Product Name

  • Name

    YTTRIUM NITRATE HEXAHYDRATE

  • EINECS 233-802-6
  • CAS No. 13494-98-9
  • Article Data128
  • CAS DataBase
  • Density 2.682 g/mL at 25 °C(lit.)
  • Solubility Soluble in water.
  • Melting Point 51.8°C
  • Formula YN3O9.6H2O
  • Boiling Point 83 °C at 760 mmHg
  • Molecular Weight 274.921
  • Flash Point
  • Transport Information UN 1477 5.1/PG 3
  • Appearance white adhering crystals or crystalline powder
  • Safety 17-26-36/37/39
  • Risk Codes 8-36/37/38
  • Molecular Structure Molecular Structure of 13494-98-9 (YTTRIUM NITRATE HEXAHYDRATE)
  • Hazard Symbols IrritantXi; OxidizingO
  • Synonyms Yttriumnitrate hexahydrate;Yttrium trinitrate hexahydrate;Yttrium(III) nitratehexahydrate;
  • PSA 262.02000
  • LogP 0.46650

Synthetic route

yttrium(III) oxide

yttrium(III) oxide

nitric acid
7697-37-2

nitric acid

barium carbonate

barium carbonate

copper(II) oxide

copper(II) oxide

A

barium(II) nitrate

barium(II) nitrate

B

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

C

copper(II) hydroxynitrate

copper(II) hydroxynitrate

Conditions
ConditionsYield
In water nitrates of Ba and Y and a basic nitrate of Cu obtained on treatment of CuO, BaCO3 and Y2O3 with HNO3; soln. evapd. to dryness; X-ray diffraction;
yttrium barium copper oxide

yttrium barium copper oxide

nitric acid
7697-37-2

nitric acid

A

barium(II) nitrate

barium(II) nitrate

B

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

C

copper(II) nitrate

copper(II) nitrate

Conditions
ConditionsYield
In nitric acid byproducts: H2O; dissoln.;
yttrium(III) oxide

yttrium(III) oxide

nitric acid
7697-37-2

nitric acid

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Conditions
ConditionsYield
Y2O3 dissolved in conc. HNO3;
In water Y2O3 dissolved in dil. HNO3 to pH 2;
In nitric acid Y2O3 dissolved in min. amt. dild. nitric acid (1:1), evapd. to dryness; cooled to room temp.;
yttrium(III) oxide

yttrium(III) oxide

dinitrogen tetraoxide
10544-72-6

dinitrogen tetraoxide

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Conditions
ConditionsYield
steel bomb, 150°C, 80 atm, 24 h;>99
In neat (no solvent) byproducts: N2O3; heating at 150°C, 80 atm;;
yttrium(III) nitrate hydrate

yttrium(III) nitrate hydrate

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Conditions
ConditionsYield
In neat (no solvent) heating (160-140°C), vac.;
yttrium(III) oxide

yttrium(III) oxide

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Conditions
ConditionsYield
With nitric acid In water Dissolving the oxide into reagent grade conc. nitric acid.; Heating the soln. to remove excess HNO3.;
With HNO3 In nitric acid aq. HNO3; dissoln. of oxide in boiling nitric acid;
yttrium(III) oxide

yttrium(III) oxide

Nitrogen dioxide
10102-44-0

Nitrogen dioxide

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Conditions
ConditionsYield
In neat (no solvent) heating at 150°C in a closed tube for 24 hours;;>99
2NH4(1+)*Y(3+)*5(NO3)(1-)=(NH4)2Y(NO3)5

2NH4(1+)*Y(3+)*5(NO3)(1-)=(NH4)2Y(NO3)5

A

ammonium nitrate

ammonium nitrate

B

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Conditions
ConditionsYield
In neat (no solvent) thermic decomposition on heating at 232°C (decomposition of NH4NO3 not above 270°C);; thermoanalysis;;
In neat (no solvent) thermic decomposition on heating at 232°C (decomposition of NH4NO3 not above 270°C);; thermoanalysis;;
yttrium(III) oxide

yttrium(III) oxide

neodymium(III) oxide

neodymium(III) oxide

nitric acid
7697-37-2

nitric acid

A

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

B

neodymium(III) nitrate
16454-60-7

neodymium(III) nitrate

Conditions
ConditionsYield
Heating;
yttrium(lll) nitrate hexahydrate

yttrium(lll) nitrate hexahydrate

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Conditions
ConditionsYield
With nitric acid Heating;
barium(II) nitrate

barium(II) nitrate

ammonium oxalate

ammonium oxalate

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

copper(II) nitrate

copper(II) nitrate

yttrium barium cuprate

yttrium barium cuprate

Conditions
ConditionsYield
In water soln. of Y3+, Ba2+ and Cu2+ nitrates mixed to ratio of 1:2:3 = Y3+:Ba2+:Cu2+, 30% excess satd. soln. of (NH4)2C2O4 added at 25°C, pH = 2.38-2.53, pptn. of YBa2Cu3(C2O4(2-))n, centrifuged, dried (100°C), calcinated 860°C for 6 h;100%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

terbium(III) nitrate

terbium(III) nitrate

Y2O3#dotTb(3+)

Y2O3#dotTb(3+)

Conditions
ConditionsYield
In water; ethylene glycol stoich. amt. of Y and Tb salts stirred with H2O; heated at 140°C for 1 h; mixed by stirring for 4 h in refluxing diethylene glycol at 180°C; water removed; filtered; washed (MeOH); dried at 100°Cfor 1 h; heat treated for 3 h at ...;100%
With citric acid; formaldehyde In 2-methoxy-ethanol nitrates dissolved in 2-methoxyethanol; citric acid added, then formaldehyde added; placed on sapphire filtrate; spun at 2000 rpm for 100 s; dried in air at 100°C, baked at 600°C; repeated up to 15 times, annealed at 900°C for 2 h;
methanol
67-56-1

methanol

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

2,2'-[pyridine-2,6-dyilbis(methan-1-yl-1-ylidene)]bis(hydrazinecarboxamide)

2,2'-[pyridine-2,6-dyilbis(methan-1-yl-1-ylidene)]bis(hydrazinecarboxamide)

water
7732-18-5

water

[Y(NO3)3(2,2'-[pyridine-2,6-diylbis(methan-1-yl-1-ylidene)]bis(nydrazinecarboxamide))]*4H2O*MeOH

[Y(NO3)3(2,2'-[pyridine-2,6-diylbis(methan-1-yl-1-ylidene)]bis(nydrazinecarboxamide))]*4H2O*MeOH

Conditions
ConditionsYield
In acetonitrile 1:1 mixt. stirred overnight; filtered, evapd. (vac.), elem. anal.;99%
methanol
67-56-1

methanol

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

(2S,2'S)-N,N'-[pyridine-2,6-diylbis(methan-1-yl-1-ylidene)]bis[2-(methoxymethyl)pyrrolidin-2-amine]

(2S,2'S)-N,N'-[pyridine-2,6-diylbis(methan-1-yl-1-ylidene)]bis[2-(methoxymethyl)pyrrolidin-2-amine]

water
7732-18-5

water

[Y(NO3)3(2S,2'S-N,N,-[pyridine-2,6-diylbis(methan-1-yl-1-ylidene)]bis(2-methoxymethyl)pyrrolidin-1-amine)]*MeOH*H2O

[Y(NO3)3(2S,2'S-N,N,-[pyridine-2,6-diylbis(methan-1-yl-1-ylidene)]bis(2-methoxymethyl)pyrrolidin-1-amine)]*MeOH*H2O

Conditions
ConditionsYield
In methanol 1:1 mixt. stirred overnight; evapd. (vac.), elem. anal.;99%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

ethylene glycol
107-21-1

ethylene glycol

squaric acid
2892-51-5

squaric acid

Y(squarate)1.5(ethylene glycol)

Y(squarate)1.5(ethylene glycol)

Conditions
ConditionsYield
In water; ethylene glycol High Pressure; mixt. Ln(NO3)3, squaric acid, ethylene glycol and water were heated in Teflon-lined autoclave at 180°C for 3 days and cooled to room temp. at 12°C/h; product was filtered, washed with water, rinsed with EtOH and dried in desiccator at room temp.; elem. anal.;99%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

oxalic acid
144-62-7

oxalic acid

yttrium oxalate monohydrate

yttrium oxalate monohydrate

Conditions
ConditionsYield
In water addn. of soln. of H2C2O4 (0.20 M) to soln. of Y salt (0.025 M) (room temp., pH = 2.32+-0.20; pptn.);96.36%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

(21S,25S)-8,15,23-trioxo-1-((4-((1,4,7,10-tetrakis(carboxymethyl)-1,4,7,10-tetraazacyclododecan-2-yl)methyl)phenyl)amino)-1-thioxo-2,7,16,22,24-pentaazaheptacosane-21,25,27-tricarboxylic acid

(21S,25S)-8,15,23-trioxo-1-((4-((1,4,7,10-tetrakis(carboxymethyl)-1,4,7,10-tetraazacyclododecan-2-yl)methyl)phenyl)amino)-1-thioxo-2,7,16,22,24-pentaazaheptacosane-21,25,27-tricarboxylic acid

C48H72N10O17S(86)Y(1-)

C48H72N10O17S(86)Y(1-)

Conditions
ConditionsYield
With nitric acid; sodium acetate; ascorbic acid at 95℃; for 0.333333h; pH=Ca. 5.5 - 6; Inert atmosphere;95%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

copper(II) nitrate

copper(II) nitrate

barium(II) hydroxide

barium(II) hydroxide

3Cu(2+)*2Ba(2+)*Y(3+)*5CH3COCHCOCH3(1-)*8CH3O(1-)*CH3OH=Cu3Ba2YC34H63O19

3Cu(2+)*2Ba(2+)*Y(3+)*5CH3COCHCOCH3(1-)*8CH3O(1-)*CH3OH=Cu3Ba2YC34H63O19

Conditions
ConditionsYield
With acetylacetone In methanol methanolic soln. contg. equimolar amts. Cu(NO3)2, rare earth nitrate, Ba(OH)2 and acetylacetone (pH 8, piperidine) heated (60°C) and stirred until a homogeneous lilac ppt. started to settle; ppt. filtered out, washed (MeOH and ether), dried (vac. desiccator, silica gel), elem. anal.;92%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

N-(4-benzoylidene-3-methyl-1-phenylpyrazol-5-one)isonicotinylhydrazine
329247-15-6

N-(4-benzoylidene-3-methyl-1-phenylpyrazol-5-one)isonicotinylhydrazine

Y(N-(4'-benzoylidene-3'-methyl-1'-phenylpyrazol-5'-one)isonicotinylhydrazine)2(NO3)3

Y(N-(4'-benzoylidene-3'-methyl-1'-phenylpyrazol-5'-one)isonicotinylhydrazine)2(NO3)3

Conditions
ConditionsYield
In ethanol refluxing (4 h); concentration, washing (hot C6H6), dissoln. in hot EtOH, pptn. on Et2O addn. (stirring), collection, drying (vac., over P2O5); elem. anal.;92%
zirconyl nitrate

zirconyl nitrate

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

yttria stabilized zirconia

yttria stabilized zirconia

Conditions
ConditionsYield
With urea In water High Pressure; hydrothermal treatment at 80 °C for 24 h and at 180 °C for48 h under autogenous pressure; ppt. filtered, washed with water, ethanol, dried at vac. at 60 °C; powder XRD;90%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

ammonia
7664-41-7

ammonia

water
7732-18-5

water

oxalic acid
144-62-7

oxalic acid

A

ammonium dioxalatoyttrate(III)

ammonium dioxalatoyttrate(III)

B

Y(3+)*OH(1-)*C2O4(2-)=Y(OH)C2O4

Y(3+)*OH(1-)*C2O4(2-)=Y(OH)C2O4

Conditions
ConditionsYield
In water addn. of aq. NH3 soln. within 1 min to a sol. of Y(NO3)3 and H2O (in a glass vessel under agitation with a paddle mixer), addn. of oxalic acid to the Y(OH)3 slurry (concn. of acid 0.1 mol/dm**3, addn. time 10 s, molar ratio H2C2O4:Y(OH)3=1.75); filtration (vac. suction), washing with H2O, drying on a hot plate;A 89%
B 11%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

1,2-dihydro-1,5-dimethyl-2-phenyl-4-formyl(benzhydrazide)-3H-pyrazol-3-one
76644-54-7

1,2-dihydro-1,5-dimethyl-2-phenyl-4-formyl(benzhydrazide)-3H-pyrazol-3-one

nitratobis[N'-((2,3-dimethyl-5-oxo-1-phenyl-3-pyrazolin-4-yl)methylidene)benzohydrazide-κ3-N'O,O]yttrium(III) dinitrate

nitratobis[N'-((2,3-dimethyl-5-oxo-1-phenyl-3-pyrazolin-4-yl)methylidene)benzohydrazide-κ3-N'O,O]yttrium(III) dinitrate

Conditions
ConditionsYield
In methanol; ethanol soln. Y(NO3)3 in MeOH added dropwise with stirring to a boiling soln. ofN'-((2,3-dimethyl-5-oxo-1-phenyl-3-pyrazolin-4-yl)methylidene)benzohydr azide (1:2.1 mol) in EtOH; reflux about 4 h; cooling; ppt. filtered off; washed (i-PrOH, hot C6H6); crystd. (MeOH); dried (vac., P2O5); elem. anal.;89%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

silver nitrate

silver nitrate

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

potassium iodide
7681-11-0

potassium iodide

lead(II) iodide

lead(II) iodide

16C3H7NO*2Y(3+)*Pb3Ag10I22(6-)

16C3H7NO*2Y(3+)*Pb3Ag10I22(6-)

Conditions
ConditionsYield
at 60℃; for 3h;87%
Tetraisopropyl methylenediphosphonate
1660-95-3

Tetraisopropyl methylenediphosphonate

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

bis(tetrakis(O-isopropyl)methylenediphosphonate)yttrium(III) nitrate

bis(tetrakis(O-isopropyl)methylenediphosphonate)yttrium(III) nitrate

Conditions
ConditionsYield
In acetonitrile in air; soln. was concd., ppt. was washed with ether, dried in vac., elem. anal.;86%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

2-(pyridin-2-yl)-3-((pyridin-2-ylmethylene)-amino)-2,3-dihydroquinazolin-4(1H)-one
55137-76-3

2-(pyridin-2-yl)-3-((pyridin-2-ylmethylene)-amino)-2,3-dihydroquinazolin-4(1H)-one

[Y(2-pyridine-2-yl-3-[pyridine-2-carboxylideneamino]-1,2-dihydroquinazolin-4-(3H)-one)2(H2O)2NO3](NO3)2

[Y(2-pyridine-2-yl-3-[pyridine-2-carboxylideneamino]-1,2-dihydroquinazolin-4-(3H)-one)2(H2O)2NO3](NO3)2

Conditions
ConditionsYield
With NH3 In methanol soln. of nitrate and ligand in MeOH was refluxed for 2 h; alcoholic NH3 was added to pH 6.5; refluxed for 3-4 h; concd.; residue macerated with petroleum ether; filtered; washed (H2O, ether); dried in air; elem. anal.;84%
3-phenyl-4-benzoyl-isoxazol-5-one
41836-94-6

3-phenyl-4-benzoyl-isoxazol-5-one

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Yb(PBI)3

Yb(PBI)3

Conditions
ConditionsYield
In ethanol; water addn. of alc. soln. of ligand to hot aq. soln. of metal salt (dropwise, stirring), heating (water bath, 10 min), pptn.; sepn. (filtration under suction), drying (air), storing (over fused CaCl2); elem. anal.;80%
1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

isophthalic acid
121-91-5

isophthalic acid

[Y2(1,10-phenanthroline)2(1,3-benzenedicarboxylate)3]

[Y2(1,10-phenanthroline)2(1,3-benzenedicarboxylate)3]

Conditions
ConditionsYield
With NaOH In water High Pressure; Y-salt was dissolved in water, isophthalic acid and phenanthroline were added under stirring, pH was adjusted to 5 (NaOH), the mixt. was honogenized for 30 min at room temp., sealed, heated at 180°C for 72 h under autogeneous pressure; crystals were filtered under vac., dried at ambient temp.; elem. anal.;80%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

4-formyl-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one
950-81-2

4-formyl-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one

[Y(4-formyl-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one)2(NO3)2]NO3
230976-36-0

[Y(4-formyl-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one)2(NO3)2]NO3

Conditions
ConditionsYield
In ethyl acetate dropwise addn. of soln. of Ln(NO3)3 to soln. of pyrazolinone, refluxing (10 min), pptn. on cooling to room temp.; filtration, washing (hot EtOAc, hot benzene), recrystn. (MeCN), drying (vac., over P2O5); elem. anal.;80%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

C30H38Cu2N6O4
1620000-99-8

C30H38Cu2N6O4

water
7732-18-5

water

acetone
67-64-1

acetone

C30H40Cu2N9O14Y*C3H6O

C30H40Cu2N9O14Y*C3H6O

Conditions
ConditionsYield
for 0.166667h; Heating;80%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

1,2-bis(pyrrolidin-2-on-1-yl)-1-etane
15395-91-2

1,2-bis(pyrrolidin-2-on-1-yl)-1-etane

Y2(N,N'-ethylenebis(pyrrolidin-2-one))3(NO3)6

Y2(N,N'-ethylenebis(pyrrolidin-2-one))3(NO3)6

Conditions
ConditionsYield
In acetonitrile 2 equiv. of ligand; pptn. on mixing or after concn. at room temp. (not specified), collection, washing (MeCN), drying (vac., over silica gel); elem. anal.;76%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

Ethane-1-phosphono-2-sulphonic acid
75407-14-6

Ethane-1-phosphono-2-sulphonic acid

yttrium 2-phosphonatoethanesulfonate
1099630-58-6

yttrium 2-phosphonatoethanesulfonate

Conditions
ConditionsYield
With NaOH In water H2O added to mixt. of aq. solns. of Y salt, (HO)2P(O)C2H4SO3H and NaOH (molar ratio 1:1:2); homogenized by shaking for 2 min; heated at 170°C for 24 h; detd. by X-ray powder diffraction;76%
With NaOH In water other Radiation; H2O added to mixt. of aq. solns. of Y salt, (HO)2P(O)C2H4SO3H and NaOH (molar ratio 1:1:2); microwave heated at 170°C for 2-24 h with stirring (0-900 1/min); detd. by X-ray powder diffraction;32%
With NaOH In water High Pressure; under hydrothermal conditions; aq. soln. contg. Y salt, (HO)2P(O)C2H4SO3H and NaOH (molar ratio 1:1:2 or 1:1:3) heated at 170°C for 24 h; detd. by X-ray powder diffraction;
[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

2-hydroxyl-4-carboxylbenzenesulfonic acid
88122-95-6

2-hydroxyl-4-carboxylbenzenesulfonic acid

water
7732-18-5

water

Y(3+)*H2O*C7H3O6S(3-)*C10H8N2

Y(3+)*H2O*C7H3O6S(3-)*C10H8N2

Conditions
ConditionsYield
With sodium hydroxide at 120℃; for 72h; pH=5; Autoclave; High pressure;76%
1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

water
7732-18-5

water

benzene-1,2-dicarboxylic acid
88-99-3

benzene-1,2-dicarboxylic acid

[Y2(1,10-phenanthroline)2(1,2-benzenedicarboxylate)3]*H2O

[Y2(1,10-phenanthroline)2(1,2-benzenedicarboxylate)3]*H2O

Conditions
ConditionsYield
With NaOH In water High Pressure; Y-salt was dissolved in water, phthalic acid and phenanthroline were added under stirring, pH was adjusted to 5 (NaOH), the mixt. was honogenized for 30 min at room temp., sealed, heated at 180°C for 72 h under autogeneous pressure; crystals were filtered under vac., dried at ambient temp.; elem. anal.;75%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

tris(2-[(3,4-dihydroxybenzylidene)imino]ethyl)amine
1070776-25-8

tris(2-[(3,4-dihydroxybenzylidene)imino]ethyl)amine

[Y(tris(2-[(3,4-dihydroxybenzylidene)imino]ethyl)amine)(NO3)2]NO3*H2O
1070776-40-7

[Y(tris(2-[(3,4-dihydroxybenzylidene)imino]ethyl)amine)(NO3)2]NO3*H2O

Conditions
ConditionsYield
In methanol a soln. of Y salt added slowly to a soln. of ligand, stirred for 2 h at room temp.; filtered, washed (MeOH), dried (vac.); elem. anal.;75%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

ethanol
64-17-5

ethanol

C13H12N2O5

C13H12N2O5

C13H10N2O5(2-)*NO3(1-)*3C2H6O*Y(3+)

C13H10N2O5(2-)*NO3(1-)*3C2H6O*Y(3+)

Conditions
ConditionsYield
With sodium acetate for 8h; pH=5; Reflux;75%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

periciazine
2622-26-6

periciazine

Y(3+)*2C21H23N3OS*3NO3(1-) = [Y(C21H23N3OS)2(NO3)2](NO3)

Y(3+)*2C21H23N3OS*3NO3(1-) = [Y(C21H23N3OS)2(NO3)2](NO3)

Conditions
ConditionsYield
In ethanol 15 min; pptn. washing (EtOH), drying (vac.); elem. anal.;74%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

N,N''-bis[(benzylcarbamoyl)methyl]diethylenetriamine-N,N',N''-triacetic acid

N,N''-bis[(benzylcarbamoyl)methyl]diethylenetriamine-N,N',N''-triacetic acid

{Y(N,N''-bis(benzylcarbamoylmethyl)diethylenetriamine-N,N',N''-triacetate)(H2O)}*3H2O

{Y(N,N''-bis(benzylcarbamoylmethyl)diethylenetriamine-N,N',N''-triacetate)(H2O)}*3H2O

Conditions
ConditionsYield
With HCl; H2O In hydrogenchloride addn. of the Y salt in aq. HCl to a soln. of the triacetic acid in H2O, refluxing the mixt. until complete clearness of the soln., cooling to room temp.; crystn. on adjusting the pH to 4 and standing, filtration, washing (cold H2O), drying under vac., elem. anal.;74%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

p-chlorobenzoyl-di-(2-pyridyl)ketohydrazone
93418-36-1

p-chlorobenzoyl-di-(2-pyridyl)ketohydrazone

water
7732-18-5

water

[Y(NO3)2(ClC6H4CONHNC(C5H4N)2)2](1+)*NO3(1-)*2H2O=[Y(NO3)2(ClC6H4CONHNC(C5H4N)2)2]NO3*2H2O

[Y(NO3)2(ClC6H4CONHNC(C5H4N)2)2](1+)*NO3(1-)*2H2O=[Y(NO3)2(ClC6H4CONHNC(C5H4N)2)2]NO3*2H2O

Conditions
ConditionsYield
In methanol; water addn. dropwise of methanolic soln. of ClC6H4CONHNC(C5H4N)2 (2 equiv.) to water soln. of Y(NO3)3 (1 equiv.); stirring for 4 h; filtration, washing with MeOH; drying in vac. over anhyd. CaCl2; elem. anal.;74%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

trifluoperazine hydrochloride
1250-26-6

trifluoperazine hydrochloride

Y(3+)*2C21H24N3SF3*3NO3(1-) = [Y(C21H24N3SF3)2(NO3)2](NO3)

Y(3+)*2C21H24N3SF3*3NO3(1-) = [Y(C21H24N3SF3)2(NO3)2](NO3)

Conditions
ConditionsYield
In ethanol 15 min; pptn. washing (EtOH), drying (vac.); elem. anal.;73%
1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

benzenephosphono-3-sulphonic acid
126180-64-1

benzenephosphono-3-sulphonic acid

Y(1,10-phenanthroline)(3-phosphonobenzesulfonic acid(3-))(H2O)2*2H2O

Y(1,10-phenanthroline)(3-phosphonobenzesulfonic acid(3-))(H2O)2*2H2O

Conditions
ConditionsYield
In water High Pressure; mixt. of Y(NO3)3, 3-phosphonobenzesulfonic acid, 1,10-phenanthroline in H2O placed in autoclave, pH adjusted to 4.0 by NaOH, heated to 150°C for 4 d; collected; elem. anal.;73%

Yttrium (III) nitrate hexahydrate (1:3:6) Standards and Recommendations

ACGIH TLV: TWA 1 mg(Y)/m3

Yttrium (III) nitrate hexahydrate (1:3:6) Specification

The Yttrium Nitrate Hexahydrate, with the CAS registry number 13494-98-9 and EINECS registry number 233-802-6, has the systematic name of yttrium nitrate hydrate (1:3:6). It is a kind of white adhering crystals or crystalline powder, and belongs to the following product categories: Metal and Ceramic Science; Salts; Yttrium Salts. And the molecular formula of this chemical is YN3O9.6H2O. What's more, it should be stored at 0-6°C.

The physical properties of Yttrium Nitrate Hexahydrate are as followings: (1)ACD/LogP: -0.13; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -0.13; (4)ACD/LogD (pH 7.4): -0.13; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)#H bond acceptors: 4; (8)#H bond donors: 1; (9)#Freely Rotating Bonds: 0; (10)Polar Surface Area: 66.05 Å2; (11)Enthalpy of Vaporization: 37.72 kJ/mol; (12)Boiling Point: 83 °C at 760 mmHg; (13)Vapour Pressure: 49.8 mmHg at 25°C.

The preparation of Yttrium Nitrate Hexahydrate: Excessive Y2O3 react with hot concentrated nitric acid. After filtration, remove unreacted oxide, then by cooling crystallization, suction filtration and drying, you can get the product.

You can still convert the following datas into molecular structure:
(1)SMILES: [Y+3].O=[N+]([O-])[O-].[O-][N+]([O-])=O.[O-][N+]([O-])=O.O.O.O.O.O.O
(2)InChI: InChI=1/3NO3.6H2O.Y/c3*2-1(3)4;;;;;;;/h;;;6*1H2;/q3*-1;;;;;;;+3
(3)InChIKey: QBAZWXKSCUESGU-UHFFFAOYAY

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
frog LDLo subcutaneous 350mg/kg (350mg/kg)   Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 141, Pg. 273, 1929.
mouse LDLo subcutaneous 16600mg/kg (16600mg/kg)   Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 141, Pg. 273, 1929.

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