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品質等級
化驗
99.0-101.0% (T)
損耗
≤2.0% loss on drying
pH值
0.9-1.4
mp
103-109 °C
105-107 °C (lit.)
溶解度
H2O: 2.88 g in 30 mL, clear, colorless
正離子痕跡
Al: ≤5 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg
紫外吸收
λ: 260 nm Amax: ≤0.05
λ: 280 nm Amax: ≤0.04
SMILES 字串
CP(O)(O)=O
InChI
1S/CH5O3P/c1-5(2,3)4/h1H3,(H2,2,3,4)
InChI 密鑰
YACKEPLHDIMKIO-UHFFFAOYSA-N
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應用
Highly pure methylphosphonic acid for phosphoproteome analysis
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 2
閃點(°F)
>392.0 °F - Pensky-Martens closed cup
閃點(°C)
> 200 °C - Pensky-Martens closed cup
其他客户在看
Nucleic acids research, 22(13), 2592-2600 (1994-07-11)
The HIV-1 regulatory proteins tat and rev are both RNA binding proteins which recognize sequences in duplex RNA which are close to structural distortions. Here we identify phosphate contacts which are critical for each binding reaction by use of a
Journal of chromatography. A, 782(1), 55-62 (1998-01-24)
A new two-step high-performance liquid chromatography (HPLC) procedure has been developed to separate modified histone H1 subtypes. Reversed-phase (RP) HPLC followed by hydrophilic-interaction liquid chromatography (HILIC) was used for analytical and semi-preparative scale fractionation of multi-phosphorylated H1 histone subtypes into
Journal of proteome research, 11(8), 4269-4276 (2012-07-10)
In large-scale phosphoproteomics studies, fractionation by strong cation exchange (SCX) or electrostatic repulsion-hydrophilic interaction chromatography (ERLIC) is commonly used to reduce sample complexity, fractionate phosphopeptides from their unmodified counterparts, and increase the dynamic range for phosphopeptide identification. However, these procedures
Journal of proteome research, 10(8), 3474-3483 (2011-06-21)
Reversible phosphorylations play a critical role in most biological pathways. Hence, in signaling studies great effort has been put into identification of a maximum number of phosphosites per experiment. Mass spectrometry (MS)-based phosphoproteomics approaches have been proven to be an
Analytical chemistry, 87(3), 1596-1604 (2014-11-19)
In the past decade, several strategies for comprehensive phosphoproteome analysis have been introduced. Most of them combine different phosphopeptide enrichment techniques and require starting material in the milligram range, as a consequence of their insufficient sensitivity. This limitation impairs the
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