GB894752A - Improvements in or relating to citric acid derivatives - Google Patents

Improvements in or relating to citric acid derivatives

Info

Publication number
GB894752A
GB894752A GB10124/60A GB1012460A GB894752A GB 894752 A GB894752 A GB 894752A GB 10124/60 A GB10124/60 A GB 10124/60A GB 1012460 A GB1012460 A GB 1012460A GB 894752 A GB894752 A GB 894752A
Authority
GB
United Kingdom
Prior art keywords
citryl
acid
trigluconic
calcium
iron
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB10124/60A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Reheis Co Inc
Original Assignee
Reheis Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Reheis Co Inc filed Critical Reheis Co Inc
Publication of GB894752A publication Critical patent/GB894752A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/67Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
    • C07C69/675Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
    • C07C69/704Citric acid esters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises citryl trigluconic acid, isolated as a syrup which has not been completely freed from water, and metal salts including calcium, magnesium and iron citryl trigluconates. Citryl trigluconic acid is made by reacting citric acid and gluconic acid or glucono-8-lactone in the proportion of approximately three moles of gluconic acid or lactone per mole of citric acid in aqueous solution at a temperature within the range from about 80 DEG C. to 110 DEG C. The metal salts may be made by reacting the citryl trigluconic acid in aqueous solution with an alkaline compound of the corresponding metal, for example, an oxide, hydroxide or carbonate, diluting the resulting solution with a watermiscible organic liquid in which the salt is insoluble in sufficient amount to precipitate the salt, and recovering the resulting precipitate. Citryl trigluconic acid finds many uses as a sequestering agent, and the metal salts may be used to remedy nutritive deficiencies.ALSO:Metal salts of citryl trigluconic acid may be used in aqueous solutions in compositions used to remedy nutritive deficiencies, such as calcium, magnesium and iron deficiencies, by injection or oral administration. For example, the calcium salt may be supplied in physiological saline containing 1 gm. of calcium citryl trigluconate per 10 c.c. A composition for injection may contain thiamine hydrochloride, liver extract and calcium citryl trigluconate. The magnesium salts are useful as laxatives alone and in conjunction with antacid mixtures. They may also be employed for parenteral administration as anticonvulsants, central depressants or dehydrants. The iron salts may be used as iron supplements for oral or intravenous administration.
GB10124/60A 1959-05-20 1960-03-22 Improvements in or relating to citric acid derivatives Expired GB894752A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US894752XA 1959-05-20 1959-05-20

Publications (1)

Publication Number Publication Date
GB894752A true GB894752A (en) 1962-04-26

Family

ID=22217850

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10124/60A Expired GB894752A (en) 1959-05-20 1960-03-22 Improvements in or relating to citric acid derivatives

Country Status (1)

Country Link
GB (1) GB894752A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992016493A1 (en) * 1991-03-16 1992-10-01 Basf Aktiengesellschaft Citric acid esters of polyhydroxyle compounds and their use in washing and cleaning products

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992016493A1 (en) * 1991-03-16 1992-10-01 Basf Aktiengesellschaft Citric acid esters of polyhydroxyle compounds and their use in washing and cleaning products
US5508394A (en) * 1991-03-16 1996-04-16 Basf Aktiengesellschaft Citric esters of polyhydroxy compounds and use thereof in detergents

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