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质量水平
检测方案
99.99% trace metals basis
形式
solid
杂质
≤150.0 ppm Trace Metal Analysis
pKa (25 °C)
(1) 2.15, (2) 6.82, (3) 12.38 (phosphoric acid)
mp
252.6 °C (lit.)
密度
2.338 g/mL at 25 °C (lit.)
SMILES字符串
[K+].OP(O)([O-])=O
InChI
1S/K.H3O4P/c;1-5(2,3)4/h;(H3,1,2,3,4)/q+1;/p-1
InChI key
GNSKLFRGEWLPPA-UHFFFAOYSA-M
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一般描述
磷酸二氢钾晶体无色,可溶于水,具有吸湿性。在加热至 187℃ 时,KH2PO4 发生相转换,晶系统由四方向单斜转变,195℃ 时的晶格参数为 α=7.47Å, b =7.33Å, c =14.49Å, α= ß = 90° 和 γ=92.2.
应用
可能使用过
- 产生荧光发射的碳点
- 缓冲剂
- pH 控制剂
- 乳化剂
- 稳定剂
- 保水剂,
- 食品中的抗氧化剂
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
X-Ray Study of High-Temperature Phase Transitions in KH2PO4
Journal of the Physical Society of Japan, 39, 843-849 (1975)
Chemical communications (Cambridge, England), 47(42), 11615-11617 (2011-09-21)
A facile method is developed to synthesize intrinsically fluorescent carbon dots by hydrothermal treatment of glucose in the presence of monopotassium phosphate. The fluorescence emission of the carbon dots thus produced is tunable by simply adjusting the concentration of monopotassium
IUCrJ, 2(Pt 2), 168-176 (2015-04-14)
Lipidic cubic phases (LCPs) have emerged as successful matrixes for the crystallization of membrane proteins. Moreover, the viscous LCP also provides a highly effective delivery medium for serial femtosecond crystallography (SFX) at X-ray free-electron lasers (XFELs). Here, the adaptation of
Journal of applied physiology (Bethesda, Md. : 1985), 117(10), 1097-1109 (2014-09-06)
The purpose of this study was to examine whether speed endurance training (SET, repeated 30-s sprints) and heavy resistance training (HRT, 80-90% of 1 repetition maximum) performed in succession are compatible and lead to performance improvements in moderately trained endurance
Nature communications, 5, 4961-4961 (2014-09-24)
The PIK3CA gene is frequently mutated in human cancers. Here we carry out a SILAC-based quantitative phosphoproteomic analysis using isogenic knockin cell lines containing 'driver' oncogenic mutations of PIK3CA to dissect the signalling mechanisms responsible for oncogenic phenotypes induced by
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