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Journal articles on the topic '3-Amino-1-propanol'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Blanco, Antonio, Alicia García-Abuín, Diego Gómez-Díaz, and José M. Navaza. "Density, Speed of Sound, Viscosity and Surface Tension of 3-Dimethylamino-1-propylamine + Water, 3-Amino-1-propanol + 3-Dimethylamino-1-propanol, and (3-Amino-1-propanol + 3-Dimethylamino-1-propanol) + Water from T = (293.15 to 323.15) K." Journal of Chemical & Engineering Data 62, no. 8 (July 13, 2017): 2272–79. http://dx.doi.org/10.1021/acs.jced.7b00042.

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2

Cacela, C., A. Baudot, M. L. Duarte, A. M. Matos-Beja, M. Ramos Silva, J. A. Paixão, and R. Fausto. "Low temperature polymorphism in 3-amino-1-propanol." Journal of Molecular Structure 649, no. 1-2 (April 2003): 143–53. http://dx.doi.org/10.1016/s0022-2860(03)00049-8.

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3

Gol'dshleger, N. F., A. S. Lobach, A. S. Astakhova, M. G. Kaplunov, A. V. Kulikov, A. P. Moravskii, O. S. Roschupkina, and Yu M. Shul'ga. "Interaction of fullerene C60 with 3-amino-1-propanol." Russian Chemical Bulletin 43, no. 6 (June 1994): 1081–83. http://dx.doi.org/10.1007/bf01558086.

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4

Badalova, K. K., A. R. Mamedova, R. A. Alieva, A. M. Magerramov, and M. A. Allakhverdiev. "Reaction of 1-Amino-3-propoxy-2-propanol with Aldehydes." Russian Journal of Applied Chemistry 78, no. 10 (October 2005): 1656–58. http://dx.doi.org/10.1007/s11167-005-0580-9.

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5

Podjed, Nina, Petra Stare, Romana Cerc Korošec, María M. Alcaide, Joaquín López-Serrano, and Barbara Modec. "3-Amino-1-propanol and N-methylaminoethanol: coordination to zinc(ii) vs. decomposition to ammonia." New Journal of Chemistry 44, no. 2 (2020): 387–400. http://dx.doi.org/10.1039/c9nj05005a.

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6

Wang, Ke-dong, Ying-bin Jia, Zhen-jiang Lai, and Yu-fang Liu. "Ab initio Study on Ionization Energies of 3-Amino-1-propanol." Chinese Journal of Chemical Physics 24, no. 3 (June 2011): 315–18. http://dx.doi.org/10.1088/1674-0068/24/03/315-318.

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7

Dong, Lihu, Jian Chen, and Guanghua Gao. "Solubility of Carbon Dioxide in Aqueous Solutions of 3-Amino-1-propanol." Journal of Chemical & Engineering Data 55, no. 2 (February 11, 2010): 1030–34. http://dx.doi.org/10.1021/je900492a.

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8

Korotkii, Yu V., N. A. Vrynchanu, Yu N. Maksimov, and M. O. Lozinskii. "Synthesis and antimicrobial activity of 1-[4-(1-adamantyl)phenoxy]-3-amino-2-propanol." Pharmaceutical Chemistry Journal 43, no. 6 (June 2009): 301–4. http://dx.doi.org/10.1007/s11094-009-0299-7.

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9

Scheel, Rebecca, Kathrin Louven, and Carsten Strohmann. "Crystal structures of [Li7(i-PrO)3(C4H10NO)3]2O and [Na(i-PrOH)2(C8H18NO2)]2." Acta Crystallographica Section E Crystallographic Communications 76, no. 6 (May 29, 2020): 948–53. http://dx.doi.org/10.1107/s2056989020006659.

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The title compounds, hexakis[μ3-2-(dimethylamino)ethanolato]hexa-μ2-isopropanolato-μ4-oxido-tetradecalithium(I), [Li7(i-PrO)3(C4H10NO)3]2O (1), and {3-[(2-methoxyethyl)(methyl)amino]-1,1-dimethylpropanolato}diisopropanolsodium(I), [Na(i-PrOH)2(C8H18NO2)] (2), were crystallized in the presence of 2-propanol (i-PrOH, C3H7OH). The structure 1 has monoclinic symmetry (C2/c) and the asymmetric unit contains half of the compound. Title compound 2 has triclinic symmetry (P\overline{1}) and the asymmetric unit is half of an inversion-symmetric aggregate. Both compounds consist of an alkali metal, an aminoalkoxide and a 2-propanol compound. Furthermore, the dimeric sodium aggregate 2 is build up by hydrogen bonding through the 2-propanol and the alkoxides. Compound 1 does not exhibit hydrogen bonding, due to the fact that the 2-propanol is deprotonated. In compound 1, benzene appeared as co-crystallate, but was suppressed by solvent masking because of strong disorder. The formula mass and density do not take account of the solvent.

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10

Álvarez, Estrella, Fernando Cerdeira, Diego Gómez-Diaz, and José M. Navaza. "Density, Speed of Sound, Isentropic Compressibility, and Excess Volume of Binary Mixtures of 1-Amino-2-propanol or 3-Amino-1-propanol with 2-Amino-2-methyl-1-propanol, Diethanolamine, or Triethanolamine from (293.15 to 323.15) K." Journal of Chemical & Engineering Data 55, no. 7 (July 8, 2010): 2567–75. http://dx.doi.org/10.1021/je900739x.

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11

Sánchez-Bautista, Alfredo, Ester M. Palmero, Alberto J. Moya, Diego Gómez-Díaz, and M. Dolores La Rubia. "Characterization of Alkanolamine Blends for Carbon Dioxide Absorption. Corrosion and Regeneration Studies." Sustainability 13, no. 7 (April 3, 2021): 4011. http://dx.doi.org/10.3390/su13074011.

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There are a lot of research programs focusing on the development of new solvents for carbon dioxide capture. The most important priority should be reducing the energy consumption needed at the regeneration step, but minimizing solvent degradation and its corrosivity is also considered as a priority. In this research, the aqueous blends of 2-amino-2-methyl-1-propanol (AMP: 1 kmol·m−3) and 1-amino-2-propanol (MIPA: 0.1–0.5 kmol·m−3) are characterized in terms of density, viscosity, and surface tension. The carbon dioxide absorption rate and capacity, the regeneration capacity, and the corrosivity of these solvents are also evaluated.

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12

Kadiwala, Salim, Aravind V. Rayer, and Amr Henni. "Kinetics of carbon dioxide (CO2) with ethylenediamine, 3-amino-1-propanol in methanol and ethanol, and with 1-dimethylamino-2-propanol and 3-dimethylamino-1-propanol in water using stopped-flow technique." Chemical Engineering Journal 179 (January 2012): 262–71. http://dx.doi.org/10.1016/j.cej.2011.10.093.

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13

Álvarez, Estrella, Ángeles Cancela, Rocío Maceiras, José M. Navaza, and Rubén Táboas. "Surface Tension of Aqueous Binary Mixtures of 1-Amino-2-Propanol and 3-Amino-1-Propanol, and Aqueous Ternary Mixtures of These Amines with Diethanolamine, Triethanolamine, and 2-Amino-2-methyl-1-propanol from (298.15 to 323.15) K." Journal of Chemical & Engineering Data 48, no. 1 (January 2003): 32–35. http://dx.doi.org/10.1021/je020048n.

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14

Harnisch, Henrik, and Gerhard K. E. Scriba. "Capillary electrophoresis method for the determination of (R)-dapoxetine, (3S)-3-(dimethylamino)-3-phenyl-1-propanol, (S)-3-amino-3-phenyl-1-propanol and 1-naphthol as impurities of dapoxetine hydrochloride." Journal of Pharmaceutical and Biomedical Analysis 162 (January 2019): 257–63. http://dx.doi.org/10.1016/j.jpba.2018.09.039.

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15

Benmaarouf-khallaayoun, Z., M. Baboulene, V. Speziale, and A. Lattes. "Hydroboration of Unsaturated Amines VIII A Convenient Synthesis of Amino-3 Propanol-1." Synthetic Communications 15, no. 3 (March 1985): 233–41. http://dx.doi.org/10.1080/00397918508063793.

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16

Bentes, Jessica, Alicia García-Abuín, Allen G. Gomes, Diego Gómez-Díaz, José M. Navaza, and Antonio Rumbo. "CO2 chemical absorption in 3-amino-1-propanol aqueous solutions in BC reactor." Fuel Processing Technology 137 (September 2015): 179–85. http://dx.doi.org/10.1016/j.fuproc.2015.03.030.

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17

Omrani, Abdollah, Abbas Ali Rostami, and Maryam Mokhtary. "Densities and volumetric properties of 1,4-dioxane with ethanol, 3-methyl-1-butanol, 3-amino-1-propanol and 2-propanol binary mixtures at various temperatures." Journal of Molecular Liquids 157, no. 1 (November 2010): 18–24. http://dx.doi.org/10.1016/j.molliq.2010.07.015.

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18

Hvidt, Torsten, Walter A. Szarek, and David B. Maclean. "Synthesis of enantiomerically pure β-amino-α-methylene-γ-butyrolactones by way of ozonolysis of aromatic α-amino acids." Canadian Journal of Chemistry 66, no. 4 (April 1, 1988): 779–82. http://dx.doi.org/10.1139/v88-135.

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The (R) and (S) isomers of β-amino-α-methylene-γ-butyrolactone hydrochloride (4-amino-dihydro-3-methylene-2(3H)-furanone hydrochloride) have been synthesized from (R)- and (S)-tryptophan, respectively. A key step is the ozonolysis of N,O-diacetyl-2-amino-3-(3′-indolyl)-1-propanol. (S)-β-Amino-α-methylene-γ-butyrolactone hydrochloride has been synthesized also by an analogous route starting with (S)-phenylalanine.

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19

Scheers, Ellen M., Anna Forsby, and Paul J. Dierickx. "Cytotoxicity of Amino Alcohols to Rat Hepatoma-derived Fa32 Cells." Alternatives to Laboratory Animals 30, no. 3 (May 2002): 309–12. http://dx.doi.org/10.1177/026119290203000308.

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Amino alcohols are used as emulsifying agents in dry-cleaning soaps, wax removers, cosmetics, paints and insecticides. The cytotoxicities of 12 amino alcohols, which differed in chain length, position of the amino and alcohol groups, and the presence of an additional phenyl group, were determined by the neutral red uptake inhibition assay with normally cultured, glutathione-depleted or antioxidant-enriched Fa32 rat hepatoma-derived cells. Glutathione depletion and antioxidant enrichment were achieved by including 50μM L-buthionine- S,R-sulphoximine (BSO) or 100μM α-tocopherol acetate (vitamin E) in the culture medium for 24 hours before and during the assay. The cytotoxicity of the amino alcohols observed after treatment for 24 hours was expressed as the concentration of compound needed to induce a 50% reduction in neutral red uptake (NI50). The observed NI50 values ranged from 3mM to 30mM. The individual stereoisomers and a racemic mixture of 1-amino-2-propanol exhibited similar cytotoxicities (with normally cultured Fa32 cells, and vitamin E- and BSO-treated cultures). Similar NI50 values for D-(+)-2-amino-1-propanol, 3-amino-1-propanol and the L-, D- or DL- forms of 1-amino-2-propanol, indicated that the position of the amino group had little influence on the cytotoxicities of the amino alcohols. In contrast, the position of the hydroxyl group appeared to play an important role for the toxicity of the compound, as indicated by the significantly different NI50 values for 4-amino-1-butanol and 4-amino-2-butanol. An additional phenyl group greatly increased the cytotoxicity of 2-amino-1,3-propanediol. For most of the compounds, cytotoxicity increased when GSH was depleted, and decreased when the cells were enriched with vitamin E. This indicated that most of the tested chemicals interact with GSH, either directly or indirectly, by processes which generate oxygen free-radicals. Decreased toxicity was found for most of the chemicals administered to vitamin E-enriched cells, indicating that reactive oxygen species could be involved in the toxicity of the amino alcohols.

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20

Begeç, Saliha, Sümeyya Alatas, and Adem Kiliç. "The Reactions of Phenoxy Substituted Phosphazenes with 1,3-Propanediol and 3-Amino-1-propanol." HETEROCYCLES 71, no. 2 (2007): 281. http://dx.doi.org/10.3987/com-06-10915.

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21

Peeters, O. M., N. M. Blaton, and C. J. De Ranter. "(+)-(S)-1-{4-[(2-Benzothiazolyl)(methyl)amino]piperidyl}-3-(3,4-difluorophenoxy)-2-propanol (Lubeluzole)." Acta Crystallographica Section C Crystal Structure Communications 51, no. 10 (October 15, 1995): 2129–32. http://dx.doi.org/10.1107/s0108270195005439.

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22

Idris, Zulkifli, Nithin B. Kummamuru, and Dag A. Eimer. "Viscosity Measurement and Correlation of Unloaded and CO2-Loaded 3-Amino-1-propanol Solution." Journal of Chemical & Engineering Data 63, no. 5 (April 30, 2018): 1454–59. http://dx.doi.org/10.1021/acs.jced.7b01035.

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23

Cho, Chan Sik, Byoung Ho Oh, and Sang Chul Shim. "Synthesis of quinolines by ruthenium-catalyzed heteroannulation of anilines with 3-amino-1-propanol." Journal of Heterocyclic Chemistry 36, no. 5 (September 1999): 1175–78. http://dx.doi.org/10.1002/jhet.5570360510.

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24

Shirazi, Sanaz Gharehzadeh, and Fakhri Kermanpour. "Density and Viscosity of 2-Butanol + (1-Propanol, 2-Propanol, or 3-Amino-1-propanol) Mixtures at Temperatures of (293.15 to 323.15) K: Application of the ERAS Model." Journal of Chemical & Engineering Data 64, no. 6 (April 29, 2019): 2292–302. http://dx.doi.org/10.1021/acs.jced.8b01097.

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25

Hu, Ai-Xi, Gao Cao, Xin-Rong Xiao, and Hong-Yan Wu. "(2S,3S,5R)-2-(3-Chlorophenyl)-2-hydroxy-3,5-dimethyl-2-morpholinium chloride." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 29, 2006): o1584—o1585. http://dx.doi.org/10.1107/s1600536806010361.

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The title compound, C12H17ClNO2 +·Cl−, was synthesized by the reaction of (R)-(−)-2-amino-1-propanol and 2-bromo-1-(3-chlorophenyl)propan-1-one. The morpholine ring has a chair conformation; the 3,5-dimethyl and 2-hydroxy groups are on the same side of the morpholine ring with the 2-(3-chlorophenyl) group on the opposite side.

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26

Das, Bisweswar, Binay Deogam, and Bishnupada Mandal. "Experimental and theoretical studies on efficient carbon dioxide capture using novel bis(3-aminopropyl)amine (APA)-activated aqueous 2-amino-2-methyl-1-propanol (AMP) solutions." RSC Advances 7, no. 35 (2017): 21518–30. http://dx.doi.org/10.1039/c7ra01286a.

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The present study investigates the absorption of CO₂, into novel bis(3-aminopropyl)amine (APA)-activated aqueous solutions of 2-amino-2-methyl-1-propanol (AMP), using a wetted-wall column absorber.

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27

Idris, Zulkifli, Nataliia Peresunko, Klaus J. Jens, and Dag A. Eimer. "Equilibrium solubility of carbon dioxide in aqueous solutions of 3-amino-1-propanol, 4-amino-1-butanol and 5-amino-1-pentanol at low partial pressures." Fluid Phase Equilibria 387 (February 2015): 81–87. http://dx.doi.org/10.1016/j.fluid.2014.11.028.

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28

Henni, Amr, Juelin Li, and Paitoon Tontiwachwuthikul. "Reaction Kinetics of CO2in Aqueous 1-Amino-2-Propanol, 3-Amino-1-Propanol, and Dimethylmonoethanolamine Solutions in the Temperature Range of 298−313 K Using the Stopped-Flow Technique." Industrial & Engineering Chemistry Research 47, no. 7 (April 2008): 2213–20. http://dx.doi.org/10.1021/ie070587r.

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29

Camacho, F., S. Sánchez, and R. Pacheco. "Thermal Effects During the Absorption of CO2 in Aqueous Solutions of 3-Amino-1-Propanol." Chemical Engineering & Technology 23, no. 12 (December 2000): 1073–80. http://dx.doi.org/10.1002/1521-4125(200012)23:12<1073::aid-ceat1073>3.0.co;2-z.

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30

White, Gregory J., and Michael E. Garst. "Cyclic sulfamate from N-substituted 2-amino-3-phenyl-1-propanol and its nucleophilic reactions." Journal of Organic Chemistry 56, no. 9 (April 1991): 3177–78. http://dx.doi.org/10.1021/jo00009a045.

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31

Cho, Chan Sik, Byoung Ho Oh, and Sang Chul Shim. "ChemInform Abstract: Synthesis of Quinolines by Ruthenium-Catalyzed Heteroannulation of Anilines with 3-Amino-1-propanol." ChemInform 31, no. 12 (June 9, 2010): no. http://dx.doi.org/10.1002/chin.200012149.

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32

Jovanovic, Slobodanka, Milanka Vico-Stevanovic, Dragana Ugljesic-Kilibarda, Dragica Popadic, Slobodanka Simic, and Dijamanda Dzeletovic. "Catalysis in the alkylation reaction of 1-naphthol with epichlorohydrin." Journal of the Serbian Chemical Society 71, no. 8-9 (2006): 867–77. http://dx.doi.org/10.2298/jsc0609867j.

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Two new and improved procedures were developed for the synthesis of 1-(1-naphthyloxy)-2,3-epoxypropane as an important intermediate in the production of the beta-blocker and antioxidant 1-[(1-methylethyl)amino]-3-(1-naphthyloxy)- 2-propanol (propranolol). Both base homogeneous and heterogeneous PTC catalysis were employed. High yields and remarkable selectivity were achieved. The improved purity is particularly important, in view of the quality requirements for propranolol hydrochloride as an active pharmaceutical ingredient.

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33

Ghabbour, Hazem A., Mohamed N. Aboul-Enein, Aida A. El-Azzouny, Rasha M. Hassan, Mohamed I. Attia, and Hoong-Kun Fun. "Crystal structure of 1-({4-[(3-nitrobenzyl)oxy]benzyl}amino)-2,3-dihydro- 1H-indene-1-carboxamide hydrochloride - 2-propanol(1:1), C27H32ClN3O5." Zeitschrift für Kristallographie - New Crystal Structures 229, no. 4 (December 1, 2014): 309–10. http://dx.doi.org/10.1515/ncrs-2014-0156.

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34

Belabbaci, Aouicha, Nouria Chiali-Baba Ahmed, Ilham Mokbel, and Latifa Negadi. "Investigation of the isothermal (vapour+liquid) equilibria of aqueous 2-amino-2-methyl-1-propanol (AMP), N-benzylethanolamine, or 3-dimethylamino-1-propanol solutions at several temperatures." Journal of Chemical Thermodynamics 42, no. 9 (September 2010): 1158–62. http://dx.doi.org/10.1016/j.jct.2010.04.015.

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35

Haufa, Krzysztof Zdzisław, and Mirosław Antoni Czarnecki. "Molecular Structure and Hydrogen Bonding of 2-Aminoethanol, 1-Amino-2-Propanol, 3-Amino-1-Propanol, and Binary Mixtures with Water Studied by Fourier Transform Near-Infrared Spectroscopy and Density Functional Theory Calculations." Applied Spectroscopy 64, no. 3 (March 2010): 351–59. http://dx.doi.org/10.1366/000370210790918445.

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36

Iijima, Kinya, and Takahiro Unno. "Molecular structure and conformation of gaseous 3-amino-1-propanol from electron diffraction data and rotational constants." Journal of Molecular Structure 445, no. 1-3 (April 1998): 179–85. http://dx.doi.org/10.1016/s0022-2860(97)00423-7.

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37

Kovács, P., L. Kõhidai, and G. Csaba. "Effect of 3-Amino-1-Propanol on the Phosphatidylinositol (PI) and Glycosyl Phosphatidylinositol (GPI) Systems of Tetrahymena." Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology 118, no. 1 (September 1997): 83–87. http://dx.doi.org/10.1016/s0742-8413(97)00001-7.

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38

Fadnavis, Nitin W., Kasiraman R. Radhika, and A. Vedamayee Devi. "Preparation of enantiomerically pure (R)- and (S)-3-amino-3-phenyl-1-propanol via resolution with immobilized penicillin G acylase." Tetrahedron: Asymmetry 17, no. 2 (January 2006): 240–44. http://dx.doi.org/10.1016/j.tetasy.2005.12.022.

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39

Ramasubramanian, A. S., Ramachandra Bhat, Ramakrishna Dileep, and Sandya Rani. "Transition metal complexes of 5-bromosalicylidene-4-amino-3-mercapto-1,2,4-triazine-5-one: Synthesis, characterization, catalytic and antibacterial studies." Journal of the Serbian Chemical Society 76, no. 1 (2011): 75–83. http://dx.doi.org/10.2298/jsc100212136r.

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Transition metal complexes of 5-bromosalicylidene-4-amino-3- mercapto-1,2,4-triazine-5-one with metal precursors, such as Cu(II), Ni(II), Co(II) and Pd(II), were synthesized and characterized by physicochemical and spectroscopic techniques. All the complexes are of the ML type. Based on analytical, spectral data and magnetic moments, the Co(II) and Ni(II) complexes were assigned octahedral geometries, while the Cu (II) and Pd(II) complexes square planar. A study on the catalytic oxidation of benzyl alcohol, cyclohexanol, cinnamyl alcohol, 2-propanol and 2- methyl-1-propanol was performed with N-methylmorpholine-N-oxide (NMO) and molecular oxygen as co-oxidants. All the complexes and their parent organic moiety were screened for their biological activity on several pathogenic bacteria and were found to possess appreciable bactericidal properties.

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40

Al Mamari, Hamad H., and Yousuf Al Lawati. "N-(2-Hydroxy-1,1-dimethylethyl)-3-methylbenzamide." Molbank 2020, no. 1 (December 19, 2019): M1099. http://dx.doi.org/10.3390/m1099.

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The title compound, N-(2-hydroxy-1,1-dimethylethyl)-3-methylbenzamide was synthesized by reacting 3-methylbenzoyl chloride or 3-methylbenzoic acid with 2-amino-2-methyl-1-propanol. In the present report, the synthesized target compound was fully characterized by various spectroscopic methods (1H NMR, 13C NMR, IR, GC-MS), its composition confirmed by elemental analysis, and its structure determined and confirmed by X-ray analysis. The importance of this compound lies in its possession of an N,O-bidentate directing group. Such a structural motif is potentially suitable for metal-catalyzed C–H bond functionalization reactions.

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41

Agayan, Galina M., Nikolay K. Balabaev, and Margarita N. Rodnikova. "Description of the hydrogen bond network in liquid 3-amino-1-propanol by graph theory and percolation methods." Radioelectronics. Nanosystems. Information Technologies 12, no. 1 (March 17, 2020): 61–68. http://dx.doi.org/10.17725/rensit.2020.12.061.

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42

Idris, Zulkifli, and Dag A. Eimer. "Density Measurements of Unloaded and CO2-Loaded 3-Amino-1-propanol Solutions at Temperatures (293.15 to 353.15) K." Journal of Chemical & Engineering Data 61, no. 1 (December 21, 2015): 173–81. http://dx.doi.org/10.1021/acs.jced.5b00412.

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43

Rádl, Stanislav, Lenka Kovářová, Jaroslav Moural, and Radoslava Bendová. "Structural modification and new methods for preparation of ofloxacin analogs." Collection of Czechoslovak Chemical Communications 56, no. 9 (1991): 1937–43. http://dx.doi.org/10.1135/cccc19911937.

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Reaction of ethyl 2-(2,4-dichloro-5-fluoro-3-nitrobenzoyl)-3-ethoxyacrylate IIb with 2-amino-1-propanol provided corresponding compound IIIb which under alkaline conditions underwent an aromatic denitrocyclization reaction which after alkaline saponification provided 10-chloro-9-fluoro-3-methyl-7-oxo-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid Vd. Treatment of 8-hydroxyquinolone VIII with 3-bromopropyne in the presence of sodium hydrogen carbonate provided methylene derivative VIIb which was saponified into a appropriate acid VIIc. Compound VIIb treated with N-methylpiperazine and then saponified yielded VIIa. Hydrogenation of 3-methylene derivative VIIb provided 3-methyl derivative Va.

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44

HUSZTHY, P., J. S. BRADSHAW, K. E. KRAKOWIAK, T. WANG, and N. K. DALLEY. "ChemInform Abstract: Efficient Synthesis of Azetidine Through N-Trityl- or N- Dimethoxytritylazetidines Starting from 3-Amino-1-propanol or 3- Halopropylamine Hydrohalides." ChemInform 25, no. 16 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199416136.

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Keswani, Neelam, and Nand Kishore. "Interaction of some hydrophobic amino acids, peptides, and protein with aqueous 3-chloro-1,2-propanediol and 3-chloro-1-propanol: Biophysical studies." Journal of Chemical Thermodynamics 43, no. 4 (April 2011): 591–602. http://dx.doi.org/10.1016/j.jct.2010.11.015.

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Hammadi, Akli, and Christian Crouzel. "Stereoselective synthesis of the (R)- and (S)-1-(2-amino-3-nitrophenoxy)-3-(tert-butylamino)-2-propanol from the enantiomeric glycidyl tosylates." Tetrahedron: Asymmetry 1, no. 9 (January 1990): 579–82. http://dx.doi.org/10.1016/0957-4166(90)80005-j.

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Zhang, Ya-Wen, Zong-Xuan Shen, De-Ben Gu, Wei-Yi Chen, Zheng-Hao Fei, and Qing-Fei Dai. "(S)-2-Amino-3-(2,5-dimethylphenyl)-1,1-diphenyl-1-propanol: Synthesis and Application in Enantioselective Reduction of Prochiral Ketones." Synthetic Communications 26, no. 23 (December 1996): 4415–20. http://dx.doi.org/10.1080/00397919608003844.

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Shan, H., H. Y. Wang, C. Y. Song, and F. Wang. "Kinetics and mechanism of oxidation of 2-Aminoethanol and 3-Amino-1-propanol by diperiodatoargentate(III) in alkaline medium." Journal of the Iranian Chemical Society 6, no. 2 (June 2009): 393–98. http://dx.doi.org/10.1007/bf03245849.

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Viswanathan, C. L., M. M. Kodgule, and A. S. Chaudhari. "Design, synthesis and evaluation of racemic 1-(4-hydroxyphenyl)-2-[3-(substituted phenoxy)-2-hydroxy-1-propyl]amino-1-propanol hydrochlorides as novel uterine relaxants." Bioorganic & Medicinal Chemistry Letters 15, no. 15 (August 2005): 3532–35. http://dx.doi.org/10.1016/j.bmcl.2005.05.047.

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HEATH, E., S. OLUSANYA, and G. PIJANOWSKI. "Initial Experiments with Cyproterone Acetate and 1-Amino-3-Chloro-2-Propanol Hydrochloride in the Male Virginia Opossum (Didelphis virginiana)." Andrologia 15, no. 1 (April 24, 2009): 50–56. http://dx.doi.org/10.1111/j.1439-0272.1983.tb00114.x.

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