What Does Dmg Stand For Chemistry
- What Does Dmg Stand For Chemistry Table
- What Does Dmg Stand For Chemistry Pdf
- What Does Dmg Stand For Chemistry In Education
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File TypeApple Disk Image
| Developer | Apple |
| Popularity | |
| Category | Disk Image Files |
| Format | Binary |
What is a DMG file?
A DMG file is a mountable disk image used to distribute software to the macOS operating system. The file is typically downloaded from the Internet by a Mac user, then double-clicked to install an application on the computer.
Today, software developers typically build and distribute applications for Mac users as DMG, .APP, or .PKG files. DMG files are especially common since their contents can be verified upon installation to ensure they have not been tampered with and they can also be compressed to reduce the size of the installer.
When a Mac user downloads a DMG file, he can simply double-click it to open it with the DiskImageMounter utility that comes with macOS. When the DMG file is opened, it mounts a virtual disk on the desktop and in an Apple Finder window as if it was a CD or a USB flash drive that was just inserted into the computer.
In the Finder window, the Mac user can double-click the program icon, which is an APP file, to run the app. Or the Mac user can drag the program icon to the 'Applications' folder icon to move it to the 'Applications' directory in macOS.
After the software stored in the DMG file is installed, the DMG file is no longer needed. Therefore, DMG files can be deleted after installing the software.
While DMG files are Mac-specific and not intended for use in Windows, there are several Windows programs that can extract their contents or convert them to other formats. Some programs include 7-Zip, PeaZip, and DMG2IMG.
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NOTE: The DMG format replaced the .IMG file format, which was previously used in Mac OS Classic.
Unknown files on your Mac? Try File Viewer.| Mac |
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What Does Dmg Stand For Chemistry Table
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| ChEMBL | |
| ChemSpider |
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| ECHA InfoCard | 100.002.201 |
| EC Number | |
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CompTox Dashboard(EPA) | |
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| Properties | |
| C4H8N2O2 | |
| Molar mass | 116.120 g·mol−1 |
| Appearance | White/Off White Powder |
| Density | 1.37 g/cm3 |
| Melting point | 240 to 241 °C (464 to 466 °F; 513 to 514 K) |
| Boiling point | decomposes |
| low | |
| Structure | |
| 0 | |
| Hazards | |
| Main hazards | Toxic, Skin/Eye Irritant |
| Safety data sheet | External MSDS |
| GHS pictograms | |
| GHS Signal word | Danger |
| H228, H301 | |
| P210, P240, P241, P264, P270, P280, P301+310, P321, P330, P370+378, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Related compounds | |
| Hydroxylamine salicylaldoxime | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
What Does Dmg Stand For Chemistry Pdf
Dimethylglyoxime is a chemical compound described by the formula CH3C(NOH)C(NOH)CH3. Its abbreviation is dmgH2 for neutral form, and dmgHFinal cut pro 6 dmg. for anionic form, where H stands for hydrogen. This colourless solid is the dioxime derivative of the diketone butane-2,3-dione (also known as diacetyl). DmgH2 is used in the analysis of palladium or nickel. Its coordination complexes are of theoretical interest as models for enzymes and as catalysts. Many related ligands can be prepared from other diketones, e.g. benzil.
Preparation[edit]
Dimethylglyoxime can be prepared from butanone first by reaction with ethyl nitrite to give biacetyl monoxime. The second oxime is installed using sodium hydroxylamine monosulfonate:[1]
Complexes[edit]
Dimethylglyoxime is used to detect and quantify nickel, which forms the bright red complex nickel bis(dimethylglyoximate) (Ni(dmgH)2). The reaction was discovered by L. A. Chugaev in 1905.[2]
Cobalt complexes have also received much attention. In chloro(pyridine)cobaloxime[3] the macrocycle [dmgH]22− mimics the macrocyclic ligand found in vitamin B12.
What Does Dmg Stand For Chemistry In Education
References[edit]
- ^Semon, W. L.; Damerell, V. R. (1930). 'Dimethylglyoxime'. Organic Syntheses. 10: 22. doi:10.15227/orgsyn.010.0022.CS1 maint: multiple names: authors list (link)
- ^Lev Tschugaeff (1905). 'Über ein neues, empfindliches Reagens auf Nickel'. Berichte der Deutschen Chemischen Gesellschaft. 38 (3): 2520–2522. doi:10.1002/cber.19050380317.
- ^Girolami, G. S.; Rauchfuss, T.B.; Angelici, R. J. (1999). Synthesis and Technique in Inorganic Chemistry: A Laboratory Manual (3rd ed.). pp. 213–215.