131222-81-6

Basic information

• Product Name: (R)-4-HYDROXY-2,5-DIMETHYLFURAN-3(2H)-ONE
• Synonyms: (R)-4-HYDROXY-2,5-DIMETHYLFURAN-3(2H)-ONE
• CAS NO: 131222-81-6
• Molecular Formula: C₆H₈O₃
• Molecular Weight: 128.13
• EINECS: 222-908-8
• Mol File: 131222-81-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 215.5°Cat760mmHg
• Flash Point: 90.5°C
• Appearance: /
• Density: 1.249g/cm³
• Vapor Pressure: 0.032mmHg at 25°C
• Refractive Index: 1.512
• CAS DataBase Reference: (R)-4-HYDROXY-2,5-DIMETHYLFURAN-3(2H)-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-4-HYDROXY-2,5-DIMETHYLFURAN-3(2H)-ONE(131222-81-6)
• EPA Substance Registry System: (R)-4-HYDROXY-2,5-DIMETHYLFURAN-3(2H)-ONE(131222-81-6)

Safety Data

• Hazardous Substances Data: 131222-81-6(Hazardous Substances Data)

Usage

Description

(R)-4-HYDROXY-2,5-DIMETHYLFURAN-3(2H)-ONE, commonly known as furfuryl alcohol, is a furan derivative with the molecular formula C6H8O3. It is a chemical compound that possesses a characteristic odor and is recognized for its applications in various industries due to its unique properties.

Uses

Used in Chemical Production:
(R)-4-HYDROXY-2,5-DIMETHYLFURAN-3(2H)-ONE is used as a key compound in the production of resins, polymers, and pharmaceuticals. Its chemical structure allows it to be a versatile building block for creating a wide range of materials with specific properties.
Used in Flavor and Fragrance Industry:
Furfuryl alcohol is utilized as a flavoring agent in the food and beverage industry, where its distinct odor adds a unique taste and aroma to various products.
Used in Laboratory and Industrial Settings:
Although it is known for its potential toxicity and carcinogenic properties, (R)-4-HYDROXY-2,5-DIMETHYLFURAN-3(2H)-ONE is still used in certain laboratory and industrial applications. However, it is crucial to handle this compound with caution and follow safety protocols to minimize health risks.

InChI:InChI=1/C6H8O3/c1-3-5(7)6(8)4(2)9-3/h3,8H,1-2H3

Upstream product

• 3658-77-3 furaneol 

Relevant articles and documents

Stereochemical study of chiral tautomeric flavorous furanones by vibrational circular dichroism

(Equation Presented) 2-Substituted-3(2H)-furanone derivatives are industrially significant aroma compounds possessing a unique keto - enol tautomeric feature causing their racemization. Absolute configurations of two flavorous furanones, which have remained unclear for the past 40 years since their discovery, were clarified by the vibrational circular dichroism technique as well as chemical relay reactions. Odor evaluation of each enantiomer revealed relationships between their configurations and their odor activities.