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4075-81-4

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4075-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4075-81-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4075-81:
(6*4)+(5*0)+(4*7)+(3*5)+(2*8)+(1*1)=84
84 % 10 = 4
So 4075-81-4 is a valid CAS Registry Number.
InChI:InChI=1/2C3H6O2.Ca/c2*1-2-3(4)5;/h2*2H2,1H3,(H,4,5);/q;;+2/p-2

4075-81-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A14994)  Calcium propionate hydrate, 97%   

  • 4075-81-4

  • 500g

  • 255.0CNY

  • Detail
  • Alfa Aesar

  • (A14994)  Calcium propionate hydrate, 97%   

  • 4075-81-4

  • 2500g

  • 1008.0CNY

  • Detail
  • Aldrich

  • (18104)  Calciumpropionate  99.0-100.5% (in dried substance), meets analytical specification of E 282

  • 4075-81-4

  • 18104-1KG-R

  • 577.98CNY

  • Detail
  • Aldrich

  • (21230)  Calciumpropionate  ≥97.0% (dry substance, NT)

  • 4075-81-4

  • 21230-250G-F

  • 202.41CNY

  • Detail
  • Aldrich

  • (21230)  Calciumpropionate  ≥97.0% (dry substance, NT)

  • 4075-81-4

  • 21230-1KG-F

  • 547.56CNY

  • Detail

4075-81-4Synthetic route

propiononitrile
107-12-0

propiononitrile

A

calcium propionate
4075-81-4

calcium propionate

B

Propionamid
79-05-0

Propionamid

Conditions
ConditionsYield
With calcium hydroxide; water at 160 - 200℃; under 516.802 - 13445.8 Torr; for 2.66 - 12.33h; Conversion of starting material;A 24.2%
B 0.0114%
With calcium hydroxide; water at 160 - 200℃; under 7328 - 14206.3 Torr; for 2 - 12.33h; Product distribution / selectivity;
propionic acid
802294-64-0

propionic acid

calcium propionate
4075-81-4

calcium propionate

Conditions
ConditionsYield
With calcium oxide at 180℃; under 3750.38 Torr; Reagent/catalyst; Pressure; Temperature; Autoclave; Large scale;52.1 kg
propionic acid
802294-64-0

propionic acid

calcium oxide

calcium oxide

calcium propionate
4075-81-4

calcium propionate

Conditions
ConditionsYield
at 26 - 170℃; for 0.3h; Product distribution / selectivity;
In water at 125℃; for 0.183333h; Product distribution / selectivity;
propionic acid
802294-64-0

propionic acid

calcium carbonate

calcium carbonate

calcium oxide

calcium oxide

calcium propionate
4075-81-4

calcium propionate

Conditions
ConditionsYield
In water at 115℃; for 0.25h; Product distribution / selectivity;
propionic acid
802294-64-0

propionic acid

Propionamid
79-05-0

Propionamid

calcium propionate
4075-81-4

calcium propionate

Conditions
ConditionsYield
Stage #1: Propionamid With calcium hydroxide; water at 60 - 103℃;
Stage #2: propionic acid In water pH=8.1;
tributyl-amine
102-82-9

tributyl-amine

carbon dioxide
124-38-9

carbon dioxide

calcium propionate
4075-81-4

calcium propionate

A

propanoic acid tributylamine salt
75775-31-4

propanoic acid tributylamine salt

B

calcium carbonate

calcium carbonate

Conditions
ConditionsYield
In water for 0.5h; Product distribution / selectivity;A n/a
B 90.8%
calcium propionate
4075-81-4

calcium propionate

L-carnitine
541-15-1

L-carnitine

L-carnitine calcium propionate

L-carnitine calcium propionate

Conditions
ConditionsYield
In water for 0.25h;90%
calcium propionate
4075-81-4

calcium propionate

potassium sorbate
24634-61-5

potassium sorbate

calcium propionate sorbate

calcium propionate sorbate

Conditions
ConditionsYield
In water at 25℃; for 0.0333333h;75%
manganese(II) perchlorate hexahydrate

manganese(II) perchlorate hexahydrate

2-hydroxyacetophenoneoxime
1196-29-8

2-hydroxyacetophenoneoxime

calcium propionate
4075-81-4

calcium propionate

acetonitrile
75-05-8

acetonitrile

A

Mn4(2-hydroxyphenylethanone oxime(-2H))4(2-hydroxyphenylethanone oxime(-1H))4*3.5MeCN

Mn4(2-hydroxyphenylethanone oxime(-2H))4(2-hydroxyphenylethanone oxime(-1H))4*3.5MeCN

B

poly[[Mn(III)6Ca2O2(2-hydroxyphenylethanone oxime(-2H))6(propionato)6(H2O)2]*2MeCN*0.95H2O]

poly[[Mn(III)6Ca2O2(2-hydroxyphenylethanone oxime(-2H))6(propionato)6(H2O)2]*2MeCN*0.95H2O]

Conditions
ConditionsYield
In acetonitrile Mn(ClO4)2*6H2O, oxime ligand, Ca-propionate (1:1:1 mol) stirred in MeCN overnight; filtered; crystd. from filtrate over few ds; XRD;A n/a
B 40%
sodium benzoate
532-32-1

sodium benzoate

calcium propionate
4075-81-4

calcium propionate

C3H5O2(1-)*C7H5O2(1-)*Ca(2+)

C3H5O2(1-)*C7H5O2(1-)*Ca(2+)

Conditions
ConditionsYield
In water at 25℃; for 0.0333333h;
carbon dioxide
124-38-9

carbon dioxide

calcium propionate
4075-81-4

calcium propionate

A

propanoic acid tributylamine salt
75775-31-4

propanoic acid tributylamine salt

B

calcium carbonate

calcium carbonate

Conditions
ConditionsYield
Stage #1: tributyl-amine; calcium propionate With acetic acid In water
Stage #2: carbon dioxide In water under 760.051 Torr; for 0.5h; Product distribution / selectivity;
Reaxys ID: 11350085

Reaxys ID: 11350085

calcium propionate
4075-81-4

calcium propionate

A

propanoic acid tributylamine salt
75775-31-4

propanoic acid tributylamine salt

B

calcium carbonate

calcium carbonate

Conditions
ConditionsYield
Stage #1: tributyl-amine; calcium propionate With acetic acid In water
Stage #2: In water under 760.051 Torr; for 0.5h; Product distribution / selectivity;
calcium propionate
4075-81-4

calcium propionate

propionic acid
802294-64-0

propionic acid

manganese(ll) chloride

manganese(ll) chloride

barium(II) oxide

barium(II) oxide

dicalcium barium propionate#dotMn(2+)

dicalcium barium propionate#dotMn(2+)

Conditions
ConditionsYield
In water crystn.; recrystn. from water for 3 times during 2 or 3 weeks;
tricalcium aliminate

tricalcium aliminate

calcium propionate
4075-81-4

calcium propionate

calcium oxide

calcium oxide

3CaO*Al2O3*CH3(CH2)CO2(1-)*99H2O

3CaO*Al2O3*CH3(CH2)CO2(1-)*99H2O

Conditions
ConditionsYield
With H2O In water
strontium(II) oxide

strontium(II) oxide

calcium propionate
4075-81-4

calcium propionate

propionic acid
802294-64-0

propionic acid

manganese(ll) chloride

manganese(ll) chloride

2Ca(2+)*Sr(2+)*6(C2H5COO)(1-)=Ca2Sr(C2H5COO)6#dotMn(2+)

2Ca(2+)*Sr(2+)*6(C2H5COO)(1-)=Ca2Sr(C2H5COO)6#dotMn(2+)

Conditions
ConditionsYield
In water dissolving SnO slowly in an aq. soln. of propionic acid, adding the Ca salt, adding small amts. of MnCl2; dissolved, recrystd. two to three times;
lead (II) propionate
814-70-0, 19183-30-3, 42558-73-6

lead (II) propionate

calcium propionate
4075-81-4

calcium propionate

dicalcium lead propionate
13832-22-9, 17203-66-6, 54993-40-7

dicalcium lead propionate

Conditions
ConditionsYield
In water heating a soln. of Ca(CH3CH2CO2)2 and Pb(CH3CH2CO2)2 with the molar ratio of 2:1 from 30 to 50°C; recrystn. (three times);
lanthanum propionate

lanthanum propionate

calcium propionate
4075-81-4

calcium propionate

manganese(II) propanoate
21129-18-0

manganese(II) propanoate

lanthanum calcium manganes oxide

lanthanum calcium manganes oxide

Conditions
ConditionsYield
In propionic acid spin-coating of quartz substrates, pyrolysis (550-850°C, 30 min, O2);
lanthanum propionate

lanthanum propionate

calcium propionate
4075-81-4

calcium propionate

manganese(II) propanoate
21129-18-0

manganese(II) propanoate

La0.90Ca0.10MnO3

La0.90Ca0.10MnO3

Conditions
ConditionsYield
In propionic acid spin-coating of quarts substrate, pyrolysis (550-850°C, 30 min, O2); electron microscopy;
lanthanum propionate

lanthanum propionate

calcium propionate
4075-81-4

calcium propionate

manganese(II) propanoate
21129-18-0

manganese(II) propanoate

La0.8Ca0.2MnO3

La0.8Ca0.2MnO3

Conditions
ConditionsYield
In propionic acid spin-coating of quartz substrate, pyrolysis (550-850°C, 30 min, O2);
barium(II)

barium(II)

calcium propionate
4075-81-4

calcium propionate

barium propionate
5908-77-0

barium propionate

Conditions
ConditionsYield
In not given addition of Ba(2+) to a concd. Ca(C2H5CO2)-solution ppts. Ba(C2H5CO2)2;;
In not given addition of Ba(2+) to a concd. Ca(C2H5CO2)-solution ppts. Ba(C2H5CO2)2;;
calcium propionate
4075-81-4

calcium propionate

lead(II) oxide

lead(II) oxide

manganese(ll) chloride

manganese(ll) chloride

dicalcium lead propionate

dicalcium lead propionate

Conditions
ConditionsYield
With propionic acid In water dissolving PbO in an aq. soln. of C2H5COOH, addn. of Ca(C2H5COO)2, (soln. containing MnCl2 (one Mn(2+) per thousand Ca(2+)); slow evapn., recrystn. (water);
lanthanum propionate

lanthanum propionate

calcium propionate
4075-81-4

calcium propionate

manganese(II) propanoate
21129-18-0

manganese(II) propanoate

La0.6Ca0.4MnO3.000

La0.6Ca0.4MnO3.000

Conditions
ConditionsYield
In propionic acid spin-coating of quartz substrates, pyrolysis (550-850°C, 30 min, O2);
lanthanum propionate

lanthanum propionate

calcium propionate
4075-81-4

calcium propionate

manganese(II) propanoate
21129-18-0

manganese(II) propanoate

La0.50Ca0.50MnO3.00

La0.50Ca0.50MnO3.00

Conditions
ConditionsYield
In propionic acid spin-coating of quartz substrate, pyrolysis (550-850°C, 30 min, O2);
lanthanum propionate

lanthanum propionate

calcium propionate
4075-81-4

calcium propionate

manganese(II) propanoate
21129-18-0

manganese(II) propanoate

lanthanum calcium manganite

lanthanum calcium manganite

Conditions
ConditionsYield
In propionic acid chemical soln. deposition on LaAlO3 substrate; spin coating the precursor soln. (metals propionates in stoich. proportion in propionic acid) on substrate; pyrolysing the precurso films, annealing at 950°C; detd. by XRD;
calcium propionate
4075-81-4

calcium propionate

copper(II) sulfate
7758-99-8

copper(II) sulfate

Ca(2+)*2C2H5CO2(1-)=(C2H5CO2)2Ca#dotCu(2+)

Ca(2+)*2C2H5CO2(1-)=(C2H5CO2)2Ca#dotCu(2+)

Conditions
ConditionsYield
In water slow evapn. of aq. soln. of (C2H5CO2)2Ca and 1-2 drops of CuSO4;
calcium propionate
4075-81-4

calcium propionate

strontium(II) propionate
23287-50-5

strontium(II) propionate

Ca2Sr(C2H5COO)6, low temperature, triclinic

Ca2Sr(C2H5COO)6, low temperature, triclinic

Conditions
ConditionsYield
In water twice recrystn. of Ca(C2H5COO) and Sr(C2H5COO)2 soln. (in molar ratio 2:1); cooled to 50 K;
tributyl-amine
102-82-9

tributyl-amine

calcium acetate
62-54-4

calcium acetate

calcium propionate
4075-81-4

calcium propionate

A

propanoic acid tributylamine salt
75775-31-4

propanoic acid tributylamine salt

B

tributylammonium acetate
7204-64-0

tributylammonium acetate

Conditions
ConditionsYield
With carbon dioxide In 2-Ethylhexyl alcohol; 2-ethylhexyl acetate; water under 12929 Torr; for 0.666667h;
tributyl-amine
102-82-9

tributyl-amine

calcium propionate
4075-81-4

calcium propionate

propionic acid
802294-64-0

propionic acid

propanoic acid tributylamine salt
75775-31-4

propanoic acid tributylamine salt

Conditions
ConditionsYield
With carbon dioxide In 2-Ethylhexyl alcohol; 2-ethylhexyl acetate; water; iso-butanol at 35℃; under 12929 Torr; for 0.5h; Product distribution / selectivity;

4075-81-4Downstream Products

4075-81-4Relevant academic research and scientific papers

PROCESS FOR PREPARATION OF TERT-BUTYLAMINE AND PROPIONIC ACID SALTS FROM N-TERTIARY BUTYL ACRYLAMIDE

-

Page/Page column 15; 16;, (2021/11/13)

Disclosed is a process (100) for conversion of N-tertiary butyl acrylamide to tert-butylamine and salts of propionic acid. The process comprises of first selectively reducing the vinylic double bond in N-tertiary butyl acrylamide by catalytic hydrogenation of an alcoholic solution of N-tertiary butyl acrylamide to provide N-tertiary buyl propanamide; recovering the hydrogenation catalyst by filtering the solution and treating the solution with an alkali to produce N-tertiary butylamine and corresponding alkali salt of propionic acid. The process converts of N-tertiary butyl acrylamide into value added products at milder reaction conditions, without producing any hazardous byproducts and effluents.

METHOD FOR PRODUCING CALCIUM DIPROPIONATE

-

Paragraph 0010, (2018/07/26)

The invention relates to a solid-material method for producing calcium dipropionate in a pressure-resistant solid-state mixing reactor by charging calcium oxide, calcium hydroxide or calcium carbonate or mixtures of these calcium compounds, and adding propionic acid by a reaction directly in the solid phase under a pressure that is increased above normal pressure.

Process for producing a calcium carboxylate

-

Page/Page column 7-8, (2010/02/10)

A process for producing a calcium carboxylate comprising contacting a nitrile compound, a calcium compound selected from calcium hydroxide, calcium oxide or mixtures thereof, and water at a temperature of about 90°C to about 250°C at a sufficient pressure and for a sufficient time to produce a reaction mixture comprising calcium carboxylate.

PROCESS FOR PRODUCING A CALCIUM CARBOXYLATE

-

Page 5; 6, (2008/06/13)

A process for producing a calcium carboxylate comprising contacting a nitrile compound, a calcium compound selected from calcium hydroxide, calcium oxide or mixtures thereof, and water at a temperature of about 90° C. to about 250° C. at a sufficient pressure and for a sufficient time to produce a reaction mixture comprising calcium carboxylate.

A METHOD OF MAKING SALT

-

Page/Page column 14, (2008/06/13)

A method of making the salt of an acid, includes the steps of combining and mixing the acid and a base selected from the oxides, hydroxides and carbonates of sodium, potassium, calcium and magnesium, in a first reaction zone over a first period to produce a reaction mixture. The reaction mixture is transferred at the end of the first period from the first reaction zone to a second reaction zone the transferring step being carried out over a second period. Heat generated by reaction between the acid and the base in the second reaction zone drives off sufficient water to produce a product mixture containing less than about 8 % (m/m) water. The first period is between about 1 and 180 seconds and the second period is between about 2 and 60 seconds.

Solid phase synthesis of salts of organic acid

-

, (2008/06/13)

A process for the solid-phase synthesis of salts of organic acids in a granular, free-flowing, and dust-free form particularly suited for use as animal feed additives. A liquid organic acid is applied to an inert, absorbent carrier. A solid base is then added during stirring. The acid is slowly released from the carrier preventing the fast reactions that lead to the formation of clumps. The exothermic reaction releases heat which assists in reducing the moisture content of the product.

Methods of preparation and using antimicrobial products

-

, (2008/06/13)

Novel antimicrobial products and methods of making and using the same are shown, whereby the products can be used in the same or greater percentages as conventional microbial growth inhibitors without imparting an off-flavor, taste, color or odor to the products in which they are used. The antimicrobial products are formed by reacting azodicarbonamide or an ammonia gas with a compound selected from the group consisting of benzoic acid, sodium benzoate, calcium benzoate, potassium benzoate, acetic acid, sodium diacetate, paraben, niacin, calcium acetate, calcium diacetate, citric acid, lactic acid, fumaric acid, sorbic acid, sodium sorbate, calcium sorbate, potassium sorbate, propionic acid, sodium propionate, calcium propionate, potassium propionate and mixtures thereof. In one embodiment, the product is prepared by placing a layer of azodicarbonamide on a substrate and covering the layer with a gas permeable separator. The antimicrobial compound is then added on top of the separator, and the combination is heated to form the final product. In another embodiment, the product is prepared by exposing the antimicrobial compound to an ammonia gas. The ammonia gas reacts with free acids in the antimicrobial compound to convert the free acids into ammonium salts, thereby eliminating off-flavor and off-odor of the resulting antimicrobial product. The antimicrobial products prepared according to the present invention are suitable for use in foodstuffs, sanitation products, cosmetics, pharmaceuticals, and so forth.

Method for preparing antimicrobial salts

-

, (2008/06/13)

Novel antimicrobial products and methods of making and using the same are disclosed, whereby the products can be used in the same or greater percentages as conventional microbial growth inhibitors without imparting an off-flavor, taste, color or odor to the products in which they are used. The antimicrobial products are formed by exposing a compound selected from the group consisting of benzoic acid, sodium benzoate, calcium benzoate, potassium benzoate, acetic acid, sodium diacetate, paraben, niacin, calcium acetate, calcium diacetate, citric acid, lactic acid, fumaric acid, sorbic acid, sodium sorbate, calcium sorbate, potassium sorbate, propionic acid, sodium propionate, calcium propionate, potassium propionate and mixtures thereof, to an ammonia gas. In one embodiment, the product is prepared by placing a layer of azodicarbonamide on a substrate and covering the layer with a gas permeable separator. The antimicrobial compound is then added on top of the separator, and the combination is heated to cause the azodicarbonamide to decompose and release ammonia gas to form the final product. In another embodiment, the product is prepared by exposing the antimicrobial compound to an ammonia gas. The ammonia gas reacts with free acids in the antimicrobial compound to convert the free acids into ammonium salts, thereby eliminating off-flavor and off-odor of the resulting antimicrobial product. The antimicrobial products prepared according to the present invention are suitable for use in foodstuffs, sanitation products, cosmetics, pharmaceuticals, and so forth.

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