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
Agency
USP/NF
tested according to Ph. Eur.
方案
99-101% anhydrous basis
表单
solid
mp
275 °C (dec.) (lit.)
应用
pharmaceutical (small molecule)
SMILES字符串
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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储存分类代码
13 - Non Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
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
Hulya Nalcacioglu et al.
Journal of pediatric urology, 9(1), e58-e63 (2012-10-27)
Bilateral obstructive nephrolithiasis is a rare cause of acute kidney injury (AKI) in early childhood. As soon as the identification of AKI secondary to ureteral stone is made, it will necessitate an emergency treatment. We report three infants with AKI
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.
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
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