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Potassium citrate tribasic monohydrate

Name: Potassium citrate tribasic monohydrate
Brand: SIGMA

suitable for cell culture

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About This Item

Empirical Formula (Hill Notation):

C₆H₅K₃O₇ · H₂O

CAS Number:

6100-05-6

Molecular Weight:

324.41

NACRES:

NA.25

PubChem Substance ID:

24892561

UNSPSC Code:

12161700

EC Number:

231-905-0

MDL number:

MFCD00150442

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Properties

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

Description

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1 of 1

This Item	25107	P1722	1.04956
Sigma-Aldrich C3029 Potassium citrate tribasic monohydrate	Sigma-Aldrich 25107 Potassium citrate tribasic monohydrate	Sigma-Aldrich P1722 Potassium citrate tribasic monohydrate	SAFC 1.04956 tri-Potassium citrate monohydrate
assay ≥98% (GC)	assay 99-100.5% (calc with ref. to anhyd. subst.)	assay 100.10%	assay -
technique(s) cell culture \| mammalian: suitable	technique(s) -	technique(s) -	technique(s) -
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 500
form powder	form powder or crystals	form crystals	form solid
pH 8.0-9.5	pH 7-9 (20 °C, 5%)	pH -	pH 7.5-9.0 (20 °C, 50 g/L in H₂O)
solubility H₂O: 100 mg/mL, clear, colorless	solubility glycerol: soluble 1 gm in 2.5 ml, water: soluble 1 gm in 0.65 ml, alcohol: insoluble	solubility -	solubility -

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Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number

0000547739

0000504156

0000310586

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Cystinuria: mechanisms and management.

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

Hypercalciuria associated with high dietary protein intake is not due to acid load.

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

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment.

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.

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Global Trade Item Number

SKU	GTIN
C3029-500G	04061833485187

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