Ammonium iodide | CAS:12027-06-4
Ammonium iodide
- Name:Ammonium iodide
- CAS:12027-06-4
- Synonyms:
- Molecular Formula:NH4I
- Molecular Weight:144.94
- EINESC:234-717-7
Description
Properties
Melting point | 551 ºC |
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Density | 2.514 |
Safety
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SDS
Source | SDS/MSDS Samples |
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Alfa-Aesar | View & Download |
Sigma-Aldrich | View & Download |
Acros-Organics | View & Download |
Synthetic Route
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More
Articles
Peer-Reviewed Papers
Neurotoxic effects of trans-glutaconic acid in rats.Patrícia F Schuck et al.Oxidative medicine and cellular longevity, 2013, 607610-607610 (2013-04-23)
Sodium ion-dependent hydrogen production in Acidaminococcus fermentans.U Härtel et al.Archives of microbiology, 166(5), 350-356 (1996-11-01)
Glutaric acid and its metabolites cause apoptosis in immature oligodendrocytes: a novel mechanism of white matter degeneration in glutaryl-CoA dehydrogenase deficiency.Bettina Gerstner et al.Pediatric research, 57(6), 771-776 (2005-03-19)
6-Chloro-2(2H)-pyranone: a new 2(2H)-pyranone synthon.Biagetti M, et al. Tetrahedron Letters, 44(3), 607-610 (2003)
Alkaline Partial Wet Oxidation of Lignin for the Production of Carboxylic Acids.Demesa AG, et al. Chemical Engineering & Technology, 38(12), 2270-2278 (2015)
Nerve cell lesions caused by 3-hydroxyglutaric acid: a possible mechanism for neurodegeneration in glutaric acidaemia I.B Flott-Rahmel et al.Journal of inherited metabolic disease, 20(3), 387-390 (1997-07-01)
99mTc-labeling and in vitro and in vivo evaluation of HYNIC- and (Nalpha-His)acetic acid-modified [D-Glu1]-minigastrin.E von Guggenberg et al.Bioconjugate chemistry, 15(4), 864-871 (2004-07-22)
On the neurotoxicity of glutaric, 3-hydroxyglutaric, and trans-glutaconic acids in glutaric acidemia type 1.T M Lund et al.Journal of neuroscience research, 77(1), 143-147 (2004-06-16)
Chronic subdural hematoma, as an initial manifestation of glutaric aciduria type-1.H Osaka et al.Brain & development, 15(2), 125-127 (1993-03-01)
Stereodifferentiation of 3-hydroxyisobutyric- and 3-aminoisobutyric acid in human urine by enantioselective multidimensional capillary gas chromatography-mass spectrometry.F Podebrad et al.Clinica chimica acta; international journal of clinical chemistry, 292(1-2), 93-105 (2000-02-25)
Efficient synthesis and neuroprotective effect of substituted 1,3-diphenyl-2-propen-1-ones.Jae-Chul Jung et al.Journal of medicinal chemistry, 51(13), 4054-4058 (2008-06-04)
Theoretical studies of molecular structure and vibrational spectra of glutaconic acid.Atalay Y, et al. Journal of Molecular Structure, 787(1), 90-95 (2006)
The reversible dehydration of (R)-2-hydroxyglutarate to (E)-glutaconate.W Buckel European journal of biochemistry, 106(2), 439-447 (1980-05-01)
Glutaconate CoA-transferase from Acidaminococcus fermentans.W Buckel et al.European journal of biochemistry, 118(2), 315-321 (1981-08-01)
Plausible molecular mechanism for activation by fumarate and electron transfer of the dopamine beta-mono-oxygenase reaction.D Shyamali Wimalasena et al.The Biochemical journal, 367(Pt 1), 77-85 (2002-06-01)
Biochemical characterization of human 3-methylglutaconyl-CoA hydratase and its role in leucine metabolism.Matthias Mack et al.The FEBS journal, 273(9), 2012-2022 (2006-04-28)
Adaptive laboratory evolution of tolerance to dicarboxylic acids in Saccharomyces cerevisiae.Rui Pereira et al.Metabolic engineering, 56, 130-141 (2019-09-25)
A biotin-dependent sodium pump: glutaconyl-CoA decarboxylase from Acidaminococcus fermentans.W Buckel et al.FEBS letters, 148(1), 35-38 (1982-11-01)
Crystal and molecular structure of glutaconic acid.Thomas L and Srikrishnan T. Journal of Chemical Crystallography, 33(9), 689-693 (2003)
Induction of the mitochondrial permeability transition in vitro by short-chain carboxylic acids.C M Palmeira et al.Biochemical and biophysical research communications, 272(2), 431-435 (2000-06-02)
Production of glutaconic acid in a recombinant Escherichia coli strain.Ivana Djurdjevic et al.Applied and environmental microbiology, 77(1), 320-322 (2010-11-03)
Remarks
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Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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