Diazald
Diazald structure
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Common Name | Diazald | ||
|---|---|---|---|---|
| CAS Number | 80-11-5 | Molecular Weight | 214.242 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 320.5±35.0 °C at 760 mmHg | |
| Molecular Formula | C8H10N2O3S | Melting Point | ~58 °C | |
| MSDS | Chinese USA | Flash Point | 147.6±25.9 °C | |
| Symbol |
GHS02, GHS07 |
Signal Word | Danger | |
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Anaerobic activation of p-cymene in denitrifying betaproteobacteria: methyl group hydroxylation versus addition to fumarate.
Appl. Environ. Microbiol. 80(24) , 7592-603, (2014) The betaproteobacteria "Aromatoleum aromaticum" pCyN1 and "Thauera" sp. strain pCyN2 anaerobically degrade the plant-derived aromatic hydrocarbon p-cymene (4-isopropyltoluene) under nitrate-reducing conditions. Metabolite analysis of p-cymene-adapted "A. arom... |
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Diazald, a newly recognized antimicrobial agent and its spectrophotometric determination.
Acta Microbiol. Hung. 39(3-4) , 317-22, (1992) Diazald, a chemical intermediate for the synthesis of biologically active compounds, was found to be a potent in vitro antimicrobial agent against yeasts, yeast-like and filamentous fungi as well as Gram-positive and Gram-negative bacterial strains. Its activ... |
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Transnitrosating activity of N-nitroso-N-methyl-p-toluenesulfonamide in rats and human gastric juice.
Neoplasma 35(3) , 257-62, (1988) N-nitroso-N-methyl-p-toluenesulfonamide (NMTS, diazald, CAS 80-11-5) is a widely used compound for laboratory production of diazomethane. The present results showed that the noncarcinogenic NMTS reacts as a transnitrosating agent with amino nitrogen of second... |
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Contact dermatitis from Diazald.
Contact Dermatitis 50(5) , 315-6, (2004)
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Organometallics 12 , 1029, (1993)
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J. Chem. Soc., Perkin Trans. II , 29, (1993)
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J. Chem. Soc., Perkin Trans. II , 1233, (1993)
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J. Chromatogr. Sci. 29 , 8, (1991)
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