Product Name

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  • Name

    Sulfuric(VI) acid

  • EINECS 231-639-5
  • CAS No. 7664-93-9
  • Article Data1730
  • CAS DataBase
  • Density 2.2 g/cm3
  • Solubility miscible with water
  • Melting Point 10 °C
  • Formula H2O4S
  • Boiling Point 330.001 °C at 760 mmHg
  • Molecular Weight 98.0795
  • Flash Point 11°C
  • Transport Information UN 3264 8/PG 3
  • Appearance clear colorless oily liquid
  • Safety 26-30-45-36/37-16
  • Risk Codes 36/38-35-39-23/24/25-11
  • Molecular Structure Molecular Structure of 7664-93-9 (Sulfuric(VI) acid)
  • Hazard Symbols CorrosiveC
  • Synonyms Dihydrogen sulfate;Dipping acid;NSC 248648;Oil of vitriol;Sulphuric acid;Vitriol brown oil;Sulfuricacid;
  • PSA
  • LogP

Synthetic route

sulfur dioxide
7446-09-5

sulfur dioxide

water
7732-18-5

water

iodine
7553-56-2

iodine

A

sulfuric acid
7664-93-9

sulfuric acid

B

hydrogen iodide
10034-85-2

hydrogen iodide

Conditions
ConditionsYield
0 - 25 °C; part of a Mg-S-I water splitting cycle;A 100%
B 100%
sulfur dioxide
7446-09-5

sulfur dioxide

water
7732-18-5

water

A

sulfuric acid
7664-93-9

sulfuric acid

B

sulfur
7704-34-9

sulfur

Conditions
ConditionsYield
at 170-180°C; in very dilute soln. complete decompn. in 2 h, incomplete decompn. in concd. solns.;A n/a
B 100%
byproducts: H2S4O6;
sodium thiosulfate In water 100°C;
carbon oxide sulfide
463-58-1

carbon oxide sulfide

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

A

carbon dioxide
124-38-9

carbon dioxide

B

sulfuric acid
7664-93-9

sulfuric acid

C

water
7732-18-5

water

Conditions
ConditionsYield
With potassium sulfate; potassium hydrogensulfate; potassium peroxomonosulfate In water Kinetics; oxidation of OCS studied in round-bottom Pyrex bulbs, acid-water mixtures introduced into bulbs and degassed, bulb reactors filled with with a gas mixture slightly above 1 atm total pressure with a typical mixing ratio of OCS:Ar:He=40:60:700 Torr; gas chromy. and mass spectroscopy applied for determination of product content;A 100%
B n/a
C n/a
With sulfuric acid In water Kinetics; oxidation of OCS studied in round-bottom Pyrex bulbs, acid-water mixtures introduced into bulbs and degassed, bulb reactors filled with with a gas mixture slightly above 1 atm total pressure with a typical mixing ratio of OCS:Ar:He=40:60:700 Torr; gas chromy. and mass spectroscopy applied for determination of product content;A 100%
B n/a
C n/a
sulfur dioxide
7446-09-5

sulfur dioxide

oxygen
80937-33-3

oxygen

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
With sulfuric acid; ammonia absorption of dild. SO2 in aq. soln. of NH3, eliberation with H2SO4, O2 from water electrolysis, 3-layer contact bed, heat exchanger, 3 H2SO4 absorbers, coke filter, tail gas recirculation, 528-682°C;99.5%
With NH3; H2SO4; catalyst: V compd. absorption of dild. SO2 in aq. soln. of NH3, eliberation with H2SO4, O2 from water electrolysis, 3-layer contact bed, heat exchanger, 3 H2SO4 absorbers, coke filter, tail gas recirculation, 528-682°C;99.5%
ferric hydroxide In not given 125-130°C, Fe(OH)3 on pumice or asbestos;
sulfur
7704-34-9

sulfur

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
With air moist air introductions into four-stage contact furnace, 2-stage drum absorber, washing of tail gas in Venturi app.; 93-95 % acid concn.;99%
With air moist air introductions into four-stage contact furnace, 2-stage drum absorber, washing of tail gas in Venturi app.; 93-95 % acid concn.;99%
With catalyst: V compd. moist S roaster gas, absorption in concd. acid;
Marshall's acid
13445-49-3

Marshall's acid

tin(ll) chloride

tin(ll) chloride

A

sulfuric acid
7664-93-9

sulfuric acid

B

tin(IV) chloride
7646-78-8

tin(IV) chloride

Conditions
ConditionsYield
In hydrogenchloride room temp.; 10-15 min.;A n/a
B 99%
In hydrogenchloride room temp.; 10-15 min.;A n/a
B 99%
bromic acid
7789-31-3

bromic acid

A

sulfuric acid
7664-93-9

sulfuric acid

B

bromine
7726-95-6

bromine

Conditions
ConditionsYield
With sulphurous acid byproducts: H2O;A n/a
B 99%
With H2SO3 byproducts: H2O;A n/a
B 99%
sulfur dioxide
7446-09-5

sulfur dioxide

A

sulfuric acid
7664-93-9

sulfuric acid

B

sulfur
7704-34-9

sulfur

Conditions
ConditionsYield
In not given Electrolysis; Pt anode, graphite cathode, area of the electrodes 30 cm^2, 1 A, 20 min, 0.208 mg/l SO2 soln.;A 98.16%
B 70.87%
In not given Electrolysis; Pt anode, graphite cathode, area of the electrodes 30 cm^2, 1 A, 20 min, 0.420 mg/l SO2 soln.;A 98.52%
B 74.28%
In not given Electrolysis; Pt anode, graphite cathode, area of the electrodes 30 cm^2, 1 A, 20 min, 1.123 mg/l SO2 soln.;A 98.86%
B 74.2%
pyrite

pyrite

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
3-stage contact with heat exchangers, for pyrite roaster gas;98%
With air burning at 820°C in rotating furnace, elec. filter, washing, air addn., wet elec. filter, drying, heat exchanger, two-stage inner cooling, cooler, absorption, cooling;
With nitric acid formation of H2SO4 by reaction of HNO3 with pyrite; faster reaction at 100 °C than at higher temperature;;
With air; catalyst: V2O5 - K2O - SiO2 burning at 820°C in rotating furnace, elec. filter, washing, air addn., wet elec. filter, drying, heat exchanger, two-stage inner cooling, cooler, absorption, cooling;
sulfur dioxide
7446-09-5

sulfur dioxide

water
7732-18-5

water

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
With (CN)2 In water byproducts: HCN; with (CN)2 excess for 4-5 days at room temp.;94%
contact oven with intermediate heat exchangers, temp. regulation by fresh air addn., H2O to inlet gas, SO2 recycling;80%
condensation after contact furnace at 175. degree.C; 66.3 % acid concn.;46.7%
sodium sulfate
7757-82-6

sodium sulfate

A

sulfuric acid
7664-93-9

sulfuric acid

B

sodium hydroxide
1310-73-2

sodium hydroxide

Conditions
ConditionsYield
In water Electrolysis; formation of PbSO4 on Pb-anode; electrolysis of PbSO4;A 91%
B 91%
With H2O Electrolysis;
In water Electrolysis;
sulphurous acid
7782-99-2

sulphurous acid

chloric acid
7790-93-4

chloric acid

A

sulfuric acid
7664-93-9

sulfuric acid

B

chlorine dioxide
10049-04-4, 25052-55-5

chlorine dioxide

C

water
7732-18-5

water

Conditions
ConditionsYield
With air; sulfur dioxide In sulfuric acid byproducts: HClO, HCl, Cl2; Holst-process;;A n/a
B 90%
C n/a
chlorosulfonic acid
7790-94-5

chlorosulfonic acid

A

sulfuryl dichloride
7791-25-5

sulfuryl dichloride

B

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
uranyl chloride In neat (no solvent) equilibrium on thermal decompn.;; distillation;;A 90%
B n/a
mercury In neat (no solvent) equilibrium on thermal decompn.;; distillation;;A 90%
B n/a
bismuth(III) chloride In neat (no solvent) equilibrium on thermal decompn.;; distillation;;A 90%
B n/a
vanadyl(IV) sulphate pentahydrate

vanadyl(IV) sulphate pentahydrate

5-Chloro-1,10-phenanthroline
4199-89-7

5-Chloro-1,10-phenanthroline

bromanilic acid
4370-59-6

bromanilic acid

(VO)2(Br2C6O4)(C12H7ClN2)2(2+)*SO4(2-)=[(VO)2(Br2C6O4)(C12H7ClN2)2](SO4)
230953-51-2

(VO)2(Br2C6O4)(C12H7ClN2)2(2+)*SO4(2-)=[(VO)2(Br2C6O4)(C12H7ClN2)2](SO4)

B

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
In methanol dropwise addn. of soln. of VOSO4 to soln of bromanilic acid, addn. of soln. of N-ligand (stirring, room temp.), refluxing (8 h; crystn.); filtration, washing (MeOH, Et2O), drying (vac., over P2O5), recrystn. (DMF/EtOH); elem. anal.;A 88%
B n/a
chlorosulfonic acid
7790-94-5

chlorosulfonic acid

A

pyrosulfuryl chloride
7791-27-7

pyrosulfuryl chloride

B

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
Stage #1: chlorosulfonic acid With Acetanilid at 26 - 45℃; for 9.2h;
Stage #2: With thionyl chloride at 55℃; for 6.4h; Temperature; Further stages;
A 87%
B n/a
vanadyl(IV) sulphate pentahydrate

vanadyl(IV) sulphate pentahydrate

2.9-dimethyl-1,10-phenanthroline
484-11-7

2.9-dimethyl-1,10-phenanthroline

bromanilic acid
4370-59-6

bromanilic acid

(VO)2(Br2C6O4)((CH3)2C12H6N2)2(2+)*SO4(2-)=[(VO)2(Br2C6O4)((CH3)2C12H6N2)2](SO4)
230953-49-8

(VO)2(Br2C6O4)((CH3)2C12H6N2)2(2+)*SO4(2-)=[(VO)2(Br2C6O4)((CH3)2C12H6N2)2](SO4)

B

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
In methanol dropwise addn. of soln. of VOSO4 to soln of bromanilic acid, addn. of soln. of N-ligand (stirring, room temp.), refluxing (8 h; crystn.); filtration, washing (MeOH, Et2O), drying (vac., over P2O5), recrystn. (DMF/EtOH); elem. anal.;A 85%
B n/a
1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

vanadyl(IV) sulphate pentahydrate

vanadyl(IV) sulphate pentahydrate

bromanilic acid
4370-59-6

bromanilic acid

(VO)2(Br2C6O4)(C12H8N2)2(2+)*SO4(2-)=[(VO)2(Br2C6O4)(C12H8N2)2](SO4)
230953-47-6

(VO)2(Br2C6O4)(C12H8N2)2(2+)*SO4(2-)=[(VO)2(Br2C6O4)(C12H8N2)2](SO4)

B

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
In methanol dropwise addn. of soln. of VOSO4 to soln of bromanilic acid, addn. of soln. of N-ligand (stirring, room temp.), refluxing (8 h; crystn.); filtration, washing (MeOH, Et2O), drying (vac., over P2O5), recrystn. (DMF/EtOH); elem. anal.;A 81%
B n/a
aminosulfonic acid
5329-14-6

aminosulfonic acid

A

sulfuric acid
7664-93-9

sulfuric acid

B

nitrogen
7727-37-9

nitrogen

C

sodium chloride
7647-14-5

sodium chloride

Conditions
ConditionsYield
With chlorine In water introduction of chlorine into alkaline soln.; intermediates (NaSO3NCl2/NaSO3NHCl) decompose after short time in this soln.;;A n/a
B 79.65%
C n/a
With Cl2 In water introduction of chlorine into alkaline soln.; intermediates (NaSO3NCl2/NaSO3NHCl) decompose after short time in this soln.;;A n/a
B 79.65%
C n/a
[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

vanadyl(IV) sulphate pentahydrate

vanadyl(IV) sulphate pentahydrate

bromanilic acid
4370-59-6

bromanilic acid

(VO)2(Br2C6O4)(NC5H4C5H4N)2(2+)*SO4(2-)=[(VO)2(Br2C6O4)(NC5H4C5H4N)2](SO4)
230953-45-4

(VO)2(Br2C6O4)(NC5H4C5H4N)2(2+)*SO4(2-)=[(VO)2(Br2C6O4)(NC5H4C5H4N)2](SO4)

B

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
In methanol dropwise addn. of soln. of VOSO4 to soln of bromanilic acid, addn. of soln. of N-ligand (stirring, room temp.), refluxing (8 h; crystn.); filtration, washing (MeOH, Et2O), drying (vac., over P2O5), recrystn. (DMF/EtOH); elem. anal.;A 72%
B n/a
trisulfimide
13954-94-4

trisulfimide

A

ammonium bisulfate
7803-63-6

ammonium bisulfate

B

sulfuric acid
7664-93-9

sulfuric acid

C

SULFAMIDE
7803-58-9

SULFAMIDE

Conditions
ConditionsYield
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
trisulfimide
13954-94-4

trisulfimide

A

sulfuric acid
7664-93-9

sulfuric acid

B

aminosulfonic acid
5329-14-6

aminosulfonic acid

C

SULFAMIDE
7803-58-9

SULFAMIDE

Conditions
ConditionsYield
With water in the cold, 48 h, 2 M HCl;A 33%
B n/a
C n/a
With H2O in the cold, 48 h, 2 M HCl;A 33%
B n/a
C n/a
In water decompn. in aq. soln.; 0 and 22°C discussed; presece of acid discussed;;
dithionic acid
14970-71-9

dithionic acid

A

sulfuric acid
7664-93-9

sulfuric acid

B

sulfur dioxide
7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In water 0.2362 mM/g decompn. 46.8°C, 245 h.;A 19.96%
B n/a
In water 0.2401 mM/g decompn. 25.3°C, 945.25 h.;A 2.96%
B n/a
In water Kinetics;
water
7732-18-5

water

sulfur
7704-34-9

sulfur

sulfuric acid
7664-93-9

sulfuric acid

Conditions
ConditionsYield
condensation of humidified S burner gas;
absorption of moist gas to H2SO4;
In water in sealed tube;at 150°C;under 20 atm O2;;0.06%
4-bromo-5-methyl-2-phenyl-2H-pyrazole-3-sulfonic acid

4-bromo-5-methyl-2-phenyl-2H-pyrazole-3-sulfonic acid

bromine
7726-95-6

bromine

sulfuric acid
7664-93-9

sulfuric acid

bromine
7726-95-6

bromine

5,7,5',7'-tetrabromo-3,3'-dioxo-1,3,1',3'-tetrahydro-[2,2']biindolyl-2,2'-disulfonic acid

5,7,5',7'-tetrabromo-3,3'-dioxo-1,3,1',3'-tetrahydro-[2,2']biindolyl-2,2'-disulfonic acid

sulfuric acid
7664-93-9

sulfuric acid

trichloroisocyanuric acid
87-90-1

trichloroisocyanuric acid

sulphurous acid
7782-99-2

sulphurous acid

sulfuric acid
7664-93-9

sulfuric acid

bismuth
7440-69-9

bismuth

aqueous H2 O2

aqueous H2 O2

sulfuric acid
7664-93-9

sulfuric acid

pyrographite
7440-44-0

pyrographite

2-butyl-5-hydroxymethyl-1H-imidazole
68283-19-2

2-butyl-5-hydroxymethyl-1H-imidazole

platinum
7440-06-4

platinum

2-butyl-1H-imidazole-5-carboxaldehyde
68282-49-5

2-butyl-1H-imidazole-5-carboxaldehyde

Conditions
ConditionsYield
With sodium hydroxide In water100%
With sodium hydroxide In water98.2%
With sodium hydroxide In methanol; water94.5%
7-Chloro-4-hydroxy-2-(4-carboxyphenyl)-1,2,5,10-tetrahydropyridazino [4,5-b]quinoline-1,10-dione
170142-44-6

7-Chloro-4-hydroxy-2-(4-carboxyphenyl)-1,2,5,10-tetrahydropyridazino [4,5-b]quinoline-1,10-dione

sulfuric acid
7664-93-9

sulfuric acid

7-Chloro-4-hydroxy-2-(4-carboxymethylphenyl)-1,2,5,10-tetrahydropyridazino [4,5-b]quinoline-1,10-dione

7-Chloro-4-hydroxy-2-(4-carboxymethylphenyl)-1,2,5,10-tetrahydropyridazino [4,5-b]quinoline-1,10-dione

Conditions
ConditionsYield
In methanol100%
sulfuric acid
7664-93-9

sulfuric acid

cadmium(II) sulphide

cadmium(II) sulphide

cadmium sulfate

cadmium sulfate

Conditions
ConditionsYield
In hydrogenchloride; sulfuric acid dissolving CdS in HCl, evapn. to dryness, dissoln. in dild. H2SO4, evapn. with a drop of concd. HNO3;100%
In hydrogenchloride; sulfuric acid aq. H2SO4; dissolving CdS in HCl, evapn. to dryness, dissoln. in dild. H2SO4, evapn. with a drop of concd. HNO3;100%
sulfuric acid
7664-93-9

sulfuric acid

hydrogen iodide
10034-85-2

hydrogen iodide

magnesium oxide

magnesium oxide

A

magnesium sulfate
7487-88-9

magnesium sulfate

B

magnesium iodide

magnesium iodide

Conditions
ConditionsYield
70 °C; 1-2. step of Mg-S-I water splitting cycle;A 100%
B 100%
[Fe(μ-S2(CH2)3)(CN)(CO)4(PMe3)](1-)
392334-61-1, 371241-08-6, 392333-87-8, 1226500-22-6

[Fe(μ-S2(CH2)3)(CN)(CO)4(PMe3)](1-)

sulfuric acid
7664-93-9

sulfuric acid

hydrogen
1333-74-0

hydrogen

Conditions
ConditionsYield
In water Electrolysis; electrolysis of soln. of Fe2(CO)4(CN)(PMe3)S2(CH2)3 with 50 equiv. H2SO4at -1.2 V for 15 min; GC analysis;100%
barium sulfate

barium sulfate

sulfuric acid
7664-93-9

sulfuric acid

Ba(2+)*SO4(2-)*2H2SO4*H2O=BaSO4*2H2SO4*H2O

Ba(2+)*SO4(2-)*2H2SO4*H2O=BaSO4*2H2SO4*H2O

Conditions
ConditionsYield
With water In sulfuric acid digesting; concn. of H2SO4 in aq. H2SO4 >93%; pptn. by adjusting H2SO4 concn. to 84.15%-93% with water;100%
With H2O In sulfuric acid aq. H2SO4; digesting; concn. of H2SO4 in aq. H2SO4 >93%; pptn. by adjusting H2SO4 concn. to 84.15%-93% with water;100%
With water In sulfuric acid uptake of water from the air;
0.34K(1+)*0.7H2O*NbS2(034-)=K0.34(H2O)0.7NbS2

0.34K(1+)*0.7H2O*NbS2(034-)=K0.34(H2O)0.7NbS2

sulfuric acid
7664-93-9

sulfuric acid

0.34H3O(1+)*NbS2(034-)=(H3O)0.34NbS2

0.34H3O(1+)*NbS2(034-)=(H3O)0.34NbS2

Conditions
ConditionsYield
In sulfuric acid aq. H2SO4; Nb-contg. compd. was treated in aq. H2SO4 for 48 h;100%
4-(3-methylimidazolium)butanesulfonate

4-(3-methylimidazolium)butanesulfonate

sulfuric acid
7664-93-9

sulfuric acid

1-methyl-3-(4-sulfobutyl)-1H-imidazol-3-ium hydrogensulfate
827320-59-2

1-methyl-3-(4-sulfobutyl)-1H-imidazol-3-ium hydrogensulfate

Conditions
ConditionsYield
In toluene at 80℃; for 24h;100%
4-(pyridinium-1-yl)butane-1-sulfonate
21876-43-7

4-(pyridinium-1-yl)butane-1-sulfonate

sulfuric acid
7664-93-9

sulfuric acid

N-(4-sulphonic acid)butylpyridinium hydrogen sulphate
827320-61-6

N-(4-sulphonic acid)butylpyridinium hydrogen sulphate

Conditions
ConditionsYield
In toluene at 80℃; for 24h;100%
ammonium sulfate

ammonium sulfate

sulfuric acid
7664-93-9

sulfuric acid

sulfur trioxide
7446-11-9

sulfur trioxide

boric acid
11113-50-1

boric acid

3H3N*3H(1+)*B(SO4)3(3-)

3H3N*3H(1+)*B(SO4)3(3-)

Conditions
ConditionsYield
at 300℃; for 3h;100%
strontium(II) carbonate
1633-05-2

strontium(II) carbonate

sulfuric acid
7664-93-9

sulfuric acid

sulfur trioxide
7446-11-9

sulfur trioxide

boric acid
11113-50-1

boric acid

Sr(2+)*2{B(SO4)2}(1-)=Sr{B(SO4)2}2

Sr(2+)*2{B(SO4)2}(1-)=Sr{B(SO4)2}2

Conditions
ConditionsYield
at 180℃; for 24h;100%
bismuth
7440-69-9

bismuth

sulfuric acid
7664-93-9

sulfuric acid

bismuth(III) sulfate

bismuth(III) sulfate

Conditions
ConditionsYield
In further solvent(s) H2SO4 was added to Bi in HNO3 with stirring and heating; more H2SO4 wasadded and suspn. was heated for 40 h; heated in a muffle furnace at 648K; elem. anal.;99.8%
In sulfuric acid byproducts: SO2; by dissolving in boiling concd. H2SO4;;
In sulfuric acid byproducts: SO2; very weak reaction with diluted H2SO4.;;
In nitric acid Bi dissolved in HNO3 and treated with H2SO4, heated for several hours at 380 °C;;
2-(bromomethyl)-3-methylbutanoic acid
24766-14-1

2-(bromomethyl)-3-methylbutanoic acid

sulfuric acid
7664-93-9

sulfuric acid

isobutene
115-11-7

isobutene

2-Bromomethyl-3-methyl-butyric acid tert-butyl ester
224178-55-6

2-Bromomethyl-3-methyl-butyric acid tert-butyl ester

Conditions
ConditionsYield
With sodium hydrogencarbonate In dichloromethane99%
2,4,6-trimethyl-pyridine
108-75-8

2,4,6-trimethyl-pyridine

N-methylcyclohexylamine
100-60-7

N-methylcyclohexylamine

sulfuric acid
7664-93-9

sulfuric acid

tetrabutylammomium bromide
1643-19-2

tetrabutylammomium bromide

N-Isobutenyloxycarbonyl-N-methylcyclohexylamine

N-Isobutenyloxycarbonyl-N-methylcyclohexylamine

Conditions
ConditionsYield
In 1,1,2,2-tetrachloroethylene99%
N-nitroso-N-cyclohexylhydroxylamine potassium salt
27697-50-3

N-nitroso-N-cyclohexylhydroxylamine potassium salt

sulfuric acid
7664-93-9

sulfuric acid

N-nitroso-N-cyclohexylhydroxylamine aluminum salt

N-nitroso-N-cyclohexylhydroxylamine aluminum salt

Conditions
ConditionsYield
In water; toluene99%
molybdenum (II) chloride

molybdenum (II) chloride

sulfuric acid
7664-93-9

sulfuric acid

Mo6Cl8(4+)*2SO4(2-)=[Mo6Cl8](SO4)2

Mo6Cl8(4+)*2SO4(2-)=[Mo6Cl8](SO4)2

Conditions
ConditionsYield
In methanol byproducts: HCl; concd. H2SO4 is added to a soln. of the cluster in MeOH, HCl is evolvedand soln. is warmed up; soln. is heated to remove HCl and concd., soln. is diluted with MeOH, ppt.is sepd., washed and dried over P2O5, elem. anal.;99%
cis-dichloro(ethylenediamine)palladium(II)
15020-99-2

cis-dichloro(ethylenediamine)palladium(II)

sulfuric acid
7664-93-9

sulfuric acid

thiourea
17356-08-0

thiourea

(Pd(Thio)4SO4)

(Pd(Thio)4SO4)

Conditions
ConditionsYield
With acetic acid In water soln. PdEnCl2 in water was treated under heating in water bath with saturated aq. thiourea acidified with acetic acid, in 30 min 2 M H2SO4 was added; ppt. was filtered, washed with diluted H2SO4 and water, and dried;99%
Pt2(6+)*2O2(2-)*2OH(1-)*32K(1+)*32HSO4(1-)=[Pt2(O2)2(OH)2]*32KHSO4

Pt2(6+)*2O2(2-)*2OH(1-)*32K(1+)*32HSO4(1-)=[Pt2(O2)2(OH)2]*32KHSO4

sulfuric acid
7664-93-9

sulfuric acid

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

Conditions
ConditionsYield
In sulfuric acid aq. H2SO4; room temp.;99%
Pt2(6+)*2O2(2-)*2OH(1-)*20K(1+)*20HSO4(1-)=[Pt2(O2)2(OH)2]*20KHSO4

Pt2(6+)*2O2(2-)*2OH(1-)*20K(1+)*20HSO4(1-)=[Pt2(O2)2(OH)2]*20KHSO4

sulfuric acid
7664-93-9

sulfuric acid

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

Conditions
ConditionsYield
In sulfuric acid aq. H2SO4; room temp.;99%
Pt2(6+)*2O2(2-)*2OH(1-)*24K(1+)*24HSO4(1-)=[Pt2(O2)2(OH)2]*24KHSO4

Pt2(6+)*2O2(2-)*2OH(1-)*24K(1+)*24HSO4(1-)=[Pt2(O2)2(OH)2]*24KHSO4

sulfuric acid
7664-93-9

sulfuric acid

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

Conditions
ConditionsYield
In sulfuric acid aq. H2SO4; room temp.;99%
Pt2(6+)*2O2(2-)*2OH(1-)*28K(1+)*28HSO4(1-)=[Pt2(O2)2(OH)2]*28KHSO4

Pt2(6+)*2O2(2-)*2OH(1-)*28K(1+)*28HSO4(1-)=[Pt2(O2)2(OH)2]*28KHSO4

sulfuric acid
7664-93-9

sulfuric acid

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

Conditions
ConditionsYield
In sulfuric acid aq. H2SO4; room temp.;99%
Pt2(6+)*2O2(2-)*2OH(1-)*10K(1+)*10HSO4(1-)=[Pt2(O2)2(OH)2]*10KHSO4

Pt2(6+)*2O2(2-)*2OH(1-)*10K(1+)*10HSO4(1-)=[Pt2(O2)2(OH)2]*10KHSO4

sulfuric acid
7664-93-9

sulfuric acid

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

2K(1+)*Pt2(6+)*4SO4(2-)*2H2O=K2[Pt2(SO4)4(H2O)2]

Conditions
ConditionsYield
In sulfuric acid aq. H2SO4; room temp.;99%

Sulfuric acid History

The discovery of sulfuric acid is credited to the 8th century Muslim chemist and alchemist, Jabir ibn Hayyan (Geber). The acid was later studied by 9th century Persian physician and alchemist Ibn Zakariya al-Razi (Rhazes), who obtained the substance by dry distillation of minerals including iron(II) sulfate heptahydrate, FeSO4·7H2O, and copper(II) sulfate pentahydrate, CuSO4·5H2O.
In the 17th century, the German-Dutch chemist Johann Glauber prepared sulfuric acid by burning sulfur together with saltpeter (potassium nitrate, KNO3), in the presence of steam
Sulfuric acid created by John Roebuck's process only approached a 35–40% concentration.
Later refinements to the lead-chamber process by French chemist Joseph-Louis Gay-Lussac and British chemist John Glover improved the yield to 78%.
Throughout the 18th century, this could only be made by dry distilling minerals in a technique similar to the original alchemical processes.
In 1831, British vinegar merchant Peregrine Phillips patented the contact process, which was a far more economical process for producing sulfur trioxide and concentrated sulfuric acid. Today, nearly all of the world's sulfuric acid is produced using this method.

Sulfuric acid Consensus Reports

Reported in EPA TSCA Inventory.

Sulfuric acid Standards and Recommendations

OSHA PEL: TWA 1 mg/m3
ACGIH TLV: TWA 1 mg/m3; STEL 3 mg/m3; Suspected Human Carcinogen (Contained in strong inorganic mists); (Proposed: TWA 0.2 mg/m3; Suspected Human Carcinogen (Contained in strong inorganic mists))
DFG MAK: 1 mg/m3
NIOSH REL: (Sulfuric Acid) TWA 1 mg/m3
DOT Classification:  8; Label: Corrosive

Sulfuric acid Analytical Methods

 Sulfuric acid (CAS NO.7664-93-9) ,its occupational chemical analysis uses OSHA: #ID-113 or NIOSH: Acids, inorganic, 7903.

 

Sulfuric acid Specification

Sulfuric acid (alternative spelling sulphuric acid), with the cas number 7664-93-9, is a highly corrosive strong mineral acid with the molecular formula H2 SO4. It is a pungent-ethereal, colorless to slightly yellow viscous liquid which is soluble in water at all concentrations.Sometimes, it may be dark brown as dyed during its industrial production process in order to alert people to its hazards.

Physical properties about Sulfuric acid are: (1)ACD/LogP: -1.114; (2)ACD/LogD (pH 5.5): -5.61; (3)ACD/LogD (pH 7.4): -5.61; (4)ACD/BCF (pH 5.5): 1.00; (5)ACD/BCF (pH 7.4): 1.00; (6)#H bond acceptors: 4; (7)#H bond donors: 2; (8)Index of Refraction: 1.537; (9)Molar Refractivity: 13.925 cm3; (10)Molar Volume: 44.58 cm3; (11)Polarizability: 5.52 10-24cm3; (12)Surface Tension: 124.13500213623 dyne/cm; (13)Density: 2.2 g/cm3; (14)Enthalpy of Vaporization: 62.935 kJ/mol; (15)Boiling Point: 330.001 °C at 760 mmHg

Preparation of Sulfuric acid: The manufacture of Sulfuric acid (CAS NO.7664-93-9) by the lead chamberprocess involves oxidation of sulfur to sulfur dioxide by oxygen, further oxidation of sulfur dioxide to sulfur trioxide with nitrogen dioxide, and, finally, hydrolysis of sulfur trioxide.

S + O2 → SO2
2NO + O2→ 2NO2
SO2 + NO2 → SO3 + NO
SO3 + H2O → H2SO4

Modifications of the process include towers to recover excess nitrogen oxides and to increase the final acid concentration from 65% (chamber acid) to 78% (tower acid).
The contact process has evolved to become the method of choice for sulfuric acid manufacture because of the ability of the process to produce stronger acid.

S + O2 → SO2
2SO2 + O2 → 2SO3
SO3 + H2O → H2SO4

In the process, sulfur and oxygen are converted to sulfur dioxide at 1000 °C and then cooled to 420 °C. The sulfur dioxide and oxygen enter the converter, which contains a catalyst such as vanadium pentoxide (V2O5). About 60 to 65% of the sulfur dioxide is converted by an exothermic reaction to sulfur trioxide in the first layer with a 2 to 4-second contact time. The gas leaves the converter at 600°C and is cooled to 400°C before it enters the second layer of catalyst. After the third layer, about 95% of the sulfur dioxide is converted into sulfur trioxide. The mixture is then fed to the initial absorption tower, where the sulfur trioxide is hydrated to sulfuric acid after which the gas mixture is reheated to 420 °C and enters the fourth layer of catalyst that gives overall a 99.7% conversion of sulfur dioxide to sulfur trioxide. It is cooled and then fed to the final absorption tower and hydrated to sulfuric acid. The final sulfuric acid concentration is 98 to 99% (1 to 2% water). A small amount of this acid is recycled by adding some water and recirculating into the towers to pick up more sulfur trioxide.

Uses of Sulfuric acid: Although Sulfuric acid is the common starting raw material, other sources of Sulfuric acid (CAS NO.7664-93-9) can be used, including iron, copper, lead, nickel, and zinc sulfides. Hydrogen sulfide, a by-product of petroleum refining and natural gas refining, can be burned to sulfur dioxide. Gypsum (CaSO4) can also be used but needs high temperatures to be converted to sulfur dioxide. Other uses for it include the manufacture of fertilizers, chemicals, inorganic pigments, petroleum refining, etching, as a catalyst in alkylation processes, in electroplating baths, for pickling and other operations in iron and steel production, in rayon and film manufacture, in the making of explosives, and in nonferrous metallurgy.

When you are using this chemical, please be cautious about it as the following:
In case of contact with eyes, rinse immediately with plenty of water and seek medical advice;
Never add water to this product;
In case of accident or if you feel unwell, seek medical advice immediately (show label where possible);?
Wear suitable protective clothing and gloves;

You can still convert the following datas into molecular structure:
(1)InChI=1S/H2O4S/c1-5(2,3)4/h(H2,1,2,3,4);
(2)InChIKey=QAOWNCQODCNURD-UHFFFAOYSA-N;
(3)SmilesS(=O)(=O)(O)O;

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
guinea pig LC50 inhalation 18mg/m3 (18mg/m3) LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES Medicina del Lavoro. Industrial Medicine. Vol. 45, Pg. 590, 1954.
 
human TCLo inhalation 1mg/m3/3H (1mg/m3) LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES Inhalation Toxicology. Vol. 9, Pg. 731, 1997.
human TCLo inhalation 3mg/m3/24W (3mg/m3) MUSCULOSKELETAL: CHANGES IN TEETH AND SUPPORTING STRUCTURES British Journal of Industrial Medicine. Vol. 18, Pg. 63, 1961.
 
man LDLo unreported 135mg/kg (135mg/kg)   "Poisoning; Toxicology, Symptoms, Treatments," 2nd ed., Arena, J.M., Springfield, IL, C.C. Thomas, 1970Vol. 2, Pg. 73, 1970.
mouse LC50 inhalation 320mg/m3/2H (320mg/m3)   "Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 107, 1982.
rat LC50 inhalation 510mg/m3/2H (510mg/m3)   "Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 107, 1982.
rat LD50 oral 2140mg/kg (2140mg/kg)   American Industrial Hygiene Association Journal. Vol. 30, Pg. 470, 1969.

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