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10192-85-5

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  • High Quality POTASSIUM ACRYLATE CAS 10192-85-5 Best Price

    Cas No: 10192-85-5

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10192-85-5 Usage

General Description

Potassium acrylate is the potassium salt of acrylic acid, a common industrial chemical. It is a white, crystalline substance, typically used as a thickening agent in cosmetics and personal care products. Potassium acrylate is also known for its water-absorbing properties and is used in products such as diapers and sanitary napkins to enhance absorbency. It is considered to be a safe and non-toxic chemical when used in approved applications and concentrations. However, it can be a skin and eye irritant in its pure form, and proper safety precautions must be taken when handling and using this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 10192-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,9 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10192-85:
(7*1)+(6*0)+(5*1)+(4*9)+(3*2)+(2*8)+(1*5)=75
75 % 10 = 5
So 10192-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H4O2.K/c1-2-3(4)5;/h2H,1H2,(H,4,5);/q;+1/p-1

10192-85-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L10079)  Potassium acrylate hydrate, 95%   

  • 10192-85-5

  • 5g

  • 306.0CNY

  • Detail
  • Alfa Aesar

  • (L10079)  Potassium acrylate hydrate, 95%   

  • 10192-85-5

  • 25g

  • 1302.0CNY

  • Detail

10192-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name POTASSIUM ACRYLATE

1.2 Other means of identification

Product number -
Other names Propenoic acid potassium salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Surface active agents
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:10192-85-5 SDS

10192-85-5Synthetic route

acrylic acid
79-10-7

acrylic acid

potassium acrylate
10192-85-5

potassium acrylate

Conditions
ConditionsYield
With potassium hydroxide
ethene
74-85-1

ethene

carbon dioxide
124-38-9

carbon dioxide

potassium acrylate
10192-85-5

potassium acrylate

Conditions
ConditionsYield
With bis(1,5-cyclooctadiene)nickel(0); 1,2-bis-(dicyclohexylphosphino)ethane In toluene at 50 - 100℃; under 23272.3 Torr; Solvent; Pressure; Autoclave;
With RuP(CH2CH2P(C6H5)2)3(C2H4); potassium tert-butylate In N,N-dimethyl acetamide at 140℃; under 22502.3 Torr; for 12h; Catalytic behavior; Reagent/catalyst; Temperature; Solvent; Inert atmosphere; Autoclave;
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; 1,2-bis-(dicyclohexylphosphino)ethane at 120℃; under 7500.75 - 22502.3 Torr; for 18h; Autoclave;
ethene
74-85-1

ethene

C45H46O2P4Ru

C45H46O2P4Ru

potassium ethoxide
917-58-8

potassium ethoxide

A

RuP(CH2CH2P(C6H5)2)3(C2H4)
195048-79-4

RuP(CH2CH2P(C6H5)2)3(C2H4)

B

potassium acrylate
10192-85-5

potassium acrylate

Conditions
ConditionsYield
In N,N-dimethyl acetamide at 60℃; under 750.075 Torr; for 2h; Inert atmosphere; Sealed tube;A 96 %Spectr.
B 68 %Spectr.
2-(n-perfluorooctyl)ethyl iodide
2043-53-0

2-(n-perfluorooctyl)ethyl iodide

potassium acrylate
10192-85-5

potassium acrylate

1H,1H,2H,2H-heptadecafluorodecyl acrylate
27905-45-9

1H,1H,2H,2H-heptadecafluorodecyl acrylate

Conditions
ConditionsYield
With 4-methoxy-phenol; hydroquinone In tert-butyl alcohol at 180℃; for 6h; Conversion of starting material;99%
C9H22ClNO2Si

C9H22ClNO2Si

potassium acrylate
10192-85-5

potassium acrylate

C12H25NO4Si

C12H25NO4Si

Conditions
ConditionsYield
With tyrosamine; methyltriphenylphosphonium chloride In N,N-dimethyl-formamide at 115℃; for 2h; Inert atmosphere;98%
C10H24ClNOSi

C10H24ClNOSi

potassium acrylate
10192-85-5

potassium acrylate

C13H27NO3Si

C13H27NO3Si

Conditions
ConditionsYield
With N1,N4-di(naphthalen-1-yl)benzene-1,4-diamine; butyltriphenylphosphonium chloride In N,N-dimethyl-formamide at 120℃; for 1.5h; Inert atmosphere;98%
C11H26ClNO3Si

C11H26ClNO3Si

potassium acrylate
10192-85-5

potassium acrylate

C14H29NO5Si

C14H29NO5Si

Conditions
ConditionsYield
With 2,6-di-tert-butyl-4-methyl-phenol; ethyltriphenylphosphonium bromide In N,N-dimethyl-formamide at 125℃; for 1h; Inert atmosphere;98%
C8H20ClNO3Si

C8H20ClNO3Si

potassium acrylate
10192-85-5

potassium acrylate

C11H23NO5Si

C11H23NO5Si

Conditions
ConditionsYield
With tyrosamine; tetraphenyl phosphonium chloride In toluene at 110℃; for 2.5h; Inert atmosphere;98%
N,N'-diphenyl-1,4-phenylenediamine
74-31-7

N,N'-diphenyl-1,4-phenylenediamine

potassium acrylate
10192-85-5

potassium acrylate

N-neopentyl-4-(4-methylpiperidinyl)-pyridinium chloride
95758-27-3

N-neopentyl-4-(4-methylpiperidinyl)-pyridinium chloride

3-Chloropropyltrimethoxysilan
2530-87-2

3-Chloropropyltrimethoxysilan

3-(trimethoxysilyl)propyl acrylate
4369-14-6

3-(trimethoxysilyl)propyl acrylate

Conditions
ConditionsYield
In methanol92.7%
diethyl 3-(bromopropyl)phosphonic acid
1186-10-3

diethyl 3-(bromopropyl)phosphonic acid

potassium acrylate
10192-85-5

potassium acrylate

1,3-dibromo-propane
109-64-8

1,3-dibromo-propane

diethyl 3-acryloyloxypropylphosphonate
1224604-81-2

diethyl 3-acryloyloxypropylphosphonate

Conditions
ConditionsYield
With triethyl phosphite In N,N-dimethyl-formamide92%
triisopropylsilyl chloride
13154-24-0

triisopropylsilyl chloride

potassium acrylate
10192-85-5

potassium acrylate

tri(isopropyl)silyl acrylate
157859-20-6

tri(isopropyl)silyl acrylate

Conditions
ConditionsYield
With 2,6-di-tert-butyl-4-methyl-phenol In toluene at 45 - 50℃; for 6h; Reagent/catalyst; Inert atmosphere;86%
potassium acrylate
10192-85-5

potassium acrylate

3-Chloropropyltrimethoxysilan
2530-87-2

3-Chloropropyltrimethoxysilan

3-(trimethoxysilyl)propyl acrylate
4369-14-6

3-(trimethoxysilyl)propyl acrylate

Conditions
ConditionsYield
With tetrabutylammomium bromide at 125 - 130℃; for 5h; Temperature; Large scale;85.6%
trimethylsilyl methanesulfonate
10090-05-8

trimethylsilyl methanesulfonate

potassium acrylate
10192-85-5

potassium acrylate

trimethylsilyl acrylate
13688-55-6

trimethylsilyl acrylate

Conditions
ConditionsYield
With 2,2-diphenyl-1-picrylhydrazine at 150℃; for 1h;82.7%
potassium acrylate
10192-85-5

potassium acrylate

3-[(chlorosulfinyl)oxy]-1,1,2,2-tetrafluoropropane
110920-07-5

3-[(chlorosulfinyl)oxy]-1,1,2,2-tetrafluoropropane

acrylate de trihydro-1,1,3 tetrafluoropropyle
7383-71-3

acrylate de trihydro-1,1,3 tetrafluoropropyle

Conditions
ConditionsYield
76.2%
potassium acrylate
10192-85-5

potassium acrylate

2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl chlorosulfite
254756-56-4

2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptyl chlorosulfite

Conditions
ConditionsYield
76.1%
potassium acrylate
10192-85-5

potassium acrylate

5-[(chlorosulfinyl)oxy]-1,1,2,2,3,3,4,4-octafluoropentane
254756-55-3

5-[(chlorosulfinyl)oxy]-1,1,2,2,3,3,4,4-octafluoropentane

acrylate de trihydro-1,1,5 octafluoropentyle
376-84-1

acrylate de trihydro-1,1,5 octafluoropentyle

Conditions
ConditionsYield
76%
potassium acrylate
10192-85-5

potassium acrylate

allyl bromide
106-95-6

allyl bromide

allyl acrylate
999-55-3

allyl acrylate

Conditions
ConditionsYield
tetrabutylammomium bromide In dichloromethane at 30℃; for 50h;75%
potassium acrylate
10192-85-5

potassium acrylate

5-Bromo-pentanoic acid 4-[(R)-1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-butyl ester
173677-24-2

5-Bromo-pentanoic acid 4-[(R)-1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-butyl ester

5-Acryloyloxy-pentanoic acid 4-[(R)-1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-butyl ester
173677-25-3

5-Acryloyloxy-pentanoic acid 4-[(R)-1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-butyl ester

Conditions
ConditionsYield
With 18-crown-6 ether In N,N,N,N,N,N-hexamethylphosphoric triamide at 40℃; for 24h;73%
potassium acrylate
10192-85-5

potassium acrylate

[4-(3-Bromo-propoxy)-phenyl]-(4-trifluoromethoxy-phenyl)-diazene

[4-(3-Bromo-propoxy)-phenyl]-(4-trifluoromethoxy-phenyl)-diazene

Acrylic acid 3-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-propyl ester

Acrylic acid 3-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-propyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 60℃; for 8h;72%
tributyltin chloride
1461-22-9

tributyltin chloride

potassium acrylate
10192-85-5

potassium acrylate

tributyltin acrylate
13331-52-7

tributyltin acrylate

Conditions
ConditionsYield
In ethanol at 30-40°C;70%
In ethanol at 30-40°C;70%
potassium acrylate
10192-85-5

potassium acrylate

tripropyltin chloride
2279-76-7

tripropyltin chloride

tripropyl tin (1+); acrylate

tripropyl tin (1+); acrylate

Conditions
ConditionsYield
In ethanol byproducts: KCl; equimolar amts. of educts, gentle warming; recrystn. in petroleum ether;66%
In ethanol byproducts: KCl; equimolar amts. of educts, gentle warming; recrystn. in petroleum ether;66%
potassium acrylate
10192-85-5

potassium acrylate

[4-(5-Bromo-pentyloxy)-phenyl]-(4-trifluoromethoxy-phenyl)-diazene

[4-(5-Bromo-pentyloxy)-phenyl]-(4-trifluoromethoxy-phenyl)-diazene

Acrylic acid 5-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-pentyl ester

Acrylic acid 5-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-pentyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 60℃; for 8h;61%
2,2,2-trichloroethyl (2-(tert-butylcarbamoyl)phenyl)sulfamate

2,2,2-trichloroethyl (2-(tert-butylcarbamoyl)phenyl)sulfamate

potassium acrylate
10192-85-5

potassium acrylate

2-acrylamido-N-(tert-butyl)benzamide

2-acrylamido-N-(tert-butyl)benzamide

Conditions
ConditionsYield
In chlorobenzene at 120℃; for 10h;52%
potassium acrylate
10192-85-5

potassium acrylate

[4-(2-Bromo-ethoxy)-phenyl]-(4-trifluoromethoxy-phenyl)-diazene

[4-(2-Bromo-ethoxy)-phenyl]-(4-trifluoromethoxy-phenyl)-diazene

Acrylic acid 2-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-ethyl ester

Acrylic acid 2-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-ethyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 60℃; for 8h;41%
potassium acrylate
10192-85-5

potassium acrylate

1,3-Bis(chloromethyl)-1,1,3,3-tetramethyldisiloxane
2362-10-9

1,3-Bis(chloromethyl)-1,1,3,3-tetramethyldisiloxane

1,3-bis-acryloyloxymethyl-1,1,3,3-tetramethyl-disiloxane
4515-14-4

1,3-bis-acryloyloxymethyl-1,1,3,3-tetramethyl-disiloxane

Conditions
ConditionsYield
With hydroquinone In N,N-dimethyl-formamide for 6h; boiling;40%
potassium acrylate
10192-85-5

potassium acrylate

4-(4-bromobutyloxy)-4'-trifluoromethoxyazobenzene

4-(4-bromobutyloxy)-4'-trifluoromethoxyazobenzene

Acrylic acid 4-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-butyl ester

Acrylic acid 4-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-butyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 60℃; for 8h;36%
potassium acrylate
10192-85-5

potassium acrylate

[4-(6-Bromo-hexyloxy)-phenyl]-(4-trifluoromethoxy-phenyl)-diazene

[4-(6-Bromo-hexyloxy)-phenyl]-(4-trifluoromethoxy-phenyl)-diazene

Acrylic acid 6-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-hexyl ester

Acrylic acid 6-[4-(4-trifluoromethoxy-phenylazo)-phenoxy]-hexyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 60℃; for 8h;35%
C10H4F17Cl
133299-39-5

C10H4F17Cl

potassium acrylate
10192-85-5

potassium acrylate

1H,1H,2H,2H-heptadecafluorodecyl acrylate
27905-45-9

1H,1H,2H,2H-heptadecafluorodecyl acrylate

Conditions
ConditionsYield
With 4-methoxy-phenol; hydroquinone In tert-butyl alcohol at 180℃; for 6h;12%
2-Chlormethyl-1,4,6-trioxa-spiro-<4,4>-nonan
3660-10-4

2-Chlormethyl-1,4,6-trioxa-spiro-<4,4>-nonan

potassium acrylate
10192-85-5

potassium acrylate

2-acryloyloxymethyl-1,4,6-trioxaspiro<4,4>nonane
84298-13-5

2-acryloyloxymethyl-1,4,6-trioxaspiro<4,4>nonane

Conditions
ConditionsYield
N-benzyl-N,N,N-triethylammonium chloride In N,N-dimethyl-formamide at 110 - 115℃; for 7h;7%
potassium acrylate
10192-85-5

potassium acrylate

2-bromomethyl-1,4,6-trioxaspiro<4.4>nonane
84298-07-7

2-bromomethyl-1,4,6-trioxaspiro<4.4>nonane

2-acryloyloxymethyl-1,4,6-trioxaspiro<4,4>nonane
84298-13-5

2-acryloyloxymethyl-1,4,6-trioxaspiro<4,4>nonane

Conditions
ConditionsYield
N-benzyl-N,N,N-triethylammonium chloride In N,N-dimethyl-formamide at 110 - 115℃; for 7h;7%
diethyl phosphorylchloridite
589-57-1

diethyl phosphorylchloridite

potassium acrylate
10192-85-5

potassium acrylate

acryloyl diethyl phosphite
28303-81-3

acryloyl diethyl phosphite

Conditions
ConditionsYield
In diethyl ether
2-fluoro-2,2-dinitroethylsulfuric acid
53510-13-7

2-fluoro-2,2-dinitroethylsulfuric acid

potassium acrylate
10192-85-5

potassium acrylate

2-fluoro-2,2-dinitroethyl acrylate
16544-21-1

2-fluoro-2,2-dinitroethyl acrylate

dipropyl phosphorochloridite
20003-39-8

dipropyl phosphorochloridite

potassium acrylate
10192-85-5

potassium acrylate

Phosphorigesaeure-dipropylester-acryloylester
93228-17-2

Phosphorigesaeure-dipropylester-acryloylester

Conditions
ConditionsYield
In diethyl ether

10192-85-5Relevant articles and documents

Reactivity of a Ruthenium(0) Complex Bearing a Tetradentate Phosphine Ligand: Applications to Catalytic Acrylate Salt Synthesis from Ethylene and CO2

Ito, Tatsuyoshi,Takahashi, Kohei,Iwasawa, Nobuharu

, p. 205 - 209 (2019)

By using a zerovalent, electron-rich ruthenium complex bearing a tetradentate phosphine ligand, a five-membered ruthenalactone was generated by oxidative cyclization of ethylene and CO2. This ruthenalactone underwent thermal, reversible β-H elimination to afford an acrylato(hydrido)ruthenium(II) complex, which liberated acrylate salt on treatment with a base. The reaction was successfully applied to the first ruthenium-catalyzed synthesis of an acrylate salt from ethylene and CO2. This study demonstrated the feasibility of the electron-rich ruthenium(0) complex as a catalyst in CO2-fixation chemistry.

ACRYLATES THROUGH OLEFIN/CARBON DIOXIDE COUPLING

-

Paragraph 0067, (2019/04/11)

Methods of producing α,β-unsaturated carboxylic acid salts are described. A method can include reacting an alkene and carbon dioxide with a composition that includes a carboxylation catalyst and an inorganic base in a protic solvent under reaction conditions suitable to produce an inorganic base salt of an α,β-unsaturated carboxylic acid.

Process for the preparation of bromo-substituted aromatic esters of α,β-unsaturated acids

-

, (2008/06/13)

A process for the preparation of bromo-substituted aromatic esters of α, β-unsaturated acids of the formula STR1 wherein n is 1 or 2, x=6'n, and R and R' are hydrogen or alkyl; comprises reacting a salt of α,β-unsaturated acid and an alkali with a bromo-substituted benzyl halide in an inert substantially water-immiscible solvent and in the presence of a phase-transfer catalyst.

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