P1722
柠檬酸钾 三元 一水合物
crystals, meets USP testing specifications
别名:
柠檬酸 三钾盐, 柠檬酸三钾
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关于此项目
线性分子式:
HOC(COOK)(CH2COOK)2 · H2O
化学文摘社编号:
分子量:
324.41
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
231-905-0
MDL number:
Beilstein/REAXYS Number:
3924344
Assay:
100.10%
Form:
crystals
产品名称
柠檬酸钾 三元 一水合物, meets USP testing specifications
InChI key
PJAHUDTUZRZBKM-UHFFFAOYSA-K
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
SMILES string
O.[K+].[K+].[K+].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O
agency
USP/NF
meets USP testing specifications
Quality Level
assay
100.10%
form
crystals
mp
275 °C (dec.) (lit.)
application(s)
pharmaceutical (small molecule)
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General description
一水合柠檬酸钾 (KCTM) 是一种钾盐，据报道可与 UCON 50-HB-5100（一种无规共聚物）有效形成双水相体系 (ATPS)。该产品是符合USP（美国药典）测试规范的高质量药典产品。它可以用于科研和试验研究。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
(Liquid+ liquid) equilibria of polymer-salt aqueous two-phase systems for laccase partitioning: UCON 50-HB-5100 with potassium citrate and (sodium or potassium) formate at 23?C.
Lladosa E, et al.
The Journal of Chemical Thermodynamics, 55, 166-171 (2012)
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.
Khashayar Sakhaee et al.
Surgery for obesity and related diseases : official journal of the American Society for Bariatric Surgery, 8(1), 67-72 (2011-06-28)
Patients undergoing Roux-en-Y gastric bypass (RYGB) surgery are prone to developing bone loss and kidney stones. The goal of the present study was to test the hypothesis that an effervescent formulation of potassium calcium citrate (PCC) would avert metabolic complications
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