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inquiryItems Standard Result Assay 98%min ----------------------------------------------------------------------------------------------
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inquiryCalcium hydride Product Name: Calcium hydride Molecular Weight: 42.09 CAS NO: 7789-78-8 EC NO: -- Molecular Formula: H2Ca Sp
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inquiryProduct Description Product name Calcium hydride CAS 7789-78-8;125544-53-8 Assay 99% Appearance white p
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inquiryProduct Name Calcium Hydride CAS No. 7789-78-8 EINECS 232-189-2 Molecular Weight 42.1
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inquiryFormula: CaH2Molecular Weight : 42.10 Synonyms: Calcium hydride (CaH2);Calciumdihydride; EINECS: 232-189-2Density: 1.9Melting Point:Boiling Point: 1484oC Application:Inorganics;Adsorbents, Filter Aids and Drying Agents;Metal HydridesAlternat
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inquiryCALCIUM HYDRIDE Basic information Alkaline earth metal Toxicity Chemical Properties Application Production method Category Explosive hazardous characteristics Storage Characteristics Extinguishing agent
We do following terms : 1) Best quality 2) Many years experience in this field 3) Loyal customers in countries 4) Professional big supplier 5) Safe shipping 6) Various payment terms Calcium Hydride 98% CAS 7789-78-8
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inquiryConditions | Yield |
---|---|
In melt High Pressure; Ca melted in vac. at 350°C for 5 h, filled with H2 (5 atm) at 400°C for 5 min, at 10 atm. at 480°; elem. anal.; | 99.6% |
In neat (no solvent) hydrogenation in a closed iron tube under pressure at temperatures between 650°C and 690°C;; | 90% |
In neat (no solvent) hydrogenation in a closed iron tube under pressure at temperatures between 650°C and 690°C;; | 90% |
Conditions | Yield |
---|---|
In neat (no solvent) heating the mixture in H2-atmosphere to 420-600°C;; product-mixture;; | |
In neat (no solvent) heating the mixture in H2-atmosphere to 420-600°C;; product-mixture;; |
Conditions | Yield |
---|---|
With ammonia at red heat; | |
With NH3 at red heat; |
Conditions | Yield |
---|---|
In neat (no solvent) on evacn. of system(metal, loaded (Ar) into reactor-autoclave of the hydrogenation apparatus)at 300-350°C (0.5-1h),cooling to room temp. and feeding hydrogen into reactor (from LaNi5 "accumulator") to give pressure of 2.8MPa, 150°C, 1h;; on gas-volumetric and chemical anal.; XRD (orthorhombic, lattice parameters); react. without an induction period and forming a clinker;; | |
In neat (no solvent) on evacn. of system(metal, loaded (Ar) into reactor-autoclave of the hydrogenation apparatus)at 300-350°C (0.5-1h),cooling to room temp. and feeding hydrogen into reactor (from LaNi5 "accumulator") to give pressure of 3.5MPa, 200°C, 1h;; on gas-volumetric and chemical anal.; XRD (orthorhombic, lattice parameters); react. is running without an induction period and forming of a clinker;; |
Conditions | Yield |
---|---|
at dark red heat; |
Conditions | Yield |
---|---|
byproducts: H2, N2; vigorous reaction at 400°C; | |
byproducts: H2, N2; vigorous reaction at 400°C; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: calcium oxide; bombarding solid CaCl2 deposited on substrate with atomar H for 60 mins in plasmochemical app. described by I. Sh. Normatov, N. Shermatov, and U. Mirsaidov, Fiz. Khim. Obrab. Mater., No. 3, 141-142 (1990);; formation of metallic layer, containing oxide phase of calcium; X-ray diffraction;; | A 0% B n/a |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: HCl; bombarding periodically stirred CaCl2 (on substrate) with H for 120 mins in plasmochemical app. described by I. Sh. Normatov, N. Shermatov, and U. Mirsaidov, Fiz. Khim. Obrab. Mater., No. 3, 141-142 (1990); grinding; bombarding with H for 120 mins;; X-ray diffraction, DTA, IR spectroscopy;; |
Conditions | Yield |
---|---|
In neat (no solvent) reaction of CaCl2 with H2 formed by dissociation of CH4;; |
Conditions | Yield |
---|---|
reversible react.; | |
at dark red heat and at temperatures above it; |
Conditions | Yield |
---|---|
With hydrogen at red heat; | |
With hydrogen | A n/a B 0% |
With H2 | A n/a B 0% |
With H2 at red heat; |
ethene
calcium
A
calcium hydride
B
calcium carbide
C
pyrographite
Conditions | Yield |
---|---|
In neat (no solvent) dark red heat; crust of CaC2, C and CaH2 inhibit reaction;; | |
In neat (no solvent) dark red heat; crust of CaC2, C and CaH2 inhibit reaction;; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: H2; 375-390°C; no isolation, monitoring by thermal anal.; |
Conditions | Yield |
---|---|
platinum In neat (no solvent) at 600 - 700°C; acceleration by H2O vapor;; | |
nickel In neat (no solvent) at 600 - 700°C; acceleration by H2O vapor;; | |
iron In neat (no solvent) at 600 - 700°C; acceleration by H2O vapor;; |
Conditions | Yield |
---|---|
With magnesium In neat (no solvent) calcination of a mixture of CaO and powdered Mg in an atmosphere of H2;; | |
With aluminium In neat (no solvent) byproducts: Al2O3; | |
With magnesium In neat (no solvent) byproducts: MgO; heating mixture at 400°C in vacuum and react. takes place at 550 - 650°C;; |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) react. was carried out at hydrogen pressure around 50 bar at temp. between 170 and 200°C; |
nitrogen
calcium carbide
A
calcium hydride
C
calcium cyanamide
D
pyrographite
Conditions | Yield |
---|---|
In neat (no solvent) |
Conditions | Yield |
---|---|
With hydrogen In neat (no solvent) formation at approx. 500-1000°C;; |
Conditions | Yield |
---|---|
In neat (no solvent) smelting together metallic Ca and CaCl2 in vac., in H2- or CH4-stream or in Ar-atmosphere forms no CaCl; CaO and CaH2 are formed by reaction of Ca with H2O;; | A 0% B n/a C n/a |
In neat (no solvent) smelting together metallic Ca and CaCl2 in vac., in H2- or CH4-stream or in Ar-atmosphere forms no CaCl; CaO and CaH2 are formed by reaction of Ca with H2O;; | A 0% B n/a C n/a |
calcium
acetylene
A
calcium hydride
B
calcium carbide
C
pyrographite
Conditions | Yield |
---|---|
In neat (no solvent) dark red heat; crust of CaC2, C and CaH2 inhibit reaction;; | |
In neat (no solvent) dark red heat; crust of CaC2, C and CaH2 inhibit reaction;; |
methane
calcium
A
calcium hydride
B
calcium carbide
C
pyrographite
Conditions | Yield |
---|---|
In neat (no solvent) dark red heat; crust of CaC2, C and CaH2 inhibit reaction;; | |
In neat (no solvent) dark red heat; crust of CaC2, C and CaH2 inhibit reaction;; |
Conditions | Yield |
---|---|
In neat (no solvent) Ca form in a NH3-stream at red a mixture of Ca3N2 and CaH2;; | |
In neat (no solvent) Ca form in a NH3-stream at red a mixture of Ca3N2 and CaH2;; |
Conditions | Yield |
---|---|
In neat (no solvent) heated up to 773 K; XRD; |
Conditions | Yield |
---|---|
With pyrographite In neat (no solvent) at 800 - 900°C; acceleration C; presence of Zn;; | |
With pyrographite In neat (no solvent) at 1200°C; acceleration by C; in presence of NH3;; | |
With pyrographite In neat (no solvent) at 900°C; acceleration by C; presence of NaCl;; |
Conditions | Yield |
---|---|
In neat (no solvent) Kinetics; decomposition of Ca(NH3)6 to active Ca; different pressures and temps.;; | |
In neat (no solvent) Kinetics; decomposition of Ca(NH3)6 to active Ca; different pressures and temps.;; |
Conditions | Yield |
---|---|
In not given react. with Ca-salts of phenols at ambient temp. and 200 at;; |
Conditions | Yield |
---|---|
In neat (no solvent) ball milled at room temp. for 20 h under 1 MPa of H2; XRD, IR; |
Conditions | Yield |
---|---|
In neat (no solvent) Electric Arc; | |
In neat (no solvent) Electric Arc; |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) High Pressure; react. was carried out at hydrogen pressure around 50 bar at temp. between 170 and 200°C; |
calcium hydride
Conditions | Yield |
---|---|
In ethanol draining of CaCl2*6H2O at 10°C with alcohol under formation of aq. alcohol-solution with CaH2;; |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) ball milled at room temp., 120 min; extd. (ethylenediamine) under Ar; filtered; ethylenediamine evapd. at room temp. under 0.05 MPa; XRD; | A 100% B n/a |
lithium aluminium tetrahydride
calcium hydride
Conditions | Yield |
---|---|
With (C2H5)2O In diethyl ether a mixt. of AlH3, CaH2 and LiAlH4 in Et2O is stirred at 34°C for 5.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are washed with ether and dried in vac. at room temp.; | 100% |
In tetrahydrofuran a mixt. of AlH3, CaH2 and LiAlH4 in THF is stirred at 30°C for 5.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are washed with ether and dried in vac. at room temp.; | 0% |
Conditions | Yield |
---|---|
With LiAlH4 In diethyl ether; toluene a mixt. of AlH3, CaH2 and LiAlH4 in ether/toluene (1:1) is stirred at 52°C for 3.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are dried in vac. at room temp.; | 100% |
With LiBH4 In diethyl ether; toluene a mixt. of AlH3, CaH2 and LiBH4 in ether/toluene (1:1) is stirred at 50°C for 2.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are dried in vac. at room temp.; | 100% |
With LiBH4 In diethyl ether; toluene a mixt. of AlH3, CaH2 and LiBH4 in ether/toluene (1:1) is stirred at 52°C for 5.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are dried in vac. at room temp.; | 100% |
lithium aluminium tetrahydride
calcium hydride
Conditions | Yield |
---|---|
With (C2H5)2O In diethyl ether a mixt. of AlH3, CaH2 and LiAlH4 in Et2O is stirred at 34°C for 3.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are washed with ether and dried in vac. at room temp., elem. anal.; | 100% |
With (C2H5)2O In diethyl ether a mixt. of AlH3, CaH2 and LiAlH4 in Et2O is stirred at 34°C for 5.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are washed with ether and dried in vac. at room temp., elem. anal.; | 100% |
With (C2H5)2O In diethyl ether a mixt. of AlH3, CaH2 and LiAlH4 in Et2O is stirred at 25°C for 7.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are washed with ether and dried in vac. at room temp., elem. anal.; | 95% |
With (C2H5)2O In diethyl ether a mixt. of AlH3, CaH2 and LiAlH4 in Et2O is stirred at 33°C for 5.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are washed with ether and dried in vac. at room temp., elem. anal.; | 70% |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) placing of CaH2 and Ge in welded Ta containers, heating within evacuated, well-flamed, sealed silica jacket at 1150°C for 6 h, cooling to650°C with rate of 10-12°C/h; | 100% |
calcium hydride
(2-((2,6-diisopropylphenyl)amino)-4-((2,6-diisopropylphenyl)imino)pent-2-ene)ZnCl
({2,6-iPr2H3C6N(CH3)C}2CH)ZnH
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: CaCl2; 0.5 CaH2; | 99% |
Conditions | Yield |
---|---|
With aluminium at 75℃; for 15h; Catalytic behavior; Kinetics; Concentration; Temperature; Milling; | 97.8% |
tetrahydrofuran
ammonia borane complex
calcium hydride
B
hydrogen
Conditions | Yield |
---|---|
In tetrahydrofuran soln. NH3BH3 in THF was added to suspn. CaH2 in THF, mixt. was stirred overnight, solvent was removed in vac. at room temp. overnight; | A 96% B n/a |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) placing of CaH2 and Si in welded Ta containers, heating within evacuated, well-flamed, sealed silica jacket at 1150°C for 6 h, cooling to650°C with rate of 10-12°C/h; | 95% |
Conditions | Yield |
---|---|
In tetrahydrofuran (inert atm.); stirring suspn. of zinc compd. and CaH2 in THF at 0°C for 3 d; filtration, keeping at -30°C for 24 h, isolation of crystals, elem. anal.; | 91% |
Conditions | Yield |
---|---|
With hydrogen In neat (no solvent) in flow reactor at 180°C; the diluent used was H2; | 90% |
In neat (no solvent) Kinetics; byproducts: CaF2; mech. activated in rotating flow-through reactor; rotation frequency 100-150 rpm, CaF2 heated at temp. of 180-190°C, SiF4+H2 (1/1 v/v) flow through; gaseous products frozen out with liq. N2; detd. by gas-chromy.; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: CaF2; at 200°C; | 90% |
calcium hydride
tellurium hexafluoride
18O-labeled water
A
pentafluorotellurate(VI)
B
pyridinium hydrogen sulfate
Conditions | Yield |
---|---|
With H2SO4 In pyridine byproducts: H2, CaF2; Sonication; O2 and H2O excluded: H2(18)O added to CaH2 in pyridine, H2 evolution, reactn. mixt. stirred and sonicated (3d, room temp.), degassed, frozen (-196 ° C), TeF6 added (vac. transfer), heated and stirred (45 ° C, 12h), caution: TeF6-pressure!; pyridine and TeF6 removed (vac.), {pyH(1+)}{(18)OTeF5} extracted into warm CH2Cl2, CH2Cl2 removed (vac., white residue), (19)F NMR, concd. H2SO4 added, vac. distn., (19)F NMR; | A 88% B n/a |
Conditions | Yield |
---|---|
elem. anal.; | 85% |
calcium hydride
Conditions | Yield |
---|---|
With (C2H5)2O In diethyl ether a mixt. of AlH3, CaH2 and LiBH4 in Et2O is stirred at 20°C for 5.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are dried in vac. at room temp.; | 83% |
With (C2H5)2O In diethyl ether a mixt. of AlH3, CaH2 and LiBH4 in Et2O is stirred at 22°C for 7.0 h; flakes are sepd. from soln. and unreacted CaH2 is decanted, flakes are dried in vac. at room temp.; | 75% |
Conditions | Yield |
---|---|
With hydrogen In neat (no solvent) formation at passing a mixture of H2 and N2 over CaH2 at 730-750°C after 20 hours;; | 82% |
With H2 In neat (no solvent) formation at passing a mixture of H2 and N2 over CaH2 at 730-750°C after 20 hours;; | 82% |
In neat (no solvent) formation in N2-stream at 700-800.degree;; | |
In neat (no solvent) formation in N2-stream at 700-800.degree;; |
calcium hydride
N-tert-butyldiethanolamine
iron(III) chloride
sodium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran XRD; | 70% |
Conditions | Yield |
---|---|
In further solvent(s) acetylene carbon black reacted with CaCH2 in Ca/Li flux; sealed ampules heated to 1323 K in 2 h and kept at this temp. for 2 h; cooled to 1073 K in 24 h, cooled to 773 K in 108 h, centrifuged; elem. anal.; | A 70% B n/a |
methanol
calcium hydride
[Cu2(OAc)4(H2O)2]
1,1'-(pyridine-2,6-diyl)bis(4,4-dimethylpentane-1,3-dione)
Conditions | Yield |
---|---|
In methanol under N2; tetraketone added to suspn. of CaH2 in MeOH; mixt. stirred at 20°C for 1 h; Cu(II) acetate monohydrate added; mixt. stirred at 20°C for 16 h; suspn. filtered; solvent removed; dried under vac.; crystn. by vapor diffusion of Et2O in MeOH soln.; | 65% |
Conditions | Yield |
---|---|
With catalyst: TiCl3/Pd In neat (no solvent, solid phase) High Pressure; mixt. of CaB6, CaH2 and catalyst TiCl3/Pd ball milled for 30 min, pelletized under Ar in glove box and then placed in autoclave; H2 pressure 350bar; autoclave heated up to 400-440°C, pressure adjusted to 700 bar and kept for 48 h; XRD; | 60% |
ruthenium(III)chloride In neat (no solvent, solid phase) High Pressure; mixt. of CaB6, CaH2 and catalyst RuCl3 ball milled for 30 min, pelletized under Ar in glove box and then placed in autoclave; H2 pressure 350 bar; autoclave heated up to 400-440°C, pressure adjusted to 700 barand kept for 48 h; XRD; | |
titanium(III) chloride In neat (no solvent, solid phase) High Pressure; mixt. of CaB6, CaH2 and catalyst TiCl3 ball milled for 30 min, pelletized under Ar in glove box and then placed in autoclave; H2 pressure 350 bar; autoclave heated up to 400-440°C, pressure adjusted to 700 barand kept for 48 h; XRD; | |
In neat (no solvent, solid phase) High Pressure; mixt. of CaB6 and CaH2 ball milled for 30 min, pelletized under Ar in glove box and then placed in autoclave; H2 pressure 350 bar; autoclave heated up to 400-440°C, pressure adjusted to 700 bar and kept for 48h; no react. without catalyst; XRD; | 0% |
calcium hydride
{trans-Pt{C=C(CMe3)P(O)(CCCMe3)C=C(CMe3)(H)}(PET3)2(H2O)}{BF4}
{trans-Pt{C=C(CMe3)P(OBF3)(CCCMe3)C=C(CMe3)(H)}{PEt3}2(H)}
{trans-Pt{C=C(CMe3)P(O)(CCCMe3)C=C(CMe3)(H)}{PEt3}2(H)}
Conditions | Yield |
---|---|
With H2 In dichloromethane large molar excess of powd. CaH2 added to a soln. of Pt complex (N2), stirred (N2, room temp., 2 h), filtered (filtrate collected in flame-dried glass-ware), stream of H2 gas passed through soln. (2.5 h, -78°C); solvent removed (vac.), residue extd. with hexane and Et2O both twice, Et2O exts. evapd. (vac.), solid crystd. from CH2Cl2/hexane (-20°C); elem. anal. (*1H2O); BF3-free compd. isolated by concn. of the hexane exts. and cooling (-20°C); | A 55% B 18% |
Conditions | Yield |
---|---|
In neat (no solvent) (Ar), mixed with Li/Ca/Ge/CaH2 molar ratio 10:10:2:3 in steal crucible,sealed in silica tube, heated to1323 K in 2 h, kept for 2 h, cooled to 1073 K in 24 h, cooled to 773 K in 108 h; centrifuged, oped (under Ar), XRD; | A 50% B n/a |
calcium hydride
{trans-Pt{C=C(CMe3)P(O)(CCCMe3)C=C(CMe3)(H)}{P(n-Prop)3}2(H2O)}{BF4}
{trans-Pt{C=C(CMe3)P(OBF3)(CCCMe3)C=C(CMe3)(H)}{P(n-Pr3)}2(H)}
Conditions | Yield |
---|---|
With H2 In dichloromethane large molar excess of powd. CaH2 added to a soln. of Pt complex (N2), stirred (N2, room temp., 2 h), filtered (filtrate collected in flame-dried glass-ware), stream of H2 gas passed through soln. (2.5 h, -78°C); solvent removed (vac.), residue extd. with hexane and Et2O both twice, Et2O ext. evapd. (vac.), solid crystd. from CH2Cl2/hexane (-20°C); elem. anal. (*H2O); | 42% |
Conditions | Yield |
---|---|
With lithium at 1050℃; for 5h; Inert atmosphere; Glovebox; Sealed tube; | 42% |
Conditions | Yield |
---|---|
In neat (no solvent) fast reaction at 800°C;; | |
In neat (no solvent) fast reaction at 800°C;; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: CaO; react. in an autoclave under H2-pressure, 300-600°C, exothermic react. (formation of CaH2 from CaCl2 and H2 during the react. possible), addn. of SiO2 for absorption of CaO;; | |
In neat (no solvent) byproducts: CaO; react. in an autoclave under H2-pressure, 300-600°C, exothermic react. (formation of CaH2 from CaCl2 and H2 during the react. possible), addn. of SiO2 for absorption of CaO;; |
Conditions | Yield |
---|---|
With hydrogen byproducts: CaO; Ca hydride decompd. to nascent H and Ca, redn. with nascent H, Ca reacts with O2 originating from moisture and CaO formes; opt. circumstance of redn. 470°C; sepn. Cr from CaO with dild. aq. HNO3; |
Conditions | Yield |
---|---|
With mineral oil In tetrahydrofuran; water CaH2 dispersed in mixt. of surfactant, mineral oil, C7H8 and methanol; mixt. of THF and water added at 5°C for 5 h; detd. by TEM and SAXS; |
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