4451-30-3

Basic information

• Product Name: .beta.-D-Glucofuranose, 1,5:3,6-dianhydro-
• Synonyms: .beta.-D-Glucofuranose, 1,5:3,6-dianhydro-;1,4:3,6-Dianhydro-alpha-D-glucopyranose min. 98%;DGP, 1,5:3,6-Dianhydro-beta-D-glucofuranose;1,4:3,6-Dianhydro-alpha-D-glucopyranose
• CAS NO: 4451-30-3
• Molecular Formula: C₆H₈O₄
• Molecular Weight: 144.13
• Mol File: 4451-30-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 122-123℃
• Boiling Point: 317.3±37.0 °C(Predicted)
• Appearance: /
• Density: 1.569±0.06 g/cm3(Predicted)
• PKA: 14.10±0.20(Predicted)
• CAS DataBase Reference: .beta.-D-Glucofuranose, 1,5:3,6-dianhydro-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-Glucofuranose, 1,5:3,6-dianhydro-(4451-30-3)
• EPA Substance Registry System: .beta.-D-Glucofuranose, 1,5:3,6-dianhydro-(4451-30-3)

Safety Data

• Hazardous Substances Data: 4451-30-3(Hazardous Substances Data)

Usage

Uses

Used in Carbohydrate Chemistry:
.beta.-D-Glucofuranose, 1,5:3,6-dianhydrois used as a key intermediate for the synthesis of various complex carbohydrates and their derivatives. Its unique structure allows for the development of novel carbohydrate-based compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, .beta.-D-Glucofuranose, 1,5:3,6-dianhydrois used as a building block for the development of new drugs. Its unique structure can be exploited to design and synthesize novel drug candidates with improved pharmacological properties, such as enhanced bioavailability, selectivity, and reduced side effects.
Used in Materials Science:
.beta.-D-Glucofuranose, 1,5:3,6-dianhydrois used as a component in the development of advanced materials, such as polymers and coatings, with tailored properties. Its unique structure can contribute to the creation of materials with improved mechanical, thermal, and chemical properties, making them suitable for various applications, including packaging, electronics, and biomedical devices.

Upstream product

• 9004-34-6 microcrystalline cellulose 
• 67-56-1 methanol 

Downstream Products

• 7625-23-2 3,6-anhydro-D-glucose 

Relevant articles and documents

Revealing the chemistry of biomass pyrolysis by means of tunable synchrotron photoionisation-mass spectrometry

Imaging biomass conversion: pyrolysis is the first reaction involved in all thermal processes for biofuels and green chemicals production. Synchrotron light ionisation and mass spectrometry is used for the first time to investigate biomass pyrolysis. The soft and tunable ionisation source coupled with ab initio calculations reveals chemical mechanisms and new major intermediate species. This methodology could be extended to the thermal and catalytic conversion of all other materials. Primary volatile products are analysed online as a function of photon energy, biomass composition (cellulose, xylan, lignin), reactor temperature and time of conversion. Hydroxyacetaldehyde was detected at very minor yields for cellulose pyrolysis confirming that it is a secondary product. The effect of cellulose structure and ash content on primary tar formation was also studied. The mechanism of levoglucosan dissociative photoionisation is depicted. A new major intermediate product which could be a precursor of furanone-based species from cellulose is evidenced thanks to the soft ionisation and MSMS structural analysis of ions. Different lignin markers and evolutions upon time of conversion are shown for miscanthus and oak pyrolysis.

INFLUENCE OF SODIUM CHLORIDE ON VOLATILE PRODUCTS FORMED BY PYROLYSIS OF CELLULOSE: IDENTIFICATION OF HYDROXYBENZENES AND 1-HYDROXY-2-PROPANONE AS MAJOR PRODUCTS

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