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62-54-4/Calcium acetate

Quick Details
Molecular Formula:C4H6CaO4
Molecular Weight:158.167
Appearance:white crystals or powder
CasNo:62-54-4

  • Product Details

    Factory Sells Best Quality Calcium acetate 62-54-4 with stock

    • Molecular Formula:C4H6CaO4
    • Molecular Weight:158.167
    • Appearance/Colour:white crystals or powder 
    • Melting Point:160 °C (dec.) 
    • Refractive Index:1.5500 
    • Boiling Point:117.1 °C at 760 mmHg 
    • Flash Point:40 °C 
    • PSA:52.60000 
    • Density:1.5 g/cm3 
    • LogP:0.02760 

    Calcium acetate(Cas 62-54-4) Usage

    Chemical properties

    Calcium acetate, also known as acetate of lime or vinegar salts, is the calcium salt of acetic acid. It is an odorless powder. Calcium has an important role in the nutrition of humans and animals. Hormonal mechanisms control absorption of dietary calcium (including added calcium salts) allowing adaptation to a range of calcium intakes while maintaining a relatively constant blood calcium concentration of about 10 mg/100 mL. Major functions of calcium inside the body include the formation and maintenance of bones and teeth, the physiology of muscle contraction, the cell membrane integrity, the activity of several enzymes that have specific requirement for it, the coagulation of blood, and the regulation of acid-base balance.*

    Toxicity

    ADI is not subject to restrictive regulations (FAO/WHO, 2001). GRAS (FDA, §181.29, §182.6197, § 184.1185, 2000). LD50: 52 mg/kg (mouse, subcutaneous).

    Usage limit

    GB 14880 a 94: cereals and their products, beverages 8~16g/kg. GB 2760-2001: vinegar, 6~8g/kg (in terms of Ca). FAO/WHO (1984): Edible caseinate, GMP. FDA, § 184.1185 (2000): baked goods, gelatin, pudding, fillings, 0.2%; sweet sauce, top materials and poured, 0.15%; EEC can be used for packaging cheese powder, quick-setting jelly powder. FEMA (mg/kg): soft drinks 200; baked goods 500.

    Production method

    It is obtained by the reaction between calcium carbonate and acetic acid. Preparation method of anhydrous calcium acetate: the refined powder of calcium carbonate is added to the water, stirred into a suspension; added separately of a small amount of glacial acetic acid. After completion of the reaction, the filtrate was concentrated in a water bath and a white solid, anhydrous calcium acetate, was precipitated from the viscous filtrate. It is obtained by the neutralization between coke acid (wood acetic acid) and calcium hydroxide, followed by the evaporation of the filtrate and recrystallization. It is obtained by the reaction between the reaction between acetic acid and calcium hydroxide or calcium carbonate. Filter, concentrate and cool to obtain the dihydrate (colorless crystal), heated to 84 °C in a water salt (colorless crystal), heated to 100 °C to obtain the anhydrous salt. Shellfish can be taken as raw materials, washed, crushed and dried for 1 h, subjecting to barbecue for 2 hour at 900~l000 ℃, then being added water to make a 1.3~1.5mol/L lime milk. And then neutralized with acetic acid to clarify, filter with the filtrate concentrated, and finally dried at 120~140 °C to get the final product with a yield of 91.28%. To a 20% acetic acid solution, add calcium carbonate powder to until there is no longer any CO2 gas escaping, then add a small amount of calcium carbonate, heated? 80 ° C for reaction of 2-3h. The filtrate was heated and concentrated with water bath while adding a small amount of 80% acetic acid at the same time to precipitate the calcium acetate monohydrate (what precipitated after the cooling of the solution is dihydrate), and finally dried at 60~70 ℃to derive the products.

    Hazards & Safety Information

    Category:? Toxic substances Toxicity classification:? highly toxic Acute toxicity:? intravenous-mouse LD50: 52 mg/kg; celiac-mouse LD50: 75 mg/kg Flammability and Hazardous characteristics:? Thermal decomposition releases Pungent irritation Smoke Storage and transportation characteristics:Treasury: ventilated, low temperature drying; store it separately from food raw materials Fire extinguishing agent:? water, dry powder, foam, carbon dioxide

    Production Methods

    Calcium acetate can be prepared by soaking calcium carbonate (found in eggshells, or in common carbonate rocks such as lime stone or marble) in vinegar: CaCO3 + 2CH3COOH → Ca(CH3COO)2 + H2O + CO2 Since both reagents would have been available pre-historically, the chemical would have been observable as crystals then.

    Preparation

    Produced by calcium hydroxide neutralization of acetic acid.

    Definition

    ChEBI: The calcium salt of acetic acid. It is used, commonly as a hydrate, to treat hyperphosphataemia (excess phosphate in the blood) in patients with kidney disease: the calcium ion combines with dietary phosphate to form (insoluble) calcium phosphate, which is excreted in the faeces.

    General Description

    Calcium Acetate belongs to the group of calcium salts, widely used as phosphorus binders in patients with chronic renal failure.Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

    Pharmaceutical Applications

    Calcium acetate is used as a preservative in oral and topical formulations. Therapeutically, parenteral calcium acetate acts as a source of calcium ions for hypocalcemia or electrolyte balance. Oral calcium acetate is used as a complexing agent for hyperphosphatemia in dialysis patients. Calcium acetate is also used in the food industry as a stabilizer, buffer and sequestrant.

    Safety Profile

    Poison by intravenous and intraperitoneal routes. Mutation data reported. See also CALCIUM COMPOUNDS. When heated to decomposition it emits acrid smoke and fumes.

    Safety

    Calcium acetate is used in oral and topical formulations. The pure form of calcium acetate is toxic by IP and IV routes. LD50 (mouse, IP): 0.075 g/kg LD50 (mouse, IV): 0.052 g/kg LD50 (rat, oral): 4.28 g/kg

    Veterinary Drugs and Treatments

    Calcium acetate can be used for oral administration to treat hyperphosphatemia in patients with chronic renal failure. Secondary to its phosphorus binding efficiency and lower concentration of elemental calcium, calcium acetate is considered the most effective and having the lowest potential for causing hypercalcemia of the calcium-based phosphorus-binding agents. When compared to calcium carbonate, calcium acetate binds approximately twice as much phosphorus per gram of elemental calcium administered. Unlike calcium citrate, calcium acetate does not promote aluminum absorption.

    Metabolism

    The residual acetate will be metabolised through bicarbonate, which will be further excreted via normal metabolic routes. Any unbound calcium not involved in the binding of phosphate will be variable and may be absorbed. Calcium is absorbed mainly from the small intestine by active transport and passive diffusion. About one-third of ingested calcium is absorbed although this can vary depending upon dietary factors and the state of the small intestine. 1,25-Dihydroxycholecalciferol (calcitriol), a metabolite of vitamin D, enhances the active phase of absorption. Excess calcium is mainly excreted renally. Unabsorbed calcium is eliminated in the faeces, together with that secreted in the bile and pancreatic juice. Minor amounts are lost in the sweat, skin, hair, and nails.

    storage

    Calcium acetate is stable although very hygroscopic, and so the monohydrate is the common form. It decomposes on heating (above 1608℃) to form calcium carbonate and acetone. Store in well-closed airtight containers.

    Incompatibilities

    Calcium acetate is incompatible with strong oxidizing agents and moisture.

    Regulatory Status

    GRAS listed. Accepted for use as a food additive in Europe. Included in the FDA Inactive Ingredients Database (oral suspensions and tablets; topical emulsions, lotions, and creams). Included in nonparenteral medicines (oral tablets) licensed in the UK.

    InChI:InChI=1/C2H4O2.Ca/c1-2(3)4;/h1H3,(H,3,4);/q;+2/p-1

    62-54-4 Relevant articles

    Synthesis of CaCu3Ti4O12, Study of Physicochemical and Photocatalytic Properties

    Ivanov,Alekseeva,Agafonov

    , (2020)

    Abstract: Precursor CaCu3Ti4O12 has been...

    Synthesis, characterization and the thermal decomposition of calcium(II)bis(oxalato)calcium(II)dihydrate

    Deb,Baruah,Dass

    , p. 301 - 308 (1996)

    Calcium(II)bis(oxalato)calcium(II)dihydr...

    Dissolution of calcium carbonate in aqueous solutions of acetic acid

    Blinkova,Eliseev

    , p. 1064 - 1066 (2005)

    A kinetic equation for the calcium carbo...

    DIRECT CONVERSION OF ESTERS TO CARBOXYLATES

    -

    Paragraph 0041, (2022/03/22)

    A calcium carboxylate is prepared by rea...

    On the nature of calcium magnesium acetate road deicer

    Miller, Jennifer R.,LaLama, Matthew J.,Kusnic, Rachel L.,Wilson, Darian E.,Kiraly, Paije M.,Dickson, Samuel W.,Zeller, Matthias

    , p. 1 - 10 (2018/11/20)

    CMA (calcium magnesium acetate) road dei...

    RECOVERY OF ORGANIC ACID USING A COMPLEX EXTRACTION SOLVENT

    -

    Page/Page column 34-35, (2012/05/05)

    A method is disclosed for the recovery o...

    62-54-4 Process route

    calcium hypochlorite
    7778-54-3

    calcium hypochlorite

    acetone
    67-64-1

    acetone

    chloroform
    67-66-3,8013-54-5

    chloroform

    calcium acetate
    62-54-4

    calcium acetate

    calcium hydroxide

    calcium hydroxide

    Conditions
    Conditions Yield
    In acetone; Ca(ClO)2 reacts with acetone forming CHCl3, Ca(CH3CO2)2 and Ca(OH)2;;
    In acetone; Ca(ClO)2 reacts with acetone forming CHCl3, Ca(CH3CO2)2 and Ca(OH)2;;
    calcium diformate
    544-17-2

    calcium diformate

    calcium acetate
    62-54-4

    calcium acetate

    Conditions
    Conditions Yield
    91%

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