Isobutylamine
Isobutylamine structure
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Common Name | Isobutylamine | ||
|---|---|---|---|---|
| CAS Number | 78-81-9 | Molecular Weight | 73.13680 | |
| Density | 0.736 g/mL at 25 °C(lit.) | Boiling Point | 64-71 °C(lit.) | |
| Molecular Formula | C4H11N | Melting Point | −85 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 15 °F | |
| Symbol |
GHS02, GHS05, GHS06 |
Signal Word | Danger | |
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Supercritical fluid chromatography for GMP analysis in support of pharmaceutical development and manufacturing activities.
J. Pharm. Biomed. Anal. 117 , 316-24, (2015) Supercritical fluid chromatography (SFC) has long been a preferred method for enantiopurity analysis in support of pharmaceutical discovery and development, but implementation of the technique in regulated GMP laboratories has been somewhat slow, owing to lim... |
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The development of a semi-preparatory scale supercritical-fluid chromatograph for high-throughput purification of 'combi-chem' libraries.
J. Biochem. Biophys. Methods 43(1-3) , 87-111, (2000) A unique separator was developed which allowed automatic separation and peak collection using semi-preparative supercritical fluid chromatography (SFC). A peak detector switched the effluent between waste and special collection cassettes. Up to 50 mg of vario... |
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Effect of particle size on the speed and resolution of chiral separations using supercritical fluid chromatography.
J. Chromatogr. A. 1363 , 250-6, (2014) Fast chiral supercritical fluid chromatography (SFC) separations have become important due to the increasing use of high-throughput experimentation (HTE) in organic synthesis. These HTE experiments can generate hundreds of samples for chiral analysis that nee... |
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Structural features of peptoid-peptide hybrids in lipid-water interfaces.
FEBS Lett. 588(17) , 3291-7, (2014) The inclusion of peptoid monomers into antimicrobial peptides (AMPs) increases their proteolytic resistance, but introduces conformational flexibility (reduced hydrogen bonding ability and cis/trans isomerism). We here use NMR spectroscopy to answer how the i... |
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Caffeic acid derivatives production by hairy root cultures of Echinacea purpurea.
J. Agric. Food Chem. 54(22) , 8456-60, (2006) Inoculation of leaf explants of Echinacea purpurea (Moench) with Agrobacterium rhizogenes induced hairy roots with the capacity to produce biologically active caffeic acid derivatives (CADs), especially cichoric acid. The kinetics of growth, the uptake of mac... |
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Identification of puberty-accelerating pheromones in male mouse urine.
J. Exp. Zool. 251(3) , 300-5, (1989) Gas chromatography-mass spectrometry was employed to identify the two volatile amines in male mouse urine. These amines were much less concentrated in urine of castrated males. The identified amines, isobutylamine and isoamylamine, were assayed for the potent... |
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Essential contribution of germline-encoded lysine residues in Jgamma1.2 segment to the recognition of nonpeptide antigens by human gammadelta T cells.
J. Immunol. 167(12) , 6773-9, (2001) Human gammadelta T cells display unique repertoires of Ag specificities largely imposed by selective usages of distinct Vgamma and Vdelta genes. Among them, Vgamma2/Vdelta2(+) T cells predominate in the circulation of healthy adults and respond to various mic... |
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[Biosynthesis of nitrosopiperidine from isobutylamine and NaNo2 by some fungi].
Wei Sheng Wu Xue Bao 27(1) , 78-82, (1987)
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Analysis of puberty-accelerating pheromones.
J. Exp. Zool. 264(1) , 42-5, (1992) Two experiments were performed to test putative puberty-accelerating pheromones. In the first experiment, 37 weanling female house mice of the ICR strain were exposed to 1 of the following 3 treatments: an airborne mixture of 0.05 M isoamylamine and 0.05 M is... |
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Isopropylamino and isobutylamino groups as recognition sites for carbohydrates: acyclic receptors with enhanced binding affinity toward β-galactosides.
J. Org. Chem. 75(19) , 6416-23, (2010) Binding motifs observed in the crystal structures of protein-carbohydrate complexes, in particular the participation of the isopropyl/isobutyl side chain of valine/leucine in the formation of van der Waals contacts, have inspired the design of new artificial ... |