Hamzaoui, Malek et al. published their research in Arabian Journal for Science and Engineering in 2022 | CAS: 57-55-6

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Quality Control of 1,2-Propanediol

A Numerical and Experimental Performance Assessment of a Single-Phase Supersonic Ejector was written by Hamzaoui, Malek;Nesreddine, Hakim;Aidoun, Zine. And the article was included in Arabian Journal for Science and Engineering in 2022.Quality Control of 1,2-Propanediol This article mentions the following:

This paper proposes an integrated numerical-exptl. study of a fixed geometry ejector designed for a cooling system activated by waste heat. Ejector operation is analyzed for cases of imposed input and output sets of conditions in terms of pressures and/or temperatures Experiments with constant primary conditions and secondary temperature were conducted in a range of outlet pressures for model validation purposes. A parametric anal. was then performed for constant pressure and temperature conditions at both inputs (primary and secondary) by varying the outlet pressure. For each test case, performance in terms of entrainment ratio, local parameters distributions (P, M, τ) and the internal flow structure were analyzed in an attempt to establish a link between the external constraints, the flow structure, the operation stability and performance within the range of cooling applications. The ranges of operating conditions investigated were Pp = 4.77 bar, Tp = 83°C and, resp., 1.7 ≤ Pc ≤ 2.4 bar, 12.5°C ≤ Te ≤ 16.5°C, at saturation Exptl. entrainment ratio, ERexp in the range of 0.12-0.22 was numerically simulated within ± 10%. It was shown that both the ejector operation and the internal flow configurations were sensitive to backpressure. More particularly, an optimal backpressure exists to which corresponds an on-design conditions with maximized entrainment ratio and a shock-wave train located at the end of the mixing chamber. A backpressure increase sets the ejector in off design. This mode of operation is characterized by a shift of the shock train toward the inlets, a disturbance of the flow configuration, a diminution of the entrainment ratio and a deterioration of the operation stability. On the other hand, a backpressure decrease does not affect the ejector stability of operation at its maximum entrainment ratio for the prevailing conditions. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6Quality Control of 1,2-Propanediol).

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Quality Control of 1,2-Propanediol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Sun, Min-Fei et al. published their research in European Journal of Pharmaceutics and Biopharmaceutics in 2022 | CAS: 57-55-6

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Quality Control of 1,2-Propanediol

Identification and characterization of chemical and physical stability of insulin formulations utilizing degraded glycerol after repeated use and storage was written by Sun, Min-Fei;Xu, Youfu;Yuan, Jun-Jie;Fang, Wei-Jie. And the article was included in European Journal of Pharmaceutics and Biopharmaceutics in 2022.Quality Control of 1,2-Propanediol This article mentions the following:

Insulin treatment is currently considered to be the main strategy for controlling diabetes. Although the recombinant insulin formulation is relatively mature, we found that a batch of insulin formulation exhibited an unusual degradation rate in the stability experiment The main purposes of this article are to identify the root cause for this phenomenon and characterize of chem. and phys. degradation products. We compared the chem. and phys. stability of two batches of insulin formulations prepared sep. with simulated repeated use and freshly opened glycerol. The chem. stability of insulin was identified by liquid chromatog. coupled with tandem mass spectrometry (LC- MS/MS). Micro-flow imaging (MFI), far-UV CD (Far-UV CD) and Thioflavin T (ThT) fluorescent assays were used to reveal protein aggregation and fibrosis. The chem. and phys. stability of the insulin formulation with newly opened glycerol was much better than that with degraded glycerol, and both groups of formulations were extremely sensitive to light. The results indicated that the original batch insulin formulation with abnormal stability was indeed caused by the excipient glycerol after long-term storage and repeated usage. More attention should be paid to the quality changes of excipients during repeated usage and storage of excipients for the practical purpose. Moreover, we have discovered a novel degradation pathway for insulin and peptides in general. In addition, LC-MS/MS results suggested that the N-terminus of insulin B-chain was prone to chem. degradation which enlightens that it could be potentially modified to improve the stability of insulin formulations. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6Quality Control of 1,2-Propanediol).

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Quality Control of 1,2-Propanediol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Dong, Rachael et al. published their research in Cryobiology in 2022 | CAS: 57-55-6

1,2-Propanediol (cas: 57-55-6) 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. 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.Application In Synthesis of 1,2-Propanediol

Evaluation of the permeation kinetics of formamide in porcine articular cartilage was written by Dong, Rachael;Clark, Shannon;Laouar, Leila;Heinrichs, Luke;Wu, Kezhou;Jomha, Nadr M.;Elliott, Janet A. W.. And the article was included in Cryobiology in 2022.Application In Synthesis of 1,2-Propanediol This article mentions the following:

Cryopreservation of articular cartilage will increase tissue availability for osteochondral allografting and improve clin. outcomes. However, successful cryopreservation of articular cartilage requires the precise determination of cryoprotectant permeation kinetics to develop effective vitrification protocols. To date, permeation kinetics of the cryoprotectant formamide in articular cartilage have not been sufficiently explored. The objective of this study was to determine the permeation kinetics of formamide into porcine articular cartilage for application in vitrification. The permeation of DMSO was first measured to validate existing methods from our previously published literature. Osteochondral dowels from dissected porcine femoral condyles were incubated in 6.5 M DMSO for a designated treatment time (1 s, 1 min, 2 min, 5 min, 10 min, 15 min, 30 min, 60 min, 120 min, 180 min, 24 h) at 22 °C (N = 3). Methods were then repeated with 6.5 M formamide at one of three temperatures: 4 °C, 22 °C, 37 °C (N = 3). Following incubation, cryoprotectant efflux into a wash solution occurred, and osmolality was measured from each equilibrated wash solution Concentrations of effluxed cryoprotectant were calculated and diffusion coefficients were determined using an anal. solution to Fics law for axial and radial diffusion in combination with a least squares approach. The activation energy of formamide was determined from the Arrhenius equation. The diffusion coefficient (2.7-3.3 x 10-10 m2/s depending on temperature) and activation energy (0.9±0.6 kcal/mol) for formamide permeation in porcine articular cartilage were established. The determined permeation kinetics of formamide will facilitate its precise use in future articular cartilage vitrification protocols. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6Application In Synthesis of 1,2-Propanediol).

1,2-Propanediol (cas: 57-55-6) 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. 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.Application In Synthesis of 1,2-Propanediol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Liu, Yong et al. published their research in ACS Medicinal Chemistry Letters in 2016 | CAS: 5856-63-3

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. 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.Application of 5856-63-3

Discovery of Pyrazolo[1,5-a]pyrimidine TTK Inhibitors: CFI-402257 is a Potent, Selective, Bioavailable Anticancer Agent was written by Liu, Yong;Laufer, Radoslaw;Patel, Narendra Kumar;Ng, Grace;Sampson, Peter B.;Li, Sze-Wan;Lang, Yunhui;Feher, Miklos;Brokx, Richard;Beletskaya, Irina;Hodgson, Richard;Plotnikova, Olga;Awrey, Donald E.;Qiu, Wei;Chirgadze, Nickolay Y.;Mason, Jacqueline M.;Wei, Xin;Lin, Dan Chi-Chia;Che, Yi;Kiarash, Reza;Fletcher, Graham C.;Mak, Tak W.;Bray, Mark R.;Pauls, Henry W.. And the article was included in ACS Medicinal Chemistry Letters in 2016.Application of 5856-63-3 This article mentions the following:

This work describes a scaffold hopping exercise that begins with known imidazo[1,2-a]pyrazines, briefly explores pyrazolo[1,5-a][1,3,5]triazines, and ultimately yields pyrazolo[1,5-a]pyrimidines as a novel class of potent TTK inhibitors. An X-ray structure of a representative compound is consistent with 11/2 type inhibition and provides structural insight to aid subsequent optimization of in vitro activity and physicochem. and pharmacokinetic properties. Incorporation of polar moieties in the hydrophobic and solvent accessible regions modulates physicochem. properties while maintaining potency. Compounds with enhanced oral exposure were identified for xenograft studies. The work culminates in the identification of a potent (TTK Ki = 0.1 nM), highly selective, orally bioavailable anticancer agent (CFI-402257) for IND enabling studies. In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3Application of 5856-63-3).

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. 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.Application of 5856-63-3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Shelton, Keith L. et al. published their research in Psychopharmacology (Heidelberg, Germany) in 2022 | CAS: 57-55-6

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Reference of 57-55-6

Reinforcing effects of fentanyl and sufentanil aerosol puffs in rats was written by Shelton, Keith L.;Nicholson, Katherine L.. And the article was included in Psychopharmacology (Heidelberg, Germany) in 2022.Reference of 57-55-6 This article mentions the following:

Rapidly evolving e-cigarette technol. developed for self-administering nicotine aerosol has the potential to be utilized to self-administer other aerosolized drugs of abuse. Rodent models which mirror characteristics of human e-cigarette use are necessary to explore the degree to which this may be a public health concern. Our goal was to develop a highly translational model of discrete nose-only aerosol puff drug delivery to explore the reinforcing effects of fentanyl and sufentanil aerosols in rats. Male and female Sprague-Dawley rats were trained to perform a multiple schedule FR1 lever-press, 4-s (second) nose hold operant during which the subjects orofacial areas were exposed to drug-free glycerol/propylene glycol aerosol produced by a com. e-cigarette at a power setting of 18 W. Each completed 4-s drug-free vehicle aerosol exposure resulted in a 3-s presentation of a 0.1-mL dipper of sweetened milk solution After training, rats were then allowed to self-administer 4-s nose-only puffs of fentanyl (100-6000 μg/mL) or sufentanil (30-500 μg/mL) aerosol in the absence of paired milk dipper reinforcers. All 31 rats learned the lever-press/nose-poke multiple schedule for milk dippers alone and 25 accepted exposure to 4 s of 18 W of drug-free vehicle aerosol when paired with milk dipper presentations. In the absence of paired milk dipper presentations, fentanyl aerosol puffs at concentrations of 1000 and 3000 μg/mL as well as 100 μg/mL puffs of sufentanil served as reinforcers compared to both air puffs and drug-free vehicle aerosol puffs. There were no significant differences between males and females in number of fentanyl or sufentanil puffs self-administered. Discrete nose-only puffs of two potent opioids under exposure conditions comparable to puff durations in human e-cigarette users serve as reinforcers in rats. This outcome suggests that under appropriate conditions e-cigarettes might be a potential alternative delivery mechanism for illicit opioids. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6Reference of 57-55-6).

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Reference of 57-55-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Akhmedov, I. M. et al. published their research in Russian Journal of Organic Chemistry in 2016 | CAS: 5856-63-3

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R鈥昈鈭?. For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. 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.Application of 5856-63-3

Catalytic effect of molecular iodine in the pyrrolization of tetramethoxytetrahydrofuran with optically active amines was written by Akhmedov, I. M.;Guseinov, E. Z.;Safarova, A. S.;Sadygova, A. Z.;Kurbanova, M. M.. And the article was included in Russian Journal of Organic Chemistry in 2016.Application of 5856-63-3 This article mentions the following:

A procedure for the synthesis of optically active 3,4-dimethoxypyrroles was developed. The reaction of 2,3,4,5-tetramethoxytetrahydrofuran with optically active amines in the presence of a catalytic amount of iodine (10 mol %) at 70-75掳 (8 h) afforded 65-75% of alkoxypyrroles. In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3Application of 5856-63-3).

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R鈥昈鈭?. For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. 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.Application of 5856-63-3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Ramprasath, R. et al. published their research in Environmental Research in 2022 | CAS: 57-55-6

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Computed Properties of C3H8O2

Polyol-assisted hydrothermal synthesis of Mn-doped 伪 – Fe2O3(MFO) nanostructures: Spin disorder-induced magnetism and photocatalytic properties. was written by Ramprasath, R.;Manikandan, Velu;Aldawood, S.;Sudha, S.;Cholan, S.;Kannadasan, N.;Sampath, Sridhar;Gokul, B.. And the article was included in Environmental Research in 2022.Computed Properties of C3H8O2 This article mentions the following:

Hierarchical nanostructures play an important role in environmental clean-up and sustainability applications. The magnetic and photocatalytic characteristics of flower-like Mn-doped 伪-Fe2O3 nanostructures were prepared by using a polyol-assisted hydrothermal method. Crystallite sizes are in the range of 35-42 nm, and the existence of 3D hierarchical nanostructures was observed in FESEM pictures. The optical band gap energy varies between 2.08 and 2.16 eV, while XPS examination exposes the ions’ charge states and validates Mn3+ inclusion in the Fe3+ lattice. At room temperature, the addition of Mn to 伪-Fe2O3 results in a spin disorder ferromagnetism and coercivity of about 600 Oe was achieved. Methylene blue (MB) dye solution degraded by 92% when 2.5% Mn doped with 伪-Fe2O3 under visible conditions for 120 min irradiation time. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6Computed Properties of C3H8O2).

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Computed Properties of C3H8O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Wang, Bang-Jin et al. published their research in Molecules in 2019 | CAS: 5856-63-3

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Synthetic Route of C4H11NO

An enantioselective potentiometric sensor for 2-amino-1-butanol based on chiral porous organic cage CC3-R was written by Wang, Bang-Jin;Duan, Ai-Hong;Zhang, Jun-Hui;Xie, Sheng-Ming;Cao, Qiu-E.;Yuan, Li-Ming. And the article was included in Molecules in 2019.Synthetic Route of C4H11NO This article mentions the following:

Porous organic cages (POCs) have attracted extensive attention due to their unique structures and tremendous application potential in numerous areas. In this study, an enantioselective potentiometric sensor composed of a polyvinyl chloride (PVC) membrane electrode modified with CC3-R POC material was used for the recognition of enantiomers of 2-amino-1-butanol. After optimization, the developed sensor exhibited enantioselectivity toward S-2-amino-1-butanol (log KPotS,R = -0.98) with acceptable sensitivity, and a near-Nernstian response of 25.8 卤 0.3 mV/decade within a pH range of 6.0-9.0. In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3Synthetic Route of C4H11NO).

(R)-2-Aminobutan-1-ol (cas: 5856-63-3) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Synthetic Route of C4H11NO

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

te Molder, Thimo D. J. et al. published their research in Biofuels, Bioproducts & Biorefining in 2022 | CAS: 57-55-6

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. 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 57-55-6

Do not forget the classical catalyst poisons: The case of biomass to glycols via catalytic hydrogenolysis was written by te Molder, Thimo D. J.;Kersten, Sascha R. A.;Lange, Jean-Paul;Ruiz, M. Pilar. And the article was included in Biofuels, Bioproducts & Biorefining in 2022.Related Products of 57-55-6 This article mentions the following:

The conversion of herbaceous biomass to glycols via tungstate catalyzed hydrogenolysis is challenging owing to its high content of extractives, inorganics and S/N, compared with woody biomass. We tested the hydrogenolysis performance of hay in batch autoclave experiments in the presence of soluble sodium polytungstate and Raney Ni at 245掳C, both in excess of catalyst as well as under catalyst-starving conditions. By this method, we found that addnl. tungstate and Raney Ni poisons, or at least their much higher concentrations, are present in the hay feedstock compared with woody biomass. It turns out that N- and in particular S-containing components present in hay are the root cause for deactivation of the hydrogenation catalyst. From the exptl. data we have derived feedstock criteria for N and S that should be targeted in terms of catalyst consumption for operation in an industrially relevant window. These challenging criteria urge the development of effective pretreatments for S/N removal or the employment of S/N-tolerant catalysts in the field of catalytic biomass conversion. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6Related Products of 57-55-6).

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. 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 57-55-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Hubner, A. M. et al. published their research in Journal of Dairy Science in 2022 | CAS: 57-55-6

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. 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.Synthetic Route of C3H8O2

A randomized controlled trial examining the effects of treatment with propylene glycol and injectable cyanocobalamin on naturally occurring disease, milk production, and reproductive outcomes of dairy cows diagnosed with concurrent hyperketonemia and hypoglycemia was written by Hubner, A. M.;Canisso, I. F.;Peixoto, P. M.;Coelho, W. M. Jr.;Ribeiro, L.;Aldridge, B. M.;Lima, F. S.. And the article was included in Journal of Dairy Science in 2022.Synthetic Route of C3H8O2 This article mentions the following:

The objective of this study was to assess the effects of treatment with propylene glycol (PG) and cyanocobalamin (B12) on health, milk production, and reproductive outcomes of cows diagnosed with hyperketonemia (HK), hypoglycemia (HG), or concurrent HKHG. Glucose and 尾-hydroxybutyric acid (BHBA) concentrations were assessed in whole blood using a handheld device in lactating dairy cows (n = 2,418) between 3 and 9 d postpartum. Cows categorized as HK (n = 232, BHBA 鈮?.2 mmol/L), HG (n = 161, glucose 鈮?.2 mmol/L), and concurrent HKHG (n = 204, BHBA 鈮?.2 mmol/L, and glucose 鈮?.2 mmol/L) were randomized to receive treatment or to remain untreated (control). Treatment consisted of a single dose of B12 (10 mg, i.m.) and 300 mL of PG orally for 5 d, starting on the day of cow-side testing. Milk production, health, and reproductive outcomes were analyzed according to groups. Statistical anal. was carried out using SAS version 9.4 (SAS/STAT, SAS Institute Inc.). Treatment in HG cows decreased clin. ketosis, increased milk production in the fifth week of lactation for multiparous cows, and tended to increase 305-d mature-equivalent milk yield (305ME) for primiparous cows compared with untreated cows with the same metabolic profile. For cows with HKHG, treatment increased 305ME in multiparous cows and tended to increase 305ME in primiparous cows. No differences were found for treatment among any of the metabolic groups regarding reproductive outcomes, nor were any treatment effects found among HK cows. Glycemic status may help identify metabolically challenged early postpartum dairy cows, which may have differential response to PG and B12 treatment. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6Synthetic Route of C3H8O2).

1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. 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.Synthetic Route of C3H8O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts