magnesium
Conditions | Yield |
---|---|
With calcium oxide In neat (no solvent) distillation at 1350 °C within a period of 2 hours;; | 99% |
With SiO; CaO In neat (no solvent) distillation at 1350 °C within a period of 2 hours;; | 99% |
With silicon In neat (no solvent) |
magnesium anthracene * 3 THF
magnesium
Conditions | Yield |
---|---|
In toluene byproducts: anthracene, THF; suspn. heated to 100°C with stirring (1h); hot suspn. filtered, washed (hot toluene), dried (70°C, in vacuo); | 96% |
In neat (no solvent, solid phase) byproducts: anthracene, THF; solid magnesium anthracene*3 THF heated to 200°C (high vacuum) in several stages; | |
In toluene byproducts: anthracene, THF; other Radiation; ultrasonic irradiation of suspn.; filtered, dried (in vacuo); | |
In n-heptane byproducts: anthracene, THF; other Radiation; ultrasonic irradiation of suspn.; filtered, dried (in vacuo); | |
In n-heptane byproducts: anthracene, THF; suspn. heated; filtered, dried (in vacuo); |
magnesium
Conditions | Yield |
---|---|
With calcium carbide In neat (no solvent) equimolar amts. of CaC2 and MgF2; 4 h, 0.5 Torr, 1200°C;; | 85% |
With CaC2 In neat (no solvent) equimolar amts. of CaC2 and MgF2; 4 h, 0.5 Torr, 1200°C;; | 85% |
With calcium carbide In neat (no solvent) equimolar amts. of CaC2 and MgF2; 4 h, 0.5 Torr, 1100°C;; | 84% |
Conditions | Yield |
---|---|
In neat (no solvent) equimolar amts. of CaC2 and MgO; 1-2 Torr, 1200°C;; | A 80.05% B n/a |
In neat (no solvent) equimolar amts. of CaC2 and MgO; 1-2 Torr, 1200°C;; | A 80.05% B n/a |
In neat (no solvent) equimolar amts. of CaC2 and MgO; 1-2 Torr, 1100°C;; | A 30.52% B n/a |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) heating at 850 °C; | A 11% B 11% C 38% D 36% E 4% |
Conditions | Yield |
---|---|
In gaseous matrix deoxidn. using laser to raise temp. above 4000 K required for sepn. of Mg and O, argon gas flow prevent Mg from reoxidn.; CO2 or YAG laser, 100-1000 W, chamber pressure 500 Pa - 0.1 MPa; | A n/a B 20% |
With magnesium In neat (no solvent) partial dissociation of MgO (in a mixt. with metallic Mg) in an iron tube heated to red heat; O2 evolution is observed;; | |
In neat (no solvent) dissociation of solid MgO in metallic Mg and gaseous O2 at 2000-3000 K;; |
Conditions | Yield |
---|---|
Electrolysis; |
Conditions | Yield |
---|---|
titanium(III) chloride at 250 - 350℃; under 760.051 Torr; Product distribution / selectivity; Neat (no solvent); Balled milled; |
ethylmagnesium iodide
magnesium
Conditions | Yield |
---|---|
In diethyl ether Electrolysis; current density = 1 A/dm^2, voltage = 8 V; room temperature; addition of dimethylaniline;; | |
In diethyl ether Electrolysis; current density = 1 A/dm^2, voltage = 8 V; room temperature; addition of dimethylaniline;; |
Conditions | Yield |
---|---|
In neat (no solvent) 1200°C;; simultaneous preparation of Na and Mg;; |
Conditions | Yield |
---|---|
remarks on the technical circumstances; | |
remarks on the technical circumstances; |
Conditions | Yield |
---|---|
by heating; yields a mixt. of "amorphous" and "cryst." B; |
Conditions | Yield |
---|---|
With sodium carbonate byproducts: sodiumzinccyanide; Mg2{Fe(CN)6} ignite with Na2CO3; resulting sodiummagnesiumcyanide reduced with Zn; |
Conditions | Yield |
---|---|
at 1200-1500°C; |
magnesium
Conditions | Yield |
---|---|
With calcium carbide by heating; | |
With iron In neat (no solvent) MgS is decomposed on Fe;; not isolated;; | |
With iron In neat (no solvent) MgS is molten with iron shavings;; |
Conditions | Yield |
---|---|
at 1050°C, under 2-4Hgmm; 3% MgS; |
Conditions | Yield |
---|---|
at red heat; |
Conditions | Yield |
---|---|
Electrolysis; |
magnesium chloride
A
disulfur dichloride
B
sulfur
C
magnesium
Conditions | Yield |
---|---|
Electrolysis; |
magnesium
Conditions | Yield |
---|---|
With Al-Si-Fe alloy | |
With Al-Si alloy | |
With Al-Si-Fe alloy in the presence of alkali chloride, earth alkali chloride or fluoride; |
Conditions | Yield |
---|---|
With pyrographite In neat (no solvent) Kinetics; reduction of magnesia with charcoal powder at 1743-1883 K; |
Conditions | Yield |
---|---|
in the presence of C; |
Conditions | Yield |
---|---|
In neat (no solvent) intimate mixture of stoiichiometric amounts of MgO and Al is heated in steel tube to ca. 1200 °C;; complete separation of Mg;; |
Conditions | Yield |
---|---|
In melt solid MgO introduced in molten Al; Mg-Al-alloy separated in 2 layers of MgPb (MgCd) alloys and Al by molten Pb(Cd); | |
at 1200°C in evacuated steel pipe; | |
at >900°C; MgO and Al, powdwered, mixed and briquetted; |
Conditions | Yield |
---|---|
at 1050°C, under 2-4 Hgmm; 0.5% S; |
Conditions | Yield |
---|---|
With ferrosilicon in continuous process; |
Conditions | Yield |
---|---|
In neat (no solvent) mixt. heated to 1300°C using high-frequency induction furnace; |
Conditions | Yield |
---|---|
at 1900°C; | |
2.25 h at 1275°C; Mg distilles off; | >99 |
2.25 h at 1275°C; Mg distilles off; | >99 |
Conditions | Yield |
---|---|
In neat (no solvent) Mg (purity: 99.5%) was heated in N2 (free of O2) at 800-850 °C for 4-5 h;; | 100% |
In neat (no solvent) Mg was heated in a stream of N2 at 900 °C;; | 95% |
Conditions | Yield |
---|---|
In water reduction with Mg in neutral or acidic soln.; | 100% |
In water reduction with Mg in neutral or acidic soln.; | 100% |
In water reaction in neutral and acid solutions complete;; |
Conditions | Yield |
---|---|
In neat (no solvent) stoich. react. Mg, Th, and Te at 900°C with aid of Sn flux; | 100% |
Fe(CO)2(P(O-i-Pr)3)2I2
magnesium
μ-dinitrogenbis(dicarbonylbis(triisopropylphosphite)iron)
Conditions | Yield |
---|---|
With N2 In diethyl ether protective gas atmosphere, reduction with Mg under N2 (-20°C, 8 h); filtn. (silica gel, -20°C), crystn. (pentane, -80°C); | 100% |
Conditions | Yield |
---|---|
In water Mg (64mmol) was dissolved in a soln. of 85% phosphoric acid (128mmol) in water (50ml); after ending of evolving of gas, the solvent was removedin high vacuum with liquid N2;; after the evolving of gas has stopped, the solvent was removed in high vacuum (liq. N2), and the crystals were extracted in a Soxhlet apparatus(48h) and further dried in vacuum; elem. anal.;; | 100% |
magnesium
allyl bromide
1-Bromo-2-bromomethyl-benzene
1-bromo-2-(but-3-enyl)benzene
Conditions | Yield |
---|---|
Stage #1: magnesium; allyl bromide In diethyl ether Stage #2: 1-Bromo-2-bromomethyl-benzene In tetrahydrofuran | 100% |
Conditions | Yield |
---|---|
at 20℃; for 15h; Inert atmosphere; Schlenk technique; | 100% |
Conditions | Yield |
---|---|
at 700 - 1100℃; for 336h; Sealed tube; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide metal. Mg under O2 atm. treated with DMSO and triflic acid (2 equiv.) in3 portions, heated at 100°C for 17 h; | 99% |
Conditions | Yield |
---|---|
With oxygen In dimethyl sulfoxide metal. Mg under O2 atm. treated with DMSO and triflimidic acid (2 equiv.) in 3 portions, heated at 100°C for 18 h; | 99% |
Conditions | Yield |
---|---|
With calcium In neat (no solvent) 82kg YF3, 74kg CaCl2, 37.5 kg Ca (105 excess), 15.75kg Mg, Ti- or Zr-vessel, 800-960°C;; | 99% |
1-chloro-2,3,4,5,6-pentafluorobenzene
magnesium
pentafluorophenylmagnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran reaction at -10°C, 1 hour;; | 99% |
In tetrahydrofuran reaction at -10°C, 1.25 hours;; | 87% |
In diethyl ether (CH2Br)2- activated Mg, reaction in boiling ether;; | 67% |
Conditions | Yield |
---|---|
In ethylenediamine High Pressure; solvothermal synthesis; Mg, SbCl3, S, ethylenediamine heated in a sealedTeflon-lined stainless steel autoclave at 170°C for 10 d; coolin g to room temp.; filtered off; washed with H2O, EtOH, acetone; elem. anal.; | 99% |
Conditions | Yield |
---|---|
With triethylaluminum In ethanol; n-heptane; toluene for 2h; Heating; | 99% |
Conditions | Yield |
---|---|
Stage #1: magnesium; 6-bromo-1,4-benzodioxane; lithium chloride In tetrahydrofuran at 20℃; Inert atmosphere; Schlenk technique; Stage #2: zinc(II) chloride In tetrahydrofuran at 0 - 20℃; for 0.25h; Inert atmosphere; Schlenk technique; | 99% |
Conditions | Yield |
---|---|
With N-chloro-succinimide at 40 - 75℃; under 760.051 Torr; for 4.16667h; Product distribution / selectivity; Inert atmosphere; | 98.3% |
In neat (no solvent) with C2H5OH-vapor at 280 to 290.degree C.;; | |
In ethanol dissolution in abs. ethylalcohol in presence of CCl4 or CHCl3, and in presence of air or N2 discussed;; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: MgCl2; heating at 900-1100°C;; | 98% |
Conditions | Yield |
---|---|
In neat (no solvent) mixing Mg and autocatalytic amts. of MgH2 in an autoclave, evacuating to 133 Pa, addn. of H2 to a pressure of 0.51 MPa, heating to 350°C with continous stirring, permanent H2-pressure: 0.58 MPa, react. time: 7 h; hydrid content: 7.1% by gas volumetry; | 98% |
With chromium(III) oxide In neat (no solvent) mechanical grinding of mixt. of Mg and Cr2O3 under H2 atm.(up to 1.1 MPa) using planetary ball miller or vibratory miller, at 5 min-10 h; annealed at 200°C for 5 h or at 300°C for 5 h or at 330°Cfor 15 h; powder XRD, SEM; | |
In neat (no solvent) Mg film reacted with H2 at room temp. and 100 kPa; |
Conditions | Yield |
---|---|
byproducts: NH3, H2O, H2; at room temp.; EtOH added; elem. anal.; | 98% |
ethanol
silicon tetrafluoride
magnesium
B
tetraethoxy orthosilicate
Conditions | Yield |
---|---|
Stage #1: ethanol; magnesium With iodine at 20℃; for 3.5h; Inert atmosphere; Reflux; Stage #2: silicon tetrafluoride for 2.5h; Inert atmosphere; Reflux; Stage #3: at 300℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature; Calcination; | A 98% B 82% |
methanol
silicon tetrafluoride
magnesium
B
tetramethylorthosilicate
Conditions | Yield |
---|---|
Stage #1: methanol; magnesium With iodine at 20℃; for 1.5h; Inert atmosphere; Reflux; Stage #2: silicon tetrafluoride Inert atmosphere; Stage #3: at 300℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature; Calcination; | A 98% B 85% |
Stage #1: methanol; magnesium at 20℃; for 3h; Stage #2: silicon tetrafluoride at 20℃; for 0.5h; Temperature; |
Conditions | Yield |
---|---|
at 700 - 1100℃; for 336h; Sealed tube; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
at 700 - 1100℃; for 336h; Sealed tube; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With triethylaluminum In ethanol; n-heptane; toluene for 2h; Heating; | 98% |
Conditions | Yield |
---|---|
Stage #1: 1-bromo-4-methoxy-benzene; magnesium; lithium chloride In tetrahydrofuran at 25℃; Inert atmosphere; Schlenk technique; Stage #2: zinc(II) chloride In tetrahydrofuran at 0 - 25℃; for 0.25h; Inert atmosphere; Schlenk technique; | 98% |
Conditions | Yield |
---|---|
Stage #1: bromochlorobenzene; magnesium; lithium chloride In tetrahydrofuran at 20℃; Inert atmosphere; Schlenk technique; Stage #2: zinc(II) chloride In tetrahydrofuran at 0 - 20℃; for 0.25h; Inert atmosphere; Schlenk technique; | 98% |
Conditions | Yield |
---|---|
at 700 - 1100℃; for 336h; Sealed tube; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
With sodium chloride for 0.0333333h; Time; | 97% |
Conditions | Yield |
---|---|
for 0.0333333h; Time; | 97% |
In 1808, the metal magnesium itself was first produced in England by Sir Humphry Davy using electrolysis of a mixture of magnesia and mercury oxide.
In 1831, Antoine Bussy prepared it in coherent form.
Davy's first suggestion for a name was magnium, but the name magnesium is now used.
DOT Classification: 4.3; Label: Dangerous When Wet (UN 2950); DOT Class: 4.1; Label: Flammable Solid (UN 1869); DOT Class: 4.3; Label: Danger When Wet, Spontaneously Combustible
For occupational chemical analysis use NIOSH: Elements (ICP), 7300.
Magnesium, its cas register number is 7439-95-4. It also can be called EckaGranules PK 31; Ecka Granules PK 51; Magnesium element; Magnum Forte; Ozone magnez. Magnesium is a chemical element with the symbol Mg and atomic number 12. It is a silver or grey rod, turnings or ribbon. The more finely divided material reacts with water to liberate hydrogen, a flammable gas, though this reaction is not as vigorous as that of sodium or lithium with water. In finely divided forms is easily ignited. It burns with an intense white flame and it can be wax coated to render magnesium as nonreactive.It slowly oxidizes in moist air. Reacts very slowly with water at ordinary temperatures, less slowly at 100 °C.
Preparation of Magnesium: Magnesium is principally obtained by electrolysis of fused magnesium chloride from brines, wells, and sea water. At the cathode, the Mg2+ ion is reduced by two electrons to magnesium metal:
Mg2+ + 2 e− → Mg
Uses of Magnesium: Magnesium is the third most commonly used structural metal, following iron and aluminium. It has been called the lightest useful metal by The Periodic Table of Videos. The main applications of magnesium are, in order: component of aluminium alloys, in die-casting (alloyed with zinc), to remove sulfur in the production of iron and steel, the production of titanium in the Kroll process. The second application field of magnesium is electronic devices. Because of low weight, good mechanical and electrical properties, magnesium is widely used for manufacturing of mobile phones, laptop and tablet computers, cameras, and other electronic components.
When you are using this chemical, please be cautious about it as the following:
1. In case of fire, use ... (indicate in the space the precise type of fire-fighting equipment. If water increases the risk add - Never use water);
2. Keep container tightly closed and dry;
3. Wear suitable protective clothing;
4. Take precautionary measures against static discharges;
5. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice;
You can still convert the following datas into molecular structure:
(1)InChI=1S/Mg;
(2)InChIKey=FYYHWMGAXLPEAU-UHFFFAOYSA-N;
(3)Smiles[Mg];
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