Elmas, Gamze’s team published research in Phosphorus, Sulfur and Silicon and the Related Elements in 2019 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Nitrous acid converts secondary amines (aliphatic or aromatic) to N-nitroso compounds (nitrosamines): R2NH + HNO2 → R2N―NO. Some nitrosamines are potent cancer-inducing substances, and their possible formation is a serious consideration when nitrites, which are salts of nitrous acid, are present in foods or pharmaceutical preparations. Tertiary amines give rise to nitrosamines more slowly; an alkyl group is eliminated as an aldehyde or ketone, along with nitrous oxide, N2O.Safety of 3-Aminopropan-1-ol

Safety of 3-Aminopropan-1-olIn 2019 ,《Syntheses and structural characterizations of 2-pyridyl(N/O)spirocyclotriphosphazene derivatives》 appeared in Phosphorus, Sulfur and Silicon and the Related Elements. The author of the article were Elmas, Gamze. The article conveys some information:

The Cl exchange reaction of hexachlorocyclotriphosphazene, N3P3Cl6 (1), with one equimolar amount of sodium salt of N/O donor type bidentate ligand containing a 2-pyridyl pendant arm (2) afforded, regioselectively, the partly substituted 2-pyridyl(N/O)spirocyclotriphosphazene (3; with a yield of 65%) in THF. The reactions of 3 with excess pyrrolidine, morpholine and 1,4-dioxa-8-azaspiro[4,5]decane (DASD) gave the tetraamino-2-pyridyl(N/O)spirocyclotriphosphazenes (3a-3c) in high yields. Compound 3 also gave both tetrapiperidino (3d) and gem-bispiperidino (3e) products with excess piperidine. The structures of all the compounds were determined by elemental analyses, ESI-MS, FTIR, HSQC, HMBC and 1H, 13C, and 31P NMR techniques. The crystal structure of 3e was identified by single crystal x-ray crystallog. Besides, the compound had one stereogenic P atom, and its chirality was verified by 31P NMR spectroscopy in the presence of (S)-(+)-2,2,2-trifluoro-1-(9′-anthryl)-ethanol (CSA). In addition to this study using 3-Aminopropan-1-ol, there are many other studies that have used 3-Aminopropan-1-ol(cas: 156-87-6Safety of 3-Aminopropan-1-ol) was used in this study.

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Nitrous acid converts secondary amines (aliphatic or aromatic) to N-nitroso compounds (nitrosamines): R2NH + HNO2 → R2N―NO. Some nitrosamines are potent cancer-inducing substances, and their possible formation is a serious consideration when nitrites, which are salts of nitrous acid, are present in foods or pharmaceutical preparations. Tertiary amines give rise to nitrosamines more slowly; an alkyl group is eliminated as an aldehyde or ketone, along with nitrous oxide, N2O.Safety of 3-Aminopropan-1-ol

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Alcohols – Chemistry LibreTexts

Osawa, Shigehito’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2022 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Primary amines having a tertiary alkyl group (R3CNH2) are difficult to prepare with most methods but are made industrially by the Ritter reaction. In this method a tertiary alcohol reacts with hydrogen cyanide (HCN) in the presence of a concentrated strong acid; a formamide, RNH―CHO, is formed first, which then undergoes hydrolysis.Application In Synthesis of 3-Aminopropan-1-ol

Osawa, Shigehito; Kurokawa, Sosuke; Otsuka, Hidenori published an article in 2022. The article was titled 《Controlled polymerization of metal complex monomers – fabricating random copolymers comprising different metal species and nano-colloids》, and you may find the article in Chemical Communications (Cambridge, United Kingdom).Application In Synthesis of 3-Aminopropan-1-ol The information in the text is summarized as follows:

Acrylate monomers with metal complexes were designed to build polymer metal complexes. The ideal copolymerization of monomers with zinc and platinum was performed to obtain random copolymers with a feeding metal composition The successful nano-colloid preparation from the polymers further highlighted the potential of the method for building multimetallic materials. The experimental part of the paper was very detailed, including the reaction process of 3-Aminopropan-1-ol(cas: 156-87-6Application In Synthesis of 3-Aminopropan-1-ol)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Primary amines having a tertiary alkyl group (R3CNH2) are difficult to prepare with most methods but are made industrially by the Ritter reaction. In this method a tertiary alcohol reacts with hydrogen cyanide (HCN) in the presence of a concentrated strong acid; a formamide, RNH―CHO, is formed first, which then undergoes hydrolysis.Application In Synthesis of 3-Aminopropan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Warne, Nicole M.’s team published research in Journal of Polymer Science (Hoboken, NJ, United States) in 2021 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Acylation is one of the most important reactions of primary and secondary amines; a hydrogen atom is replaced by an acyl group (a group derived from an acid, such as RCOOH or RSO3H, by removal of ―OH, such as RC(=O)―, RS(O)2―, and so on). Reagents may be acid chlorides (RCOC1, RSO2C1), anhydrides ((RCO)2O), or even esters (RCOOR′); the products are amides of the corresponding acids.Quality Control of 3-Aminopropan-1-ol

Warne, Nicole M.; Finnegan, John R.; Feeney, Orlagh M.; Kempe, Kristian published an article in 2021. The article was titled 《Using 2-isopropyl-2-oxazine to explore the effect of monomer distribution and polymer architecture on the thermoresponsive behavior of copolymers》, and you may find the article in Journal of Polymer Science (Hoboken, NJ, United States).Quality Control of 3-Aminopropan-1-ol The information in the text is summarized as follows:

Poly(cyclic imino ether)s (PCIE) have emerged as a highly promising class of polymer for use in biomedical applications with their value being derived from their excellent biocompatibility, diverse chem., and tunable hydrophilicity. Here, we investigate the properties of poly(2-isopropyl-2-oxazine) (PiPrOz), a relatively unexplored PCIE, determining it to have a cloud point temperature (Tcp) below physiol. temperature, not to crystallize from bulk or in solution, and to be highly biocompatible. Furthermore, a series of copolymers consisting of iPrOz and 2-methyl-2-oxazine (MeOz) was investigated with regard to the effect of monomer distribution and polymer architecture on thermoresponsive properties. To this end, linear block and statistical co-poly(2-oxazine)s (co-POz), along with three comb-shaped POz with block or statistical POz side chains were prepared Each of the five polymers showed distinct thermoresponsive behavior, with the linear block co-POz undergoing micelle formation and the other polymers macroscopic phase-separation at different Tcps. The variety observed in response to heating clearly highlights the importance of monomer sequence and polymer architecture when designing thermoresponsive polymers. We anticipate that our findings will prove useful to polymer chemists seeking to prepare novel thermoresponsive biomaterials. In the part of experimental materials, we found many familiar compounds, such as 3-Aminopropan-1-ol(cas: 156-87-6Quality Control of 3-Aminopropan-1-ol)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Acylation is one of the most important reactions of primary and secondary amines; a hydrogen atom is replaced by an acyl group (a group derived from an acid, such as RCOOH or RSO3H, by removal of ―OH, such as RC(=O)―, RS(O)2―, and so on). Reagents may be acid chlorides (RCOC1, RSO2C1), anhydrides ((RCO)2O), or even esters (RCOOR′); the products are amides of the corresponding acids.Quality Control of 3-Aminopropan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Majuta, Sandra N.’s team published research in Journal of the American Society for Mass Spectrometry in 2019 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Amines have a free lone pair with which they can coordinate to metal centers. Amine–metal bonds are weaker because amines are incapable of backbonding, but they are still important for sensing applications.While stronger than hydrogen bonds, amine–metal bonds are still weaker than both covalent and ionic bonds.Category: alcohols-buliding-blocks

Category: alcohols-buliding-blocksIn 2019 ,《Rapid Solution-Phase Hydrogen/Deuterium Exchange for Metabolite Compound Identification》 was published in Journal of the American Society for Mass Spectrometry. The article was written by Majuta, Sandra N.; Li, Chong; Jayasundara, Kinkini; Kiani Karanji, Ahmad; Attanayake, Kushani; Ranganathan, Nandhini; Li, Peng; Valentine, Stephen J.. The article contains the following contents:

Rapid, solution-phase hydrogen/deuterium exchange (HDX) coupled with mass spectrometry (MS) is demonstrated as a means for distinguishing small-mol. metabolites. HDX is achieved using capillary vibrating sharp-edge spray ionization (cVSSI) to allow sufficient time for reagent mixing and exchange in micrometer-sized droplets. Different compounds are observed to incorporate deuterium with varying efficiencies resulting in unique isotopic patterns as revealed in the MS spectra. Using linear regression techniques, parameters representing contribution to exchange by different hydrogen types can be computed. In this proof-of-concept study, the exchange parameters are shown to be useful in the retrodiction of the amount of deuterium incorporated within different compounds On average, the exchange parameters retrodict the exchange level with ∼ 2.2-fold greater accuracy than treating all exchangeable hydrogens equally. The parameters can be used to produce hypothetical isotopic distributions that agree (± 16% RMSD) with exptl. measurements. These initial studies are discussed in light of their potential value for identifying challenging metabolite species. [Figure not available: see fulltext.]. In the part of experimental materials, we found many familiar compounds, such as 3-Aminopropan-1-ol(cas: 156-87-6Category: alcohols-buliding-blocks)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Amines have a free lone pair with which they can coordinate to metal centers. Amine–metal bonds are weaker because amines are incapable of backbonding, but they are still important for sensing applications.While stronger than hydrogen bonds, amine–metal bonds are still weaker than both covalent and ionic bonds.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Aizawa, Miho’s team published research in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 2021 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. The reaction of alkyl halides, R―X, where X is a halogen, or analogous reagents with ammonia (or amines) is useful with certain compounds. Not all alkyl halides are effective reagents; the reaction is sluggish with secondary alkyl groups and fails with tertiary ones. Its usefulness is largely confined to primary alkyl halides (those having two hydrogen atoms on the reacting site).Quality Control of 3-Aminopropan-1-ol

Aizawa, Miho; Akiyama, Haruhisa; Matsuzawa, Yoko published their research in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 2021. The article was titled 《Convenient preparation of stimulus-responsive molecular layers containing anthracene molecules to control surface properties》.Quality Control of 3-Aminopropan-1-ol The article contains the following contents:

For controlling the surface properties by depositing mols. on the material surface, the selection of the functional groups of the stacked mols. is crucial. By introducing anthracenes in the mol. layer, which promote photodimerization and thermal/cleavage on photoirradiation or heating, it is possible to form a stimuli-responsive surface that enables changes in the mol. layer composition In this study, we improve the fabrication process of the stimulus-responsive mol. layer with anthracene in order to facilitate the design of mol. layers according to the desired purpose. This is achieved by employing acid-base interactions for forming the mol. layers, with different functions for each layer. Thermal/photocleavage reactions of anthracene dimers are induced in the stacked mol. layer. Multilayers stacked with amine mols. exhibit different behavior on the cleavage reaction and the contact angle varies, depending on the type of mols. The wettability on the surface covered with the mol. layer changes in response to the stimulation, proving the successful fabrication of a stimuli-responsive surface. The designed thermo- and photoresponsive mol. layer can potentially expand the scope of practical application as a control system for surface conditions. The experimental process involved the reaction of 3-Aminopropan-1-ol(cas: 156-87-6Quality Control of 3-Aminopropan-1-ol)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. The reaction of alkyl halides, R―X, where X is a halogen, or analogous reagents with ammonia (or amines) is useful with certain compounds. Not all alkyl halides are effective reagents; the reaction is sluggish with secondary alkyl groups and fails with tertiary ones. Its usefulness is largely confined to primary alkyl halides (those having two hydrogen atoms on the reacting site).Quality Control of 3-Aminopropan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Hua, Weiwen’s team published research in Journal of Inorganic and Organometallic Polymers and Materials in 2021 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Many important products require amines as part of their syntheses. Methylamine is utilized in the production of the analgesic meperidine (trade name Demerol) and the photographic developer Metol (trademark), and dimethylamine is used in the synthesis of the antihistamine diphenhydramine (trade name Benadryl), the solvent dimethylformamide (DMF), and the rocket propellant 1,1-dimethylhydrazine. The synthesis of the insect repellent N,N-diethyl-m-toluamide (DEET) incorporates diethylamine while that of the synthetic fibre Kevlar requires aromatic amines.Formula: C3H9NO

Formula: C3H9NOIn 2021 ,《Ice Recrystallization Inhibition Activity of Protein Mimetic Peptoids》 appeared in Journal of Inorganic and Organometallic Polymers and Materials. The author of the article were Hua, Weiwen; Wang, Yuanguang; Guo, Cun-Yue; Wang, Jianjun; Li, Songjun; Guo, Li. The article conveys some information:

Natural antifreeze proteins are known for their excellent control of ice formation and growth, while synthetic mols. seldom have the similar effects. Here we report a series of protein mimetic peptoids with different side chains exhibiting significant ice recrystallization inhibition activity, and their structure-property relationships are also studied. The presence of peptoid can clearly slow down ice growth and decrease ice crystal grain size, but shows no thermal hysteresis, which make peptoids great antifreeze agent candidates in cryopreservation. Peptoids with Me, Et and amino groups on side chains can modulate ice crystal shape, while peptoids bearing hydroxyl and Et groups decrease ice growth rate the most. All peptoids can reduce ice crystal grain size and the one with hydroxyl groups give the smallest grain size. This study reveals peptoid structure effects on ice growth and points to the design rules for biomimetic antifreeze agents. The results came from multiple reactions, including the reaction of 3-Aminopropan-1-ol(cas: 156-87-6Formula: C3H9NO)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Many important products require amines as part of their syntheses. Methylamine is utilized in the production of the analgesic meperidine (trade name Demerol) and the photographic developer Metol (trademark), and dimethylamine is used in the synthesis of the antihistamine diphenhydramine (trade name Benadryl), the solvent dimethylformamide (DMF), and the rocket propellant 1,1-dimethylhydrazine. The synthesis of the insect repellent N,N-diethyl-m-toluamide (DEET) incorporates diethylamine while that of the synthetic fibre Kevlar requires aromatic amines.Formula: C3H9NO

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Uprety, Bhawna’s team published research in Acta Crystallographica, Section E: Crystallographic Communications in 2019 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair. Amines are formally derivatives of ammonia (NH3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group (these may respectively be called alkylamines and arylamines; amines in which both types of substituent are attached to one nitrogen atom may be called alkylarylamines).HPLC of Formula: 156-87-6

In 2019,Acta Crystallographica, Section E: Crystallographic Communications included an article by Uprety, Bhawna; Arderne, Charmaine. HPLC of Formula: 156-87-6. The article was titled 《The crystal structure of the zwitterionic co-crystal of 2,4-dichloro-6-{[(3-hydroxypropyl)azaniumyl]methyl}phenolate and 2,4-dichlorophenol》. The information in the text is summarized as follows:

The title compound, C10H13Cl2NO2.C6H4Cl2O, was formed from the incomplete Mannich condensation reaction of 3-aminopropan-1-ol, formaldehyde and 2,4-dichlorophenol in methanol. This resulted in the formation of a co-crystal of the zwitterionic Mannich base, 2,4-dichloro-6-{[(3-hydroxypropyl)azaniumyl]methyl}phenolate and the unreacted 2,4-dichlorophenol. The compound crystallizes in the monoclinic crystal system (in space group Cc) and the asym. unit contains a mol. each of the 2,4-dichlorophenol and 2,4-dichloro-6-{[(3-hydroxypropyl)azaniumyl]methyl}phenolate. Examination of the crystal structure shows that the two components are clearly linked together by hydrogen bonds. The packing patterns are most interesting along the b and the c axes, where the co-crystal in the unit cell packs in a manner that shows alternating aromatic dichlorophenol fragments and polar hydrogen-bonded channels. The 2,4-dichlorophenol rings stack on top of one another, and these are held together by π-π interactions. The crystal studied was refined as an inversion twin. The experimental part of the paper was very detailed, including the reaction process of 3-Aminopropan-1-ol(cas: 156-87-6HPLC of Formula: 156-87-6)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair. Amines are formally derivatives of ammonia (NH3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group (these may respectively be called alkylamines and arylamines; amines in which both types of substituent are attached to one nitrogen atom may be called alkylarylamines).HPLC of Formula: 156-87-6

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Alcohol – Wikipedia,
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Chaudhari, Kapil S.’s team published research in International Journal of Pharmaceutics (Amsterdam, Netherlands) in 2019 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Halogenation, in which one or more hydrogen atoms of an amine is replaced by a halogen atom, occurs with chlorine, bromine, and iodine, as well as with some other reagents, notably hypochlorous acid (HClO). With primary amines the reaction proceeds in two stages, producing N-chloro- and N,N-dichloro-amines, RNHCl and RNCl2, respectively. With tertiary amines, an alkyl group may be displaced by a halogen.Recommanded Product: 156-87-6

In 2019,International Journal of Pharmaceutics (Amsterdam, Netherlands) included an article by Chaudhari, Kapil S.; Akamanchi, Krishnacharya G.. Recommanded Product: 156-87-6. The article was titled 《Novel bicephalous heterolipid based self-microemulsifying drug delivery system for solubility and bioavailability enhancement of efavirenz》. The information in the text is summarized as follows:

There is an increasing demand for new lipidic biocompatible and safe materials for self-microemulsifying drug delivery system (SMEDDS). The present work reports the synthesis, characterization, oral mucosal irritation study, and application of novel erucic acid ester of G0-PETIM dendron based bicephalous heterolipid (BHL) as an oil phase in SMEDDS using Efavirenz (EFA), a BCS class II drug with poor water solubility and poor bioavailability. Studies were conducted to optimize EFA SMEDDS using different ratios of the BHL as oil phase and surfactant: co-surfactant weight ratios (Km). At Km (1.5), the microemulsion was spontaneously formed in water with mean globule size of 22.78 ± 0.25 nm and polydispersity index (PDI) of 0.23 ± 0.031 with high drug loading efficiency of 80.35 ± 3.1%. Standard stability tests were performed on EFA SMEDDS and the results indicated it to be highly stable. The in vitro dissolution profile of EFA SMEDDS showed >95% of the drug release within an hour and expectedly substantial enhancement in in vivo bioavailability was observed; almost 6-fold increase in bioavailability with parameters Cmax 5.2 μg/mL, Tmax 3 h, and AUC(0-∞) 23.48 μg/h/mL resp. as compared the plain suspension of the drug. In conclusion, the BHL can be used effectively as an oil phase in SMEDDS to enhance solubility and bioavailability of BCS Class II drugs. Further, it holds, in general, a great promise as a new excipient for solubility and bioavailability enhancements. The experimental part of the paper was very detailed, including the reaction process of 3-Aminopropan-1-ol(cas: 156-87-6Recommanded Product: 156-87-6)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Halogenation, in which one or more hydrogen atoms of an amine is replaced by a halogen atom, occurs with chlorine, bromine, and iodine, as well as with some other reagents, notably hypochlorous acid (HClO). With primary amines the reaction proceeds in two stages, producing N-chloro- and N,N-dichloro-amines, RNHCl and RNCl2, respectively. With tertiary amines, an alkyl group may be displaced by a halogen.Recommanded Product: 156-87-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Tzeng, Stephany Y.’s team published research in Proceedings of the National Academy of Sciences of the United States of America in 2020 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Large quantities of aliphatic amines are made synthetically. The most widely used industrial method is the reaction of alcohols with ammonia at a high temperature, catalyzed by metals or metal oxide catalysts (e.g., nickel or copper). Mixtures of primary, secondary, and tertiary amines are thereby produced.Computed Properties of C3H9NO

《In situ genetic engineering of tumors for long-lasting and systemic immunotherapy》 was written by Tzeng, Stephany Y.; Patel, Kisha K.; Wilson, David R.; Meyer, Randall A.; Rhodes, Kelly R.; Green, Jordan J.. Computed Properties of C3H9NO And the article was included in Proceedings of the National Academy of Sciences of the United States of America in 2020. The article conveys some information:

Cancer immunotherapy has been the subject of extensive research, but highly effective and broadly applicable methods remain elusive. Moreover, a general approach to engender endogenous patient-specific cellular therapy, without the need for a priori knowledge of tumor antigen, ex vivo cellular manipulation, or cellular manufacture, could dramatically reduce costs and broaden accessibility. Here, we describe a biotechnol. based on synthetic, biodegradable nanoparticles that can genetically reprogram cancer cells and their microenvironment in situ so that the cancer cells can act as tumor-associated antigen-presenting cells (tAPCs) by inducing coexpression of a costimulatory mol. (4-1BBL) and immunostimulatory cytokine (IL-12). In B16-F10 melanoma and MC38 colorectal carcinoma mouse models, reprogramming nanoparticles in combination with checkpoint blockade significantly reduced tumor growth over time and, in some cases, cleared the tumor, leading to long-term survivors that were then resistant to the formation of new tumors upon rechallenge at a distant site. In vitro and in vivo analyses confirmed that locally delivered tAPC-reprogramming nanoparticles led to a significant cell-mediated cytotoxic immune response with systemic effects. The systemic tumor-specific and cell-mediated immunotherapy response was achieved without requiring a priori knowledge of tumor-expressed antigens and reflects the translational potential of this nanomedicine. In the experiment, the researchers used 3-Aminopropan-1-ol(cas: 156-87-6Computed Properties of C3H9NO)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Large quantities of aliphatic amines are made synthetically. The most widely used industrial method is the reaction of alcohols with ammonia at a high temperature, catalyzed by metals or metal oxide catalysts (e.g., nickel or copper). Mixtures of primary, secondary, and tertiary amines are thereby produced.Computed Properties of C3H9NO

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Simple exploration of 3-Aminopropan-1-ol

Application of 156-87-6, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 156-87-6 is helpful to your research.

Application of 156-87-6, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, 156-87-6, Name is 3-Aminopropan-1-ol, SMILES is OCCCN, belongs to alcohols-buliding-blocks compound. In a article, author is Abdelmigeed, Mai O., introduce new discover of the category.

A magnetized zeolitic imidazolate framework (ZIF-8) impregnated with sodium hydroxide catalyst has been synthesized and tested as a new catalyst for biodiesel production. The new catalyst was investigated for the ethanolysis of vegetable oil to produce biodiesel. The operating conditions of the biodiesel production were optimized using the 2n design method followed by a reduced number of experimental runs. A 70% conversion of oil in the ethanolysis reaction was achieved using the new catalyst. The optimized operating conditions were found to be alcohol to oil molar ratio of 21:1, catalyst loading of 1% wt., a reaction time of 90 min, and temperature of 75 degrees C. Ethanolysis reaction was found to obey the pseudosecond-order kinetic model. In addition, the Arrhenius pre-exponential constant and activation energy were calculated to be 1.12 x 10(10) L mol(-1).min(1) and 77.27 kJ/mol, respectively. The physical properties of the product biodiesel matched the American Society for Testing and Materials (ASTM) ranges. Additionally, the product biodiesel achieved a Cetane number of 75, which is 15% higher than the upper range of the ASTM. (C) 2020 Elsevier Ltd. All rights reserved.

Application of 156-87-6, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 156-87-6 is helpful to your research.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts