Sandu, Mariya P. team published research in New Journal of Chemistry in 2021 | 527-07-1

Reference of 527-07-1, 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.

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. Reference of 527-07-1

Sandu, Mariya P.;Kovtunov, Mikhail A.;Gromov, Nikolay V.;Kurzina, Irina A. research published 《 Effects of external parameters and mass-transfer on the glucose oxidation process catalyzed by Pd-Bi/Al2O3》, the research content is summarized as follows. The catalytic properties of a bimetallic 3.5% Pd-2.4% Bi catalyst supported on Al2O3 were studied in a glucose oxidation reaction in sodium gluconate at various pHs, temperatures and [Glu] : [Pd] ratios. It was found that pH 9 and temperature 60°C are the best conditions for the Pd3Bi/Al2O3 catalytic system. These reaction parameters contribute to obtaining sodium gluconate with 56.6% yield while maintaining a selectivity of 99.9%. The calculated activation energy was 67.7 kJ mol-1. The oxygen transfer rate study allowed us to conclude that the reaction proceeds in a kinetic mode. The catalyst showed activity and stability in three catalytic cycles (XGlu = 56.6-62.8, SSGlu > 99.9%). The decrease in catalytic activity in the fourth and fifth catalytic cycles is associated with a change in the valence-phase state of the catalyst surface established using XPS.

Reference of 527-07-1, 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