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10361-46-3

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10361-46-3 Usage

Chemical Properties

heavy, white powder(s); slightly hygroscopic; uses: cosmetics, ceramic glasses, and enamel fluxes; there is a 99.99+% pure monohydrate, CAS RN 13595-83-0 [HAW93] [ALD94]

Physical properties

White powder; density 4.93 g/cm3; decomposes at 260°C; insoluble in water and ethanol; dissolves in acids.

Uses

Different sources of media describe the Uses of 10361-46-3 differently. You can refer to the following data:
1. Bismuth oxynitrate is used in cosmetics, enamel fluxes and ceramic glazes. Medical applications include treatment of diarrhea, and gastric ulcers; and opacifier in x-ray diagnosis of alimentary canal .
2. Bismuth(III) nitrate oxide is used as an organic chemical synthesis intermediate. It is also used in the spectrophotometric detection of bismuth.

Preparation

Bismuth oxynitrate is prepared by hydrolysis of bismuth nitrate using either water or sodium bicarbonate solution under mild heating (between 30 to 70°C) and stirring. The composition of the product formed can vary depending on the strength of nitric acid and the quantity of water used.

Check Digit Verification of cas no

The CAS Registry Mumber 10361-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,6 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10361-46:
(7*1)+(6*0)+(5*3)+(4*6)+(3*1)+(2*4)+(1*6)=63
63 % 10 = 3
So 10361-46-3 is a valid CAS Registry Number.
InChI:InChI=1/Bi.NO3.O/c;2-1(3)4;/q+3;-1;-2

10361-46-3 Well-known Company Product Price

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  • Detail
  • Alfa Aesar

  • (11122)  Bismuth(III) nitrate oxide, Puratronic?, 99.998% (metals basis)   

  • 10361-46-3

  • 10g

  • 385.0CNY

  • Detail
  • Alfa Aesar

  • (11122)  Bismuth(III) nitrate oxide, Puratronic?, 99.998% (metals basis)   

  • 10361-46-3

  • 50g

  • 1201.0CNY

  • Detail
  • Alfa Aesar

  • (11122)  Bismuth(III) nitrate oxide, Puratronic?, 99.998% (metals basis)   

  • 10361-46-3

  • 250g

  • 4752.0CNY

  • Detail
  • Sigma-Aldrich

  • (95379)  Bismuthnitrateoxide  for spectrophotometric det., Bi, 71-74% Bi basis (KT)

  • 10361-46-3

  • 95379-100G

  • 573.30CNY

  • Detail
  • Sigma-Aldrich

  • (95379)  Bismuthnitrateoxide  for spectrophotometric det., Bi, 71-74% Bi basis (KT)

  • 10361-46-3

  • 95379-500G

  • 1,963.26CNY

  • Detail

10361-46-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Bismuth(Iii) Nitrate Oxide

1.2 Other means of identification

Product number -
Other names Bismuth subnitrate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10361-46-3 SDS

10361-46-3Synthetic route

bismuth(III) oxide
1304-76-3

bismuth(III) oxide

A

bismuth subnitrate
10361-46-3

bismuth subnitrate

B

bismutum subnitricum

bismutum subnitricum

Conditions
ConditionsYield
In nitric acid aq. HNO3; formation of the sparingly soluble basic salts; solution of the salts if H(1+)-activity exceeds 0.06;;
In nitric acid aq. HNO3; formation of the sparingly soluble basic salts; solution of the salts if H(1+)-activity exceeds 0.06;;
bismuth (III) nitrate pentahydrate

bismuth (III) nitrate pentahydrate

bismuth subnitrate
10361-46-3

bismuth subnitrate

Conditions
ConditionsYield
In neat (no solvent) drying over H2SO4 or in a stream of CO2 or dry air to constant weight;;
In neat (no solvent) storage of the pentahydrate in a desiccator until 19 % loss of weight, then heating at 50-100°C in a dry stream of air without melting;; constant weight after 6 days;;
bismuth(III) nitrate

bismuth(III) nitrate

A

bismuth subnitrate
10361-46-3

bismuth subnitrate

B

Bi12O18*9H2O*5N2O5

Bi12O18*9H2O*5N2O5

C

bismuth oxide nitrate 0.5-hydrate

bismuth oxide nitrate 0.5-hydrate

D

bismuth oxide nitrate dihydrate

bismuth oxide nitrate dihydrate

Conditions
ConditionsYield
With H2O In nitric acid aq. HNO3; slow diffusion of H2O into a saturated solution of Bi nitrate in HNO3;; separation of different crystals;;
2Bi2O3*2CrO3

2Bi2O3*2CrO3

nitric acid
7697-37-2

nitric acid

bismuth subnitrate
10361-46-3

bismuth subnitrate

Conditions
ConditionsYield
In nitric acid dissoln. in dild. HNO3 (excess); addn. of H2O; pptn.;;
In nitric acid aq. HNO3; dissoln. in dild. HNO3 (excess); addn. of H2O; pptn.;;
bismuth chromate

bismuth chromate

nitric acid
7697-37-2

nitric acid

A

bismuth subnitrate
10361-46-3

bismuth subnitrate

B

Bi2O3*2CrO3

Bi2O3*2CrO3

C

Bi2O3*4CrO3

Bi2O3*4CrO3

Conditions
ConditionsYield
In nitric acid boiling with a small amt. of concd. HNO3; evapn.;;
In nitric acid aq. HNO3; boiling with a small amt. of concd. HNO3; evapn.;;
BiO0.5(2+)*2NO3(1-)=BiO0.5(NO3)2

BiO0.5(2+)*2NO3(1-)=BiO0.5(NO3)2

bismuth subnitrate
10361-46-3

bismuth subnitrate

Conditions
ConditionsYield
In neat (no solvent, solid phase) byproducts: N2O5; heating at 440-500°C;
bismuth
7440-69-9

bismuth

nitric acid
7697-37-2

nitric acid

bismuth subnitrate
10361-46-3

bismuth subnitrate

Conditions
ConditionsYield
With water In nitric acid byproducts: N oxide; preparation of a layer of 165 g remolten Bi (description of method given) and solvation at 60-70°C in 1040 ml 25% HNO3; vigorous reaction, form. of N oxide; filtration and evaporation in porcelain crucibles; addition of 800 ml H2O under stirring;; addition of the mass to hot water and washing the precipitate with H2O; drying with alcohol and heating at 45°C;;
With H2O In nitric acid byproducts: N oxide; aq. HNO3; preparation of a layer of 165 g remolten Bi (description of method given) and solvation at 60-70°C in 1040 ml 25% HNO3; vigorous reaction, form. of N oxide; filtration and evaporation in porcelain crucibles; addition of 800 ml H2O under stirring;; addition of the mass to hot water and washing the precipitate with H2O; drying with alcohol and heating at 45°C;;
bismuth
7440-69-9

bismuth

bismuth subnitrate
10361-46-3

bismuth subnitrate

Conditions
ConditionsYield
With nitric acid In nitric acid byproducts: NO; Bi metal was dissolved in 11 M HNO3; evapd. to dryness, baked at 115°C for several h, elem. anal.;
basic bismuth nitrate
13520-71-3

basic bismuth nitrate

bismuth subnitrate
10361-46-3

bismuth subnitrate

Conditions
ConditionsYield
In neat (no solvent) dehydration;;
In neat (no solvent) heating in a dry stream of CO2 at 100°C for 6 hours with formation of Bi2O3*N2O5*H2O and finally with formation of Bi2O3*N2O5;;
bismuth oxide nitrate 0.5-hydrate

bismuth oxide nitrate 0.5-hydrate

bismuth subnitrate
10361-46-3

bismuth subnitrate

Conditions
ConditionsYield
In neat (no solvent) dehydration;;
bismuth (III) nitrate pentahydrate

bismuth (III) nitrate pentahydrate

water
7732-18-5

water

bismuth subnitrate
10361-46-3

bismuth subnitrate

Conditions
ConditionsYield
In water byproducts: HNO3; reaction of hydrolysis; EDS;
bismuth subnitrate
10361-46-3

bismuth subnitrate

N-hydroxyethyl-N-methyl-dithiocarbamic acid
91308-51-9

N-hydroxyethyl-N-methyl-dithiocarbamic acid

tris(N-methylaminoethanoldithiocarbamato)bismuth(III)
125823-32-7

tris(N-methylaminoethanoldithiocarbamato)bismuth(III)

Conditions
ConditionsYield
With HCl; NH3 In hydrogenchloride dissoln. of BiONO3 in concd. HCl, vol. reduction, addn. og ligand (stirring), passing NH3 through soln.;70%
bismuth subnitrate
10361-46-3

bismuth subnitrate

strontium(II) acetate
543-94-2

strontium(II) acetate

tantalum pentaethoxide
150747-55-0

tantalum pentaethoxide

A

strontium(II) carbonate
1633-05-2

strontium(II) carbonate

B

bismuth(III) oxide
1304-76-3

bismuth(III) oxide

Conditions
ConditionsYield
With catalyst: CH3COOH In further solvent(s) Sr(CH3COO)2, BiONO3, and Ta(OC2H5)5 in a mole ratio of 1:2:2 dissolved in 2-methoxyethanol at 80°C; pH adjusted to 3.5; transparent gel formed; dried at 100°C; calcined at 500°C for 1 h; XRD, TEM, IR;
bismuth subnitrate
10361-46-3

bismuth subnitrate

sodium hydrogencarbonate
144-55-8

sodium hydrogencarbonate

Rochelle's salt
304-59-6

Rochelle's salt

2Bi(3+)*3C4H4O6(2-)*2C4H6O6=Bi2(C4H4O6)3*2C4H6O6

2Bi(3+)*3C4H4O6(2-)*2C4H6O6=Bi2(C4H4O6)3*2C4H6O6

Conditions
ConditionsYield
In nitric acid adding KNaC4H4O6 and NaHCO3 to a soln. of (BiO)NO3, heating mixture to drive away CO2, precipitate is digested with a hot solution of tartaric acid, and Bi2(C4H4O6)3*2C4H6O6 crystallizes from the filtrate on cooling;;
In nitric acid aq. HNO3; adding KNaC4H4O6 and NaHCO3 to a soln. of (BiO)NO3, heating mixture to drive away CO2, precipitate is digested with a hot solution of tartaric acid, and Bi2(C4H4O6)3*2C4H6O6 crystallizes from the filtrate on cooling;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

Rochelle's salt
304-59-6

Rochelle's salt

bismuth(II) oxide

bismuth(II) oxide

Conditions
ConditionsYield
With sodium hydroxide; iron(II) sulfate In water warming up an aq. soln. of FeSO4, Seignette salt and NaOH with Bi oxynitrate;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

hydrogen cation

hydrogen cation

A

water
7732-18-5

water

B

Nitrate

Nitrate

C

bismuth(III)

bismuth(III)

Conditions
ConditionsYield
In nitric acid aq. HNO3; solution of BiONO3 in diluted HNO3 at 25°C;;
In nitric acid aq. HNO3; solution of BiONO3 in diluted HNO3 at 25°C;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

hydrogen cation

hydrogen cation

A

BiHO(2+)

BiHO(2+)

B

Nitrate

Nitrate

Conditions
ConditionsYield
In nitric acid aq. HNO3; solution of BiONO3 in diluted HNO3 at 25°C;;
In nitric acid aq. HNO3; solution of BiONO3 in diluted HNO3 at 25°C;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

molybdic acid

molybdic acid

bismuth molybdate
13565-96-3

bismuth molybdate

Conditions
ConditionsYield
In water aq. slurry of neutral BiONO3 and H2MoO4 refluxed for 12 h, followed by calcination at 500°C for 40 h;
bismuth subnitrate
10361-46-3

bismuth subnitrate

molybdic acid

molybdic acid

bismuth molybdenym oxide

bismuth molybdenym oxide

Conditions
ConditionsYield
In water initial ratio of Bi to Mo was 2:1, BiO(NO3) and H2MoO4 were powdered, slurried in water, boiled under stirring for 16 h, calcined at 500°C for 4 h; filtered, dried;
bismuth subnitrate
10361-46-3

bismuth subnitrate

molybdic acid

molybdic acid

bismuth molybdate

bismuth molybdate

Conditions
ConditionsYield
In water boiling (stirring); centrifugation of ppt., drying (100°C), calcining (480°C);
In water initial ratio of Bi to Mo was 1:5, BiO(NO3) and H2MoO4 were powdered, slurried in water, boiled under stirring for 16 h, calcined at 500°C for 4 h; washed with dil. NH3 sol., filtered, dried;
bismuth subnitrate
10361-46-3

bismuth subnitrate

bismuth(III) sulfide

bismuth(III) sulfide

Conditions
ConditionsYield
With hydrogen sulfide In water reaction of Bo oxide nitrate in hydrous H2S solution;;
With H2S In water reaction of Bo oxide nitrate in hydrous H2S solution;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

bismuth(III) oxide
1304-76-3

bismuth(III) oxide

Conditions
ConditionsYield
strong heating;
In neat (no solvent, solid phase) heat treated Bi salt decomposed below 500°C;
bismuth subnitrate
10361-46-3

bismuth subnitrate

bismuth molybdenym oxide

bismuth molybdenym oxide

Conditions
ConditionsYield
With ammonium heptamolybdate In water boiling (stirring); centrifugation of ppt., drying (100°C), calcining (480°C);
selenium
7782-49-2

selenium

bismuth subnitrate
10361-46-3

bismuth subnitrate

bismuth(III) selenide

bismuth(III) selenide

Conditions
ConditionsYield
With sodium hydroxide In ethylene glycol Sonication; BiONO3 was dissolved in ethylene glycol by addn. NaOH and gentle heatingin the microwave oven for 1 min, Se was added, purged with N2, and heat ed in microwave oven for 30 min; product was centrifuged once with mother liquid, and a few times with EtOH, at 20°C and 9000 rpm, and dried overnight under vac.; X-ray diffraction;
sodium percarbonate

sodium percarbonate

bismuth subnitrate
10361-46-3

bismuth subnitrate

water
7732-18-5

water

oxalic acid
144-62-7

oxalic acid

Na(1+)*Bi(3+)*2C2O4(2-)*5H2O=NaBi(C2O4)2*5H2O

Na(1+)*Bi(3+)*2C2O4(2-)*5H2O=NaBi(C2O4)2*5H2O

Conditions
ConditionsYield
In water heating 2g Na2CO4, 2g oxalic acid, 2g BiONO3 and 100g H2O, boiling, addn. of 180g cold H2O, crystn.;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

potassium iodide
7681-11-0

potassium iodide

bismuth(III) oxide iodide
7787-63-5

bismuth(III) oxide iodide

Conditions
ConditionsYield
With sodium hydroxide In nitric acid dissolution of 30.5 g BiONO3 in 30 ml concnd. HNO3, 60 ml H2O and glycerine; addn. of 125 ml NaOH and 175 ml H2O while stirring and dilution to 1000 ml; addn. of a soln. of 33 g KI in 50 ml H2O and 60 ml glacial acetic acid;; filtration of the precipitate after 2 hours and washing; yield: 32 g, purity 91.14 %;;
With aq. NaOH In nitric acid aq. HNO3; dissolution of 30.5 g BiONO3 in 30 ml concnd. HNO3, 60 ml H2O and glycerine; addn. of 125 ml NaOH and 175 ml H2O while stirring and dilution to 1000 ml; addn. of a soln. of 33 g KI in 50 ml H2O and 60 ml glacial acetic acid;; filtration of the precipitate after 2 hours and washing; yield: 32 g, purity 91.14 %;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

water
7732-18-5

water

sodium oxalate
62-76-0

sodium oxalate

oxalic acid
144-62-7

oxalic acid

Na(1+)*Bi(3+)*2C2O4(2-)*2.5H2O=NaBi(C2O4)2*2.5H2O

Na(1+)*Bi(3+)*2C2O4(2-)*2.5H2O=NaBi(C2O4)2*2.5H2O

Conditions
ConditionsYield
In water trituration of 4g BiONO3 with 4g oxalic acid and a small amount of H2O, addn. of the mixture to a boiling soln. of 20g Na2C2O4 in 500g H2O, separation of the clear soln., pouring into 2l cold H2O, crystn.;; washing, drying in the air;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

sodium paraperiodate

sodium paraperiodate

3Bi2O34*2I2O7*7H2O

3Bi2O34*2I2O7*7H2O

Conditions
ConditionsYield
In nitric acid addition of a solution of basic Bi nitrate in concentrated HNO3 to a solution of Na3H2IO6 in diluted HNO3;; filtration and washing the precipitate with diluted HNO3 and water; drying over concentrated H2SO4 and solid KOH in a vacuum desiccator;;
In nitric acid aq. HNO3; addition of a solution of basic Bi nitrate in concentrated HNO3 to a solution of Na3H2IO6 in diluted HNO3;; filtration and washing the precipitate with diluted HNO3 and water; drying over concentrated H2SO4 and solid KOH in a vacuum desiccator;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

water
7732-18-5

water

sodium hydroxide
1310-73-2

sodium hydroxide

(x)BiNaO3*(x)H2O

(x)BiNaO3*(x)H2O

Conditions
ConditionsYield
With sodium peroxide In melt oxidation of a soln. of BiONO3 in molten NaOH with Na2O2;;
With Na2O2 In melt oxidation of a soln. of BiONO3 in molten NaOH with Na2O2;;
diammonium hydrogenphosphate

diammonium hydrogenphosphate

bismuth subnitrate
10361-46-3

bismuth subnitrate

bismuth orthophosphate

bismuth orthophosphate

Conditions
ConditionsYield
In neat (no solvent) heating a mixture of (NH4)2HPO4 and BiONO3 (Bi2O3 : P2O5 = 1 : 1) below 600°C;;
bismuth subnitrate
10361-46-3

bismuth subnitrate

potassium oxalate
583-52-8

potassium oxalate

bismuth oxalate

bismuth oxalate

Conditions
ConditionsYield
In nitric acid reaction of Bi oxide nitrate and K2C2O4 in aq. HNO3;;
In nitric acid aq. HNO3; reaction of Bi oxide nitrate and K2C2O4 in aq. HNO3;;

10361-46-3Relevant articles and documents

Synthesis of Bi2O3 architectures in DMF-H 2O solution by precipitation method and their photocatalytic activity

Yang, Li-Li,Han, Qiao-Feng,Zhao, Jin,Zhu, Jun-Wu,Wang, Xin,Ma, Wei-Hua

, p. 353 - 359 (2014)

Well-crystalline flowerlike α-Bi2O3 hierarchical architectures with pineapple-shaped petals have been synthesized by precipitation method at a volume ratio of DMF/H2O of 5, where DMF and H2O were used to dissolve Bi(NO3)3 and KOH, respectively. If the DMF/H2O ratio was decreased to 2:1, 1:1 and 0:30, flower-, bundle- and dendrite-shaped α-Bi2O3 microcrystallites aggregated by nanorods were formed, respectively. The simple synthetic route and thus obtained Bi2O3 architectures of various morphologies provide a basis insight for their formation mechanism. The photocatalytic activity of the as-prepared Bi2O3 particles for degradation of Rhodamine B (RhB) under visible-light irradiation was obviously influenced by their morphologies. Bi2O3 of nanorod-based microstructures exhibited higher photodegradation activity than nanobrick-based ones, owing to higher light absorption and carrier separation efficiency in one-dimensional (1D) nanostructured materials.

Surface Modifications of (ZnSe)0.5(CuGa2.5Se4.25)0.5to Promote Photocatalytic Z-Scheme Overall Water Splitting

Chen, Shanshan,Vequizo, Junie Jhon M.,Pan, Zhenhua,Hisatomi, Takashi,Nakabayashi, Mamiko,Lin, Lihua,Wang, Zheng,Kato, Kosaku,Yamakata, Akira,Shibata, Naoya,Takata, Tsuyoshi,Yamada, Taro,Domen, Kazunari

, p. 10633 - 10641 (2021)

Charge separation is crucial for an efficient artificial photosynthetic process, especially for narrow-bandgap metal sulfides/selenides. The present study demonstrates the application of a p-n junction to particulate metal selenides to enhance photocatalytic Z-scheme overall water splitting (OWS). The constructed p-n junction of CdS-(ZnSe)0.5(CuGa2.5Se4.25)0.5 significantly boosted charge separation. A thin TiO2 coating layer also was introduced to inhibit photocorrosion of CdS and suppress the backward reaction of water formation from hydrogen and oxygen. By employing Pt-loaded TiO2/CdS-(ZnSe)0.5(CuGa2.5Se4.25)0.5 as a hydrogen evolution photocatalyst (HEP), we assembled a Z-scheme OWS system, together with BiVO4:Mo and Au as an oxygen evolution photocatalyst and electron mediator, respectively. An apparent quantum yield of 1.5% at 420 nm was achieved, which is by far the highest among reported particulate photocatalytic Z-scheme OWS systems with metal sulfides/selenides as HEPs. The present work demonstrates that a well-tailored p-n junction structure is effective for promoting charge separation in photocatalysis and opens new pathways for the development of efficient artificial photosynthesis systems involving narrow bandgap photocatalysts.

Thermal synthesis of the ZnO-Bi2O3 pigments

Sulcova,Trojan

, p. 209 - 213 (2000)

A zinc oxide pigment with an admixture of bismut oxide has been prepared as new yellow pigment for colouring of plastics and paints. The effect of the Bi2O3 in the starting mixture on the colour hue of the pigment has been evaluated. The calcination conditions of the pigment synthesis have been established. The synthesis of these pigments was followed by thermal analysis using a derivatograph apparatus in our laboratory. The optimum conditions for the synthesis of pigments and the properties of the products have been estimated.

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