Category: 527-07-1

COA of Formula: C6H11NaO7, In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl functional group (−OH) bound to a saturated carbon atom. 527-07-1, name is Sodium Gluconate, An important class of alcohols, of which methanol and ethanol are the simplest examples, includes all compounds which conform to the general formula CnH2n+1OH.

Santos, T. Jr.;Machado, V. V. S.;Borges, O. H.;Salvini, V. R.;Parr, C.;Pandolfelli, V. C. research published 《 Calcium aluminate cement aqueous suspensions as binders for Al₂O₃-based particle stabilised foams》, the research content is summarized as follows. Macroporous refractory ceramics were prepared with Al₂O₃-based particle stabilized foams in which ceramic particles were partially hydrophobized with propionic acid or L-leucine. Calcium aluminate cement (CAC) as dry powder or stable aqueous suspension were added as binders. Cement addition resulted in solid foams whereby setting took place in less than 24 h. Highly porous samples were attained with leucine-based foams whereas the propionic-acid ones were not stable after CAC addition For leucine-based foams, fired samples with homogeneous microstructures, both high porosity (∼80%) and cold crushing strength (∼30 MPa) were attained when CAC aqueous suspension was used instead of CAC dry powder. These results were associated to the better dispersion of cement particles in the foam structure when CAC liquid binder was used and pointed out the advantages of this suspension for producing solid macroporous ceramics based on particle-stabilized foams.

COA of Formula: C6H11NaO7, 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

In general, the hydroxyl group makes alcohols polar. 527-07-1, formula is C6H11NaO7, Because of hydrogen bonding, alcohols tend to have higher boiling points than comparable hydrocarbons and ethers. Application In Synthesis of 527-07-1

Sato, S.;Kunimoto, M.;Arai, K. research published 《 Quality of walleye pollack frozen surimi by adding carboxylic acid salt in place of sugar compounds》, the research content is summarized as follows. Sugar compounds and polyphosphates are typically added to frozen surimi for the maintenance of its quality. To create healthier, low-calorie frozen surimi, frozen surimi using carboxylic acid and amino acid salts as preservatives in place of sugar compounds was prepared After thawing, the surimi was salted, followed by preheating at 30°C for either 40 min or between 0 and 40 min, and then heating it at 90°C for 30 min. The breaking strength (BS) and breaking strain (bs) of the heat-induced gels of the surimi were then measured using a rheometer, and the gel strength (Gs = BS / bs) and jelly strength (JS = BS x bs) were calculated The quality of the surimi was evaluated by assessing the phys. properties of the heat-induced gels made from it, as well as the relationship between the BS and Gs during preheating for two-step heated gels. Results showed that the frozen surimi preparations made with 5% sodium gluconate and 3% sodium gluconate + 2% sodium glutamate, each with the addition of 0.1% Na3PO4, were comparable in quality to the typical preparation with 5.7% sugar compounds, remaining stable at -23°C for seven months or at -45°C for ten months. It was also found that, when comparing samples with equal BS values, the heat-induced gels of the 5% sodium gluconate and 3% sodium gluconate + 2% sodium glutamate preparations had slightly lower bs values as compared to typical frozen surimi with sugar compounds, thus exhibiting a slightly more brittle texture.

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, Application In Synthesis of 527-07-1

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

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

Serdaroglu, Goncagul;Kaya, Savas;Touir, Rachid research published 《 Eco-friendly sodium gluconate and trisodium citrate inhibitors for low carbon steel in simulated cooling water system: Theoretical study and molecular dynamic simulations》, the research content is summarized as follows. The work presented the corrosion inhibition potency of the sodium gluconate and trisodium citrate against the corrosion of low carbon steel and revealed that the TSC can be more preferment than the SG mol. In addition to exptl. investigation of the corrosion inhibition capacity of the SG and TSC mols., the quantum chem. calculations were performed by B3LYP, B3LYP-GD3BJ and M06HF functionals at three basis sets that are 6-31g(d,p), 6-311g(d,p) and 6-311++g(3df, 2pd) basis sets. The global hardness values revealed that the TSC mol. could be preferable to the SG mol. in using the design of the corrosion inhibitor materials because the SG (2.81 eV) was calculated a harder mol. than the TSC (2.70 eV). Mol. dynamic simulations were performed to investigate metal-inhibitor interactions.

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

With respect to acute toxicity, simple alcohols have low acute toxicities. Doses of several milliliters are tolerated. 527-07-1, formula is C6H11NaO7, For pentanols, hexanols, octanols and longer alcohols, LD50 range from 2–5 g/kg (rats, oral). Ethanol is less acutely toxic.All alcohols are mild skin irritants. Electric Literature of 527-07-1

Rogalski, Esther;Ehrmann, Matthias A.;Vogel, Rudi F. research published 《 Strain-specific interaction of Fructilactobacillus sanfranciscensis with yeasts in the sourdough fermentation》, the research content is summarized as follows. Fructilactobacillus (F.) sanfranciscensis is a key bacterium in traditional (type 1) sourdough fermentations It typically occurs in combination with the sourdough yeast Kazachstania (K.) humilis or the generalist Saccharomyces (S.) cerevisiae. Previous studies revealed intra-species diversity in competitiveness or dominance in sourdoughs of F. sanfranciscensis, as well as preferences for a life with or without a specific yeast. In this study representative, differently behaving strains were studied in media with different sugars and electron acceptors, and in rye sourdough fermentations in the presence and absence of K. humilis or S. cerevisiae. Strain-specific differences were observed in sugar and organic acids spectra in media, and in sourdoughs with F. sanfranciscensis strains in combination with K. humilis or S. cerevisiae. F. sanfranciscensis TMW 1.1150 proved dominant in the presence and absence of any yeast because it most effectively used maltose. Its maltose fermentation was unaffected by electron acceptors. F. sanfranciscensis TMW 1.2138 was the weakest maltose fermenter and incapable of glucose fermentation, and evidently not competitive against the other strains. F. sanfranciscensis TMW 1.392 was the most versatile strain regarding the utilization of different carbohydrates and its ability to exploit electron acceptors like fructose and oxygen. In sourdoughs without yeasts, it outcompeted other strains. The metabolism of F. sanfranciscensis TMW 1.907 was stimulated in combination with S. cerevisiae. In competitive trials, it was assertive only with S. cerevisiae. The intra-species differences in carbohydrate metabolism can widely explain the differences in their behavior in sourdough fermentation Interaction between F. sanfranciscensis and the yeasts was strain specific and supposedly commensal with K. humilis and rather competitive with S. cerevisiae.

Electric Literature 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

Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 527-07-1, formula is C6H11NaO7, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , Category: alcohols-buliding-blocks

Rogalski, Esther;Ehrmann, Matthias A.;Vogel, Rudi F. research published 《 Intraspecies diversity and genome-phenotype-associations in Fructilactobacillus sanfranciscensis》, the research content is summarized as follows. In this study the intraspecies diversity of Fructilactobacillus (F.) sanfranciscensis (formerly Lactobacillus sanfranciscensis) was characterized by comparative genomics supported by physiol. data. Twenty-four strains of F. sanfranciscensis were analyzed and sorted into six different genomic clusters. The core genome comprised only 43,14% of the pan genome, i.e. 0.87 Mbp of 2.04 Mbp. The main annotated genomic differences reside in maltose, fructose and sucrose as well as nucleotide metabolism, use of electron acceptors, and exopolysacchride formation. Furthermore, all strains are well equipped to cope with oxidative stress via NADH oxidase and a distinct thiol metabolism Only ten of 24 genomes contain two maltose phosphorylase genes (mapA and mapB). In F. sanfranciscensis TMW 1.897 only mapA was found. All strains except those from genomic cluster 2 contained the mannitol dehydrogenase and should therefore be able to use fructose as external electron acceptor. Moreover, six strains were able to grow on fructose as sole carbon source, as they contained a functional fructokinase gene. No growth was observed on pentoses, i.e. xylose, arabinose or ribose, as sole carbon source. This can be referred to the absence of ribose pyranase rbsD in all genomes, and absence of or mutations in numerous other genes, which are essential for arabinose and xylose metabolism Seven strains were able to produce exopolysaccharides (EPS) from sucrose. In addition, the strains containing levS were able to grow on sucrose as sole carbon source. Strains of one cluster exhibit auxotrophies for purine nucleotides. The physiol. and genomic analyses suggest that the biodiversity of F. sanfranciscensis is larger than anticipated. Consequently, “original” habitats and lifestyles of F. sanfranciscensis may vary but can generally be referred to an adaptation to sugary (maltose/sucrose/fructose-rich) and aerobic environments as found in plants and insects. It can dominate sourdoughs as a result of reductive evolution and cooperation with fructose-delivering, acetate-tolerant yeasts.

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, Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

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

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 (X_Glu = 56.6-62.8, S_SGlu > 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

Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 527-07-1, formula is C6H11NaO7, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , Computed Properties of 527-07-1

Raman, Ganesan;Das, Jagannath;Mantri, Kshudiram;Krishna Reddy, Jakkidi;Jasra, Raksh Vir research published 《 Layered silicate formation during chiral acid templated ZSM-5 synthesis》, the research content is summarized as follows. Silicate anion forms four, five, and six coordinate complexes with chiral polyhydroxy alc. and polyhydroxy acids in aqueous alkali media. The chem. of organosilicate complexes is well established but its effect on zeolite synthesis has not been explored. When chiral acid is used as a template in ZSM-5 synthesis, a new partially crystalline layered silicate is formed whose basal spacing value do not match with any of the known layered silicates. Chiral acids are necessary to induce layered silicate formation and it is not formed in absence of any template or tetrapropylammonium bromide (TPABr) as a template. In presence of chiral acid, layered silicates are not precursors to ZSM-5 formation as observed normally in ZSM-5 synthesis. This method is new and it paves the way for generating layered silicates using simple chiral acids as a template.

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, Computed Properties of 527-07-1

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Some low molecular weight alcohols of industrial importance are produced by the addition of water to alkenes. 527-07-1, formula is C6H11NaO7, Ethanol, isopropanol, 2-butanol, and tert-butanol are produced by this general method. Two implementations are employed, the direct and indirect methods. Name: Sodium Gluconate

Rbaa, Mohamed;Benhiba, Fouad;Dohare, Parul;Lakhrissi, Loubna;Touir, Rachid;Lakhrissi, Brahim;Zarrouk, Abdelkader;Lakhrissi, Younes research published 《 Synthesis of new epoxy glucose derivatives as a non-toxic corrosion inhibitors for carbon steel in molar HCl: Experimental, DFT and MD simulation》, the research content is summarized as follows. The purpose of this study was to examine the effect of inhibiting corrosion of two biodegradable newly synthesized compound derivatives of D-glucose for carbon steel in 1 M HCl. These compounds were characterized by IR (IR), NMR (1H and 13C NMR) and Elementary anal. (EA) spectroscopy. The evaluation of the corrosion inhibiting effect was studied using Usual electrochem. methods, DFT calculations and MD simulations. The morphol. of the metal surface was characterized by SEM/EDS. However, the gravimetric solutions were analyzed by ICP-OPS and UV-visible spectrometry. This study has shown that these compounds provide good protection for carbon steel against corrosion inhibition in the 1 M HCl. Analyzes by scanning electron spectroscopy coupled with energy dispersion spectroscopy (SEM/EDS) show that the two inhibitors have been well adsorbed on the metal surface. The theoritical studies are in good agreement with those obtained from Electrochem. methods.

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, Name: Sodium Gluconate

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 527-07-1, formula is C6H11NaO7, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , Formula: C6H11NaO7

Reiter, Lex;Wangler, Timothy;Anton, Ana;Flatt, Robert J. research published 《 Setting on demand for digital concrete – Principles, measurements, chemistry, validation》, the research content is summarized as follows. Digital fabrication with concrete is a field of rapidly developing building processes – including layered extrusion – where specific yield stress evolution over time is needed, owing to concrete loading during fabrication. By combining physico-chem. principles of concrete yield stress evolution with strength requirements imposed by the building process an avenue is devised for an effective development of these processes. Most notably, strength should grow linearly with time to ensure strength-based self-support, while it should growth with its third power to avoid self-weight induced buckling. It is argued that the needed evolution can be achieved by adequately controlling cement hydration during fabrication. Specifically, we outline the Set on Demand approach, relying on a combination of admixtures adequate for the process under study. This strategy is implemented with newly developed methods capable of measuring concrete yield stress evolution at rest, thus providing the link from chem. to processing and mech. stability.

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, Formula: C6H11NaO7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts