507 References Supporting Oral EDTA
And
this is just a small sampling!
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1.
Toyota H, Shibata S (Kyoto University). Supplementary studies on pharmacology
of disodium ethylenediaminetetraacetate (EDTA salt). Nippon Yakuriguku Zasshi.
1956;52:1-9. (CA51:11567e)
2.
Uhl HSM, Brown HH, Zlatkis A, Zak, B, Myers GB, Boyle AJ. Effect of ethylenediamine-tetraacetic
acid (EDT) on cholesterol metabolism in man. Preliminary report of effect of parenteral
and oral administration of disodium and calcium salts. Am J Clin Pathol. 1953;
23:1226-1233. (CA48:2257d)
3.
Vasil'eva OG. (Inst Ind Hyg Occup Dis, Acad Med Sci, USSR) Side effects of CaNa2
ethylene-diaminetetraacetate in experimental lead intoxication. Gigiena 1 Sanitariya.
1961;26:22-5 (Mar.). (979)
4.
Vozar L. Complexons in food products and their effect on the metabolic processes.
Prumysl potravin. 1958; 9:649-653. (CA53:8461i)
5.
Vozar L. Effect of complexon III on the distribution of calcium and phosphorus
in bones. Biologia. 1958; 13:695-699. (CA55:5762e)
6.
Williams JD, Leigh DA. (Edgware General Hospital) Lead poisoning. Letters to the
editor. British Med J. 1964; 1:1511 (June 6). (2841)
7.
Williams JD, Matthews GA, Judd AW. (St. Paul's Hospital) Oral calcium disodium
versenate in treatment of lead poisoning. British J Ind Med. 1962; 19-211-215
(July). (2491)
8. Windsor E, Cronheim GE (Riker Labs,
Inc.). Gastrointestinal absorption of heparin and synthetic heparinoids. Nature.
1961; 190:203-204. (CA55:23818a) [Heparin Na U.S.P. and the K salt of sulfopolyglucin
can be absorbed from the gastrointestinal tract when given orally with an alk.
salt of ethylenediaminetetraacetic acid (I). The chelation of Ca and (or) Mg ions
by I may be involved.]
9.
Windsor E (to Riker Laboratories). Orally active therapeutic compositions, especially
polysaccharide sulfates. U.S. 3,088,868 (Cl 167-55). May 7, 1963, Appl Aug. 18,
1958. (CA59:12598d)
10.
Wynn JE, Van't Riet B, Borzelleca JF (Med. Coll. of Virginia). Toxicity and pharmaco-dynamics
of EGTA: oral administration to rats and comparisons with EDTA. Toxicol Appl Pharmacol.
1970; 16(3):807-817. (CA73)
11. Yang SS. Toxicological
investigations of ethylenediaminetetraacetic acid. Dissertation. Univ. Mass. 1952:94
p.
12.
Rieders F, Copeland JE (Jefferson Med Coll). Inhibition of accumulation of chronically
ingested lead in rats by simultaneous feeding of edathamil calcium disodium (Na2CaEDTA).
Federation Proceedings. 1956; 15:Abstract No. 1541 (Mar.). (693)
13.
Schuttmann C, Schuttmann W (Inst. Of Occup Med, Berlin-Lichtenberg). The medical
prevention of occupational lead poisoning by oral administration of calciumdinatrium
ethylenediaminetetraacetate. Zeitschrift fur Arztliche Fortbildung. 1963; 57:1301-1307
(Dec.). (2621)
14.
Shiels DO, Thomas DLG, Kearley E. Treatment of lead poisoning by edathamil calcium-disodium.
AMA Arch of Ind Health. 1956; 13:489-498 (May). (1718)
15.
Savicevic M, Petrovic L. Prevention of industrial lead poisoning. Vojnosanitetski
Pregled. 1962; 19:531-535 (July-Aug.). (3191)
16.
Salvini M (Univ. Padua). The calcium chelate of disodium ethylenediamine tetraacetate
in the treatment of saturnism. Folia Medica (Naples). 1955; 38:2:111-126. (1616)
17.
Saruta N, Yamaguchi S. A new diagnostic method of occupational lead poisoning
for group inspection. J Sci of Labour (Japan). 1957; 33:540 (July). (1855)
18.
Ritter J, Dacquet J (Inst. Hyg. Rabat, Morocco). Detection and ambulatory treatment
of lead poisoning by oral administration of calcium di-sodium versenate. Maroc
Medical. 1961; 40:377-382 (Apr.). (2323)
19.
Remy R (Inst. Physiol. Vet. Coll.). Experimental studies on lead poisoning in
animals. I. Toxicology. II. Therapy and prophylaxis. Deutsche Tierurztliche Wochenschrift.
1956; 63:385-388; 405-408 (Oct. 1; 15). (692)
20.
Pott R. Control of lead exposure as practiced in a lead foundry. Zentralplatt
fur Arbeltsmedizin Arbeitsschutz. 1961; 11:211-214 (Sept.). (2317)
21.
Pott R. Is prophylaxis of lead poisoning with EDTA possible? Archiv fur Gewerbe-pathologie
Gewerbehygiene. 1959; 17:4:354-364. (2053)
22.
Pettinati L, Gribaudo C, Rasetti L. Oral and intravenous versenate in the therapy
of chronic lesions caused by lead. Minerva Medica. 1962; 53:2092-2097 (July).
(2458)
23. Pendergrass JC. The effects of the chronic
ingestion of low levels of inorganic mercury(11) and mercury(11) complexed with
EDTA on the rodent neuronal cytoskeleton: possible role of these forms of environmental
mercury exposure in the etiology of Alzheimer's disease. Diss Abstr Int B (Avail.
Univ. Microfilms Int., Order No. DA9527428. 1975; 1995:56(4). (CA)
24.
Oser BL, Oser M, Spencer HC. Safety evaluation studies of calcium EDTA. Toxicol
Appl Pharmacol. 1963; 5:142-162. (CA59: 9223a)
25.
Moeschlin S. The clinical picture and therapy of lead poisoning. Zeitschrift fur
Unfallmedizin Berufskrankheiten 51. 1958; 2:129-149. (1936)
26.
Myslak Z, Buczkowski M. The effect of calcium versenate (Ca-EDTA) on the kidney
in the treatment of lead poisoning. Polskie Archiwum Medycyny Wewnetrznej. 1961;
31:853-856. (2304) [Kidney function tests (creatinine clearance, RN) were carried
out on 20 out of 120 cases of chronic Pb poisoning treated by oral administration
of CaEDTA. The results showed no harmful effect of EDTA on the kidneys during
treatment.]
27. Myslak Z. Treatment of chronic saturnism
by oral administration of calcium versenate. Medycyna Pracy. 1960; 11:353-368.
(2169)
28.
Nakaue HS, Thomas JM, Reid BL. Comparison of EDTA, terephthalic acid, sodium sulfate
and acetyl-salicylic acid as antibiotic potentiating agents in broiler chicks.
Poultry Sci. 1967; 46:417-421. (NA38)
29.
Vozar L. Relation between peroral application of complexon 3 (ethylenediaminetetraacetic
acid disodium salt) and the activity of alkaline phosphatase of blood serum. Biologia.
1960; 15:208-211. Z Inn Med. 1959; 14:676. (CA54:25290h)
30.
Thomsen MK, Jacobsen C, Skibsted L II. Mechanism of initiation of oxidation in
mayonnaise enriched with fish oil as studied by electron spin resonance spectroscopy.
Eur Food Res Technol. 2000; 211(6):381-386. (CA)
31.
Sidbury JB Jr., Bynum JC, Fetz LL. (US Public Health Serv.) Effect of chelating
agent on urinary lead excretion. Comparison of oral and intravenous administration.
Proceedings of Soc Experimental Biol and Med. 1953; 82:226-228. (1444)
32.
McMahon FG. Comparison of the effect of Fe 3-specific (N, N-dihydroxyethylglycine),
versenol, and calcium disodium versenate on urinary iron excretion in a patient
with hemochromatosis. J Lab Clin Med. 1956; 48:589-602. (CA51:3027c)
33.
McPhail AP, Patel RC, Bothwell TH, Lamparelli RD. EDTA and the absorption of iron
from food. Amer J Clin Nutr. 1994; 59(3):644-648. (NA64)
34.
Manville IA, Moser R. Recent developments in the care of workers exposed to lead.
The effect of the calcium chelate of disodium ethylenediamine-tetraacetic acid
on led in the blood and urine of battery workers. AMA Arch Ind Health. 1955; 12:528-538
(Nov.). (1587)
35.
Heimbach J, Rieth S, Mohamedshah F, Slesinski R, Samuel-Fernando P, Sheehan T,
Dickmann R, Borzelleca J. Safety assessment of iron EDTA (sodium iron (Fe3+) ethylenediaminetetraacetic
acid): summary of toxicological, fortification and exposure data. Food Chem Toxicol.
2000; 38(1):99-111. (CA) [A review with many refs. Iron EDTA
36.
Davidsson L, Kastenmayer P, Hurrell RF. Sodium iron EDTA (NaFe(III)EDTA) as a
food fortification: the effect on the absorption and retention of zinc and calcium
in women. Amer J Clin Nutr. 1994; 60(2):231-237. (NA64)
37.
Foreman H, Trujillo TT. Metabolism of carbon14-labeled ethylenediaminetetraacetic
acid in human beings. J Lab Clin Med. 1954; 43:566-571. (CA48: 8949a)
38.
Foreman H. The pharmacology of some useful chelating agents. Metal Binding Med,
Proc Symposium, Philadelphia 1959. 1960; 82:94. (CA54:17719e)
39.
Bradley JE, Powell AM Jr. Oral calcium EDTA in lead intoxication of children.
J Ped. 1954; 45:297-301 (Sept.). (2882)
40.
Capellaro F, Galdo PC, Alliod R. Possibility of treating saturnism by versenate
by the oral route. Minerva Medica. 1963; 54:474-477. (2508)
41.
Calabrese A, Astolfi E, Mariani F. Oral treatment of lead intoxication with calcium
versenate. Clinical and experimental study. Dia Medico. 1961; 33:2292-2294 (Oct.
5). (2239)
42. Cotter LH. Treatment of lead poisoning
by chelation. JAMA. 1954; 155:906-908. (CA52:10388a)
43.
Choie DD, Copley MP, Gindhart TD. Mitigation of intestinal cytotoxicity of cisplatin
by EDTA in rats. Cancer Lett. 1983; 19(2):195-198. (CA)
44.
Cohn SH. The effect of chemical agents on the skeletal content and excretion of
internally deposited fission products. US Atomic Energy Comm. ANL-5584. 1956;
144-149. (CA51:4557f)
45.
Flanagan PR, Chamberlain MJ, Valberg LS. The relationship between iron and lead
absorption in humans. Am J Clin Nutr. 1982; 36(5):823-9. (CA)
46.
Forbes RM. Excretory patterns and bone deposition of zinc, calcium, and magnesium
in the rat as influenced by zinc deficiency, EDTA, and lactose. J Nutr. 1961;
74:194-200. (CA59:7921b)
47.
Davidson L, Almgren A, Hurrell RF. Sodium iron EDTA (NaFe(III) EDTA) as a food
fortificant does not influence absorption and urinary excretion of manganese in
healthy adults. J Nutr. 1998; 128(7): 1139-1143. (CA)
48.
Desoille H, Albahary C, Truhaut R, Boudene C. The lead mobilization test using
CaNa2EDTA. XII Intern Cong Occup Health. Helsinki, Finland. 1957; Vol. 111, Proceedings,
pp. 287-290. (1773)
49.
Davies NM, Jamali F. Pharmacological protection of NSAID-induced intestinal permeability
in the rat: effect of tempo and metronidazole as potential free radical scavengers.
Hum Exp Toxicol. 1997; 16(7):345-349. (CA)
50.
Kalz F, Quastel J II, Telner P, Schafer A, MacIntyre W. Changes in the electrophoretic
patterns of the serums of psoriatics under various forms of therapy. J Invest
Dermatol. 1958; 31:161-166. (CA53:20529a)
51.
Kehoe RA. Misuse of edathamil calcium-disodium for prophylaxis of lead poisoning.
J Amer Med Assoc. 1955; 157:341-342 (Jan. 22). (1582)
52.
Mariani B, Bisetti A, Romeo V. Blood-cholesterol-lowering action of the sodium
salt of calciumethylenediaminetetraacetic acid. Gazs Intern Med Chir. 1957; 62:1812-1823.
(CA51:16953c) [Two g. daily of the drug, in 2 intravenous administrations, or
(with a lower effect) by mouth or rectum, caused in humans a decrease of blood
cholesterol, especially of its free fraction.]
53.
Stankovic M, Petrovic LJ, Poleti D (Inst. Public Health, Belgrade, Serbia). A
contribution to the laboratory diagnostics of early saturnism. Arhiv za Higijenu
Rada 1 Toksikologiju. 1962; 13:189-194. (2480)
54.
Srbova J, Telsinger J (Clinic Occup. Dis., Prague). Absorption of calcium disodium
salt of ethylenediaminetetraacetic acid after oral administration in the treatment
of lead poisoning. Archiv fur Gewerbepatholgie und Gewerbehygiene 15. 1957; 6:572-580.
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55.
Suenaka T, Kosaka H, Miyama K, Tabuchi T, Hirata M, Hara I, Masumoto D, Akaboshi
S (Osaka Prefect Inst. Public Health, Osaka). The effects of repeated oral administration
of calcium-EDTA on patients with chronic lead poisoning. Osaka-furitsu Koshu Eisei
Kenkyusho Kenkyu Hokoku, Rodo Eisei Hen. 1979; 17:1-9. (CA)
56.
Suenaka T, Miyajima K, Kosaka H, Tbuchi T, Hara I. Urinary excretion of heavy
metals following oral administration of calcium EDTA. Osaka furitsu Koshu Eisei
Kenkyusho Kenkyu Hokoku, Rodo Eisei Hen. 1976; 14:19-23. (CA)
57.
Swenerton H, Hurley L S (Dept. Nutr. Univ. Calif., Davis, Calif.). Teratogenic
effects of a chelating agent and their prevention by zinc. Science. 1971; 173
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58. Telsinger J, Srbova
J. Effect of D-penicillinamine on the urinary excretion of mercury and lead. Pracovni
Lekarstvi 16. 1964; 10:433-435. (2827) [Seven patients with chronic Pb poisoning
were treated with daily oral doses of 150 mg D-penicillinamine for 4-7 days. Urinary
excretion of Pb increased about 4-fold which is practically as much as after administration
of 0.5-g tablets of CaEDTA, 4 times/day. If future studies confirm its lower toxicity
in long-term administration, D-penicillinamine may replace EDTA.]
59.
Tripod J. General pharmacodynamic aspects of mobilizing iron with chelators. Atti
Acad Med Lombarda, Suppl 20. 1965; 2025-2027. (CA67)
60.
Tufft LS, Nockels CF. The effects of stress, escherichia coli, dietary ethylenediamine-tetraacetic
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61.
Tolot F, Jaquis GM, Soubrier R, Bresson JR. Lead mobilization in, and the &-aminolevulinic
acid (ALA) content of the urine of lead-exposed subjects. Egesesegiudomany. 1966;
10(4):375-380. (CA66)
62.
Tolot F, Jaquis GM, Soubrier R, Bresson JR. The use of chelating agents "per
os" in the treatment of prophylaxis of lead poisoning. Proceedings of the
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63.
Perrault M. Truhaut R, Klotz B, Boudene C, Dreux C, Clavel B, Chain F. The effectiveness
of CaEDTA, in occupational lead poisoning. Archiv des Maladies Professionelles
de Medecine du Travail et de Securite Sociale. 1956; 17:423-429; discussion 470-472.
(1702)
64. Mitchell Jr PH, Schroeder HA. Depression
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Prasad T, Chhabra A, Atreja PP. Effect of feeding chelating agent (EDTA) on trace
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66.
Rodriguez A. Substances that potentiate the absorption of vitamin B12 administered
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67.
Rotta C, Parigi A. Prevention of lead intoxication by oral administration of calcium
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68.
Saita G, Moreo L. Lead and porphyrins in the bile of patients with lead poisoning
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70.
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Bersworth Chemical Co. The versenes for exacting chemical control of cations in
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72.
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73.
British Industrial Biological Research Association. The metabolism of EDTA. Food
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74.
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Montpellier Medical. 1962; 61:12-27 (Jan.). (2401)
75.
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76.
Teisinger J, Zumanova R, Zezula I. Effect of calcium salt of ethylenediaminetetraacetic
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77.
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78.
Taucin EJ, Svilane ABV. Effect of EDTA and chlortetracycline on assimilation of
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79. Suenaka T, Miyajima
K, Kosaka H, Tabuchi T, Hara I. Urinary excretion of heavy metals following oral
administration of calcium-EDTA. Osaka-furitsu Koshu Eisei Kenkyusho Kenkyu Hokoku,
Rodo Eisei Hen. 1977; 15:27-31. (CA) [Ca EDTA, administered to workers dealing
with Pb, significantly increased Pb and Zn excretion in urine. There was a high
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80.
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82.
Pagnotto LD, Elkins HB, Bayka I. Oral administration of edathamil calcium disodium
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(P1943)
83.
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the porphyrinic precursors in lead poisoning. Lavoro e Medicina 16. 1962; 3:44-50.
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84.
Peters HA, Eichman PL, Price JM, Kozelka FL, Reese HH. Abnormal copper and trytophan
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Petrovic LJ, Stankovic M, Savicevic M, Poleti D. Our experiences with calcium
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86. Pilat L, Moscovici
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88.
Reinl W. Prophylaxis of lead workers with orally administered Ca2EDTA. Zentralblatt
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Bell RF, Gilliland JC, Boland JR, Sullivan BR. Effect of oral edathamil calcium-disodium
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96.
Blomquist L, Bark T, Hedenborg G, Norman A. Evaluation of lactulose/mannitol and
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Gehres RF, Raymond S. A new chemical approach to the solution of urinary calculi.
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Makashev KK. Effect of calcium and disodium salts of ethylenediaminetetraacetic
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MacPhail AP, Bothwell TH, Torrance JD, Derman DP, Bezwoda WR, Charlton RW, Mayet
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113.
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Stankovic M, Petrovic LJ, Poleti D. Application of Ca2EDTA (dicalcium ethylenediamine-tetraacetate)
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The compound was administered orally to 24 printers, 18 persons with severe Pb
poisoning, and 8 controls with no Pb exposure. The upper limit of Pb excretion
in urine after 3 g CaEDTA was 0.340 mg/24 hr.
115.
Suso FA, Edwards Jr HM. Influence of various chelating agents on absorption of
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116.
Vozar L. The action of complexon 3 on the copper balance and level in the organism
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117.
Nielsen FH, Sunde ML, Hockstra WG. Effect of some dietary synthetic and natural
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118.
Pedinelli M, Stringari M. Observations on the treatment "per os" with
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119. Preda N,
Niculescu T, Rafaila E. The treatment of lead intoxication with chelating agents.
Igiena (Bucharest)13. 1964; 3:233-242. (2784) Treatment of Pb-poisoned patients
in the Clinic for Occupational Diseases, Bucharest, with iv injections of 2 g
CaNa2EDTA/day for 2-20 days markedly increased urinary excretion of Pb. Oral doses
of 4-6 g EDTA/day were less effective.
120.
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Anon. Dressings for foods. Food additives. Calcium disodium ethylenediamine-tetraacetate,
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order amending identity standard to permit calcium disodium ethylenediaminetetraacetate
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225. Anon. Food additives.
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226. Anon. Food additives. Calcium disodium
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227. Anon.
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228.
Anon. Food additives. Calcium disodium ethylenediaminetetraacetate. Federal Register,
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p.p.m. in or on cooked, canned shrimp to retard struvite formation and to promote
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229. Anon. Food additives. Calcium
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230.
Anon. food additives. Calcium disodium ethylenediaminetetraacetate. Federal Register,
cf. CA 55, 10737c. July 13, 1961; 26:6271-6272. (CA55:20243a)
231.
Anon. Food additives. Chelating agents. Federal Register, cf. CA 55, 20246a.
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food.]
232. Anon. Food additives. Calcium disodium
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Federal Register, cf. CA 58, 3822b. Sept. 25, 1963; 28:10377-10378. (CA59:14495e)
[The title compd. may be used as a stabilizer of the color of canned clams under
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233.
Anon. Food additives. Disodium EDTA. Federal Register, cf. CA 62, 3316c. Nov.
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234. Anon. Food additives. Disodium
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235. Anon. Food additives. Disodium
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[The previous regulation under the Federal Food, Drug, and Cosmetic Act is revised
to permit the use of di-Na EDTA to promote color retention in dried banana products
(315 p.p.m. max.) used as a component of cereal products and in canned cooked
chickpeas (165 p.p.m. max.).]
236. Anon. Food additives.
Disodium EDTA. Federal Register. June 18, 1965; 30:7895. (CA63:6238b) [Disodium
EDTA, min. 99% dihydrate, may be used under the Federal Food, Drug, and Cosmetic
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237. Anon. Food additives.
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238.
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