-(+)-Glycidol丨57044-25-4 is a versatile and important compound in the fields of organic synthesis, pharmaceutical manufacturing, and polymer chemistry. Its chiral nature makes it indispensable for the synthesis of enantiomerically pure products in various applications, including the production of drugs, biodegradable polymers, and specialty chemicals. As an intermediate in pharmaceutical and fine chemical synthesis, (R)-(+)-glycidol plays a crucial role in advancing the development of new materials and therapies.

