Month: December 2022

Jakhmola, Vikash published the artcileSynthesis and in-vivo activity of some antihypertensive agent based on pyridazine scaffold design, Related Products of catalysis-chemistry, the publication is International Journal of Pharmaceutical Sciences and Research (2022), 13(2), 786-792, database is CAplus.

The main objective presents research work to synthesize, characterization, and in-vivo evaluation of Pyridazine derivatives To study the different synthesized derivatives by using different anal. parameters like IR, Mass, and NMR anal. And also find out the antihypertensive activity. The studies on the hydralazine group drugs led to the synthesis of many Pyridazine derivatives with a wide activity spectrum on the cardiovascular system. Pyridazine derivatives, a class of compounds containing the N-N bond, exhibit a wide range of pharmacol. activities such as antidepressant, antihypertensive and cardiotonic, etc. Some 7-phenyl-3, 4, 8, 9-tetrahydro-2H-pyridazino [1, 6-a] [1, 3, 5] triazin-2-imine were synthesized by reacting 6-Ph substituted 2, 3, 4, 5-Tetrahydro pyridazin-3-one with cyclic secondary amine under Mannich reaction conditions. The total seven compounds (vj1-vj7) were synthesized under Mannich reaction conditions. All the synthesized derivatives were selected for evaluation of antihypertensive activities by a noninvasive method using Tail Cuff method. Most of the compounds showed good antihypertensive activity. Few compounds like vj4, vj5, and vj6 were found to show a highly significant reduction in mean arterial blood pressure but at a higher dose in comparison to standard drugs like proponolol and hydralazine. The substituted pyridazine derivatives discovered in this study may provide valuable therapeutic intervention for the treatment of hypertension.

International Journal of Pharmaceutical Sciences and Research published new progress about 2051-95-8. 2051-95-8 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene,Ketone, name is 3-Benzoylpropionicacid, and the molecular formula is C10H10O3, Related Products of catalysis-chemistry.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Ivanov, Evgeniy V. published the artcileVolumetric properties of some asymmetrically methyl-N-substituted thioureas in water between (278.15 and 318.15) K at ambient pressure, Application of 1,1-Dimethylthiourea, the publication is Journal of Molecular Liquids (2014), 426-431, database is CAplus.

Densities of dilute aqueous solutions of 1-monomethyl-2-thiourea and 1,1,3-trimethyl-2-thiourea have been measured using an Anton Paar DMA 5000 M vibrating-tube densimeter. The apparent molar volumes and expansibilities (down to infinite dilution) have been calculated from the obtained d. data. The experiments have been performed in the temperature range between (278.15 and 318.15) K, with a step of 10 K, at p ? 0.1 MPa. The influence of a nature of methyl-N-sited substituents on the structure-packing properties of aqueous thioureas has been discussed. A possibility to estimate the standard (limiting apparent or partial) molar volumes for asym. substituted 1,1-dimethyl-2-thiourea in water has been considered, too.

Journal of Molecular Liquids published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C3H8N2S, Application of 1,1-Dimethylthiourea.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Huang, Zhongfang published the artcileDepressing effect of SPF on quartz, Computed Properties of 2016-56-0, the publication is Kuangye Gongcheng (1983), 3(1), 33-5, database is CAplus.

S.P.F. (not defined) had a better depressing effect on quartz when dodecylamine?acetate??[2016-56-0] or Na?oleate??[143-19-1] are used as collectors. The depressing effect is dependent on the preactivation of quartz.

Kuangye Gongcheng published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Computed Properties of 2016-56-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Horioka, Masakazu published the artcileStudies on the treatment of high level radioactive wastewater. 2. Adsorption characteristic of DAA for zeolite, Quality Control of 2016-56-0, the publication is Yamagata-ken Eisei Kenkyushoho (1980), 35-8, database is CAplus.

A high level radioactive wastewater containing ¹³⁷Cs was adsorbed on fine zeolite which was separated by flotation by dodecylamine acetate [2016-56-0] (DAA). DAA reached an equilibrium adsorption on zeolite within 5 min but Cs⁺ equilibrium adsorption took ?48 h. DAA adsorption on zeolite is mainly surface adsorption.

Yamagata-ken Eisei Kenkyushoho published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Quality Control of 2016-56-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Horioka, Masakazu published the artcileFundamental study on the treatment of toxic substances in wastewater. Removal and calcination of cesium(Cs⁺), HPLC of Formula: 2016-56-0, the publication is Yamagata-ken Eisei Kenkyushoho (1981), 19-25, database is CAplus.

In connection with the treatment of high-level radioactive waste, a useful procedure was sought for the removal and calcination of Cs (as Cs⁺) in wastewater. First, the cation exchange capacities of the selected samples of domestic natural clay minerals were tested by a column method. Second, amine flotation was investigated with zeolite and dodecylammonium?acetate??[2016-56-0] as a collector. Subsequently, the adsorption amounts of Cs⁺, the characteristics of calcination, x-ray diffraction trace and leaching rates of Cs⁺ from calcined zeolite were measured in other tests for zeolite.

Yamagata-ken Eisei Kenkyushoho published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, HPLC of Formula: 2016-56-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Horioka, Masakazu published the artcileStudy on the refining of natural zeolite by adsorbing particle flotation, Application of Dodecylamineacetate, the publication is Yamagata-ken Eisei Kenkyushoho (1982), 9-15, database is CAplus.

The floatabilities of natural zeolite, quartz feldspar, 1:1 mixture of natural zeolite-quartz, and 1:1 mixture of natural zeolite-feldspar were investigated by the Denver-type laboratory flotation machine using dodecylammonium acetate (I) and pine oil as a collector. The Cs adsorption capacity of zeolite recovered by I flotation in the acidic state < pH 2, was less than that of the natural zeolite. However, the capacity was improved when treated with 1N NaOH or 1N KCl. Quartz and feldspar were separated from natural zeolite by I flotation in a HCl or H₂SO₄ circuit at pH 0.5-2, but not in neutral or alk. pH range. The selective separation of zeolite from the mixture of natural zeolite-quartz or natural zeolite-feldspar was achieved by using I (100 mg/L) at pH 1.1 together with pine oil (46 mg/L) as a collector. The recovery and the content of zeolite as froth were about 83 and 77%, resp.

Yamagata-ken Eisei Kenkyushoho published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Application of Dodecylamineacetate.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Hohenlohe-Oehringen, K. published the artcile1-Methoxy-l-buten-3-one and primary amines, Application In Synthesis of 28056-87-3, the publication is Monatshefte fuer Chemie (1962), 586-99, database is CAplus.

MeOCH:CHAc (I) condensed with primary aliphatic amines and treated with HCl gave via the non-isolated alkylaminobutenones 40-50% N-alkyl2-methyl-5-acetylpyridinium salts (II). These were reducible directly or through intermediate stages to N-alkylcopellidines or N-alkylisocopellidines (1-alkyl-2-methyl-5-ethylpiperidines) (III). The structure of the II was proved by synthesis of the N-Me derivatives and the structure of the III by degradation. Homoveratrylamine (IIIa) (35 g.) in 90 ml. Et₂O treated with 53 g. I, when the reaction subsided the solution kept 3 hrs. at room temperature, treated with Et₂O-HCl, the gummy solid separated by decanting the supernatant solution, refluxed 2 hrs. in 100 ml. CHCl₃, the solution diluted with 200 ml. Me₂CO, and cooled gave 32 g. N-homoveratryl-2-methyl-5-acetylpyridinium chloride (IV), m. 220-30¡ã (decomposition); phenylhydrazone decompose 138-9¡ã (Me₂CO). Aqueous IV poured into Me₂CO containing NaI gave the corresponding iodide, m. 188¡ã. Aqueous IV treated with concentrated aqueous NH₃ gave an unstable anhydro base, reconverted with Et₂O-HCl into IV. IV (12 g.) in 50 ml. AcOH hydrogenated with Pd-C at room temperature and atm. pressure (970 ml. H absorbed), filtered, the filtrate evaporated in vacuo, and the residue recrystallized from EtOH-Me₂CO gave 9.7 g. N-homoveratryl-2-methyl-5-(¦Á-hydroxyethyl)pyridinium chloride (V), m. 170¡ã. Alc.-V treated with Me₂CO containing NaI gave the corresponding iodide, m. 175¡ã. IV (3.5 g.) in H₂O treated with concentrated aqueous NH₃, the precipitate filtered off, washed with H₂O, dissolved in MeOH, the solution treated with MeI, heated 2 hrs. on a H₂O bath in a glass autoclave, and cooled gave 1.6 g. unidentified compound, C₁₉H₂₄NO₃I, m. 207¡ã (MeOH). IV (5 g.) and 10 ml. N₂H₄.H₂O in 15 ml. EtOH boiled 45 min., evaporated in vacuo the residue treated with concentrated aqueous HCl, the mixture evaporated, the residue crystallized from EtOH, and the solid filtered off gave 3.1 g. compound, m. 170-92¡ã; evaporation of the mother liquor gave 2.1 g. IIa.HCl, m. 156¡ã (EtOH-Me₂CO). PtO₂ (2 g.) hydrogenated in 10 ml. H₂O, the mixture treated with 15 g. IV in N HCl, hydrogenated at room temperature and atm. pressure (every 4 hrs. the mixture was shaken with air to reactivate the catalyst; after 30-40 hrs. 5300 ml. H was absorbed), the catalyst filtered off, extracted with boiling H₂O, the extract filtered while hot, the combined filtrates evaporated in vacuo, and the residue crystallized from Me₂CO gave 5.7 g. N-homoveratrylcopellidine-HCl (VI.HCl), m. 200¡ã (EtOH-Me₂CO). VI.HCl in H₂O treated with aqueous Na₂CO₃ gave VI, b₇ 160-70¡ã; HBr salt m. 212¡ã; HI salt m. 190¡ã; picrate m. 153¡ã. The Me₂CO mother liquor from the above reduction kept several days at -20¡ã and the resulting solid (3.6 g.) repeatedly crystallized from EtOH-Et₂O gave N-homoveratrylisocopellidine-HCl (VII.HCl) (isomeric with VI.HCl), m. 185¡ã; VII b₇ 160-70¡ã. Homoveratryl bromide [prepared by LiAlH₄ reduction of 3,4-(MeO)₂C₆H₃CH₂CO₂Et followed by treatment with PBr₃] (2 g.) and 1 g. dl-coniine in 10 ml. C₆H₆ heated 4 hrs. on a H₂O bath in a glass autoclave, cooled, filtered, the filtrate converted to bases, and the bases fractionated in vacuo gave N-homoveratrylconiine, b_0.05 120¡ã, which was nonidentical with either VI or VII; HCl salt m. 95¡ã; picrate m. 104¡ã (EtOH). VI (2 g.) and excess MeI in Et₂O kept 16 hrs. at room temperature and the oily precipitate crystallized from MeOH gave VI.MeI, m. 146¡ã. VI.Mel (1 g.) in 40 ml. H₂O shaken 1 hr. with Ag₂O (from 2 g. AgNO₃), filtered, the filtrate evaporated in vacuo, the residue distilled in vacuo (H₂O pump), and the distillate worked up gave a neutral (VIII) and basic (IX) fraction; VIII treated with Et₂O-picric acid gave N-methylcopellidine (X) picrate (XI), X. 169¡ã; IX was identified as 3,4-(MeO)₂C₆H₃CH:CH₂ by its spectrum, by formation of its bromide, m. 101¡ã, and by KMnO₄ oxidation to veratric acid, m. 178-80¡ã. MeNH₂ (3.1 g.) and 20 g. I in 100 ml. Et₂O kept 4 hrs. at room temperature and treated with Et₂O-HCl gave 2.7 g. 2-methyl-5-acetylpyridine-MeCl (XII.MeCl) sesquihydrate, decompose 207-15¡ã (EtOH-EtOAc); phenylhydrazone hemihydrate decompose 237¡ã. I (170 g.) in 300 ml. Et₂O cooled to -20¡ã, the solution mixed with a cooled (-20¡ã) solution of 35 ml. MeNH₂ in 100 ml. Et₂O, kept 1 hr. in an ice-salt mixture and then 15 min. at room temperature, treated with Et₂O-HCl, the precipitate separated by decanting the supernatant Et₂O solution, dissolved in AcOH, and the solution treated with AcOH-Br at 10-15¡ã gave 112 g. perbromide (XIII), needles [HCONMe₂ (XIV)-AcOH], decomposing slowly at room temperature and rapidly at 70¡ã. XIII in XIV treated portionwise with PhOH in XIV with cooling and diluted with Et₂O gave 61 g. XII.MeBr, m. 204¡ã (decomposition). XIII heated above 70¡ã (HBr was evolved; self-bromination occurred) gave a Br derivative of XII.MeBr hydrate, m. 200¡ã (decomposition) (H₂OMe₂CO). XII.MeBr was stable in neutral and acid solution and towards oxidation agents, but was unstable in the alk. range, forming in aqueous NaHCO₃ a carmine-red dye. XII.MeBr heated with MeI and NaHCO₃ gave the carmine-red dye mentioned above; if the NaHCO₃ was omitted, XII.MeI, m. 157¡ã, was formed. XII.MeBr (20 g.) in 40 ml. H₂O and 12 ml. HCl hydrogenated with 3 g. PtO₂ at room temperature and atm. pressure (the catalyst was frequently reactivated by shaking with air; after 35 hrs. 11,200 ml. H was absorbed), filtered, the filtrate evaporated in vacuo, the residue dissolved in a little H₂O, the solution treated with KOH, extracted with Et₂O, the extract evaporated, the residual base (XV) dissolved in 50 ml. EtOH, the solution treated with warm EtOH containing 19 g. picric acid and the product (25 g.) recrystallized twice from EtOH gave 21 g. XI, m. 169¡ã (EtOH). XV treated with Et₂O-HCl gave X.HCl, m. 205¡ã (sublimed above 160¡ã) (EtOH-Et₂O); X.HBr m. 198-200¡ã. XI in aqueous suspension treated with dilute aqueous NaOH gave X, b₇ 60¡ã, mol. weight (mass spectrometry) 141. The mother liquor of XI (m. 169¡ã) concentrated, the residue dissolved in petr. ether, and the solution kept 24 hrs. deposited 8 g. N-methylisocopellidine (XVI) picrate (XVII), m. 98¡ã (EtOH-Et₂O); XVI b₇ 60¡ã. XII.MeBr (15 g.) in 50 ml. H₂O containing 8 g. NaOAc.3H₂O hydrogenated 6 hrs. with Raney Ni at 150-60¡ã and 100 atm., the catalyst filtered off, washed with EtOH, the combined filtrate and washing treated with HCl, evaporated in vacuo, the residue dissolved in H₂O, the solution made strongly alk. with KOH, the product isolated with Et₂O, and distilled gave 3.3 g. isomer of X and XVI, C₉H₁₉N, b₇ 54-6¡ã [picrate m. 205-10¡ã (EtOH)], and 3.5 g. 1,2-dimethyl-b-(¦Á-hydroxyethyl)piperidine (XVIII), b₇ 115-17¡ã [picrate m. 158¡ã (EtOH Et₂O)]. XVIII (1 g.) treated with Et₂O-HCl, the resulting XVIII.HCl dissolved in excess SOCl₂, the solution boiled 1 hr., evaporated, the residue treated with C in Me₂CO-H₂O, the solution hydrogenated with Raney Ni at room temperature, after H absorption ceased the mixture filtered, the filtrate treated with a few ml. HCl, evaporated, the residue made alk., the product isolated with Et₂O, and treated with pieric acid gave XI, m. 169¡ã (EtOH). XII.MeBr (9.5 g.) in AcOH hydrogenated with Pd-C at room temperature and atm. pressure (after 1 hr. 1300 ml. H was absorbed, when absorption ceased), filtered, and the filtrate evaporated in vacuo gave crude 1,2-dimethyl-5-(¦Á-hydroxyethyl)pyridinium bromide (XIX), which could not be crystallized Crude XIX refluxed 3 hrs. with excess SOCl₂, the solution evaporated in vacuo on a H₂O bath, the residue heated 1 hr. at 100¡ã in vacuo, and the product recrystallized from EtOHEt₂O gave dichloropyridinium chloride compound (XX), C₉H₁₂Cl₃N, having the double m.p. 160¡ã and 169¡ã. XX in H₂O hydrogenated with Pd-C at room temperature and atm. pressure, filtered, the filtrate evaporated, the residue dissolved in a little EtOH, the solution treated with some Me₂CO, decanted from precipitated oily byproducts, and diluted with Et₂O gave 1,2-dimethyl-5-ethylpyridinium chloride, very hygroscopic; picrate m. 112¡ã (EtOH). XI (12 g.) suspended in 50 ml. H₂O, treated with dilute NaOH (from 3 g. NaOH), steam distilled, the distillate treated with Et₂O, the Et₂O phase separated, and kept 1 day at room temperature with excess MeI gave 8.2 g. X.MeI, m. 230-3¡ã (EtOH-Me₂CO). X.MeI (4.5 g.) in 50 ml. H₂O shaken 0.5 hr. at room temperature with Ag₂O (from 8 g. AgNO₃), filtered, the filtrate evaporated in vacuo, and the residue distilled in vacuo (80 mm.) and 140¡ã (bath temperature) gave CH₂:CH(CH₂)₂CHEtCH₂NMe₂ (XXI); picrate (XXII) m. 69¡ã (EtOH-Et₂O); methiodide (XXIII) m. 190-2¡ã (Me₂COEt₂O). XVII (20 g.) converted as above to XVI.MeI [m. 286-8¡ã (decomposition)] and the latter subjected to similar Hofmann degradation gave 5.7 g. XXI (XXII m. 69¡ã; XXIII m. 193¡ã); these products from XVI.MeI were identical with the analogous products obtained from X.MeI. XXI (2 g.) in 15 ml. dilute HCl hydrogenated with Pd C at room temperature and atm. pressure (H absorption ceased after 0.5 hr.), filtered, the filtrate made alk., the product isolated with Et₂O, and distilled gave Me(CH₂)₃CHEtCH₂NMe₂, b₇ 62¡ã; methiodide (XXIV) m. 217¡ã (Me₂CO-EtOAc). XXIV (10 g.) in 200 ml. H₂O shaken 0.5 hr. with Ag₂O (from 15 g. AgNO₃), filtered, the filtrate evaporated in vacuo, the residue decomposed at 155¡ã (bath temperature) and atm. pressure (Widmer column), the distillate diluted with Et₂O, the solution extracted with dilute HCl, dried, and fractionated gave 1.2 g. Me(CH₂)₃CEt: CH₂ (XXV), b. 117¡ã/740 mm. XXV (0.5 g.) in EtOAc ozonized at -15¡ã until no more O₃ was absorbed, the solution hydrogenated with Pd-C at room temperature and atm. pressure until H absorption ceased, filtered, the EtOAc filtrate and the catalyst extracted with H₂O, and the combined extracts treated with dimedon in EtOH gave 0.65 g. dimedon derivative of CH₂O, m. 192¡ã. XXV (0.6 g.) in 5 ml. HCO₂Me hydrogenated with Pd-C at 50 atm. and room temperature, filtered, and the filtrate fractionated gave Me(CH₂)₃CHMeEt, b. 116¡ã/740 mm. Infrared and ultraviolet spectral data were presented.

Monatshefte fuer Chemie published new progress about 28056-87-3. 28056-87-3 belongs to catalysis-chemistry, auxiliary class Amine,Aliphatic hydrocarbon chain, name is 2-Ethyl-N,N-dimethylhexan-1-amine, and the molecular formula is C10H23N, Application In Synthesis of 28056-87-3.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Hoefler, F. published the artcileModel calculations on the vibrational spectra of phenylsilanes and some related compounds, Recommanded Product: Difluorodiphenylsilane, the publication is Monatshefte fuer Chemie (1976), 107(3), 705-19, database is CAplus.

Normal coordinate calculations on symmetric vibrations of PhnMX4-n type mols. (M = C, Si, Ge, Sn, Pb, P and X = H, F, Cl, Br, OH) were performed by using a simplified model for M-sensitive modes of the Ph group. A good agreement of calculated and observed frequencies was obtained with reasonable and transferable force constants Significant effects of vibrational coupling are illustrated.

Monatshefte fuer Chemie published new progress about 312-40-3. 312-40-3 belongs to catalysis-chemistry, auxiliary class Organic Silicones, name is Difluorodiphenylsilane, and the molecular formula is C12H10F2Si, Recommanded Product: Difluorodiphenylsilane.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Hodge, E. B. published the artcile7-Nitro-1,3,5-triazaadamantane and derivatives. Reactions of azaadamantanes with anhydrides, COA of Formula: C7H14N4, the publication is Journal of Organic Chemistry (1972), 37(2), 320-1, database is CAplus.

A new method of preparation and a number of reactions of 7-nitro-1,3,5-triazaadamantane (I) are given. The reactions of I with anhydrides leads to 3,7-diacyl-5-nitro-1,3,7-triazabicyclo[3.3.1]nonanes. This same reactions was studied with hexamethylenetetramine, which, with propionic anhydride, gave 1,3,5,7-tetrapropionyloctahydro-tetrazocine.

Journal of Organic Chemistry published new progress about 14707-75-6. 14707-75-6 belongs to catalysis-chemistry, auxiliary class Triazinanes, name is 1,3,5-Triazaadamantan-7-amine, and the molecular formula is C7H14N4, COA of Formula: C7H14N4.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Herrmann, K. published the artcileEffects of the anticonvulsant drug valproic acid and related substances on the early development of the zebrafish (Brachydanio rerio), Category: catalysis-chemistry, the publication is Toxicology in Vitro (1993), 7(1), 41-54, database is CAplus and MEDLINE.

The early development of the zebrafish Brachydanio rerio is being investigated as a possible test system for prescreening drugs suspected to be hazardous to humans. Experiments have been carried out to evaluate the teratogenic effect of the human antiepileptic drug valproic acid (VPA) and several chem. related substances. The experiments show the highly synchronous development of zebrafish embryos, even of batches laid by different parents. Effects due to drug treatment can be easily and accurately determined VPA causes retardation and cessation of development. It generate malformations such as edema, brain deformities, a shortened and bent tail, and bipartite axiation of the posterior trunk. The effects of the various substances tested were estimated and compared by measuring retardation of development. The related substances display similar effects, but differ in their effectiveness as they do in other test systems: 2-en-valproic acid and 4-en-valproic acid display weaker effects than VPA and propylhexanoic acid. Valpromide, methylhexanoic acid, pentenoic acid and diethylacetic acid display a weak effect or no effect at all. The effects in zebrafish appear to be more similar to those observed in hydroids and in mammalian whole embryo culture systems than to the effects in mammals in vivo. Differences may be best explained by differences in uptake and degradation of the drugs, and by the influence of the maternal organism in mammals.

Toxicology in Vitro published new progress about 3115-28-4. 3115-28-4 belongs to catalysis-chemistry, auxiliary class Aliphatic Chain, name is 2-Butylhexanoic acid, and the molecular formula is C10H20O2, Category: catalysis-chemistry.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia