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7646-93-7
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???(??):
????;????(POTASSIUMHYDROGENSULFATE);??????(VI)
???:
Potassium bisulfate
???(??):
KHSO4;POTASSIUM HYDROGEN SULFATE;POTASSIUM BISULPHATE;POTASSIUM HYDROGEN SULPHATE;Kaliumhydrogensulfat;POTASSIUM HYDROGEN SULPHATE pure;salenixum;Potassium bisuL;POTASSIUM BISULFATE;monopotassiumsulfate
CBNumber:
CB9370612
???:
HKO4S
??? ??:
136.16884
MOL ??:
7646-93-7.mol

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214 °C(lit.)
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decomposes [STR93]
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2.32 g/mL at 25 °C(lit.)
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1140kg/m3
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Store at +5°C to +30°C.
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H2O: 1 M at 20 °C, ??, ??
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Specific Gravity
2.322
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??????(pH)
1 (50g/l, H2O, 20℃)
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Hygroscopic
Merck
14,7613
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InChI
1S/K.H2O4S/c;1-5(2,3)4/h;(H2,1,2,3,4)/q+1;/p-1
InChIKey
CHKVPAROMQMJNQ-UHFFFAOYSA-M
SMILES
[K+].OS([O-])(=O)=O
CAS ??????
7646-93-7(CAS DataBase Reference)
EPA
Potassium bisulfate (7646-93-7)
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  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? C
?? ???? ?? 34-37
????? 26-36/37/39-45
????(UN No.) UN 2509
WGK ?? 1
RTECS ?? TS7200000
F ?????? 3
TSCA TSCA listed
HS ?? 2833 29 80
?? ?? 8
???? II
???? ??? 8B - Non-combustible corrosive hazardous materials
Hazard Classifications Eye Dam. 1
Skin Corr. 1B
STOT SE 3
?? LD50 orally in Rabbit: 2340 mg/kg
???? ?? KE-32642
????(GHS): Corrosion (GHS05)Exclamation Mark (GHS07)
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H303 ??? ??? ? ?? ?? ?? ?? - ?? ?? 5 P312
H314 ??? ?? ??? ?? ??? ??? ????? ?? ????? ?? 1A, B, C ?? P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
H335 ?? ???? ??? ? ?? ?? ???? ?? - 1? ??;???? ?? ?? 3 ??
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P260 ??·?·??·???·??·...·????? ???? ???.
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P271 ?? ?? ??? ? ?? ???? ?????.
P280 ????/???/???/?????? ?????.
P301+P330+P331 ???? ?? ?????. ??? ?? ?? ???.
P303+P361+P353 ??(?? ????)? ??? ??? ?? ??? ??? ????? ??? ?? ????/?????.
P312 ???? ??? ????(??)? ??? ????.
P363 ?? ??? ??? ??? ?????.
P403+P233 ??? ??? ? ?? ?? ??? ???? ?????.
P405 ???? ?????.
P501 ...? ??? / ??? ?? ???.
NFPA 704
0
3 1

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Potassium bisulfate, also known as potassium hydrogen sulfate and potassium acid sulfate, KHS04 is water soluble, white deliquescent crystals,which melt at 214°C. Potassium bisulfate dissolved in water undergoes ionization to form K+, H+, SO42-. It is used in wine making, fertilizer manufacture, and as a flux and food preservative.

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Potassium bisulfate may be used:
As a catalyst for the preparation of butyl paraben from p-hydroxybenzoic acid and n-butyl alcohol.
As a promoter for the synthesis of 3,4-dihydropyrimidin-2(1H)-one derivatives via Biginelli reaction in ethylene glycol.
As an acid catalyst for the synthesis of ethyl tert-butyl ether (ETBE) from ethanol and tert-butyl alcohol via reactive distillation.
As a dehydrating agent for the synthesis of pyruvic acid from tartaric acid.

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Potassium bisulfate is typically made by heating potassium sulfate (K2SO4) with sulfuric acid. The acid provides the hydrogen needed to convert the salt (K2SO4) to the corresponding acid salt (KHSO4).

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Potassium hydrogen sulfate is a colorless crystalline solid with a sulfur odor. It may cause illness from ingestion. If heated to high temperatures it may emit toxic fumes. It is used as flux in analysis of ores and siliceous Compounds.

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Fused salt is deliquescent, Soluble in water, yielding a corrosive acidic solution.

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Acidic salts, such as Potassium bisulfate , are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They 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.

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TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

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Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Safety Profile

Moderately toxic by ingestion. A corrosive irritant to the skin, eyes, and mucous membranes. When heated to decomposition it emits toxic fumes of SOx and K2O. Can form an explosive mixture. See also SULFATES.

Purification Methods

Crystallise it from H2O (1mL/g) between 100o and 0o. It is also formed when a warm solution of K2SO4 in conc H2SO4 is cooled down.

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