562-73-2

Usage

Uses

Used in Pharmaceutical Industry:
1,3,4,5-tetrahydroxycyclohexanecarboxylic acid is used as a chelating agent and a sequestering agent for its ability to bind and remove metal ions from solutions, which is crucial in various pharmaceutical formulations and processes.
Used in Food and Beverage Industry:
1,3,4,5-tetrahydroxycyclohexanecarboxylic acid is used as a food preservative due to its ability to inhibit the growth of microorganisms, thereby extending the shelf life of food products.
Used in Polymer Production:
1,3,4,5-tetrahydroxycyclohexanecarboxylic acid is utilized in the production of certain polymers, where its chemical properties contribute to the formation of desired polymer characteristics.
Used in Industrial and Research Applications:
Due to its unique chemical properties and bioavailability, 1,3,4,5-tetrahydroxycyclohexanecarboxylic acid is a valuable compound in a range of industrial and research applications, including the development of new materials and chemical processes.

InChI:InChI=1/C7H12O6/c8-3-1-7(13,6(11)12)2-4(9)5(3)10/h3-5,8-10,13H,1-2H2,(H,11,12)

Upstream product

• 1049703-62-9 chlorogenic acid 
• 640-06-2 1,3,4-trihydroxy-6-oxa-bicyclo[3.2.1]octan-7-one 
• 202650-88-2 3-caffeoylquinic acid 
• 7647-01-0 hydrogenchloride 
• 7664-93-9 sulfuric acid 
• 7732-18-5 water 
• 144-62-7 oxalic acid 
• 25514-46-9 (1S,3S,4R,5R)-3-((3-(3,4-dihydroxyphenyl)propanoyl)oxy)-1,4,5-trihydroxycyclohexane-1-carboxylic acid 
• 896-60-6 (+/-)-1,3t,4t-triacetoxy-5c-hydroxy-cyclohexane-r-carboxylic acid-lactone 
• 770-67-2 (+/-)-γ-Quinide 
• 32384-33-1 quinic acid 1,5-lactone triacetate 
• 213250-58-9 (3R,5R)-3,5-bis[(tert-butyldimethylsilyl)oxy]-1-hydroxy-4-oxocyclohexanecarboxylic acid methyl ester 
• 135711-62-5 methyl quinicate 
• 191916-39-9 methyl (-)-quinate 

Downstream Products

• 99-50-3 3,4-Dihydroxybenzoic acid 
• 1768-31-6 pentachloroacetone 
• 81010-88-0 2,5-dihydroxy-benzene-1,3-disulfonic acid 
• 618-46-2 m-Chlorobenzoyl chloride 
• 90-02-8 salicylaldehyde 
• 123-31-9 hydroquinone 
• 65-85-0 benzoic acid 
• 106-51-4 p-benzoquinone 
• 71-43-2 benzene 
• 99-96-7 4-hydroxy-benzoic acid 
• 14210-97-0 1,4-dibenzoyloxybenzene 
• 2688-77-9 (S)-laudanosine 
• 665-27-0 1,5-quinide 
• 1246364-48-6 (R)-3-[(tert-Butyldimethylsilyl)oxy]-4-methylene-cyclohexanone 

Relevant academic research and scientific papers

Synthesis, Structure, and Tandem Mass Spectrometric Characterization of the Diastereomers of Quinic Acid

(-)-Quinic acid possess eight possible stereoisomers, which occur both naturally and as products of thermal food processing. In this contribution, we have selectively synthesized four isomers, namely, epi-quinic acid, muco-quinic acid, cis-quinic acid, and scyllo-quinic acid, to develop a tandem LC-MS method identifying all stereoisomeric quinic acids. Four derivatives have been unambiguously characterized by single-crystal X-ray crystallography. The missing diastereomers of quinic acid were obtained by nonselective isomerization of (-)-quinic acid using acetic acid/concentrated H2SO4 allowing chromatographic separation and assignment of all diastereomers of quinic acid. We report for the first time that a full set of stereoisomers are reliably distinguishable on the basis of their tandem mass spectrometric fragment spectra as well as their elution order. A rationale for characteristic fragmentation mechanisms is proposed. In this study, we also observed that muco-quinic acid, scyllo-quinic acid, and epi-quinic acid are present in hydrolyzed Guatemalan roasted coffee sample as possible products of roasting.