79466-34-5

Basic information

• Product Name: 2R,3S,4S,5S-hexitol hexaacetate
• Synonyms: 2R,3S,4S,5S-hexitol hexaacetate
• CAS NO: 79466-34-5
• Molecular Weight: 434.397
• Mol File: 79466-34-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2R,3S,4S,5S-hexitol hexaacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2R,3S,4S,5S-hexitol hexaacetate(79466-34-5)
• EPA Substance Registry System: 2R,3S,4S,5S-hexitol hexaacetate(79466-34-5)

Safety Data

• Hazardous Substances Data: 79466-34-5(Hazardous Substances Data)

Upstream product

• 50-70-4 D,L-iditol 
• 108-24-7 acetic anhydride 
• 50-70-4 D-glucitol 
• 6706-59-8 L-Sorbitol 
• 108-05-4 vinyl acetate 
• 643-01-6 L-mannitol 
• 7208-47-1 1,2,3,4,5,6-hexa-O-acetyl-D-glucitol 
• 79466-34-5 2R,3S,4S,5S-hexitol hexaacetate 
• 13443-46-4 L-iditol hexaacetate 
• 75879-31-1 2R,3S,4S,5R-hexitol hexaacetate 
• 50-70-4 sorbitol 

Downstream Products

• 642-00-2 DL-glucitol hexa-acetate 

Relevant articles and documents

Compounds from flowers of Daucus carota L. SSp. carota and their antioxidant activity

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Enumeration of hydroxyl groups of sugars and sugar alcohols by aqueous-based acetylation and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

RATIONALE The properties of carbohydrates are determined in part by the number and stereochemical arrangement of their hydroxyl groups. To facilitate their analysis, rapid methods are needed to identify and enumerate hydroxyl groups in sugars and polyalcohols, especially methods that are water-based. METHODS The present report details the results of an alternative method for identification and enumeration of hydroxyl groups in aqueous media. It employs vinyl acetate to selectively derivatize hydroxyl groups in analytes, followed by analysis of the reaction mixtures by matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry (MALDI-TOF-MS). RESULTS The method has been applied to several single and multi-component mixtures of monosaccharides and polyalcohols. The O-acetylated products were analyzed without chromatographic separation or purification by MALDI-TOF-MS. The mass spectra revealed consecutive ion peaks that are separated by 42 mass units as a consequence of displacement of one hydroxyl hydrogen by one acetyl group. CONCLUSIONS A rapid and aqueous-based method is described to enumerate the hydroxyl groups in carbohydrates. The number of ion peaks due to derivatized products is determined by MALDI-TOF-MS, and corresponds to the number of free hydroxyl groups in the analyte. The method is applicable to both single and multi-component mixtures. Published 2011. This article is a US Government work and is in the public domain in the USA. Published 2012. This article is a US Government work and is in the public domain in the USA.

The use of 1-methylimidazole as a solvent and catalyst for the preparation of aldonitrile acetates of aldoses

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