产品名称
柠檬酸钾 三元 一水合物, purum p.a., ≥99.0% (NT)
等级
purum p.a.
质量水平
方案
≥99.0% (NT)
表单
liquid
pH值(酸碱度)
7.5-9.0 (25 °C, 50 mg/mL in H2O)
mp
275 °C (dec.) (lit.)
溶解性
H2O: 0.5 g/10 mL, clear, colorless
痕量阴离子
chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤50 mg/kg
痕量阳离子
Ca: ≤50 mg/kg
Cd: ≤50 mg/kg
Co: ≤50 mg/kg
Cu: ≤50 mg/kg
Fe: ≤50 mg/kg
Na: ≤1500 mg/kg
Ni: ≤50 mg/kg
Pb: ≤50 mg/kg
Zn: ≤50 mg/kg
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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一般描述
柠檬酸钾三元一水合物是柠檬酸的三钾盐。其已成为用于形成水两相体系(ATPS)的非常有前景的有机盐。UCON(温度响应聚合物)+柠檬酸钾ATPS已有研究。
应用
柠檬酸钾三水合一水合物(柠檬酸三钾)可在制备活性炭负载的CuCl2 + PdCl2 + NaOH 催化剂的过程中作为促进剂加入。该催化剂可用于将乙醇转化为碳酸二乙酯(DEC)。1 它可用于组成黑曲霉 72-4发酵培养基。 它可以作为标准品,用于研究 佛手菜根茎(BLR)对CaC2O4 结晶的影响。
储存分类代码
11 - 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)
Carbon dioxide fixation by cell-free extracts of Aspergillus niger.
Woronick CL and Johnson MJ.
The Journal of Biological Chemistry, 235(1), 9-15 (1960)
Antiurolithic effect of Bergenia ligulata rhizome: an explanation of the underlying mechanisms.
Bashir S and Gilani AH.
Journal of Ethnopharmacology, 122(1), 106-116 (2009)
(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
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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