Conditions | Yield |
---|---|
With air In solid by standing in air for 24 h; | 99% |
trisulfimide
A
ammonium bisulfate
B
sulfuric acid
C
SULFAMIDE
Conditions | Yield |
---|---|
With water heat of evapn., 2 h, 2 M HCl; | A n/a B 67% C n/a |
With H2O heat of evapn., 2 h, 2 M HCl; | A n/a B 67% C n/a |
Conditions | Yield |
---|---|
In sulfuric acid heating with an excess of H2SO4;; |
Conditions | Yield |
---|---|
With ammonia; water; oxygen; vanadia In further solvent(s) 150-200 °C, in molten equimolar mixture of NH4HSO4 and NaHSO4 dissolving V2O5; transition metal sulfates enhances activity; |
Conditions | Yield |
---|---|
With water; chlorine byproducts: NH4Cl, HCl; with NH3 excess; |
Conditions | Yield |
---|---|
heating at 180°C; |
hydrogen
nitrogen(II) oxide
A
nitrous oxide
B
ammonium bisulfate
C
hydroxylamine sulfate
Conditions | Yield |
---|---|
With palladium on activated charcoal In sulfuric acid Kinetics; 40 °C, P(H2) = 50 kPa, P(NO) = 10 kPa; |
ammonium bisulfate
Conditions | Yield |
---|---|
With hydrogenchloride In water satd. soln. of neutral sulfate is distd. with aq. HCl;; | |
With sulfuric acid In sulfuric acid cooling a warm solution of (NH4)2SO4 in H2SO4; | |
Pt boat; 300 to 320 ° C and for a short period at red heat; |
Conditions | Yield |
---|---|
200 to 250°C; | |
heating in open vessel; ambient or reduced pressure; | |
In neat (no solvent) Kinetics; Thermal decomposition.; | |
200 to 250°C; | |
In neat (no solvent) decompn. of (NH4)2SO4 into NH3 and NH4HSO4 at 300-455°C was studied; TG and DSC; |
B
ammonium bisulfate
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: NH3, H2O; 150°C; IR spectroscopy, X-ray diffraction; |
A
ammonium bisulfate
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: NH3, H2O; 250°C; IR spectroscopy, X-ray diffraction; |
Conditions | Yield |
---|---|
In water byproducts: H2O, CuSO4; |
sulfuric acid
urea
A
ammonium bisulfate
B
aminosulfonic acid
C
disulfuric acid
Conditions | Yield |
---|---|
In sulfuric acid byproducts: CO2; heating with excess H2SO4 (100%/130-140°C); evolution of CO2;; |
hydroxyl ammonium amidosulfonate
A
ammonium bisulfate
B
nitrogen
C
nitrogen(II) oxide
D
dinitrogen monoxide
Conditions | Yield |
---|---|
in a larger amt. at 95°C, in a smaller amt. at 110°C; | |
in a larger amt. at 95°C, in a smaller amt. at 110°C; |
Conditions | Yield |
---|---|
In not given byproducts: HCl; | |
In not given byproducts: HCl; |
sulfur dioxide
hydroxylamine
A
ammonium bisulfate
B
sulfamic acid
Conditions | Yield |
---|---|
In water Kinetics; at pH=5; followed by polarography; |
Conditions | Yield |
---|---|
With H2O In water byproducts: H2O2; hydrolysis on boiling;; |
(hydroxylamino)sulfonic acid
A
ammonium bisulfate
B
dihydrogen peroxide
C
oxygen
Conditions | Yield |
---|---|
With water In water hydrolysis on boiling;; | A 0% B 0% C 0% |
With H2O In water hydrolysis on boiling;; | A 0% B 0% C 0% |
Conditions | Yield |
---|---|
With H2O In water decompn.;; |
Conditions | Yield |
---|---|
by hydrolysis; purification from NH4HSO4 by precipitation with baryta water,then evapn.over H2SO4 under reduced pressure; | |
by hydrolysis; purification from NH4HSO4 by precipitation with baryta water,then evapn.over H2SO4 under reduced pressure; |
Conditions | Yield |
---|---|
In melt passing dry ammonia through molten (NO)2S2O7;; | |
In melt passing dry ammonia through molten (NO)2S2O7;; |
Conditions | Yield |
---|---|
In neat (no solvent) passing dry ammonia(NO)2S2O7 (liquidation);; |
ammonium bisulfate
Conditions | Yield |
---|---|
deliquescent by air;ammonium hydrosulfate crystallizes from the liquid so formed; | |
deliquescent by air;ammonium hydrosulfate crystallizes from the liquid so formed; |
Conditions | Yield |
---|---|
In water by slow evapn. of aq. solns. of (NH4)2SO4:H2SO4 stoich. mixt. at room temp.; detd. by XRD; | |
In water slow evapn. from aq. soln.; |
Conditions | Yield |
---|---|
With air In neat (no solvent) vigorous hydrolysis on heating to 130-140°C in common (moist) air;; | |
With water In water hydrolysis described; degree of hydrolysis depending on temp. and time;; | |
With water In water hydrolysis on heating for longer period;; |
ammonium bisulfate
Conditions | Yield |
---|---|
heating by 10 Hgmm; at 300 °C melting and foaming; no more changing until 300 °C.; | |
With water In water byproducts: O2; slow by room temp.,fast at elevated temp.; | |
With water In water Kinetics; byproducts: O2; |
Conditions | Yield |
---|---|
In neat (no solvent) decompn. by heating (1h/400°C);; |
Conditions | Yield |
---|---|
With air In melt two salts was reacted in melt in air; | A n/a B n/a C 92% |
Conditions | Yield |
---|---|
byproducts: H2SO4; after 6 hours; | 30% |
byproducts: H2SO4; after 6 hours; | 30% |
Conditions | Yield |
---|---|
In water ZnS (pptd. in the heat, hot washed, well dried and pulverized); amount of H2S depends on concn. of acidic soln.; dilution: 1 mol NH4HSO4 in 4 l;; | 2.06% |
In water ZnS (pptd. in the heat, hot washed, well dried and pulverized); amount of H2S depends on concn. of acidic soln.; dilution: 1 mol NH4HSO4 in 8 l;; | 2.16% |
In water ZnS (pptd. in the heat, hot washed, well dried and pulverized); amount of H2S depends on concn. of acidic soln.; dilution: 1 mol NH4HSO4 in 1 l;; | 1.7% |
In water ZnS (pptd. in the heat, hot washed, well dried and pulverized); amount of H2S depends on concn. of acidic soln.; dilution: 1 mol NH4HSO4 in 2 l;; | 1.85% |
ammonium bisulfate
ethanolamine
sulfuric acid mono-(2-amino-ethyl ester)
Conditions | Yield |
---|---|
With ammonium sulfate |
Conditions | Yield |
---|---|
In neat (no solvent) heating;; | |
In water distillation of HCl;; | |
In neat (no solvent) heating at 280°C;; | |
In neat (no solvent) passing NH4Cl vapor over NH4HSO4;; | |
In water |
Conditions | Yield |
---|---|
With potassium sulfate In sulfuric acid byproducts: K2S2O8; Electrolysis; Pietzsch-Adolph process: anode: Pt/cathode: carbon (asbestos cord wound); presence of small amount of KHSO4;; | |
With K2SO4 In sulfuric acid byproducts: K2S2O8; aq. H2SO4; Electrolysis; Pietzsch-Adolph process: anode: Pt/cathode: carbon (asbestos cord wound); presence of small amount of KHSO4;; |
Conditions | Yield |
---|---|
With fluorine In water reaction by influence of F2 on the aq. soln., higher yields at decreasing influence times of F2;; |
Conditions | Yield |
---|---|
With potassium hydrogensulfate In sulfuric acid byproducts: K2S2O8; Electrolysis; Pietzsch-Adolph process: electrolytically yielded (NH4)2S2O8 is reacted with KHSO4 to form solid K2S2O8;; | |
In sulfuric acid Electrolysis; Loewenstein Riedel process: hydrolysis to H2O2 on distillation; Pt anode/diaphragm;; | |
In sulfuric acid Electrolysis; Loewenstein-Riedel process: hydrolysis to H2O2 by distillation;; |
Conditions | Yield |
---|---|
220°C, 15 to 60 min; |
ammonium bisulfate
sodium chloride
A
sodium hydrogen sulfate
B
ammonia
Conditions | Yield |
---|---|
In neat (no solvent) addn. of NaCl to molten NH4HSO4 leads to the formation of NH4NaSO4 and HCl, which reacts to NH3 and NaHSO4 by further heating;; | |
In neat (no solvent) addn. of NaCl to molten NH4HSO4 leads to the formation of NH4NaSO4 and HCl, which reacts to NH3 and NaHSO4 by further heating;; |
Conditions | Yield |
---|---|
220°C, 15 to 60 min; |
Conditions | Yield |
---|---|
In neat (no solvent) iron shavings are added to molten (NH4)HSO4;; product mixture obtained;; | |
In neat (no solvent) iron shavings are added to molten (NH4)HSO4;; product mixture obtained;; |
Conditions | Yield |
---|---|
In melt Co(II)-salt is molten in 5 - 6 parts of NH4HSO4;; crystn.;; |
calcium hydrogen phosphate
ammonium bisulfate
ammonium dihydrogen phosphate
Conditions | Yield |
---|---|
CaHPO4 was treated with equivalent amount of NH4HSO4;; | |
CaHPO4 was treated with equivalent amount of NH4HSO4;; |
ammonium bisulfate
Conditions | Yield |
---|---|
In neat (no solvent) FeSO4 is added to molten (NH4)HSO4;; product mixture obtained;; | |
In neat (no solvent) FeSO4 is added to molten (NH4)HSO4;; product mixture obtained;; |
ammonium bisulfate
sodium chloride
A
hydrogenchloride
B
sodium hydrogen sulfate
C
ammonia
Conditions | Yield |
---|---|
In not given formation of NaNH4SO4 on heating NH4HSO4 with NaCl at 400 °C; reaction of NaNH4SO4 forming NH3 and NaHSO4;; formation of a ammonia-free product;; | |
In not given formation of NaNH4SO4 on heating NH4HSO4 with NaCl; reaction of NaNH4SO4 forming NH3 and NaHSO4;; | |
In not given formation of NaNH4SO4 on heating NH4HSO4 with NaCl at 400 °C; reaction of NaNH4SO4 forming NH3 and NaHSO4;; formation of a ammonia-free product;; | |
In not given formation of NaNH4SO4 on heating NH4HSO4 with NaCl; reaction of NaNH4SO4 forming NH3 and NaHSO4;; |
IUPAC Name: Azanium hydrogen sulfate
The MF of Azanium hydrogen sulfate (CAS NO.7803-63-6) is H5NO4S.
The MW of Azanium hydrogen sulfate (CAS NO.7803-63-6) is 115.11.
Synonyms of Azanium hydrogen sulfate (CAS NO.7803-63-6): Ammonium bisulfate ; Ammonium hydrogensulfate ; Ammonium sulfate monobasic ; Sulfuric acid, monoammonium salt
Product Categories: Inorganics
Apperance: white crystalline powder or chunks
Boiling Point: 330 °C
Melting Point: 146.9 °C
Density; 1.79 g/mL at 25 °C(lit.)
Solubility in H2O: 1 M at 20 °C, clear, colorless
Sensitive: Hygroscopic
Merck: 13,500
Stability: Stable.Hygroscopic
EINECS: 232-265-5
Azanium hydrogen sulfate (CAS NO.7803-63-6) can be further neutralized with ammonia to form ammonium sulfate, a valuable fertilizer.Also used as analytical reagent and in the pharmaceutical industry.
Reported in EPA TSCA Inventory.
Moderately toxic by ingestion. A corrosive. See also SULFATES. Dangerous; when heated to decomposition it emits highly toxic fumes of sulfuric acid and SOx, NH3, and NOx.Safety information of Azanium hydrogen sulfate (CAS NO.7803-63-6):
Hazard Codes C
Risk Statements
34 Causes burns
Safety Statements
26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36/37/39 Wear suitable protective clothing, gloves and eye/face protection
45 In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
RIDADR UN 2506 8/PG 2
WGK Germany 1
F 3
HazardClass 8
PackingGroup II
DOT Classification: 8; Label: Corrosive
Ammonium bisulfate, also known as ammonium hydrogen sulfate, is a white, crystalline solid when it is completely pure, with formula (NH4)HSO4. It is commonly collected as a byproduct of flue gas desulfurization, formed by partial neutralization of sulfuric acid (H2SO4) aerosols by gaseous ammonia, NH3. Indeed, the solid material can collect on and foul solid surfaces in the flues. It is too acidic for most end uses, and is corrosive to the skin.
It react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.
When heated to high temperatures, Ammonium hydrogen sulfate may release toxic sulfur oxide and nitrogen oxide fumes. Ammonium hydrogen sulfate is soluble in water. Ammonium hydrogen sulfate is a chemical catalyst, used in hair preparations.
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