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Calcium lactate is a black or white crystalline salt produced by the reaction of lactic acid with calcium carbonate or calcium hydroxide. It is commonly found in aged cheeses and is used in various applications, including food, medicine, and dental care.
Used in Food Industry:
Calcium lactate is used as a stabilizer and texture improver for canned fruits and vegetables, preventing structural collapse during cooking. It is also used in angel food cake, whipped toppings, and meringues to increase protein extensibility, resulting in an increased foam volume.
Used in Bakery:
Calcium lactate is used as an ingredient in baking powder, helping to leaven the dough and improve the texture of baked goods.
Used in Medicine:
Calcium lactate is used as an antacid to neutralize stomach acid and treat calcium deficiencies. It can be absorbed at various pH levels and does not require food for absorption.
Used in Dental Care:
Calcium lactate is added to sugar-free foods and chewing gum containing xylitol to prevent tooth decay and increase the remineralization of tooth enamel.
Used in Food Preservation:
Calcium lactate is used as a preservative in foods and beverages to extend their shelf life, as well as in fresh-cut fruits like cantaloupes to keep them firm without imparting a bitter taste.
Used in Personal Care:
Calcium lactate is used in dentifrices to promote oral health and prevent tooth decay.
Used in Calcium Fortified Foods:
Calcium lactate is used in calcium-fortified foods such as infant foods and to improve the properties of dry milk powder.

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  • 814-80-2 Structure
  • Basic information

    1. Product Name: Calcium lactate
    2. Synonyms: CALCIUM LACTATE, TRIHYDRATE;LACTIC ACID CALCIUM SALT, TRIHYDRATE;2-HYDROXYPROPANOIC ACID CALCIUM SALT, TRIHYDRATE;2-hydroxy-propanoicacicalciumsalt(2:1);calciumlactate(1:2);calphosan;conclytecalcium;-Hydroxypropanoicacidcalciumsaltpentahy-drate
    3. CAS NO:814-80-2
    4. Molecular Formula: 2C3H5O3*Ca
    5. Molecular Weight: 218.22
    6. EINECS: 212-406-7
    7. Product Categories: Nutritional fortification substances;Food additve and acidulant;Food additives
    8. Mol File: 814-80-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 227.6 °C at 760 mmHg
    3. Flash Point: 109.9 °C
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: Soluble in water, freely soluble in boiling water, very slightly soluble in ethanol (96 per cent).
    9. CAS DataBase Reference: Calcium lactate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Calcium lactate(814-80-2)
    11. EPA Substance Registry System: Calcium lactate(814-80-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. TSCA: Yes
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 814-80-2(Hazardous Substances Data)

814-80-2 Usage

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.

Highly Efficient Iridium-Catalyzed Production of Hydrogen and Lactate from Glycerol: Rapid Hydrogen Evolution by Bimetallic Iridium Catalysts

Cheong, Yeon-Joo,Sung, Kihyuk,Kim, Jin-A,Kim, Yu Kwon,Jang, Hye-Young

, p. 4064 - 4068 (2020/09/12)

Mono- and bimetallic iridium complexes involving novel triscarbene ligands were synthesized and applied to the dehydrogenation of biomass-derived glycerol. This resulted in affording hydrogen and lactate with the excellent turnover number (TON; 3,240,000) and turnover frequency (TOF; 162,000 h–1). The triscarbene ligand in a single frame allowed the formation of bimetallic iridium complexes. This induced the cooperative effect of two iridium ions and rendered excellent TONs and TOFs in the production of hydrogen and lactate.

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

A polylactic acid waste recovery method (by machine translation)

-

Paragraph 0081-0082, (2017/08/30)

The present invention provides a polylactic acid (PLA) waste recovery method, comprises the following steps, first the PLA dissolved in the lactide in waste heat, and then adding water after the reaction, thereby obtaining a reaction mixture; then the above-mentioned step the obtained product with the calcium source after mixing and reacting, get the calcium lactate. The preparation process using high boiling point of lactide dissolved PLA waste, the high molecular weight of the PLA in the not too high temperature condition, can be at the molecular level with the water contact undergo rapid hydrolysis reaction of generating lactic acid, calcium lactate product finally obtained. The present invention provides a method for recovery of the process is simple, mild condition, high conversion rate, without the use of a catalyst, can reduce the waste emission, safety and environmental protection; and the present invention provides the preparation method also can cycle the feeding, the continuity is good, is more suitable for large-scale industrial production, it has certain economic and social benefits. (by machine translation)

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.

A GLYCEROL DERIVED MATERIAL

-

Page/Page column 56 - 58, (2010/04/03)

A method of producing a solid glycerol derived material includes the steps of combining glycerol with a metal oxide, the glycerol having a water content of between about 5 and 50%, and the rate of combination of the glycerol and the metal oxide and the amount of the metal oxide being selected so that at least part of the water present in the glycerol reacts with the metal oxide in an exothermic reaction and at least part is driven off by heat produced in the exothermic reaction to produce the solid glycerol derived material.

Nutritional and pharmaceutical compositions

-

Page/Page column 3, (2008/06/13)

Th present invention relates to nutritional and pharmaceutical compositions. More particularly it is concerned with improving compositions which due to the presence of an efflorescent component may be unstable and prone to decomposition and/or spoilage. The problem is overcome by incorporating one or mote anhydrous compounds into the composition in an amount capable of sequestering any water which may be released from one or more water containing components. The preferred anhydrous compounds are anhydrous or calcined MgSO4 and CaO.

Highly acidic metalated organic acid

-

Page/Page column 11, (2008/06/13)

A highly acidic metalated organic acid composition and its preparation. The acidic composition can be prepared by mixing a monovalent or polyvalent cation and an organic acid in the presence of a strong oxyacid, wherein the resultant acidic composition is less corrosive to a ferrous metal than a solution of a mineral acid having the same acidic pH value as that of the acidic composition, and where in the acid composition is more biocidal than a mixture of the organic acid and a metal salt of the organic acid which mixture has the same acid normality value as that of the acidic composition. The acidic composition can be prepared by mixing at least one regenerating acid, at least one metal base, and at least one organic acid, wherein the amount of the regenerating acid is in excess of the equivalent amount of the metal base.

COMPOSITION CONTAINING READILY ABSORBABLE CALCIUM AND PROCESS FOR PRODUCING THE SAME

-

, (2008/06/13)

A composition containing readily absorbable calcium which comprises a calcium salt and 0.2 to 5% by weight of chondroitin sulfate based on the calcium content in the calcium salt. A calcium salt preferably used in this composition is obtained by, for example, baking external skeletons of sea urchins in an oven to thereby give calcium oxide, hydrating it into calcium hydroxide and then reacting it with an organic carboxylic acid to thereby give a calcium salt. The absorption of calcium in vivo is highly promoted by adding chondroitin sulfate. As a calcium source various natural and synthetic calcium can be used.

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