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De novo design of signal sequences to localize cargo to the 1,2-propanediol utilization microcompartment. [PDF]
Jakobson CM +2 more
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Vitrification and crystallization in the R(−)1,2-propanediol-S(+)1,2-propanediol system
Thermochimica Acta, 1995Abstract Differential scanning calorimetry (DSC) was used to investigate the thermal behaviour of 1,2-propanediol enantiomers and to study the R(−)1,2-propanediol-S(+)1,2-propanediol phase diagram. The melting temperature of the pure enantiomers was determined as 240 K and their melting heat as 8400 J mol−1.
P Claudy, J M Létoffé
exaly +2 more sources
Bulletin of the Chemical Society of Japan, 1992
Abstract Ester formations of borate ion with 1,2-propanediol, 3-amino-1,2-propanediol, and (±)-3-dimethylamino-1,2-propanediol and stabilities of the formed esters were studied by 11B NMR spectroscopy. For each of the boric acid–diol systems, esters with the 1 : 1 mole ratio of borate ion and diol and with the 1 : 2 mole ratio were ...
Takao Oi +2 more
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Abstract Ester formations of borate ion with 1,2-propanediol, 3-amino-1,2-propanediol, and (±)-3-dimethylamino-1,2-propanediol and stabilities of the formed esters were studied by 11B NMR spectroscopy. For each of the boric acid–diol systems, esters with the 1 : 1 mole ratio of borate ion and diol and with the 1 : 2 mole ratio were ...
Takao Oi +2 more
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The metabolism of 1,2-propanediol
Biochimica et Biophysica Acta, 1961Abstract 1. 1. Lactaldehyde has been identified as the product of the oxidation of dl -1.2-propanediol by a rabbit-liver alcohol dehydrogenase preparation. 2. 2. The K s values for (a) oxidation of ethanol, l -1,2-propanediol, and d -1,2-propanediol are respectively 0.63, 3.6, and 33.3 μmoles/ml; and for (b) reduction of acetaldehyde,
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Microwave spectrum of 1,2-propanediol
Journal of Molecular Spectroscopy, 2009Abstract The microwave spectrum of the sugar alcohol 1,2-propanediol (CH3CHOHCH2OH) has been measured over the frequency range 6.5–25.0 GHz with several pulsed-beam Fourier-transform microwave spectrometers. Seven conformers of 1,2-propanediol have been assigned and ab initio electronic structure calculations of the 10 lowest energy forms have been ...
F.J. Lovas +5 more
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Toxicology, metabolism, and biochemistry of 1,2-propanediol
Toxicology and Applied Pharmacology, 1972Abstract The toxicity of 1,2-propanediol is reviewed, and a table of the LD50 values for the rat, rabbit, mouse, guinea pig, and dog is presented. Metabolic and chronic studies demonstrate that 1,2-propanediol can be used as a substitute for carbohydrate in the diet of rats and young chicks. The glycol is primarily oxidized to lactate or pyruvate.
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1,2-Propanediol-2-Phosphate in Ascaris lumbricoides
Science, 1966No phosphagen is present in the body-wall muscle of Ascaris lumbricoides . A stable phosphorus compound, which on the basis of its chemical reactions seems to be 1,2-propanediol-2-phosphate, constitutes more than half of the acid-soluble phosphorus compounds.
J, Kubistovà, D, Seth
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The production of 1,2-propanediol in ethanol treated rats
Biochemical and Biophysical Research Communications, 1985Chronic administration of ethanol in the most commonly used experimental diet (Lieber, C. S., and DeCarli, L. M. (1976) Fed. Proceed. 35, 1232-1236) resulted in the production of 1,2-propanediol within one week of initiation of alcohol feeding. After two weeks 1,2-propanediol levels were 8.8 +/- 1.6 nmol/ml in alcohol treated animals.
J P, Casazza, R L, Veech
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2001
[4704-77-2] C3H7BrO2 (MW 154.99) InChI = 1S/C3H7BrO2/c4-1-3(6)2-5/h3,5-6H,1-2H2 InChIKey = SIBFQOUHOCRXDL-UHFFFAOYSA-N (carbonyl protecting group which can be cleaved under neutral conditions2) Physical Data: bp 92–94 °C/1.5 mmHg; d 1.769 g cm−3.
Michael A. Walters, Hélène R. Arcand
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[4704-77-2] C3H7BrO2 (MW 154.99) InChI = 1S/C3H7BrO2/c4-1-3(6)2-5/h3,5-6H,1-2H2 InChIKey = SIBFQOUHOCRXDL-UHFFFAOYSA-N (carbonyl protecting group which can be cleaved under neutral conditions2) Physical Data: bp 92–94 °C/1.5 mmHg; d 1.769 g cm−3.
Michael A. Walters, Hélène R. Arcand
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