In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 527-07-1, formula is C6H11NaO7, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. Recommanded Product: Sodium Gluconate
Rojo, Henar;Gaona, Xavier;Rabung, Thomas;Polly, Robert;Garcia-Gutierrez, Miguel;Missana, Tiziana;Altmaier, Marcus research published 《 Complexation of Nd(III)/Cm(III) with gluconate in alkaline NaCl and CaCl2 solutions: Solubility, TRLFS and DFT studies》, the research content is summarized as follows. The effect of gluconate on the solubility and aqueous speciation of An(III) and Ln(III) was studied using a combination of Nd(III) solubility experiments, Cm(III) time-resolved laser fluorescence spectroscopy (TRLFS) and d. functional theory (DFT) calculations Solubility experiments were performed under an Ar-atm. using a well-defined Nd(OH)3(s) solid phase equilibrated in NaCl (0.1-5.0 M) and CaCl2 (0.1-3.5 M) solutions with 9 ≤ pHc ≤ 13 and 10-6 M ≤ [GLU]tot ≤ 10-2 M. The solubility of Nd(OH)3(s) remains mostly unaffected in NaCl solutions with [GLU]tot = 10-3 M, whereas a clear increase in solubility is observed in dilute CaCl2 solutions with the same [GLU]tot and pHc ≥ 11. In concentrated CaCl2 solutions, gluconate does not affect the solubility of Nd(III) due to the competition with Ca-GLU complexes. Cm(III) TRLFS spectra collected in NaCl solutions with pHc ≈ 12 confirm the formation of weak Cm(III)-GLU complexes. The very strong red shift observed in dilute CaCl2 solutions in connection with high fluorescence intensities supports the formation of ternary Ca-Cm(III)-GLU complexes. The speciation of Cm(III) in 3.5 M CaCl2 solutions is mostly dominated by the complex Ca3[Cm(OH)6]3+, although the formation of ternary Ca-Cm(III)-GLU species is hinted at high gluconate concentrations DFT calculations provide addnl. support to the formation of stable ternary Ca-Cm(III)-GLU aqueous complexes. This work provides key information to understand the chem. speciation and relevant equilibrium processes of An(III) and Ln(III) in the presence of gluconate under conditions relevant for nuclear waste disposal.
Recommanded Product: Sodium Gluconate, Sodium Gluconate is the sodium salt of gluconic acid with chelating property. Sodium gluconate chelates and forms stable complexes with various ions, preventing them from engaging in chemical reactions.
Sodium gluconate is an organic sodium salt having D-gluconate as the counterion. It has a role as a chelator. It contains a D-gluconate.
D-Gluconic acid sodium salt is a glycol ether that is used as an injection solution. It has been shown to have antibacterial efficacy against wild-type strains of bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. The in vitro antimicrobial action of D-gluconic acid sodium salt was found to be due to its ability to inhibit bacterial growth by interfering with the synthesis of DNA. D-gluconic acid sodium salt also has been shown to have antihypertensive effects in rats through the inhibition of angiotensin II type 1 receptor (AT1) signaling pathway and erythrocyte proliferation. This drug also has been shown to bind benzalkonium chloride and x-ray diffraction data show that it is crystalline in nature. The analytical method for determining the concentration of D-gluconic acid sodium salt is by electrochemical impedance, 527-07-1.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts