yttrium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) byproducts: H2O; Schlenk techniques; heating Y compd. under vacuum (1E-3 Torr); | 99% |
Conditions | Yield |
---|---|
With pyrographite In gas byproducts: CO; by chlorination-chem. vapor transport react.; mixt. of Er2O3 and Y2O3 with carbon and KCl (1:1:6:1 at. ratio) placed in alumina reactor and chlorinated with dry Cl2 (20 cm**3/min) at 800 K for 2 h; gas replace by Ar:Cl2 at 800-1300 K; detn. of separation factor; | A 31.74% B 21.33% |
Conditions | Yield |
---|---|
In hydrogenchloride Y2O3 dissolved in 10 ml HCl (6m); addn. of solid NH4Cl (n(NH4Cl):n(Y2O3) approx. 15), addn. of 10 ml concd. HCl, heating to near dryness, cooling, ground; transferred to a quartz tube with a side arm, evacuation to ca. 10 Pa, heated to 373 K for 15-18 h, then temp. rise to 673 K (sublimation of NH4Cl), then temp. rise to 1223 K (sublimation of YCl3); elem. anal.; |
Conditions | Yield |
---|---|
Y2O3 is reacted with NH4Cl; purified by two distn. in tantalum crucibles under high vac.; | |
In hydrogenchloride react. of oxide and excess NH4Cl in concd. HCl at 100°C; sublimation at 360°C/0.1 mmHg; | |
In not given extd. with THF; |
Conditions | Yield |
---|---|
In neat (no solvent) heating (70°C, vac.; 100-250°C, HCl atm.); |
yttrium(III) chloride
Conditions | Yield |
---|---|
With NH4Cl In neat (no solvent) heating of YCl3*99H2O in the presence of NH4Cl (Handbuch der preparativen anorganischen Chemie, Herausg. G. Brauer, Studgardt, 1975); |
yttrium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) thermolysis (vac., 400°C); sublimation (870°C, 1E-5 torr); | |
In neat (no solvent) Y compd. transferred to platinum crucible under dry conditions, evacuation temp. raised slowly to 350-400°C, complete decompn. after fewhs.; |
chlorine
aluminium
A
aluminum oxide
B
yttrium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) heating (200°C, vac.; 300°C, 2 d); separated by chemical transport; |
Conditions | Yield |
---|---|
In melt exchange reaction (KCl/NaCl melt, 1073 K); | |
In melt exchange reaction (KCl-NaCl melt, 1073 K); |
Conditions | Yield |
---|---|
at 300°C, 1-2 d, sealed tube; |
Conditions | Yield |
---|---|
In neat (no solvent) passing stream of COCl2 over Y2O3 at 600 °C;; |
Conditions | Yield |
---|---|
In neat (no solvent) vac., 573 K; vapour trasportion; |
Conditions | Yield |
---|---|
In neat (no solvent) in streaming Cl2-gas at 200-300°C;; |
Conditions | Yield |
---|---|
at 500°C, 6 h; | |
In neat (no solvent) chlorination of Y2O3 with carbon tetrachloride at 955 K for 10 h; elem. anal.; |
Conditions | Yield |
---|---|
With Cl2 In neat (no solvent) 250-300°C, 1 d; Cl2 atm., 600°C; |
Conditions | Yield |
---|---|
In water dissolving Y2O3 in HCl soln.; evapn.; | |
In neat (no solvent) oxide was treated with concd. HCl; evapd.; residue dissolved in H2O; evapd.; | |
In hydrogenchloride metal oxide dissolved in slight excess of HCl; solvent evapd.; |
B
yttrium(III) chloride
C
tin(IV) chloride
Conditions | Yield |
---|---|
In neat (no solvent) thermic decomposition;; |
Conditions | Yield |
---|---|
With pyrographite In solid byproducts: CO; at 800°C for 2 h; | |
With aluminium trichloride; pyrographite In neat (no solvent) chlorinating of rare earth/carbon (molar ration 3/1) mixt. (Cl2 flow rate 20 ml/min, 800 K, 2 h), heating in CO/HCl flow (800-1200 K), chemical vapor transport (AlCl3, 1300 K, 6 h, CO carrier gas, 40 ml/min); atomic emission spectrometric monitoring; | |
With sucrose carbon In neat (no solvent) byproducts: CO, CO2, O2; mixt. of Y2O3 and sucrose carbon kept under flowing Ar for 1 h and heated at 100°C; Cl2 introduced; mixt. heated in Ar/Cl2 atm. up to 950°C at 3.8°C/min; X-ray diffraction; | |
With sucrose carbon In further solvent(s) Kinetics; byproducts: CO, CO2; the chlorination kinetics of Y2O3/sucrose carbon studied by thermogravimetry at 550-950°C; Cl2 used in a mixt. with Ar; |
Conditions | Yield |
---|---|
With chlorine byproducts: CO; at 1100°C; YCl3 removed from the reaction zone with a stream of He; | |
With Cl2 byproducts: CO; at 1100°C; YCl3 removed from the reaction zone with a stream of He; |
yttrium(III) chloride
Conditions | Yield |
---|---|
With ammonium chloride In neat (no solvent) heating of mixt. of YCl3-hydrate and NH4Cl in Cl2/HCl stream; |
yttrium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) 300°C, 2 d;; | |
In neat (no solvent) 300°C, 2 d;; |
Conditions | Yield |
---|---|
With HCl In hydrogenchloride byproducts: O2, H2O; dissolution in excess concd. HCl; |
Conditions | Yield |
---|---|
With HCl In hydrogenchloride byproducts: O2, H2O; dissolution in excess concd. HCl; |
Conditions | Yield |
---|---|
With HCl In hydrogenchloride byproducts: O2, H2O; dissolution in excess concd. HCl; |
Conditions | Yield |
---|---|
With HCl In hydrogenchloride byproducts: O2, H2O; dissolution in excess concd. HCl; |
A
Carbonyl fluoride
B
yttrium(III) chloride
Conditions | Yield |
---|---|
byproducts: SO2; above 400°C; | |
byproducts: SO2; above 400°C; |
yttrium(III) chloride
Conditions | Yield |
---|---|
thermal decompn. at 500-1000°C; | |
thermal decompn. at 500-1000°C; | |
thermal decompn. at 500-1000°C; |
Conditions | Yield |
---|---|
In neat (no solvent) 335°C; thermogravimetric anal.; |
Conditions | Yield |
---|---|
With HCl In hydrogenchloride byproducts: O2, H2O; dissolution in excess concd. HCl; |
Y((SiMe3)2)2Cl(tetrahydrofuran)2
B
yttrium(III) chloride
Conditions | Yield |
---|---|
byproducts: THF; decompn. in absence of THF; |
methyl methylphenylphosphinate
yttrium(III) chloride
Conditions | Yield |
---|---|
In further solvent(s) byproducts: MeCl; slow heating in neat Ph(Me)P(O)OMe until complete pptn.; particle size and polymerization degree depending on heating rate; | 100% |
In not given byproducts: chloromerhane; heating with the excess of methylphenylphosphinic acid methyl ester; filtering, washing with ethanol; |
Conditions | Yield |
---|---|
In water stoich., YCl3 and 1,4-benzenedicarboxylate disodium salt mixed in H2O atroom temp.; filtered, dried (air), elem. anal.; | 100% |
In water stoich. amt. of YCl3 and Na salt of terephthalic acid mixed in H2O; filtered; ppt. dried in air; detd. by X-ray powder diffraction and inductively coupled plasma-atomic emission spectra; |
erbium(III) chloride
water
yttrium(III) chloride
disodium terephthalate
Conditions | Yield |
---|---|
In water stoich., ErCl3, YCl3 and 1,4-benzenedicarboxylate disodium salt mixed inH2O at room temp.; filtered, dried (air), elem. anal.; | 100% |
erbium(III) chloride
water
yttrium(III) chloride
disodium terephthalate
Conditions | Yield |
---|---|
In water stoich., ErCl3, YCl3 and 1,4-benzenedicarboxylate disodium salt mixed inH2O at room temp.; filtered, dried (air), elem. anal.; | 100% |
erbium(III) chloride
water
yttrium(III) chloride
disodium terephthalate
Conditions | Yield |
---|---|
In water stoich., ErCl3, YCl3 and 1,4-benzenedicarboxylate disodium salt mixed inH2O at room temp.; filtered, dried (air), elem. anal.; | 100% |
erbium(III) chloride
water
yttrium(III) chloride
disodium terephthalate
Conditions | Yield |
---|---|
In water stoich., ErCl3, YCl3 and 1,4-benzenedicarboxylate disodium salt mixed inH2O at room temp.; filtered, dried (air), elem. anal.; | 100% |
yttrium(III) chloride
Conditions | Yield |
---|---|
In isopropyl alcohol byproducts: isopropyl acetate; molar ratio chloride:isopropoxide=2:1, refluxing; solvent removal (reduced pressure), drying (28°C, 0.1 torr); elem. anal.; | 99.9% |
Conditions | Yield |
---|---|
In water byproducts: CO2, NH4Cl, H2O; to stirred soln. of YCl3 (5 mmol) was added NH4HCO3 (15 mmol) at 25° C; the soln. was maintained at 25°C for 1 wk; the resulting ppt. was filtered, washed with H2O and air-dried; chem. anal.; | 99.24% |
yttrium(III) chloride
Conditions | Yield |
---|---|
In isopropyl alcohol byproducts: isopropyl acetate; molar ratio chloride:isopropoxide=1:2, refluxing; solvent removal (reduced pressure), drying (28°C, 0.1 torr); elem. anal.; | 99.2% |
yttrium(III) chloride
Conditions | Yield |
---|---|
With lithium In neat (no solvent) reduction of YCl3 (distd. in vac. at 900-950°C), 16.56kg YCl3, 2.040 kg Li (15.5% excess);; | 99% |
With calcium In neat (no solvent) YCl3 free from H2O and oxide-halogenides, 10% excess Ca, under Ar, start of react. at 1350-1400.degreee.C;; heating to 1550°C for 5min after end of react., purity 99.-+.0.5%;; | 90% |
With sodium In neat (no solvent) distn. of Na into a vessel containing YCl3 at 800-850°C and 0.07 atm Ar-pressure, 5-7h at 800-850°C, pouring off NaCl-slag;; distn. at 850°C; contaminations in wt.-%: 0.012-0.090 O, 0.002-0.03 N, 0.01-0.03 C;; | 85% |
yttrium(III) chloride
niobium pentachloride
Conditions | Yield |
---|---|
In neat (no solvent) Ar, stoichiometric mixture sealed in a quartz tube, heated at 1023 K for4 d, the heating and cooling ramps were 20 and 10 K*h**-1, respectively; | 99% |
Conditions | Yield |
---|---|
In not given hot soln.; | 99% |
In not given hot soln.; | 99% |
yttrium(III) chloride
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide byproducts: KCl; YCl3 and Pd-complex were stirred in DMF at room temp. over 5 ds; filtered, DMF was pumped, 24 h at room temp., dried under vac. for 12-14h; elem. anal.; | 99% |
Conditions | Yield |
---|---|
With NaH In tetrahydrofuran byproducts: NaCl; inert atmosphere; treatment of 6 equiv. of ligand with slight excess ofNaH, filtration, addn. to suspn. of YCl3, refluxing for 24 h; solvent removal (vac.), dissoln. in MePh, filtration (Celite), concn., crystn. (-30°C); elem. anal.; | 99% |
sodium 2-(N,N-dimethylaminomethyl)phenolate
yttrium(III) chloride
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: NaCl; N2-atmosphere; dropwise addn. of 3 equiv. ligand to metal chloride (roomtemp.), stirring overnight; solvent removal (vac.), extn. into CH2Cl2, solvent removal (vac.), washing (pentane); elem. anal.; | 99% |
IUPAC Name: Trichloroyttrium
The MF of Yttrium(III) chloride (CAS NO.10361-92-9) is Cl3Y.
The MW of Yttrium(III) chloride (CAS NO.10361-92-9) is 195.26.
Synonyms of Yttrium(III) chloride (CAS NO.10361-92-9): Yttrium chloride ; Yttrium chloride (YCl3) ; Yttrium chloride solution ; Yttrium trichloride
Product Categories: Inorganics;Catalysis and Inorganic Chemistry;Chemical Synthesis;Crystal Grade Inorganics;Metal and Ceramic Science;Salts;Yttrium Salts
Density: 2.67 g/mL at 25 °C
Melting Point: 721 °C
Storage temp: 2-8 °C
Sensitive: Hygroscopic
EINECS: 1036-192-9
Merck: 14,10107
Form: powder
Yttrium(III) chloride (CAS NO.10361-92-9) is used as analytical reagent.It is also used as a catalyst and in superconductors and has been linked to pulmonary edema and liver damage.
Yttrium(III) chloride can be formed by reacting yttrium(III) oxide with hydrochloric acid, among other methods.
1. | ipr-rat LD50:45 mg/kg | AMIHAB AMA Archives of Industrial Health. 16 (1957),475. | ||
2. | ipr-mus LD50:88 mg/kg | AMIHAB AMA Archives of Industrial Health. 16 (1957),475. | ||
3. | ipr-gpg LD50:85 mg/kg | AEHLAU Archives of Environmental Health. 5 (1962),437. |
Reported in EPA TSCA Inventory.
Poison by intraperitoneal route. When heated to decomposition it emits toxic fumes of Cl−. See also YTTRIUM and RARE EARTHS.Safety information of Yttrium(III) chloride (CAS NO.10361-92-9):
Hazard Codes Xi
Risk Statements
36/37/38 Irritating to eyes, respiratory system and skin
Safety Statements
26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
37/39 Wear suitable gloves and eye/face protection
WGK Germany 3
RTECS ZG3150000
ACGIH TLV: TWA 1 mg(Y)/m3
Yttrium(III) chloride is an ionic compound of yttrium and chlorine. It is a salt that is solid at room temperature, highly soluble in water, and deliquescent. YCl3 in the solid state has a crystal structure with cubic close packed chloride ions and yttrium ions filling one third of the octahedral holes and the resulting YCl6 octahedra sharing three edges with adjacent octahedra give a layer structure. This structure is shared by a range of compounds notably AlCl3
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