573-35-3

Usage

Uses

Used in Water Treatment Industry:
(2,3,4,5,6-pentahydroxycyclohexyl)oxyphosphonic acid is used as a corrosion inhibitor for preventing the oxidation and chemical reactions that lead to metal corrosion in water treatment processes. Its strong bonding capability with metal surfaces ensures effective protection against corrosion.
Used in Metalworking Industry:
In the metalworking industry, (2,3,4,5,6-pentahydroxycyclohexyl)oxyphosphonic acid serves as a corrosion inhibitor, safeguarding metal components and tools from the detrimental effects of corrosion during manufacturing and processing stages. This contributes to the longevity and performance of metal equipment.
Used in Oilfield Applications:
(2,3,4,5,6-pentahydroxycyclohexyl)oxyphosphonic acid is utilized as a scale inhibitor in oilfield operations to prevent the formation of mineral deposits that can obstruct pipelines and other equipment. By inhibiting scaling, it ensures smooth operation and efficiency in oil extraction and transportation processes.
Overall, (2,3,4,5,6-pentahydroxycyclohexyl)oxyphosphonic acid is a valuable compound in industrial settings due to its multifunctional properties as both a corrosion and scale inhibitor, enhancing the reliability and longevity of metal equipment and systems in various sectors.

InChI:InChI=1/C6H13O9P/c7-1-2(8)4(10)6(5(11)3(1)9)15-16(12,13)14/h1-11H,(H2,12,13,14)

Upstream product

• 441311-55-3 2-O-phosphono-1,3,4,5,6-penta-O-acetyl-myo-inositol 
• 87-89-8 D-myo-inositol 
• 75194-94-4 3,3,7,7-tetramethyl-2,8-dioxa-5-aza-1λ³-phosphabicyclo(3,3,0)octane 
• 125288-06-4 4,6-di-O-benzyl-myo-inositol 2-dibenzylphosphate 
• 26326-85-2 Ins(1,2,3,4,6)P5 
• 26326-86-3 Ins(1,2,3,4,5)P₅ 
• 114418-96-1 Ins(1,2,4,5,6)P₅ 
• 864372-89-4 1,4,5-tri-O-acetyl-3,6-di-O-benzyl-2-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864372-74-7 (1S,2R,3R,4S)-2,3-di-O-acetyl-1,4-di-O-benzylconduritol B 
• 864372-76-9 4,5-di-O-acetyl-3,6-di-O-benzyl-D-myo-inositol 
• 864372-88-3 1,4,5-tri-O-acetyl-3,6-di-O-benzyl-D-myo-inositol 
• 864372-83-8 2,4,5-tri-O-acetyl-3,6-di-O-benzyl-D-myo-inositol 
• 98510-20-4 myo-Inositol orthoformate 
• 120268-33-9 4/6-O-benzyl-myo-inositol 1,3,5-monoorthoformate 

Downstream Products

• 33608-52-5 DL-O¹,O²-hydroxyphosphoryl-myo-inositol 
• 551-72-4 inositol 
• 86119-84-8 phosphoric acid 

Relevant academic research and scientific papers

Flexible stereo- and regioselective synthesis of myo-inositol phosphates (part 1): Via symmetrical conduritol B derivatives

A practical route is described for the preparation of myo-inositol polyphosphates. Optically pure myo-inositol derivatives can be prepared from p-benzoquinone in both forms by enzymatic resolution of a C2- symmetric diacetoxyconduritol B key in

Pathway of dephosphorylation of myo-inositol hexakisphosphate by phytases of legume seeds

Using a combination of high-performance ion chromatography analysis and kinetic studies, the pathway of dephosphorylation of myo-inositol hexakisphosphate by the phytases purified from faba bean and lupine seeds, respectively, was established. The data demonstrate that the legume seed phytases under investigation dephosphorylate myo-inositol hexakisphosphate in a stereospecific way. The phytase from faba bean seeds and the phytase LP2 from lupine seeds degrade phytate by sequential removal of phosphate groups via D-Ins(1,2,3,5,6)P5, D-Ins(1,2,5,6)P4, D-Ins(1,2,6)P3, and D-Ins(1,2)P2 to finally Ins(2)P, whereas the phytases LP11 and LP12 from lupine seeds generate the final degradation product Ins(2)P via D-Ins(1,2,4,5,6)P5, D-Ins(1,2,5,6)P4, D-Ins(1,2,6)P3, and D-Ins(1,2)P2.

The pathway of dephosphorylation of myo-inositol hexakisphosphate by phytases from wheat bran of Triticum aestivum L. cv. Nourin #61

Phytases are the primary enzymes responsible for the hydrolysis of phytic acid, myo-inositol-1, 2, 3, 4, 5, 6-hexakisphosphate (InsP6). The pathway of hydrolysis of InsP6 by phytase from wheat bran of Triticum aestivum L. cv. Nourin #61 is proved in this study. Structures of the intermediates were established by a variety of nuclear magnetic resonance techniques (1H-, two-dimensional 1H-1H coupling-correlation spectra and two-dimensional 31P-1H correlation spectra), gas chromatography, and bioassay. On the basis of the structures identified, initial hydrolysis of the phosphate ester occurs at the D/L-4 position of InsP6 to yield D/L-Ins (1, 2, 3, 5, 6) P5. After the dephosphorylation, the pathway of dephosphorylation is divided into two routes. The main route proceeds via D/L-Ins (1, 2, 5, 6) P4, D/L-Ins (1, 2, 6) P3 and D/L-Ins (1, 2) P2, while the minor route proceeds via D/L-Ins (1, 2, 3, 6) P4, Ins (1, 2, 3) P3 and D/L-Ins (1, 2) P2. D/L-Ins (1, 2) P2 is hydrolyzed at the D/L-1 or 2-position, and finally myo-inositol is produced.

myo-Inositol 1,4,5-Triphosphate and Related Compounds' Protonation Sequence: Potentiometric and 31P NMR Studies

The protonation sequence of myo-inositol 1,4,5-triphosphate 3>, of its dehydroxylated analogue, Cyhx(1,2,4)P3, of two diphosphorylated inositol phosphates, Ins(1,4)P2 and Ins(4,5)P2 and of one inosit

Derivatives of cyclohexane

New derivatives of cyclohexane in substantially pure form suitable as a pharmaceutical, foodstuff or as a stabilizer.

The Total Synthesis of myo-Inositol Phosphates via myo-Inositol Orthoformate

Novel selective alkylations of myo-inositol orthoformate (4) have been used to prepare a series of protected myo-inositol derivatives, (5a-e), (7), (10), (12), and (16).These intermediates have been used in efficient total syntheses of myo-inositol 2-phosphate, (9); myo-inositol 4-phosphate, (6); myo-inositol 1,3-bisphosphate, (18); and myo-inositol 1,3,4,5-tetrakisphosphate (14).This report represents the first total synthesis of the important natural metabolites (14) and (18) and significantly improved methods of preparation of (6) and (9).

Highly Efficient Protection by the Tetraisopropyldisiloxane-1,3-diyl Group in the Synthesis of myo-Inositol Phosphates as Inositol 1,3,4,6-tetrakisphosphate

Regioselective introduction of the tetraisopropyldisiloxane-1,3-diyl group onto myo-inositol and 1,2-O-cyclohexylidene-myo-inositol realised the efficient synthesis of various myo-inositol phosphates.

Phosohoranylation de polyols: Voie d'acces aux phosphates d'interet biologique. I. Cas du myo-inositol

An original method for the phosphorylation of an unprotected myo-inositol is described, which yields several myo-inositol phosphates at the same time.The reaction proceeds via a partial or complete phosphoranylation of the cyclitol by means of the aminobicyclophosphane 8, followed by oxidation of the resulting bicyclophosphoranes bearing a P-H bond and acid hydrolysis of the neutral phosphates thus formed.In the case of the tris-phosphoranylation we identified, among the HPLC fractions, the myo-inositol-1,2-(cycl)phosphate 22, the myo-inositol-1-phosphate 23, and the myo-inositol-2-phosphate 24.

Synthesis of myo-Inositol 1-Phosphate and 4-Phosphate, and of their Individual Enantiomers

New methodology is described which allows the synthesis of myo-inositol 1-phosphate completely free of contamination by the 2-isomer, and novel resolution procedures have been developed for the preparation of the enantiomers of myo-inositol 1- and 4-phosp