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Merck
CN

60155

Sigma-Aldrich

Potassium citrate tribasic monohydrate

tested according to Ph. Eur.

Synonym(s):

Kalii citras, Citric acid tripotassium salt, Tripotassium citrate

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About This Item

Linear Formula:
HOC(COOK)(CH2COOK)2 · H2O
CAS Number:
6100-05-6
Molecular Weight:
324.41
Beilstein:
3924344
EC Number:
231-905-0
MDL number:
MFCD00150442
UNSPSC Code:
12352300
PubChem Substance ID:
329758775

Key Documents

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Agency

USP/NF
tested according to Ph. Eur.

Assay

99-101% anhydrous basis

form

solid

mp

275 °C (dec.) (lit.)

application(s)

pharmaceutical (small molecule)

SMILES string

O.[K+].[K+].[K+].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O

InChI

1S/C6H8O7.3K.H2O/c7-3(8)1-6(13,5(11)12)2-4(9)10;;;;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);;;;1H2/q;3*+1;/p-3

InChI key

PJAHUDTUZRZBKM-UHFFFAOYSA-K

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Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBT5295

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Andrea Zatelli et al.
TheScientificWorldJournal, 2012, 219082-219082 (2012-05-18)
Chitosan and alkalinizing agents can decrease morbidity and mortality in humans with chronic kidney disease (CKD). Whether this holds true in dog is not known. Objective of the study was to determine whether a commercial dietary supplement containing chitosan, phosphate
Donna J Claes et al.
Pediatric nephrology (Berlin, Germany), 27(11), 2031-2038 (2012-01-28)
Cystinuria is a relatively uncommon cause of pediatric stone disease, but has significant morbidity if not properly controlled because of its significant stone recurrence rate. Cystinuria is caused by the inability of the renal tubules to reabsorb filtered cystine, which
Naim M Maalouf et al.
The Journal of clinical endocrinology and metabolism, 96(12), 3733-3740 (2011-10-07)
Dietary intake of animal proteins is associated with an increase in urinary calcium and nephrolithiasis risk. We tested the hypothesis that the acid load imposed by dietary proteins causes this hypercalciuria. In a short-term crossover metabolic study, an alkali salt
Pierre Cochat et al.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 27(5), 1729-1736 (2012-05-02)
Primary hyperoxaluria Type 1 is a rare autosomal recessive inborn error of glyoxylate metabolism, caused by a deficiency of the liver-specific enzyme alanine:glyoxylate aminotransferase. The disorder results in overproduction and excessive urinary excretion of oxalate, causing recurrent urolithiasis and nephrocalcinosis.
Zeynep Aygun
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 130-133 (2012-12-26)
Electron paramagnetic resonance (EPR) studies of single crystals and powder samples of Cu(2+) and VO(2+) doped potassium dihydrogen citrate (PDHC) have been carried out at different temperatures. The temperature-dependant g and A values have been obtained for powder spectra of
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