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Cas:10025-93-1
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inquiryUranium(III) chloride. CAS:10025-93-1 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic in
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Cas:10025-93-1
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:10025-93-1
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou
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Cas:10025-93-1
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inquiry1. Product advantages? High purity, all above 98.5%, no impurities after dissolution? We will test each batch to ensure quality? OEM and private brand services designed for free? Various cap colors available? We can also provide MT1 peptide powder2.
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquirygood quality, competitive price, thoughtful after sale serviceAppearance:White to Off-White Solid Storage:Keep it in dry,shady and cool place Package:as your requirement Application:Pharma;Industry;Agricultural;chemical reaserch Transportation:by Sea
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
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inquiryShanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por
Uranium chloride (UCl3)(8CI,9CI) Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen
Uranium chloride (UCl3)(8CI,9CI)Appearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Pr
uranium(IV) chloride
uranium(III) chloride
Conditions | Yield |
---|---|
With zinc redn. of UCl4 by metallic Zn at 450 to 480°C in vacuum;; | 86% |
In neat (no solvent) on sublimation of UCl4, in part dissocn. and forming of UCl3 (not volatile ppte.);; | |
With H redn. by hydrogen; using of absolutely pure H;; |
A
uranium(III) chloride
Conditions | Yield |
---|---|
In tetrahydrofuran Ar atm; 1 equiv. of amalgam, 20°C, 4.5 h; | A n/a B n/a C 85% |
benzocyclooctene
uranium(IV) chloride
A
uranium(III) chloride
B
dibenzouranocene
Conditions | Yield |
---|---|
With potassium In tetrahydrofuran under Ar; to a soln. of benzocyclooctatetraene potassium was added; mixt. stirred for 48 h, added to a soln. of UCl4 and refluxed for 2 days; evapn., washing a residue with hexane, extn. (THF); | A n/a B 20% |
Conditions | Yield |
---|---|
In neat (no solvent) at 700°C for 7 days; |
Conditions | Yield |
---|---|
in evacuated quartz tube at 1130 K for 1 h;; | |
In neat (no solvent, solid phase) at 800°C for 7 d; | |
In neat (no solvent) fused in evacuated ampule at 860-870°C for 1 h; slowly cooled, elem. anal.; | |
In neat (no solvent) 400°C, several h; heating (615°C); |
Conditions | Yield |
---|---|
In not given equilibrium; | |
In not given equilibrium; |
potassium 6,6-dimethylcyclohexadienide
uranium(IV) chloride
A
uranium(III) chloride
Conditions | Yield |
---|---|
In tetrahydrofuran under Ar; evapn. of solvent, extn. (pentane), pentane evapd. off: (Me2C6H5)2; |
Conditions | Yield |
---|---|
In neat (no solvent) at 250-300°C;; | |
In neat (no solvent) at 250-300°C;; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: Ag; Ar atmosphere; heating (sealed tantalum crucible, 1172-1223 K); sublimation; |
uranium(III) chloride
Conditions | Yield |
---|---|
With zinc In hydrogenchloride on redn. of UO2Cl2 by Zn;; not isolated;; | |
With Zn In hydrogenchloride on redn. of UO2Cl2 by Zn;; not isolated;; |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) byproducts: LiCl; at 700°C for 7 d; |
uranium(III) chloride
Conditions | Yield |
---|---|
With H2; HCl In neat (no solvent) hydriding of metal (470 K), conversion to trichloride with gaseouc HCl (470 K); sublimation (ca. 1170 K); |
Conditions | Yield |
---|---|
In melt byproducts: Cd; formation in LiCl-NaCl-CaCl2-BaCl2 melt (455°C, 30 min); not isolated; | |
With LiCl; KCl In melt (Ar); in glove box; prepd. in LiCl-KCl melt at 773 K; ref.: D. S. Poa, Z. Tomczuk, R. K. Steunenberg. J. Electrochem. Soc.,135, 1161(1988); |
Conditions | Yield |
---|---|
With H2 In neat (no solvent) hydriding metal with H2 at 473 K, converting it to UCl3 with HCl at 473 K; subliming under high vacuum at 1173 K; |
hydrogenchloride
hydrogen
A
uranium(III) chloride
B
uranium(IV) chloride
Conditions | Yield |
---|---|
U reacted with hydrogen at 250°C to yield UH3, whichis dehydrogeated at 330°C in a stream of dry Ar, the obtained powder reacted with HCl gas at 250°C; |
Conditions | Yield |
---|---|
on heating U3O8 in mixture with S2Cl2 vapor and S in excess;; | 0% |
on heating U3O8 in mixture with S2Cl2 vapor and S in excess;; | 0% |
Conditions | Yield |
---|---|
In hydrogenchloride Electrolysis; electrolysis of a soln. of UO3 in HCl (d: 1.12, 15%) in a stream of CO2 with diaphragma and Hg cathode (110V, 1.5 up to 2 A); liquid at anode: HCl (d: 1.12); when react. soln. is getting green brown colored: 0.75 up to 1A, further electrolysis untill; react. soln. is getting red colored; redn.;; | |
In hydrogenchloride Electrolysis; electrolysis of a soln. of UO3 in HCl (d: 1.12, 15%) in a stream of CO2 with diaphragma and Hg cathode (110V, 1.5 up to 2 A); liquid at anode: HCl (d: 1.12); when react. soln. is getting green brown colored: 0.75 up to 1A, further electrolysis untill; react. soln. is getting red colored; redn.;; |
Conditions | Yield |
---|---|
In not given Ar atm.; |
Conditions | Yield |
---|---|
In not given react. at 523K, distn. of UCl4 at 813K; |
uranium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) non-static high vac. system:heating slowly from 20-300 ° C, 1E-5 - 1E-7 Pa; | |
With NH4Cl In neat (no solvent) moisture- and oxygen-free conditions, thermal high vac. decompn., in a sealed quartz tube, 1.5-fold excess of NH4Cl, pumped off to ca. 1E-6 Pa, 25-80°C for 7 h, temp. slowly raised to 400°C; elem. anal.; |
Conditions | Yield |
---|---|
With hydrogenchloride uranium hydride heating with HCl forms UCl3 and UCl4 at 623-673 K; treated the sample with purified H2 at 600 to 793 the UCl4 impurity was converted into UCl3; treated the sample with purified H2 at 600 to 793 K the UCl4 impurity was converted into UCl3; characterized by X-ray diffraction and elem. anal.; |
uranium(III) chloride
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: AlCl3, benzene; decompn. in THF soln.; | |
In tetrahydrofuran byproducts: AlCl3, benzene; decompn. in THF soln.; |
uranium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) in non-static vac. (1-10*0.000001 kPa), temp. increasing from 20 to 300°C; |
uranium(III) chloride
Conditions | Yield |
---|---|
byproducts: water; heating the UCl3*7H2O dimer in a non-static high vacuum system at 25, 60 and 100°C, final heat treatment at about 200°C; IR spectroscopy; |
Conditions | Yield |
---|---|
In gas byproducts: Ca(g); 1967 - 2181 K; mass spectrometry; |
uranium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: water; 600 - 700 K, vac.; |
uranium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: water; 600 - 700 K, vac.; |
uranium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: water; 600 - 700 K, vac.; |
uranium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: water; 600 - 700 K, vac.; |
uranium(III) chloride
trifluorormethanesulfonic acid
Conditions | Yield |
---|---|
In neat (no solvent) Ar atmosphere, 180°C (3 d); distillation of TfOH, drying (150°C, vacuum, 60 h); | 100% |
Conditions | Yield |
---|---|
In neat (no solvent) Ar atmosphere, 120°C (3 d); distillation of TfOH, drying (120°C, vacuum, 30 h); elem. anal.; | 96% |
uranium(III) chloride
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: NaCl; (N2); stirring for 6 h; removal of solvent (reduced pressure); warming to 50-60°C for 1.5 h (reduced pressure); extn. of solid (diethyl ether); filtration and concn. of ext.; cooling to -80°C; elem. anal.; | 50% |
Conditions | Yield |
---|---|
With potassium In tetrahydrofuran glovebox, under N2 or Ar: addn. of potassium (69.5mmol) to a dry and degassed THF soln. of indene and further addn. of a stoichiometric amt. of UCl3 when react. was complete, stirring of mixture at room temp. for 4d at room temp.;; on removal of solvent in vacuo and extraction of the brown residue with pentane for 8 days; elem. anal.;; | 35% |
uranium(III) chloride
(η5-MeC5H4)3U(tetrahydrofuran)
Conditions | Yield |
---|---|
In tetrahydrofuran crystn. (hexane/THF); | 33% |
Conditions | Yield |
---|---|
In benzene refluxing for 7 d, drying; extn. with benzene; | 10% |
uranium(III) chloride
sodium chloride
Conditions | Yield |
---|---|
In neat (no solvent) a well ground stoichiometric mixture of CsCl, NaCl and UCl3 sealed in a quartz tube under vacuum; the mixture next heated at 400°C for 3 days; | |
In melt fusion of stoichiometric amts. of UCl3, CsCl and NaCl at 1073 - 1173 K in sealed tube; | |
In melt melting a mixt. of CsCl, NaCl and UCl3 at 1050 K for 1 h (Ar) under periodic stirring in evacuated quartz capsules; |
Conditions | Yield |
---|---|
In neat (no solvent) heating (high vacuum, quartz tube, 1070-1170 K); |
Conditions | Yield |
---|---|
In melt Electrolysis; electrolysis of molten CaCl2, BaF2 or BaCl2 with UCl3 at 900-1050 °C, (0.4-5A, current density: 0.1-1 A/cm*cm), Ni cathode, U anode);; the alloy is dropping from the cathode to the bottom;; | |
In melt Electrolysis; electrolysis of molten CaCl2, BaF2 or BaCl2 with UCl3 at 900-1050 °C, (0.4-5A, current density: 0.1-1 A/cm*cm), Ni cathode, U anode);; the alloy is dropping from the cathode to the bottom;; |
Conditions | Yield |
---|---|
byproducts: HCl, H2; 450°C; anhydrous HF; |
uranium(III) chloride
Conditions | Yield |
---|---|
With water In water byproducts: H; dissolving of UCl3 in H2O, purple react. soln., immediately evolving of H, changing to green colored, then forming of ppte. of uranium(IV)hydroxide (probably);; | |
With H2O In water byproducts: H; dissolving of UCl3 in H2O, purple react. soln., immediately evolving of H, changing to green colored, then forming of ppte. of uranium(IV)hydroxide (probably);; |
uranium(III) chloride
Conditions | Yield |
---|---|
With ammonia In hydrogenchloride | |
With NH3 In hydrogenchloride |
uranium(III) chloride
Conditions | Yield |
---|---|
With H3PO4 or H2C2O4 In hydrogenchloride pptg. of U(IV)salts;; | |
With H3PO4 or H2C2O4 In hydrogenchloride pptg. of U(IV)salts;; |
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