Category: 115-84-4

Inhibition of acid undercutting of inorganic/organic hybrid polyurethane coatings was written by He, Zhouying;Li, Ximing;Soucek, Mark D.;Castaneda, Homero. And the article was included in Progress in Organic Coatings in 2019.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

This study investigated the corrosion resistance of inorganic/organic hybrid polyurethane based coatings by using a mixture of sol-gel precursors. Four sol-gel precursor, tetra-Et orthosilicate (TEOS), titanium(IV) isopropoxide (TIP), and zirconium(IV) propoxide (ZRP), were utilized in this study. Salt spray, acid undercutting, and electrochem. impedance spectroscopy (EIS) were conducted to study the anticorrosion behavior of the coatings. Generally, samples based on mixed sol-gel precursors exhibited better protection compared to the urethane coating without sol-gel precursors or the coating with only TEOS as the single sol-gel precursor. In acid undercutting experiments, mixed sol-gel precursor samples provided the best results compared to the control and TEOS-based samples. Comparison of parameters extracted by EIS describing water uptake indicates mixed sol-gel precursor composition had the best anticorrosion performance, which was consistent with acid undercutting results. The impedance of the hybrid coatings, at the order of 1010 Ω cm² at 0.01 Hz, were ca. 3 orders higher than the control sample. Coating capacitance for all the hybrid coatings were stable throughout the immersion time while that for the control sample had a significant change after short time. The water uptake for the control sample was close to 2.5% while that for all the hybrid coatings were about or lower than 0.5%. Morphol. from SEM revealed that the organic inorganic sample with TEOS/TIP/ZRP mixed precursors maintained the coating integrity while higher porosity was developed in the control sample. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Name: 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Name: 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Uncertainties in monitoring of SVOCs in air caused by within-sampler degradation during active and passive air sampling was written by Melymuk, Lisa;Bohlin-Nizzetto, Pernilla;Prokes, Roman;Kukucka, Petr;Pribylova, Petra;Vojta, Simon;Kohoutek, Jiri;Lammel, Gerhard;Klanova, Jana. And the article was included in Atmospheric Environment in 2017.Related Products of 115-84-4 The following contents are mentioned in the article:

Degradation of semivolatile organic compounds (SVOCs) occurs naturally in ambient air due to reactions with reactive trace gases (e.g., ozone, NO_x). During air sampling there is also the possibility for degradation of SVOCs within the air sampler, leading to underestimates of ambient air concentrations We investigated the possibility of this sampling artifact in commonly used active and passive air samplers for seven classes of SVOCs, including persistent organic pollutants (POPs) typically covered by air monitoring programs, as well as SVOCs of emerging concern. Two active air samplers were used, one equipped with an ozone denuder and one without, to compare relative differences in mass of collected compounds Two sets of passive samplers were also deployed to determine the influence of degradation during longer deployment times in passive sampling. In active air samplers, comparison of the two sampling configurations suggested degradation of particle-bound polycyclic aromatic hydrocarbons (PAHs), with concentrations up to 2× higher in the denuder-equipped sampler, while halogenated POPs did not have clear evidence of degradation In contrast, more polar, reactive compounds (e.g., organophosphate esters and current use pesticides) had evidence of losses in the sampler with denuder. This may be caused by the denuder itself, suggesting sampling bias for these compounds can be created when typical air sampling apparatuses are adapted to limit degradation Passive air samplers recorded up to 4× higher concentrations when deployed for shorter consecutive sampling periods, suggesting that within-sampler degradation may also be relevant in passive air monitoring programs. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Related Products of 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Related Products of 115-84-4

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Adsorption of 2-Butyl-2-ethyl-1,3-propanediol from Aqueous Solutions on Activated Carbon: Salt-Out Effect on Equilibrium, Kinetics, and Dynamics was written by Chang, Ganggang;Bao, Zongbi;Zhang, Zhiguo;Xing, Huabin;Su, Baogen;Yang, Yiwen;Ren, Qilong. And the article was included in Industrial & Engineering Chemistry Research in 2014.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

In recent decades, 2-butyl-2-ethyl-1,3-propanediol (BEPD) was extensively evaluated as an efficient extractant for the recovery of B from brine solutions commonly present in Mg chloride. The BEPD leaked into the raffinate must be recovered to make the process of solvent extraction cost-efficient. The present study examined the feasibility of a commercialized coal-based activated C to recover BEPD from brine solutions The salt-out effect on adsorption isotherms and kinetics of BEPD from brine solutions with salt concentrations up to 100 g/L were reported at different temperatures (20°, 30°, 40°, and 50°). The saturated adsorption capacities were significantly enhanced from 192 mg/g in the deionized H₂O to 238 mg/g in the brine solution with an MgCl₂ concentration of 100 g/L at 30°. Kinetic anal. indicated that the adsorption kinetics of BEPD followed the pseudo-second-order equation, and the pseudo-second rate constant (k₂) affected by the varied salt concentrations complied with the following order: MgCl₂ (100 g/L) > MgCl₂ (25 g/L) ≈ CaCl₂ (20 g/L) > deionized H₂O. Also, the benefit from the salt-out effect was also verified by the extended dynamic breakthrough volume as well as the amount adsorbed. The dynamic adsorption capacity was much higher in a saline H₂O, i.e., 235 vs. 191 mg/g in the deionized H₂O. The Thomas model was further applied to predict the exptl. breakthrough data, and the obtained model parameters could be useful for future process design. The activated C has the potential for practical adsorption applications for BEPD recovery from aqueous solutions This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
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Intrinsically stretchable naphthalenediimide-bithiophene conjugated statistical terpolymers using branched conjugation break spacers for field-effect transistors was written by Lin, Yan-Cheng;Matsuda, Megumi;Sato, Kei-ichiro;Chen, Chun-Kai;Yang, Wei-Chen;Chueh, Chu-Chen;Higashihara, Tomoya;Chen, Wen-Chang. And the article was included in Polymer Chemistry in 2021.Computed Properties of C9H20O2 The following contents are mentioned in the article:

The development of conjugated polymers through the statistical terpolymn. of conjugation break spacers (CBSs) has received great attention because of their synergistic potential in enhancing fracture strain and tensile strength. In this study, a series of bulky and branched CBSs with ester functional groups and di-Me (P1), methyl/propyl (P2), ethyl/butyl (P3), and di-Bu (P4) alkyl groups were incorporated into naphthalenediimide-bithiophene-based conjugated polymers through statistical terpolymn. Morphol. studies, including at. force microscopy (AFM) and grazing incidence X-ray diffraction (GIXD) studies, were applied to pristine and stretched polymer films to decipher the structure-stretchability relationship; further, their mobility-stretchability relationship was investigated by studying their field-effect transistor (FET) characteristics. We found that polymers with bulky and branched CBSs exhibit reduced backbone rigidity, allowing polymer chains to entangle more easily than those of stiffer polymers with similar mol. weights Therefore, the polymer film exhibits a more uniform load distribution throughout the channel layer, and the branched CBSs serve as lubricants that deter crack propagation during deformation. Consequently, P4 with sym. extended alkyl groups shows good ductility and mobility-stretchability properties, with orthogonal μe,‖/μe,⊥ retention of approx. 20-30% with 60% strain and 30-40% after 400 stretching-releasing cycles with 60% strain. Our results indicated that statistical terpolymn. with branched CBSs is a versatile and effective methodol. for controlling orientational and stacking patterns to achieve good mobility-stretchability properties in conjugated polymers. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Computed Properties of C9H20O2).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Computed Properties of C9H20O2

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Alcohol – Wikipedia,
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Decrease in activity caused by hydrogen in Ziegler-Natta ethene polymerisation was written by Garoff, T.;Johansson, S.;Pesonen, K.;Waldvogel, P.;Lindgren, D.. And the article was included in European Polymer Journal in 2001.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

In this study we prepared seven different Ziegler-Natta catalysts and polymerized them at different hydrogen concentrations in order to investigate their kinetic behavior during polymerization The objective was to see whether the results corresponded to what could be expected on the basis of Kissin’s β-agostic deactivation theory. According to this theory, hydrogen causes the formation of dormant sites due to the formation of β-agostic coordination from the Et groups formed after hydrogen termination. According to this theory, the more hydrogen that is used, the more β-agostic coupling and the smaller percentage of Ti in a polymerizing state. This β-agostic coupling would thus explain the lower activity level seen in polymerization where more hydrogen has been used.The results of this study showed that none of the catalysts showed the kind of behavior that would correspond to what could be predicted on the basis of Kissin’s theory. Deactivation could be detected only when a lower amount of hydrogen was used. When higher amounts of hydrogen were used in polymerization there was a clear delay in activation time of the catalysts. This particularly seemed to be the case for catalysts where Ti was present as Ti(IV). This delay in the activation of the catalyst caused a decrease in activity in addition to the normal decrease in activity due to hydrogen replacing C₂” in the polymerization process. The only catalyst showing no delay in activation was a silica-based PE Ziegler-Natta catalyst where the Ti was already in trivalent form. In this case no decrease in activity was observed in addition to the normal decrease in activity caused by hydrogen replacing C₂” in the polymerization process. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Safety of 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Safety of 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
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Intramolecular hydrogen bonding and rotation isomerism in β-diols in carbon tetrachloride solution was written by Buc, H.. And the article was included in Ann. Chim. (Paris) in 1963.COA of Formula: C9H20O2 The following contents are mentioned in the article:

In order to attempt to evaluate mol. interactions in polymers, the interactions in a series of β and α,ω-aliphatic linear glycols dissolved in a non-polar solvent (CCl₄) were studied by means of determinations of the IR spectra of very dilute solutions at 25, 35, 45, 55, and 65°. With the β-diols it was concluded that the H of the OH on the least substituted C atom is present in the H-bond. The number of H-bonds per mol. decreases as the temperature increases. The stabilization of mols, joined by an intramol. H bond is due in part to the H-bond and in part to the conformation of the chain. Graphic integration of the absorption bands permits the evaluation of the free energies and enthalpies characteristic of the equilibrium; it appeared that the magnitudes are influenced by the intensity of the Van der Waals repulsions between the different groups of the mols. The thermodn. values associated with the reaction shown are clearly different from those RCH(OH)CH₂C(OH)R’R” ⇌ RCHCH₂CR’R” characterizing an intermol. H-bond, since the values of the entropy and the enthalpy of reaction are both less than the corresponding values for the formation of an intermol. H bond. With α,ω-diols, the intramol. attraction between the OH groups diminishes progressively as n (the number of C atoms between) increases up to a value of n = 6. On the basis of these results and of other considerations, privileged conformations of the aliphatic skeletons of these compounds are determined The diastereoisomers of 2,4-pentanediol were separated, and one of them (b₁₃ 102.5°) was identified as the d,d,l,l-form by comparison with the product obtained by an asym. biochem. reduction of MeCOCH₂COMe with a strain of Saccharomyces cerevisiae. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4COA of Formula: C9H20O2).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.COA of Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Trends in the Athermal Entropy of Mixing of Polymer Solutions was written by Vahid, Amir;Gray, Neil H.;Elliott, J. Richard. And the article was included in Macromolecules (Washington, DC, United States) in 2014.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Polymeric mixtures of hydrocarbons and alcs. have been simulated with discontinuous potential models to characterize the Helmholtz energy of the repulsive reference fluids. This quantity is equivalent to the athermal mixture entropy. The reference compressibility factor and Helmholtz free energy have been correlated for various mol. structures from single to infinite chain lengths. The mixtures included small n-alkanes, branched alkanes, aromatics, and alcs., with polymeric mols. of: n-alkanes, ethyl-styrenes, ethyl-propylenes, and isoprenes. We find that the athermal entropy of mixing at constant packing fraction deviates significantly from ideality as the volume ratio increases, but the nonideality is fairly insensitive to structural details like branching and rings. Volume ratio alone does not provide a complete characterization, however. For example, a mixture of C40 and C80 would yield a small deviation whereas a mixture of C2 and C4 would provide a relatively large deviation. This observation leads to the introduction of a characteristic parameter in terms of entropy d., designated as an entropic solubility parameter. In both ideal and nonideal solutions, the trends still follow van der Waals (vdW) mixing. This leads to an accurate characterization of the entropic contribution to the χ parameter (χ^S) of Flory-Huggins theory for mixtures of all sizes, shapes, and compositions of mol. structures. A general rule is developed for predicting the athermal entropy of mixing based on knowledge of the volume ratios and entropic solubility parameter of the constituent mols. The simulations are compared to Flory-Huggins (FH), group contribution lattice fluid theory (GCLF), statistical associating fluid theory (SAFT), Sanchez-Lacombe (SL), and Guggenheim-Staverman (GS) theories of polymer chains. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Quality Control of 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Quality Control of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Restricted Ion Transport by Plasticizing Side Chains in Polycarbonate-Based Solid Electrolytes was written by Ebadi, Mahsa;Eriksson, Therese;Mandal, Prithwiraj;Costa, Luciano T.;Araujo, C. Moyses;Mindemark, Jonas;Brandell, Daniel. And the article was included in Macromolecules (Washington, DC, United States) in 2020.Related Products of 115-84-4 The following contents are mentioned in the article:

Increasing the ionic conductivity has for decades been an overriding goal in the development of solid polymer electrolytes. According to fundamental theories on ion transport mechanisms in polymers, the ionic conductivity is strongly correlated to free volume and segmental mobility of the polymer for the conventional transport processes. Therefore, incorporating plasticizing side chains onto the main chain of the polymer host often appears as a clear-cut strategy to improve the ionic conductivity of the system through lowering of the glass transition temperature (T_g). This intended correlation between T_g and ionic conductivity is, however, not consistently observed in practice. The aim of this study is therefore to elucidate this interplay between segmental mobility and polymer structure in polymer electrolyte systems comprising plasticizing side chains. To this end, we utilize the synthetic versatility of the ion-conductive poly(trimethylene carbonate) (PTMC) platform. Two types of host polymers with side chains added to a PTMC backbone are employed, and the resulting electrolytes are investigated together with the side chain-free analog both by experiment and with mol. dynamics (MD) simulations. The results show that while added side chains do indeed lead to a lower T_g, the total ionic conductivity is highest in the host matrix without side chains. It was seen in the MD simulations that while side chains promote ionic mobility associated with the polymer chain, the more efficient interchain hopping transport mechanism occurs with a higher probability in the system without side chains. This is connected to a significantly higher solvation site diversity for the Li⁺ ions in the side-chain-free system, providing better conduction paths. These results strongly indicate that the side chains in fact restrict the mobility of the Li⁺ ions in the polymer hosts. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Related Products of 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Related Products of 115-84-4

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Comparison of different edible parts of bighead carp (Aristichthys nobilis) flavor was written by Xiao, Naiyong;Huang, Haiyuan;Liu, Junya;Jiang, Xin;Chen, Qin;Chen, Qing;Shi, Wenzheng. And the article was included in Journal of Food Biochemistry in 2021.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

The study aims to obtain the information on taste and odor among different edible parts (white dorsal meat, white abdomen meat, white tail meat, and dark meat) of bighead carp. The results showed that the white dorsal meat and white abdomen meat had the higher content of total amino acids among all edible parts of bighead carp samples. The highest inosine monophosphate and adenosine monophosphate content presented in white abdomen meat, and the highest equivalent umami concentration value presented in dark meat. The principal component anal. result of electronic tongue and electronic nose showed significant differences in the overall taste and odor characteristics among four group samples. Addnl., 41, 30, 42, and 29 volatile compounds were identified by headspace solid-phase microextraction/gas chromatog.-mass spectrometry among white dorsal meat, white abdomen meat, white tail meat, and dark meat of bighead carp, resp. Based on the data of relative olfactory activity value (ROAV ≥ 1), 12 relative olfactory activity compounds may mainly contribute to the overall odor of bighead carp, including 2-methylbutanal, hexanal, heptanal, (E)-2-octenal, nonanal, dodecanal, undecanal, decanal, 3-methyl-1-pentanol, 1-octen-3-ol, (Z)-2-octen-1-ol, and eucalyptol. Furthermore, according to the Partial Least Squares Discriminant Anal. profile derived from the ROAV of 12 characteristic volatile compounds, significant variations in the odor of different edible parts of bighead carp. Overall, there was a significant difference in taste and odor among different edible parts of bighead carp, and this study may provide useful information for unraveling the flavor characteristics of each edible part of raw bighead carp. The comprehensive information on taste and odor among different edible parts (white dorsal meat, white abdomen meat, white tail meat, and dark meat) of bighead carp were obtained using liquid chromatog.-mass spectrometry, automatic amino acid analyzer, electronic tongue (E-tongue), headspace solid-phase microextraction/gas chromatog.-mass spectrometry (HS-SPME/GC-MS), and electronic nose (E-tongue), resp. This study may provide useful information for unraveling the flavor characteristics of each edible part of raw bighead carp and improving the flavor of bighead carp products. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4HPLC of Formula: 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Assessment of antidiabetic potential and phytochemical profiling of Rhazya stricta root extracts was written by Mahmood, Rashid;Kayani, Waqas Khan;Ahmed, Tanveer;Malik, Farnaz;Hussain, Shahzad;Ashfaq, Muhammad;Ali, Hussain;Rubnawaz, Samina;Green, Brian D.;Calderwood, Danielle;Kenny, Owen;Rivera, Gerardo A.;Mirza, Bushra;Rasheed, Faiza. And the article was included in BMC Complementary Medicine and Therapies in 2020.Computed Properties of C9H20O2 The following contents are mentioned in the article:

Diabetes mellitus is a chronic disease characterized by hyperglycemia that may occur due to genetic, environmental or lifestyle factors. Natural remedies have been used to treat diabetes since long and many antidiabetic compounds of varied efficacies have been isolated from medicinal plants. Rhazya stricta has been used for decades for the treatment of diabetes mellitus and associated ailments. Considering the folkloric use of R. stricta against diabetes, it was aimed to investigate the effectiveness of its root extracts against diabetes through in vitro assays and in vivo studies using animal model along with phytochem. profiling through GCMS. Various fractions of Rhazya stricta obtained through column chromatog. were evaluated for a variety of assays including α-glucosidase, Dipeptidyl peptidase-IV (DPP-IV), β-secretase and Glucagon-like peptide-1 (GLP-1) secretion studies. For the in vivo studies the alloxan-induced diabetic mice were treated with root extracts and blood glucose levels, HbA1C, and other biochem. markers along with the histol. study of the liver were done. The phytochem. identification was performed using an Agilent 7890B GC coupled to a 7010 Triple Quadrupole (MS/MS) system. GraphPad Prism software version 5.01 was used for statistical anal. Majority of the extract fractions showed excellent results against diabetes by inhibiting enzymes DPP-IV (Up to 61%) and β-secretase (Up to 83%) with IC₅₀s 979 μg/mL and 169 μg/mL resp. with increase in the GLP1 secretion. The results of in vivo studies indicated a marked reduction in blood glucose and HbA1c levels along with pos. effects on other parameters like lipid profile, liver functions and renal functions of extract-treated mice as compared to control. The histol. examination of the liver demonstrated hepatoprotective effects against diabetes led changes and various classes of phytochems. were also identified through GCMS in different fractions. The results revealed strong antidiabetic activity of R. stricta root with the potential to protect body organs against diabetic changes. Moreover, a variety of phytochems. has also been identified through GCMS that might be responsible for the antidiabetic potential of Rhazya stricta root. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Computed Properties of C9H20O2).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Computed Properties of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts