60155
柠檬酸钾 三元 一水合物
tested according to Ph. Eur.
别名:
柠檬酸钾, 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
EC Number:
231-905-0
UNSPSC Code:
12352300
PubChem Substance ID:
Beilstein/REAXYS Number:
3924344
MDL number:
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, tested according to Ph. Eur.
assay
99-101% anhydrous basis
form
solid
mp
275 °C (dec.) (lit.)
application(s)
pharmaceutical (small molecule)
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存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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
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
A comparative pilot study of litholytic properties of Celosia argental (Sitivaraka) versus potassium citrate in renal calculus disease.
Rana G Singh et al.
Journal of alternative and complementary medicine (New York, N.Y.), 18(5), 427-428 (2012-04-28)
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.
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