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C3029

Sigma-Aldrich

Potassium citrate tribasic monohydrate

suitable for cell culture

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About This Item

Fórmula empírica (notación de Hill):
C6H5K3O7 · H2O
Número de CAS:
6100-05-6
Peso molecular:
324.41
EC Number:
231-905-0
MDL number:
MFCD00150442
UNSPSC Code:
12161700
PubChem Substance ID:
24892561
NACRES:
NA.25

assay

≥98% (GC)

Quality Level

200

form

powder

technique(s)

cell culture | mammalian: suitable

pH

8.0-9.5

solubility

H2O: 100 mg/mL, clear, colorless

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

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000310586
SLCN9990
0000264634
0000292225
SLCN9371

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Sigma-Aldrich

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Sigma-Aldrich

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B Lojanapiwat et al.
International braz j urol : official journal of the Brazilian Society of Urology, 37(5), 611-616 (2011-11-22)
To evaluate the preventive effects of alkaline citrate on stone recurrence as well as stone growth post-ESWL or PCNL in patients with calcium-containing stones. A total of 76 patients with calcium calculi who were stone-free or had residual stones less
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
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.
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
Zeynep Yarbaşi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 1304-1307 (2011-06-07)
An EPR and optical studies of VO2+ doped potassium dihydrogen citrate (PDHC) single crystals have been carried out at room temperature. It crystallizes in triclinic symmetry with the unit cell dimensions: a=11.343Å, b=13.078Å, c=6.272Å, α=89.79°, β=94.36°, γ=104.2°. The angular variation
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