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814-80-2

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814-80-2 Usage

Description

Calcium lactate is a black or white crystalline salt made by the action of lactic acid on calcium carbonate. It is used in foods (as an ingredient in baking powder) and given medicinally. Its E number is E327. It is created by the reaction of lactic acid with calcium carbonate or calcium hydroxide. Calcium lactate is often found in aged cheeses. Small crystals of it precipitate out when lactic acid is converted into a less soluble form by the bacteria active during the ripening process. In medicine, calcium lactate is most commonly used as an antacid and also to treat calcium deficiencies. Calcium lactate can be absorbed at various pHs and does not need to be taken with food for absorption for these reasons. Calcium lactate is added to sugar-free foods to prevent tooth decay. When added to chewing gum containing xylitol, it increases the remineralization of tooth enamel.It is also added to fresh-cut fruits such as cantaloupes to keep them firm and extend their shelf life, without the bitter taste caused by calcium chloride, which can also be used for this purpose.

Chemical Properties

Calcium lactate occurs as white or almost white, crystalline or granular powder. It is slightly efflorescent.

Uses

Different sources of media describe the Uses of 814-80-2 differently. You can refer to the following data:
1. Calcium Lactate is the calcium salt of lactic acid which is soluble in water. it has a solubility of 3.4 g/100 g of water at 20°c and is very soluble in hot water. it is available as a monohydrate, trihydrate, and pentahydrate. the trihydrate and pentahydrate have solubili- ties of 9 g in 100 ml of water at 25°c. it contains approximately 14% calcium. it is used to stabilize and improve the texture of canned fruits and vegetables by converting the labile pectin to the less solu- ble calcium pectate. it thereby prevents structural collapse during cooking. it is used in angel food cake, whipped toppings, and meringues to increase protein extensibility which results in an increase of foam volume. it is also used in calcium fortified foods such as infant foods and is used to improve the properties of dry milk powder.
2. As a preservative in foods and beverages; in dentifrices.
3. Lactic Acid Calcium Salt is used in foods as an ingredient in baking powder. Lactic Acid Calcium Salt is also used as an antacid and also to treat calcium deficiencies.

Production Methods

Calcium lactate is prepared commercially by neutralization with calcium carbonate or calcium hydroxide of lactic acid obtained from fermentation of dextrose, molasses, starch, sugar, or whey.

Hazard

A poison.

Pharmaceutical Applications

Calcium lactate is used as a bioavailability enhancer and nutrient supplement in pharmaceutical formulations. A spray-dried grade of calcium lactate pentahydrate has been used as a tablet diluent in direct compression systems, and has been shown to have good compactability. The properties of the pentahydrate form have been considered superior to those of calcium lactate trihydrate when used in direct compression tablet formulations. Tablet properties may be affected by the hydration state of the calcium lactate and particle size of the material: reducing particle size increased crushing strength, whereas storage of tablets at elevated temperature resulted in dehydration accompanied by a reduction in crushing strength. Calcium lactate has also been used as the source of calcium ions in the preparation of calcium alginate microspheres for controlled- release delivery of active agents. It has been shown to result in lower calcium concentrations in the finished microspheres when compared with calcium acetate. Therapeutically, calcium lactate has been used in preparations for the treatment of calcium deficiency.

Safety

Calcium lactate was found to have no toxic or carcinogenic effects when dosed at levels of 0%, 2.5%, and 5% in drinking water to male and female rats for 2 years.

storage

Calcium lactate can exist in a number of hydration states, which are characterized as anhydrous, monohydrate, trihydrate, and pentahydrate. Dehydration of the pentahydrate form is rapid at temperatures of 558℃ and above. Dehydration is reported to be accompanied by some loss of crystallinity. Tablet crushing strength was reported to be reduced following dehydration of calcium lactate pentahydrate.

Purification Methods

Crystallise it from warm water (10mL/g) by cooling to 0o. [Beilstein 3 IV 636.]

Incompatibilities

Calcium salts, including the lactate, can display physical incompatibility with phosphate in the diet or therapeutic preparations, for example in enteral feed mixtures.

Regulatory Status

GRAS listed except for infant foods/formulas. Accepted as a food additive in Europe. Calcium lactate (anhydrous) is included in the FDA Inactive Ingredients Database (vaginal, tablet). It is used in oral dosage forms. Included in vaginal pessary formulations licensed in the UK.

Check Digit Verification of cas no

The CAS Registry Mumber 814-80-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 814-80:
(5*8)+(4*1)+(3*4)+(2*8)+(1*0)=72
72 % 10 = 2
So 814-80-2 is a valid CAS Registry Number.
InChI:InChI=1/2C3H6O3.Ca/c2*1-2(4)3(5)6;/h2*2,4H,1H3,(H,5,6);/q;;+2/p-2

814-80-2SDS

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 Calcium Lactate

1.2 Other means of identification

Product number -
Other names Calcium lactate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives
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:814-80-2 SDS

814-80-2Synthetic route

calcium oxide

calcium oxide

Sucrose
57-50-1

Sucrose

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
In not given heating 3 h 25% saccharose soln. with CaO in excess at 197°C;;65%
In not given
calcium hydroxide

calcium hydroxide

calcium oxide

calcium oxide

Sucrose
57-50-1

Sucrose

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
In not given at 215°C and 30 at;; addn. of CaO in autoclave and saturation in heat at pH = 8.2; treatment with active carbon; concg.;;45%
In not given at 215°C and 30 at;; addn. of CaO in autoclave and saturation in heat at pH = 8.2; treatment with active carbon; concg.;;45%
glycerol
56-81-5

glycerol

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
With water; C25H37IrN6(2+)*2F6P(1-); calcium hydroxide at 180℃; for 20h; Catalytic behavior; Reagent/catalyst; Autoclave;18%
LACTIC ACID
849585-22-4

LACTIC ACID

calcium carbonate

calcium carbonate

calcium lactate
814-80-2

calcium lactate

D-Lactic acid
10326-41-7

D-Lactic acid

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
With calcium hydroxide In water
hydrogen cyanide
74-90-8

hydrogen cyanide

sulfuric acid
7664-93-9

sulfuric acid

acetaldehyde
75-07-0

acetaldehyde

calcium hydroxide

calcium hydroxide

A

ammonia
7664-41-7

ammonia

B

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
In sodium hydroxide reaction of 98% acetaldehyde in NaOH with HCN; heating soln with 50% H2SO4 and excess of Ca(OH)2; filtration in heat; cooling down;;
D-Glucose
2280-44-6

D-Glucose

calcium oxide

calcium oxide

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
In not given heating equimolar mixture at 70°C; reaction takes place in autoclave;; ultrapure;;
In not given heating equimolar mixture at 70°C; reaction takes place in autoclave;; ultrapure;;
D-Glucose
2280-44-6

D-Glucose

calcium carbonate

calcium carbonate

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
In not given fermenting 13% glucose soln. in presence of CaCO3;;
In not given fermenting 13% glucose soln. in presence of CaCO3;;
LACTIC ACID
849585-22-4

LACTIC ACID

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
With water; calcium oxide In glycerol Product distribution / selectivity;
With calcium carbonate In ethanol; water for 0.166667h; Sonication;
glycerol
56-81-5

glycerol

calcium oxide

calcium oxide

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
With copper(II) oxide In water at 230℃; for 0.5h; Sealed tube; Inert atmosphere; Green chemistry;
D,L-lactide
95-96-5

D,L-lactide

calcium lactate
814-80-2

calcium lactate

Conditions
ConditionsYield
Stage #1: D,L-lactide In water at 130 - 170℃; for 2.83333h; Sealed tube;
Stage #2: With calcium carbonate In water for 0.166667h; Reagent/catalyst; Temperature; Heating;
calcium lactate
814-80-2

calcium lactate

A

LACTIC ACID
849585-22-4

LACTIC ACID

B

ethyl 2-hydroxypropionate
97-64-3, 2676-33-7

ethyl 2-hydroxypropionate

Conditions
ConditionsYield
With ethanol; sulfuric acid at 75℃; for 1h;A 86.6%
B n/a
methanol
67-56-1

methanol

calcium lactate
814-80-2

calcium lactate

methyl lactate
547-64-8

methyl lactate

Conditions
ConditionsYield
With carbon dioxide at 180℃; for 7.37h; Temperature; Sealed tube; Green chemistry;58.22%
With sulfuric acid at 60 - 80℃; bei pH 1-1.4;
ethanol
64-17-5

ethanol

calcium lactate
814-80-2

calcium lactate

ethyl 2-hydroxypropionate
97-64-3, 2676-33-7

ethyl 2-hydroxypropionate

Conditions
ConditionsYield
With carbon dioxide at 180℃; Temperature; Sealed tube; Green chemistry;46.5%
With sulfuric acid at 100℃; bei pH 1 bis 1.4;
calcium lactate
814-80-2

calcium lactate

sodium proprionate
137-40-6

sodium proprionate

Conditions
ConditionsYield
With bis(acetylacetonato)dioxidomolybdenum(VI) In water at 200 - 270℃; Inert atmosphere;20%
propan-1-ol
71-23-8

propan-1-ol

calcium lactate
814-80-2

calcium lactate

n-propyl lactate
616-09-1

n-propyl lactate

Conditions
ConditionsYield
With sulfuric acid
i-Amyl alcohol
123-51-3

i-Amyl alcohol

calcium lactate
814-80-2

calcium lactate

isopentyl lactate
19329-89-6

isopentyl lactate

Conditions
ConditionsYield
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers;
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers;
2-methyl-propan-1-ol
78-83-1

2-methyl-propan-1-ol

calcium lactate
814-80-2

calcium lactate

isobutyl lactate
585-24-0

isobutyl lactate

Conditions
ConditionsYield
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers;
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers;
pentan-1-ol
71-41-0

pentan-1-ol

calcium lactate
814-80-2

calcium lactate

propanoic acid, 2-hydroxy-, pentyl ester
6382-06-5

propanoic acid, 2-hydroxy-, pentyl ester

Conditions
ConditionsYield
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers;
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers;
2-ethyl-1-butanol
97-95-0

2-ethyl-1-butanol

calcium lactate
814-80-2

calcium lactate

lactic acid-(2-ethyl-butyl ester)
873997-07-0

lactic acid-(2-ethyl-butyl ester)

Conditions
ConditionsYield
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers;
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers;
1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

calcium lactate
814-80-2

calcium lactate

glycerol-1.3-dilactate
21233-15-8

glycerol-1.3-dilactate

Conditions
ConditionsYield
With water at 160℃;
1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

calcium lactate
814-80-2

calcium lactate

lauryl lactate
6283-92-7

lauryl lactate

Conditions
ConditionsYield
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers;
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers;
potassium ethyl sulfate
563-17-7

potassium ethyl sulfate

calcium lactate
814-80-2

calcium lactate

ethyl 2-hydroxypropionate
97-64-3, 2676-33-7

ethyl 2-hydroxypropionate

calcium lactate
814-80-2

calcium lactate

3-methylbutyric acid
503-74-2

3-methylbutyric acid

Conditions
ConditionsYield
bei der Einw. verschiedener Hefen;
calcium lactate
814-80-2

calcium lactate

LACTIC ACID
849585-22-4

LACTIC ACID

Conditions
ConditionsYield
With sulfuric acid In water at 72 - 75℃; for 0.75h; pH=2.0; Purification / work up;
With sulfuric acid In water at 30℃; for 2h;
With sulfuric acid; ammonium chloride In water
With sulfuric acid
calcium lactate
814-80-2

calcium lactate

1,1'-bis(1,1'-carboxyethyl) ether
19201-34-4

1,1'-bis(1,1'-carboxyethyl) ether

Conditions
ConditionsYield
at 280℃;
calcium lactate
814-80-2

calcium lactate

3-hydroxy-2-butanon
513-86-0, 52217-02-4

3-hydroxy-2-butanon

Conditions
ConditionsYield
Einw. von Bacillus subtilis;
calcium lactate
814-80-2

calcium lactate

isopropyl alcohol
67-63-0

isopropyl alcohol

Conditions
ConditionsYield
With calcium hydroxide
calcium lactate
814-80-2

calcium lactate

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
bei der Vergaerung durch eine Mischkultur von zwei nicht bezeichneten Bakterien;
calcium lactate
814-80-2

calcium lactate

2.3-butanediol
513-85-9

2.3-butanediol

Conditions
ConditionsYield
bei der Vergaerung durch Bakterien der Gruppe Bacillus subtilis; substances of butanediol-(2.3), whose stereochemical homogeneity and configuration is unknown;
calcium lactate
814-80-2

calcium lactate

acetyl chloride
75-36-5

acetyl chloride

2-acetoxypropionic acid
535-17-1

2-acetoxypropionic acid

Conditions
ConditionsYield
at 60℃;
calcium lactate
814-80-2

calcium lactate

isopropyl alcohol
67-63-0

isopropyl alcohol

isopropyl lactate
617-51-6

isopropyl lactate

Conditions
ConditionsYield
With sulfuric acid
calcium lactate
814-80-2

calcium lactate

butan-1-ol
71-36-3

butan-1-ol

n-butyl lactate
138-22-7

n-butyl lactate

Conditions
ConditionsYield
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers;
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers;
calcium lactate
814-80-2

calcium lactate

hexan-1-ol
111-27-3

hexan-1-ol

n-hexyl lactate
20279-51-0

n-hexyl lactate

Conditions
ConditionsYield
With sulfuric acid; benzene unter azeotropem Abdestillieren des Reaktionswassers;
With sulfuric acid; toluene unter azeotropem Abdestillieren des Reaktionswassers;
sulfuric acid
7664-93-9

sulfuric acid

calcium lactate
814-80-2

calcium lactate

calcium sulfate

calcium sulfate

Conditions
ConditionsYield
In water at 83 - 95℃; for 1.03333 - 1.25h;
1-butyl-3-methyl-1H-imidazol-3-iumhydrogencarbonate
366491-15-8

1-butyl-3-methyl-1H-imidazol-3-iumhydrogencarbonate

calcium lactate
814-80-2

calcium lactate

1-butyl-3-methyl-3H-imidazol-1-ium lactate
797050-71-6

1-butyl-3-methyl-3H-imidazol-1-ium lactate

Conditions
ConditionsYield
Heating / reflux;
carbon dioxide
124-38-9

carbon dioxide

calcium lactate
814-80-2

calcium lactate

A

C3H6O3*C12H27N
95399-70-5

C3H6O3*C12H27N

B

calcium carbonate

calcium carbonate

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

814-80-2Relevant articles and documents

Synthesis of calcium phosphate powder from calcium lactate and ammonium hydrogen phosphate for the fabrication of bioceramics

Safronova,Putlyaev,Andreev,Filippov, Ya. Yu.,Knotko,Shatalova,Evdokimov

, p. 859 - 868 (2017)

A calcium phosphate powder has been synthesized from aqueous 0.25, 0.5, and 1.0 M calcium lactate and ammonium hydrogen phosphate solutions atat a Ca/P = 1, without pH adjusting. According to X-ray diffraction data, the as-synthesized powder consisted of brushite (CaHPO4 · 2H2O) and octacalcium phosphate (Ca8(HPO4)2(PO4)4 · 5H2O). After heat treatment in the range 500–700°C, the powders were gray in color because of the destruction of the reaction by-product. The powders heat-treated in the range 500–700°C consisted largely of γ-Ca2P2O7. The ceramics prepared from the synthesized powders by firing at 1100°C consisted of β-Ca2P2O7 and β-Ca3(PO4)2.

PREPARATION METHOD OF THE HIGH ACTIVATED CALCIUM BY SONOCHEMISTRY

-

Paragraph 0073-0078; 0080-0081, (2019/10/29)

An objective of the present invention is to provide a method for manufacturing an organic acid calcium salt (calcium citrate, calcium lactate) having a high degree of ionization and easy to be solved in water. To achieve this, the method comprises the steps of: performing pretreatment by mixing one or more kinds selected from a group consisting of calcium carbonate and calcium oxide with solvent, and irradiating ultrasonic waves to the solution; a step of mixing an organic acid with the solution to form a mixture; and a step of irradiating ultrasonic waves to the mixture formed by mixing the organic acid. Accordingly, provided is an effect of providing an organic calcium salt having a high degree of ionization and capable of being solved by several or more times solubility of each compound. Moreover, the method for manufacturing an organic acid calcium salt has a simple process and equipment and an excellent effect of being manufactured within 10 minutes.COPYRIGHT KIPO 2019

Tandem catalytic conversion of glycerol using solid catalysts followed by transesterification to produce alkyl lactate

Ren, Shoujie,Ye, X. Philip,Ayers, Paul D.

, p. 53230 - 53239 (2015/06/30)

This study investigated alkyl lactate production from glycerol by tandem processes which included glycerol conversion to calcium lactate using solid catalysts and subsequent transesterification of calcium lactate to alkyl lactate using methanol/ethanol and carbon dioxide. The effect of reaction conditions on alkyl lactate production was systematically investigated. A central composite design (CCD) and response surface methodology were used to design the experiments and evaluate the optimum process conditions. At the optimum conditions, the methyl lactate yield reached 57 mol% with a glycerol conversion of 94 mol% using refined glycerol. A yield of approximately 42 mol% for ethyl lactate was obtained using refined glycerol at the optimum conditions. Similar glycerol conversion and alkyl lactate yields were obtained using crude glycerol, indicating that the impurities in the crude glycerol had no significant effects on alkyl lactate production. The examination of regenerated catalysts that had been reused twice showed no negative effects on glycerol conversion and methyl lactate production. Compared to the traditional lactic acid and alkyl lactate production, this two-step process for alkyl lactate production from glycerol is both economical and environmentally benign since no gypsum was produced and the solid catalysts can be regenerated and reused.

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