Names | |||
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IUPAC name | |||
Other names
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Identifiers | |||
3D model (JSmol) | |||
Abbreviations | DMF-d7[ citation needed ] | ||
1908468 | |||
ChemSpider | |||
ECHA InfoCard | 100.022.497 | ||
EC Number |
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PubChem CID | |||
UN number | 2265 | ||
CompTox Dashboard (EPA) | |||
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Properties | |||
C 32 H 7NO or C 3D 7NO | |||
Molar mass | 80.1369 g mol−1 | ||
Appearance | Colourless liquid | ||
Density | 1.03 g mL−1 | ||
Boiling point | 153 °C (307 °F; 426 K) | ||
Refractive index (nD) | 1.428 | ||
Hazards | |||
GHS labelling: | |||
Danger | |||
H312, H319, H332, H360 | |||
P280, P305+P351+P338, P308+P313 | |||
Flash point | 58 °C (136 °F; 331 K) | ||
Explosive limits | 2.2–15.2% | ||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose) |
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Related compounds | |||
Related alkanamides | |||
Related compounds | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
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Digital microfluidics (DMF) is a platform for lab-on-a-chip systems that is based upon the manipulation of microdroplets. Droplets are dispensed, moved, stored, mixed, reacted, or analyzed on a platform with a set of insulated electrodes. Digital microfluidics can be used together with analytical analysis procedures such as mass spectrometry, colorimetry, electrochemical, and electrochemiluminescense.
In organic chemistry, an acyl chloride is an organic compound with the functional group −C(=O)Cl. Their formula is usually written R−COCl, where R is a side chain. They are reactive derivatives of carboxylic acids. A specific example of an acyl chloride is acetyl chloride, CH3COCl. Acyl chlorides are the most important subset of acyl halides.
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In chemistry a donor number (DN) is a quantitative measure of Lewis basicity. A donor number is defined as the negative enthalpy value for the 1:1 adduct formation between a Lewis base and the standard Lewis acid SbCl5 (antimony pentachloride), in dilute solution in the noncoordinating solvent 1,2-dichloroethane with a zero DN. The units are kilocalories per mole for historical reasons. The donor number is a measure of the ability of a solvent to solvate cations and Lewis acids. The method was developed by V. Gutmann in 1976. Likewise Lewis acids are characterized by acceptor numbers (AN, see Gutmann–Beckett method).
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Deuterated solvents are a group of compounds where one or more hydrogen atoms are substituted by deuterium atoms.
Alcohol intolerance is due to a genetic polymorphism of the aldehyde dehydrogenase enzyme, which is responsible for the metabolism of acetaldehyde. This polymorphism is most often reported in patients of East Asian descent. Alcohol intolerance may also be an associated side effect of certain drugs such as disulfiram, metronidazole, or nilutamide. Skin flushing and nasal congestion are the most common symptoms of intolerance after alcohol ingestion. It may also be characterized as intolerance causing hangover symptoms similar to the "disulfiram-like reaction" of aldehyde dehydrogenase deficiency or chronic fatigue syndrome. Severe pain after drinking alcohol may indicate a more serious underlying condition.
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